SCIENTIFIC ABSTRACT SIDOROVA, I.I. - SIDOROVA, N.G.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001550510020-2
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 20
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

,S,IDOROVA, I.I.
. - ... --
Method for the primaz-.r selection of antibiotics produced by mold
fungi. Antibiotiki 7 no.8:679-685 Ag 162. (KRA 15:9)
1. Institut po izyskaniy novykh antibiotikov AMN SSSR.
(A3TIBIOTICS) (FUNGI)

'; lDOhOVAS ~ J-.11.
Mycoparasltism, of funv4 from the Ponlis Trichothecium Link.
'Vest. Moak. un. Ser. 6: Biol., pochv. 19 no.4-.48-.56 JI-Ag 164.
(MIRA 17,.12)
1. Kafedra nizahlkh rasteniy Moskovskogo universiteta.

STDOROVA,, I.I.; GORLENKO, Me'l.1 NALSPINArr-LAo
Systematics of the ge:aera Trichothecium Link and Arthrobotrys Corda.
Bot.zhur. 49 no,ID1592-1599 N 164-. (MIRA 18il)
1. Mo3kovskiy gosudar3tvennyy universitet,

SIDOROITA, I.S. [Sydorova, I.S.,
Gynecological massage and its use in patients with fixed
uterine displacements in general compound fargotherapy at
the Yevpatorium. healti resort. Pediat. akush. gLnek. no-3:
61-62 103 (MIRA 17:1)
1. Sanatoriy ItUdarnik* (Clavnyy vrach A.111. Step, nauclmyy
sotnidnik - prof. V.G. Dik [Dik, V.11.1 g. Yevpatoriya.

ACC NRi AP'(0003*11 SOURCE CODE: UR/0413/66/000/022/01"."4"/0158-
INVENTOR: Varenov, P. G.; Sobolev, F, P.; Sidorova, I. V.
ORG: None
TITLE: Nozzle for a ship's screw. Class 65, No. 188856
SOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki, no. 22, 1966, 158
:TOPIC TAGS: nozzle design, marine enk~ineering C'o fn P04Jr- Iv7-
,ABSTRACT: This Author's Certificate Introduces a nozzle for a ship's screw. The
~unit includes external and internal sLrfaces interconnected by reinforcing ribs. To
,reduce disturbing forces transmitted From the screw to the hull, the internal surface
;of the nozzle is mounted on shock absc-rbers in the region of the screv disc.
Card
UDC; 629.1.037.23

ACC NR3 AP7000371
;.1--externaa surface of the nozzle; 2--internal surface of the nozzle; 3-internal
isurface of the nozzle in the region of the screw d-Isc; 4-shock absorbers
i
OSUB CODE: 13/ SM DATE: 18oct65
2/2

V
at on va.,-i a 'lw~) pea varieties.
AN

:;I b0i'W'J At KOK* 1, KAI, IN I ~,A , N., . ; 117,fl IE-V A, L.P.
CY-qra ctqriu tics of mutitional. changes in pea varlaties and
forms. Genatika, no.2:136-142 Ag 165, (M11RA 18tJO)
1. Institute of Cytology and Genetics, Academy of Sciences
of the U.S.S.R., cSiberlan Delvi.rtment, Novoslbirsk.

13RKOVIGH, M.; DURGHEVIIIXOVA. S.; SWRITIA, L.; SIDOROVA. L.;
VOVIESNNSKAYA, N.
Using mineral pigments In making building mterials. Strol. mat.
4 no,4:33 Ap 158. (MIRA 11:5)
(Pigments) (Building materials)

ANDRONOV, Ivan Korlmich; OKMIV. Alsksondr InzImich; SIDOROVA, L.A..
red.; SKIRNOTA, M.I., tokha.red.
[Basic course of trigonomtry, based on practical problems;
textbook for teachers] Oenovnol kurs trigonometrii, rasvivaomyi
no tselesoobrasaykh sisdachakh; posobie dlia uchitelai. Koskvs,
Goo.uchabno-pedogog.lid-vo K-va proov.RSYSR. 196o. 365 p.
(MIRA 13:6)
(Trigonometry-Study and teaching)

KAIUIITSKIY, Pavel Nikolayevich; SID04ROVA, L.A., red.; MAKAROVA,
N.F., tekhn. red.
(Problems about the universe In mathematica Jn ttqcondbry
schools] Voprosy o vselennol v matematicheskikh zadachakh
srednei shkoly; posobie dlia uchitelei. Izd.2., dop. Mo-
skva, Uclipedgiz, 1963. 90 p. (MIRA 17:2)

ZI.al I ~jjjy irvich. ~:I i",')hOVA, L.A. red.
j(~ojjer*tion of applie" :;:-obIe=s in ;r:ecua -tY T',ec~ry; a text-
book for teachers] -,borr.~k prikIadn,;',Ji zaeach np. neravenstva;
pozoole (ilia uchitelel. Izd. 2., dop. Mo.,kva,
11)(4 . 142 p. (f,',IRA 17:7)

I Zrai i I V. IS,
red.
['Elemew:a of uathtqVAL'-,ra-l antilysiE in a mathematit's
course, a textbcok f07 teachers) Flementy maternaticheskogo
qnnlll-.a v sh~ol;nom k-irse matem.Likil, posome dhe uchl,te-
lel. Lo6kva, ; ro~-.v&snvhenle, 1964. 140 p.

ri t i c t e X't ti"kf
k_,~i p,i~obie cilia
._f-_%7-,.-k zati-ich pa ari
.111~oj 5likoly. lzd.,,,., ispr~ Vio3kva,, Pro-
urhiTfAf~i rar',~~.
277 P.

SIMNOVA 1.1%
................
?rS^tMAt Of pUlWVArY inqppwative proc,;seas by endebrowbial
adainistration of ponic!.nin. Tor. arit.., KoskTa 25 se.6:36-W
NOT-Dw 1953. (CUM 25t5)
1. of the aspital Thweventic 011210 t'Actim Had -- DaGmt
K.I. Mmgln), Novealblvek N"Ical lutitutos

!,:~fc

'At L

I A., To,)chiyev, A ~ V. , 62-58-4 -113132

TITLi,: Synthesis of rystallinc- Poly '-' )ropjlerie by 'Yeazia
Qi of Technical Propylene `..'ith Tri-iso=
bat./lala..iini,i ind Titanimi Tetrachloride (Polucheniye
kri4-,tallichesko-o polipropilena polimerizatsiyey tekh=
nichcsko-o propilena s triizobutila1yu=iniYem i chet~,=
rekliklilori3ty~.-.i titano;a)
PERIODICAL: Izvestiya Alcadenii Nauk SS3R,0tde1eniye Khimicheskikh
Nauk, 1958, Nr 4, Pi), 500-501 (US~J'Ii"
ABSTRACT: In ooriodicals nam(xous reports have been published
of late, concernin- a new high-polymeric naterial.
stereo-reGular polypropylene. The latter was produced
by the polymerisation of propylene in the presence of
the oom:ilex or-anometallic catalyst Al(C H ) +TiCl,
r-
2 5 3 s
It was of int(.xest to use instead of the 3reatly py=
rophoric triethylaluiiinum es,)ecially high-Laolecalar
and less infla.:i;-.able aluminuia alkyls. In the present
Card 1/2 pa,-Ier the a-4thors describe the carried out polyr.-eri=

Synthesis of Urv~~Lallizie by n#-,3-ns cf 62-38-4-16132
of T-1chnical Propjlcrie ith Tri-isobut j1alu-
:.dria.. r~d "'itanix.-, i'etrac.-~lloride
sation of nm-)ylene in so hi~-h crystalline paljprc=
in the presence of a com:)lc-4 organometallic
catal,,nt, (Al(iC., 11 ) fTIC1.) ---ihich iu r-luch less
3
1-T i C I..
T"v.re rare 3 fj-'are'r;.
AS00CL',.T1U,'1: 1-r;t1t(it -'C-.-? (Petroleum
Institute, AS USSR)
SUBMIT"LIT: October 2,'-'.. !').57
AVAILABLL: Libr-.ry of Co,,-,-:rc:ss
1. Fropylene-Polymcrizatiom 2. Organometallic
Card 2/2 catalyst (.41 (iC4 H9)3~ Ti C 4-Applications

AUTHORS: Topchiyev, A. V., Krentsell, B. A., SOY//62-56-5-21/zb
-.S~dorova, L. G.
TITLE: Letters to the Editor (Pis'ma redaktoru
PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk,
1958, 1',r 9, pp 1133 - 1133 (USSR)
ABSTRACT: Of late in publications several references were made
in publications in regard to the mechanism of the
ste:-euspecific polymerization of the a-olefins. In
rejard to these references the authors of this letter
wish to report some experimental data gathered in --'n-
vezti~-ations on the polymerization reaction of propylene
in the preoence of the catalytic system TiCl 4 -and Wi-c 4H9)3*
Studies on the chan-e in molecular weight of the poly-
propylene formed in the reaction show that already 15
seconds after the reaction begins an product of hi.,-h
molecular weii;ht has formed. The duration of ti-le reaction
does not chan -c the molecular weight of t',-e po-y-..I,:r formed.
I. -tr);c'ura ol-ner c un
',e , . f, 1 chain keeps adding p , i its in a
T
Card 1/2 chain reaction during the polymerization, as indeed the

Letters to the Editor
Z OV /'#'- 2 - --,~ ~_ - 5 - 2 1 /2
results of several ex?eriments carried out by tile allathorc
sho-,,.,ed t,.-l,t the propylene polymerization is a chain
reaction. At the prfsent the authors are concerned with
furt!.er inves t it-at ions on the mechanism and tile function
of t,,,e cat--lytic metallo-or(;anic complex in tl~.e propylene
poly-lerization and in the. pol.ymc,rization of o"Iner a-o.,efins.
ASSOCIATION: Institut nefti Akademii nauk SSSR (Petroleum 1nz+.-ituteAS USSR)
SUBMITTED: May 29, 1958
Card 2/2

O"TDOIROVA, L. i;., Cand Chem Sci (diss) -- "Mvestleation of the polymerization
renction of propylene with tht- catalytic system Al(lso-Cj,lr~-))34 TIC114".
I
moscow, 14 pp (Acad Sci USSR, Inst of Eetrolemi-Chem Synthesis), 1;0
copies (KT,, No 9, 190, 122)

5 (2,3)
AUTHORS: Topchiyev, A. V., Academician, SOV/20-128-4-27/65
Krentsell, B. A., Sidorova, L. G.
-----------
TITLE: Some Rules of Polymerization of Propylene With the TiCl 4 + AlR3
Catalytic System
PERIODICAL: Doklady Akademii nauk SSSR, 1959, Vol 128, Nr 4, Pp 732 - 735
(USSR)
ABSTRACT: Different opinicna were expressed in publications on the rules
and mechanism of stereospecific polymerization of a-olef�nes.
Many problems it this respect have, however, remained unclear.
Therefore, some observations made by the authors in dealing
with the sub4ect mentioned in the title are interesting.
(AIR3 - Al(Iso--C4H9)3 ). The experimental system had been de-
s,;ribed before (Ref 5). It can be assumed that an exchange re-
action takes plE~ca between TiCl4 and the metallic alkyl forming
organotitanium compounds (Ref 6). The latter decompose due to
their instabili-.y, and form free radicals. The polymerization
of styrene, for instance (Ref 7), oan be initiated in this way.
Card 1/3 The organotitan:~um compound acts as a catalyst while the metal-

Some Rules of Polymerization )f Fropylene With the SOY/20-128-4--27/65
TJC1 4 + AIR3 Catalytic System
lic alkyl is, so to speak, a "supplier" of the alkyl radical.
The propylene polymerization is a chain reaction. Already
17 seconds aft(.-r its start, a polymer with a high molecular
weight is formod (Fig 4) which remains unchanged for a long
time (up to 1.5 hours). Thus, the molecule attains a maximum
size, and does not grow any more. The catalytic activity of the
complex catalysts ,of the Tsiglor type decreases with time
(Fig 2). This is possibly due to the fact that the amount of
resulting organotitanium compounds is reduced with an increas-
ing alkylatior. of titanium chlorides. Accordingly, the ab-
sorption rate of propylene also decreases. If, however, TiCl 4
is first pouriid into the reactor, and then aluminum alkyl
evenly added it a low rate, e.g. within 3 hours, the activity
of the catalyst is maintained for a long time, and the polymer
yield is considerably increased. An explanation of these pher-c-
mena is attempted with reference to the assumption made by,
C. D. Henitze-scu (Ref 4). The polymerization process initiated
by Tsigler catalysts is highly sensitive to admixtures of va-
Card 2/3 rious types in the monomer, particularly to oxygen (Fig 3).

Some Rules of Polymerization of Propylene With the SOV/20-128-4-27/65
TiCl4 + AIR 3 Catalytic System
By very large oxygen quantities, the catalyst is fully poisoned*
Various possibLe explanations are given for this fact (Ref 8).
Figure 4 shows the temperature effect on the molecular weight
of the polymer at an optimum oxygen content in propylene. At a
temperature increase from 30 to 800, the yield decreases line-
arly as expected. The stereospecific polymerization processes
can apparently be realized by any known initiation mechanism.
The process can be imagined according to the ion- or radical
mechanism. Th.? stereospecificity in the respective class of
catalysts is only determined by the degree of orderliness of
the catalytic surface. The auzhors think that a radical meoha-
nism, is not impossible in polymerization with Taigler oatalysts
(for the firct time in Ref 4). The said catalyst has, however,
not a high stereoapecificity in the reactions of propylene poly-
merization. ~2here are 4 figures and 11 references, 2 of which
are Soviet.
SUBMITTED: April 22, 1959
Card 3/3

$11911611000100210011012
B118 B203
AUTHORSs Topchiyev, A. V., Krentsell, B. A., Sidorova, L. G.
TITLEs Polymerization of propylene with the catalytic
system Al(iso-C4A9 )3+ TiCl 4
PERIODICALs Plasticheskiye massy, no. 2, 1961, 3 - 6
TEXT: For some modes of application of polypropylene (films, tubes) a
high content of isotactic structure (produced by the catalytic complex
containing TiCl 3) is not required; the quality of the stereoblock poly-
mer obtained with the catalytic system AlR 3 + TiCl4 is sufficient. This
circumstance induced the autdors to study the polymerization of propylene
with the system Al(iso-C 4H9 )3+ TiCl 4' They proceeded from the industri-
al propylene-propane fracticn of the gas formed in petroleum pyrolysis
which contained practically no oxygen after thorough purification (Ref.1),
Triisobutyl aluminum was distilled in vacuo, and used as a 20-30 % solu-
Card 1/3

3/19 61/000/002/001/012
Polymerization of propylene ... B118YB203
tion in purified benzine fraction boiling between 90 and 110 0C. Commer-
cial titanium tetrachloride was "chemically pure". The components were
stored in a 7essel filled with pure nitrogen. The propylene polymeriza-
tion was performed in inert, carefully purified, anhydrous n-heptane as
solvent. It proceeded successfully with the complex catalyst
Al(iso-C 4H9)3 + TiCl4 which is less inflammable and better accessible
than the hitherto used We 2H5)3 + TiCl 4' The molar ratio K between the
components of the catalyst affects the yield and the molecular weight of
polypropylene. The maximum yield of polymer was obtained at K - 1-5 1
2 moles of triisobutyl aluminum/TiCl 4* The highest-molecular polypropy-
lene was formed at K = 3. The catalytic activity of the complex catalyst
decreases with time due to a change in its composition, irrespective of
whether it is in operation or stored in an inert medium. If, however,
the propylene polymerization is performed by bringing about a gradual
formation of the catalyst complex with a steady addition of small doses
of Al(i-C4 H9)31 then the high activity of the catalyst is preserved lon-
Card 2/3

KRENTSEL, B.A., SIDOFOVA. L.G..-TIOPICREVs A.V.s (Decea3ed)
Principles of conversational polyTrArisation of unsaturated bydrecarbons.
Report submitted for the International Symposium of Macromolecular Chomistr7,
Pariss 1-6 July 63

KREPTSELI, B.A.; SIDOROVA, L.P.; SHISHKINA, M.V.; KVSAKOV, M.M.; KORENEVSKAYA,
F.V.; SHCkl*!9*1-'V*V'.-- '
Conversion polymerization of ckolsfins. Neftekbixiia 2 no-5s
705-708 S-0 162. (MM 16: 1)
1. Institut neftekhimicheskogo~-;inteza AN SSSR.
(Olefins) (Polywrization)

arjktcjr
kan'-z.
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po'llpropiIen. Kiev, Tekhn:.ka,
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AUMORk. '.Vulikh,-A. Li ArichipoiOA!
dotb vC
----TITIZ:---A-method-fbr -producing 9 dLum and.cd
-brovides-and dides of rubt MILM
~Class 12, No. 169081
SOURCE: --Byulletent-izobreteniy i -J,~ovarnykh wakoyt: no 6, 1965,19
TOPIC TAGS! reducing~agdnt, -,Cesitil--inorga~i6-c6iiqi6ii~d,.-rvkidi C091
d b
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:iodide
This Author's Certificare`intr-6auci4i -a-m6thod for: prodUcin, 'twi
~ABSTRACT. g b des and
'iodides of rubidium and cesium by :Interaction of the higher hydrloidd4s-of the. _bii,
icarbonates or carbonates'of these
I tetals withbromine- or iodinii -in tha.presence'of.'
reducing agents which produce qnly~ ~ gaseous' products during oxidati6n#~ -"The used 6f
.gent i4r6v 646' the", pifrilty of tha"0~0
1hydrazine hydrate a the redu ng 'i
A-TI: ON* JIM
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"I I il. 1. Srj)iA)V, S. ".,.
!Azhnt Ii prinx-milit's--ra still -Fat-anpba%Jn kak nrotivouksusnoye,
Fr-(Iqtva? Z,IrvvooVIir-anvnjve Kazakhstana, 1949, No (), :-,. 22-24

v
AV, Jour Ref Zhur Diol., N~) 2, 1959, 9355
AutIlDr
1"3t Alyn-Ata Moxli -al Ii-stitute, Burenu -;f Main Medicoluml,
Expert Exardniti w and Chnir of Foro:-.sic Medicine
Title Mideal Pict'irc in ArsclUc
Or i ~; Pub S'). tr. Byurc GI. ekspertizy i Kafedry
s,idc-b,.. ned. 44hia-Ati-,-.sk. med. i,,-ta, 1957, VYP- 1, 46-
47
Abstract - N,) abstract.
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USSPz/I,hnrz:ac-A-)~_-y a..O. T~:,icol',),Y - T,)Xic-)lj~~ V
Abs J.,ur nef - Dio*,.., N,) 2, 1959, 9353
nc:~e:.cratioa ):* the ~;landular epitlielimi in the affected
places conies about Liai.--ly by m-Atotic a:,d, i:i the pre-
served mcosa, '),,r nit,)tic, cell division. Indifferent
epitheliu.i of --.lie stomch is c:,.iefly diffcre~-.tiated into
deloraorp!ious colls, linalizatim )f the lesions aid
is rebuii1di-.,,L;" !)f the f;landular epitheliuLi are apparently
con:iectcd with excretion of the poisor.. -- S.T. Skoruder
lov
Card 21'2

ABATUROV, P.V.; GROZNOV, S.R.; GANZTSKIY, I.D.; KOZYREVA, Ye.A.;
NOVITSKAYA, L.A.; ODINTSOV, A.I.;PROTOPOPOV, S.I.; SIDDROV,
V.A.; SIDOROVA,..L.I.,- TROFIWVA, V.I.; TRUSHINA, I.V.; SHTEYKAN,
R.A.; DLTITTSOVA, K.G., red.; KAZENOVA, A.R., red.; MARSHAK, M.S.,
prof., red.; MLCHANCVA, O.P., prof., red.; SALOMATINA, K.Z.,
red.; KAGANOVA, A.A., redl; MEDRISH, D.M.,, tekhn. red.
(Dietetic cookery In eating establishments]Dieticheskoe pitanle v
stolovykh; sbomik re:tseptur I tekhnologiia prigotovleniia bliud.
Moskva, Gos.izd-vo tc-rg.lit-ry, 1962. 262 p. (MIRA 16:1)
1. Russia (1917- R.S.F.S.R.)Ministerstvo torgovli.
(COOhwm "Wem

KAGAIER, 14. G.; VELIKJd4OVA, M. G.; SIDOROVA, L. 1.
"Heat -transfer irwestiggation hn multilayer vacuum insulation."
reporb submItted I'or 2nd Ail-UnIon Corif on Heat & Mass Transfer, Minsk, 4-12
May 1~)64
All-Union Sci Ret, Inst of Oxygen Engineering.

GREBENly L.K., akademik; BAYDUGANOVA, Ye.P., nauchnyy sotr.;
SAVCHENKO, P,ye., kand. biol. nauk; GREBENI, Ye.K.,,
kand. sellkhoz. nauk; KRYLOVA, L.F., nauchn. sotr.;
S~I~DORQ ~.' nauchn. sotr.; SOROKINA, V.I., nauchn.
sotr.; BAGMET, M.I.; LAZORENKO, Te.L.; KHOk&iUK, A.G.;
PASHKEVICH, M.K.; BRYZHNIX, K.A.; LUZHKOV, M.A., kand.
sellkhoz. nauk; BALASHOV, N.T., kand. sellkhoz. nauk;
ZHELIKHOVSKIY, V.I., rediktor; POTOTSKAYA, L.A., tekhn.
red.
[Ukrainian White Steppe swine) Ukrainskaia stepnaia belaia
poroda svinei. Pod obshchei red. L.K.Grebenia. Kiev, Gos-
sellkhozizdat USSR, 1962. 252 p. (MIRA 16:5)
1. Ukrainskiy nauchno-iseledovatellskiy institut zhivotno-
vodstya stepnykh rayonov im. M.F.Immova "Askaniya-Nova."
2. AN Ukr.SSR i Vsesoyuznaya akademiya sellskokhozyaystven-
nykh nauk im. V.I.Lenina (for L.K.Greben'). 3. Ukrainakiy
nauchno-isaledovatellskiy.institut zt4votnovodstva stepnykh
rayonov im. M.F.Ivanova IrAskanlya-Nova" (for Bayduganova).
4. MelitopollsRaya gosudarstyennaya piemennaya stantsiya
(for Bagmet, Lazorenko, Kholchlyuk)- 5. Spetsialist sovkhoza
"Komeomolets" , Stayropollskiy kray (for Bryzbnik).
(Ukraine--Swine breeding)

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late 46veimpne" cd Sim imams r-th occurred.
tier* tbr OIN istim 44 dw bind ' P but smautly,
vz%. Tb* I - of dw wimmy O/N fativio noted
ravilor thm in Site biow. (3). in sairnsis in which the
MKIC"istion 4w Not U69. tbe ratio in both WOW OW wise
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ilk UAMOI OMM wbkb OW hMCthSt6d bY = low
ww"islims of it rrveww 0 dwimige lowering OIN

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SIDOROVA, L. M. Cand. Blolog. -ci.
Jissertation: The Oxidation Coefficients of Blood and 'urine In Cases
of Malignant 'tumors." First Moscow Order of Lenin ';Iedical Inst, 16 Jun 47.
SO: Vechernyaya Moskva, Jun, 1947 (Project #17536)

SIDGROVA, L.M.
Alkaline phosphatase in blood-forming elements in cancer. Trudy
AMU SSSFL 21 no.4:103-106 152. (MIRA MW
1. Iz klinichaskoy laboratoril (zov. U.N.Shiller) TSentraltnogo
onkologichoskogo institute Im. P-A-Gertsena (dir. -ehlen-korr.
ANN SSSR prof. A.I.Savitakly)
(NIO?IASM3, blood In,
alkaline phosphatene)
(PHOSPHATASIS,
alkaline, In blood in cancer)

swaROVA, L.H., TRNGUBOVA, Kh.L.
Affect of 9,lD-dimethyl-1,2-banzanthracens on the skin in rabbits.
Trudy ANN SSSR 21 no.4;150-156 '52. (NLRA 10:8)
1. Iz TSentrallnogo onkologicheakogo instituta in. P.A.Gertmens
Ministeretva zdravookhraneniyo RSM (dir. - chlon-korrespondent
ANN SSSR Prof. A.I.Savitskiy)
(SKIN, neoplasms.
exper. 9,10-di:aethyl-1,2.-benzanthracens tumors)
(BUZANTMIAGINN. effects.
9.10-dinet 1-1,2-bensauthrecone causing skin tumors
in rabbiV
(CARCINOGINS, effects.
9,10-dinothyl-1.2-banzanthrocone causing tumors of skin
in rabbits)

SIDOROTAIL.M., starshiy nauchnyy sotrudnik (Moskva. G-117. 2-V Neopalimov-
skiy, d.4, ky.2)
Iffect of oxygen therapy on blood gas content in pulnonary cancer
[with emmary In Uglish. p.1591 Test.khIr. 77 no.7:82-86 JI 156.
(MI&A 9:10)
1. Is klinicheskoy laboratorit (save -kandidat meditainskikh nank
N.I.Shiller) Gosudarstyennoge onkologicheskoge instituts in. P.A.
Gerteens, (dir. - doktor med. nank A.N.Novikov, nauchn. rukov. -
prof.A.I.Savitekly)
(LUNG IMOPIASKS. surge
preope & pontope oxygen there)
(011YGU, there use
preope & postope, In surge of lung cancer)

SIDOROVA, L.M.
Use of Khakimle diagnostic serum reaction in cancer; preliminary
report. Lab.delo 7 no.9:26-30 S 161. (MIRA 14:10)
1. Kliniko-diagnosticheskaya laboratoriya (zav. H.N.Shiller-Volkova)
flauclino-issledavatellskogo onkologicheskogo instituta imeni Gertseva,,
Mosk-v,-..
(CANCER-DIAGNOSIS) (SERUM DIAGNOSIS)

SiDOiWAI LA-1. _
Influence of a hJgh envrionmental temperature on simultaneous complex
conditioned reflexes in dogs, Zhur. vys. nerv. deiat. 3-1 no.41697-
702 JI-Ag '61. (MIRA 15:2)
1. Cbair of Normal Physiology Medical Institute Stalino.
(CONDITIONED djjOA&;) (ffi~W--.Pfi!IOLOGICAL EFFECT)

ACCESSION Md: AP4014137
AIMHOR: Sidorova, _L9 Me
S/0247/64/ol14/ool/oo56/0060
,2ITLE: Effect of prolonged high temperature on simultaneous complex
conditioned reflexes In dogs
SOURCE: Zhurnal vyassh, norv. deyatelf.,.v. 14, no. 1,, 1964v 56-60
TO?IC TAGS: conditioned reflexo simultaneous complex conditioned
reflex, complex conditioned reflex component, prolonged high
%lemporature 450C. high temperature effect, motor defensive
conditioned reflex, conditioned reflex inhibition,, transmarginal'
inhibition
ABSTRACT: In a group of experiments on 4 dogs, the effects of
prolonged high temperature were investigated alternately with the
effects of normal temperature. Tho high temperature experi:rnents wore
conducted at 2 wk intervals and normal temperature experiments were
conducted at 1 wk intervals. The dogs were placed in a combination
hoat-conditioned reflex chamber for 2 hrs at 450C. The complex
s-'%-1imulus consisted of two components - bell and li6it - and was
applied for 10 see, then reinforced by an unconditioned stimulus, and
Cardl/2

ACCESSION NR: AP4014137
after 4 min was applied again. Each of the 2 components was also
applied separately. The complex stimulus or the components were
applied to the animals after 30 min in the chamber the first time, and
after 80-90 min the second time. Temperature of the animals was
measured before and after hoat exposure, Motor defensive conditioned
reflex oxcitation was measured by the total height that extermities of
~Che ani:-aal were raised. Findings show that motor defensive condition-
ed reflexes are inhibited by prolonged high temperature. The inhibi-
tion is more marked in the complex conditioned reflexes which indicatas
an increase in transmarginal inhibition. The inhibiting effect of one
component on the effect of the other component is sharply weakDned
with prolonged high temperature. This may be attributed to wealwned
negative induction on the part of the center which reacts to the
stronger component of the complex. Orig. art. has: 4 tables.
ASSOCIATION: Kafedra normallnoy fiziologii donetskogo maditsinskogo
Inatituta (Department of Normal Physiology of tho,Donsts Medical
ImAtitute)
SU&XITT=-: 18AYV63 DATE- ACQ: l3Kar64 ENCL: 00
SUB CODE: AX 10 REP SM: 009 OTM: 002
Cwd 2/2

S I DOROVA ; -,L'.' H-9
Development of ascarid eggs in stored vegetables. Sov.zdrav.Kir. no.2,
42-43 Xr-AP 158. (NM 12:12)
1. Iz parazitologichookoy laboratorii (zav. - kand.biol.nauk I.A.
Gontar') Kirgizslccgo institute. epidemiologii, mikrobiologii i giglyeny.
(ASCARIDS AND ASCARIASIS)

SIDOROVA, L.N. (Leningrad).
Correlation of cholesterol and phospholipids in the blood of
subjects with coronary atherosclerosis and myocardial inferote
Ilin.med. 36 no.8863-66 Ag 158 (MIRA 11:9)
1. Is fakulltetakoy terapevticheakoy kliniki (zav. kafedroy -
prof. T.S. Istamanova) Loningradskogo meditzinskogo institute
imeni I.P. Pavlova
(CORONAR; DISRASE. blood in
cholesterol & phosphollpids, correlation In arteriosclerosis
ON~))
(MTOCARDIAL INFARCT, blood In
cholesterol & phospholipids. correlation (Mus))
(CHOUST31HOL. In blood
In coronary arteriosclerosis & myocardial Infaret,
correlation with phospholipids (Rus))
(PROSPHOLIFIDS, Ivr blood
in coronary arteriosclerosis & myocardial infarct,
correlation with cholesterol (Run))

KALYUZIU,IYY, I.T.; _�~WROVA, L.N.; BURFUN, L.; Ah"rAYEV, S.; TEPLITS,
V.V.; ZUYEV, V.N.; POKROVSKMA, T.I.; KOZHOMKULOV, T.A.;
LAVROVA, prof., red.; ZUBOK, Ya.Z., tekhn. red.
I;iead this, this is u:;eful] Prochitai, eto polezno. Frunze,
1;62. 10 nos. [13otkints diseasel Bolezn' Botkina. 19 p.
[Corrmnicable CL-ifectious) diseases in children) Detskie
zaraznye (infekt3ionrye) bolezni. 18 p. (Helminths and the
harm they caure to human health) Gellminty i ikh vred dlia
zdorovIin cholov8ka. 26 p. (Work bygiene of the bcet grower)
Gigiona truda evoklovoda. 12 1). Plygienic regimen of the
schoolchild] Gigienicheskii rezhim shkollnika. 24 p. [Fungus
diseases of the skin] Gribkovye zabolevaniia kozhi. 24 p.
(Prevention and treatment of cardiac and vascular diseases)
Predupi-ezhdenie i lechenie boleznei serdtsa i sosudov. 19 p.
[Prevention and treatment of rickets) Rakhit, ego predu-
prezhderlie i lechenie. 8 p. (Old age and longevity) Starost'
i dolgoletie. 34 p. (Vitamins and their significance for
human health) Vitaminy i ikh znachenie dlia zdorovlia chelo-
veka. 22 P. (MIIRA 17:3)

SLUTSIM, S.S.. kand.ekonojo.nauk; PILIPCRUK, A.I., nauchnyy sotrudnik;
AliTONOV, N.Y., ks:id.tekhn.nauk; KALYARCHUX, G.S.. kand.tekhn.
nauk. Prinimali nehastiye: KILINIKOV, A.A., inzh.; AR IYEVA,
A.L. in2h,; TMK,(HOVA, Z.S.. takhnik;.SIDOROVA, L.W., tekhaik;
ISSMMIS, I., tijkhnik; XHAVCHRWO, A.I., inzh.--14WNIKOT,
S.A., inzh., red.; ZEMIN, V.K.. otv. za vypusk: POKHLZBKINA.
M*Isp takhnored,
Wficient distri2ution of and organization of work at cargo
transfer points] Retsionallnoe resmoshchenie i orgnnizataiis
raboty punktov perevalk-1. Pod obshchei red. S.S.Slutskogo.
Moskva. 1960. 127 p. (KIRA 14:2)
1. Moscow. TSentrallnyy nouchno-iseledovatellskiy institut
ekonomiki I ekspluntataii vodnogo transports. 2. ?Santralinyy
nauchno-iseledovetellskiy inntitut ekonomiki i ekepluatataii
vodnogo transporta (for Slutskiy, Pilipchuk, Terekhove. Sidorova,
Isserlis).-3. Institut komplekonykh transportnykh problem AN SM
(for Antonov, Nalyarchuk, Kravchanko).
(Cargo handling)

KRUTIKOV, K.T., inzh.; GIRINOV, K.A., kand. takhn. nauk; ITTENBERG, I.A.,
kand. takhn. naul:; prinimali uclmistiye: T.AKHTUROV, A.N.'etarshiy
nauchnyy sotrudnlk; VOLKOV, M.V., starsidy nauchnyy sotrudnik;
XURTSRANP L.B., ittarshiv nauchnyy sotrudnlkj BOGATYREVA, M.I.,
m1adshiy nauchn3n., sotrudnik; ZABOLCTNEVA'G.K., mladshiy nauch-
nyy sotrudnik; N(NIKOVA, V.V... m1adshiy nauchnyy sotrudnik;
ALEKSEYEVA, T.I.;, m1adshiy nauchnyy sotrudnik: PETROVA, I.A.,
m1adshly nauchny-.r sotrudnik; SEDELIKIKOVA, A.F., mladshiy
nauchny-y sotrudn-.k; KATKOVA, T.I., inzh.; ZELENKOV, P.A., inzh.;
SID9~Mj,,L49A jitarahiy laborant; KALASHNIKOVA, V.M., starshiy
Ir.
I
o~rant; VOYMUNA, A.Ye.,, starshiy tekhnik; USPENSKAYA,M.B.p
starshiy tekhrd1k; YEPIFANGV, V.K., starshiy tekhnik
[organization of the shipping of transit cargoes on the Volga-
Baltic Sea Watex-,iay.) Organizatsila perevozok tranzJtnykh gruzov
po Volgo-Baltiisicomu vadmmu puti. Moskva, Transportj, 1965.
109 p. (Moscow. rSentrallmyi nauchno-issledo-vatellskii institut
ekononLiki i ekspLuatatsii vodnogo transporta. Trudy, no.40).

8DIEWYAKOV, L.P.; VOLODGHENKO, K.G.; VINASHKIN, M.A.Prinimaii
uchastiye; TITOV, N.A.; FROSELKOV, N.L.; MINAYEV, I.Z.;
I.IKOLAYLN, S.V.; SAMICYLOVA, V.F.; SIDOROVA. L-E-4--
FOUIINJ V.F.1 red. v7puska; DO]=$ I A.T., red. vnmaka;
GHAPOVSKIY, Ye.G.p red. vypuska; FOSPELOVAj AX., red, izd-
va; GUROVA, O.A., tekhn. red.
[Collection of tnified district estimtes for geological
prospecting) Sbcrnik edinykh poraionnykh edinichnykh ras,-
tsenok na geologorazvedochnye raboty. Moskva, Gos. nauchno-
tekhn. izd-vo lit-ry po geol. i okhrane nedr. No.2. (Hydro-
geology and geological engineering] Gidrogeologicheskie i
inzhenerno-geolcgicheskie raboty. 1960. 91 p. (MIRA 14:12)
1, Russia (1923-- U.S.S.R.) Rinisterstvo geologii i okhrarW
nedr. 2. Ministerstvo geologii i okhrarq nedr SSSR (for Titov,,
Nikolayev).
(Prospecting)

PIIA-,E- I BOOK ZKPWITATION 790
Akademiya nuak SSSR. Otdelenlye khimicheskikh nauk
Deystviye ioniziruyushchikh izlucheniy na neorganicheskiye I organicheskiye
sistemy (Effect of Ionizing Radiation on Inorganic and Organic Systems)
Moscow. Ivl-vo AN SSSR, 3958. 416 P. 7,000 copies printed.
Resp. Ed.: Pshezhetskiy, S. Ya.; Ed. of Publishing House, Bugs3renko, L.T.;
Tech. Ed.; Prusakova, T. A.
PURPOSE: This publication iij for scientists working in the field of radiochemistry,
COVIN=: This collection oF articles represents contributions of Soviet scientists
in the field of radiochemlBtry. The papers are concerned with the effect of
ionizing radiation on organic and inorganic substances in solutions and In the
solid phase. These papers vere completed in the years 1951 - 1956 at the
Institute of Physical Chemistry, AS USSR, the Institute of Physics and
Chemistry imeni L. Ya. Kixpov, the Moscow State University, and other scientific
institutions. Most of these works are a continuation of those published in
"Sbornik rabot po radiatuionnoy khimii" published in 1955. Te. 1. Zalkind
and Yu. M. MalJLnskiy coopemted in the editing of this symposium.
card l/ 31

Effect of Ionizing Radiation (Cont.) 790
TABLE OF CONUMM:
pAR111 1. FMCfIOM IN AQUEOM SOLUTIOUS
AND ROIATION AND EJECT-RO-CMNICAL PROCTSSRS
Preface
Duzhenkov, V.I., Dolin, P.I. Effect of X-ray Irradiation on Aqueous
Alkali Solutions Saturated 'With Oxygen 7
The kinetics of accumulation of molecular products formed in the
radiolysis of vater are E-tudied in this paper. These products
are: hydrogen peroxide tmd hydrogen, The absorption of oxygen
in high-purity alkali so:.utions saturated with oxygen was also
taken into consideration.. It vas determined that the initial
yield of hydrogen depen&j on the concentration of the irradiated
KOH solution only for coacentrations up to 0.6 - 0.7 N Koff. ~The
saxne relation vas found Tor H 0 . The material balance of ihe
molecular products shovei a s?;&~ deviation towards excessive
absorption of oxygen. Tais fact was explained as the formation of
higher peroxides, probably H02 or the complex H292-RO2
Card 2/ 31

Effect of Ionizing Radiation (Cont.) .790
There are 4 figures and 8 references, of which 6 are Soviet and 2 Englleh.
Ovozdav, B.A., Shubin, V.N. Effect of Accelerated FJActrons on Potassium
Permanganate Solutions 12
The reduction of aqueous M04 solutions P1. accelerated electrons in
the concentration range of 10-3 to 3-10- M is discussed In this paper.
The yield of the reaction Mxi(VTI) ** M-a(IV) is determined from the
relation between the wvwit of reduced permanganate and the =Knmt of
energy absorbed by the so:~ution, The authors explain the effect of the
acidity of the solution (:,n the r=V pH - 0.4 to 12) on the rate of
reduction. The maxim= y-teld vas observed for pH = 2.05. It vae
determined that the yield of reaction does not depend on the Usage rate
In the range f - i017 -to - 1020 eV/ml-sec for electrorr energies from
0.1 to 0.7 Mev. There art 8 figuxes, 3 tables, and 7 references, of vbleh
4 are Soviet, 2 Vnig3ish,, and I Polish.
Card 3/31

Zimin, A. V. S07/78-z-12
AUTHORS: Sidorova, L j -30/36
PrO3~`urnin, 'J. A.
TITLE: The Effect of -r-Hadiation From Co 60 )n Aqueou Solutions
of Tin and TLtanium (Deystviye -p-izlucheniya Cogo na vodrM
rastvory soley olova i titana)
PERIODICAL: Zhurnal neorgan-4cheskoy kh,'mi-L*, 1958,vol 3, Nr 12,
pp 2793-2797 (USSR)
2+ 3+ 4+
ABSTRACT: The radiolyzis of aqueous solutions of Sn , Ti , Ti and
6o
suspensions of Sn (011)2 and Ti(011) 3was investigated. Co was
used as the source of the gamma radiation. The relationship
between the generation of hydrogen and the variation in the
2+-
Sn ion cocentration upon the amount of energy absorbed was
investigate-I. It was found that a change in the sulfuric acid
cor-centrati)n from 1-4 N did not influence the yield of hydrogen.
The addition of Fe 2+ (10-3 and 10- 2mole) did not interfere with
the yield of hydrogen. In the radiolysis of aqueous solutions
Card 1/3 of Sn 2+ mainly water and Sn 2+- ions arise, and these latter are

The Effect of -r--Radiation From Co 6o ,n SOV/-78--~-12-~0'36
Aquecus Solutions of Tin and Titanium
further oxidized to Sn 4+ according to the followirg reactions:
2, 4-,- -
Sn +H2 02 Sn +20H
Sn 2+-~20H Sn4++20H-
In the irrae.int-ion of thc, suspenrion o14 Sn (0H)2 in weakly alkaline
solution thc, redue--tion to metallic tin proceeds more quickly
and intensively than it does in weakly acidic solution. In
irradiating Ti3+ solution it was found that in the region of
col-centration of 1-4 N HCl and H 2 so4no significant change in
the hydrogen generation occurs. W--th an increase in the T14+
corcentration the yield cf molecular hydrogen decreases as a
result of V-ie in+erazt~on of the TZ.4+_ions with atomic hydrogen
according t) the equation-
Ti4+-F H ---),Ti3++ H+
Card 2/3 In irradiating 10- 2 molar U-4+ s-Ilutions in 4N HU hydrogen and

The Effect of r-Radiation From Co 6o ~rl SOV/78-3-12-30/36
Aqucous Solutions of Tin and Titanium
oxygen form with the following yields:
G 0
H 2 --,. 0.2 moles/100ev and 02 --, 0. 05 moles/1 DOeV
No metallic titanium forms as re-.ult of irradiating a
suspension of Ti(011) 3' 2 3+
It was found ihat in 10- and C.1m solutions of Ti in
hydrochloric z,.cid solution the radiolysic of the water amourtz
to 5.0 mole/ICOeV and in sulfuric acid solution to 4.2 mole/-iOOeV.
There are 6 f-;gures, 1 table, and 16 references, 8 of which are
Soviet
SUBMITTED: February 1, 15'58
Card 3/3

"' 5128
-c/020/62/'44/003/022/030
3119/3101
el
V., Vorina, A. D., Sidorova, L. P., and
Gubanova, A. V.
Radiochemical synthesis of organosilicon and
or~;anofluorosilicon compounds
"';azdem~ya nauk 3332. Doklady, v. 144, no. 3, 1952,
0
576-578
C C F. and 0,11 CI on the one
3o=poundz of the type C
n 2n' n 2n-m r_ 6 6 0 5
.0
h a nJ ,"S i C I.103ici ..3.;iHcl and C F. SiCl H on --he other, were made
3 ' 7- 2 C'J 2 2 5 260
r v a C '~ mutually under the action of,,., -rays (Co ) a. +200C and +700C.
"-e resul'in- reaction procucts wer-e fractionated by multiple c:)ndensation.
T*-e individual comnonents vere subjected to elementary analysis. Yolecular
e-i,-,h;,, density, refractivo index, and molar refraction viere deterzined.
20
nu--ber of known compoundi; and the new compounds (V H? (d
3 ds"15
bard 1/3-

S/020/0'2/144/003/022/030-
~~zioche,
mical synthesis of B119/3101
20
1.5170, n 1.361o, 71:1 39.o6, b. p. 3AIOC1756.5 m-" "-p ) Siol
23= 1 20 = 12 = 49-59, b. p. 160c',; (c 3 6 2 2
/d 1."2G2, n D 1.3413, HFI)Cli,sici
2
20 3 0 ') -
0
~d 1.4610, 1.3338, YR = 39.S1, b. p. 940'/749 mm ;--g);
20 - 20
~c j -Sic n 1.3710, 1~12 44-107, b~ 110-1120'
1 (d = 1.45112 D
3 u 2 ~I 2 20 20
/752 mm H an. d C 2 HF 4 Clsici 2 (d = 1.5138, n D 1.3645, ISU' 34.71a)
found . synthetlc method can be applied where the poly:aerization
rate of olefins iz lower '.---n their reaction rate with chloro silanes.
radiatiGn Chemical yieli and the quant-itative yield in reactIon
-)ro " I
uc:o depcn-i on the molar quantitative ratio of the 'nitial substances
o-) --la- : 1 olefin molecule per 1, atom of chloro silane). The change of
;eaction ter-Perature does not affect the radiation chemical yield of
)C!rf_`I.-.oro falkyl-dial'yl) chloro silanes ~G - 80 - 100 molecules/100 ev)
an,! aryl chiloro silanes (G - 6 - 10 molecules/100 ev). -With (alkyl-
chloro silanes, G increases from B-10 molecules/100 ev at 200-
to 160-210 molecule,000 ev at 700C. There is I table. The most imiortant
nl-lish-laiouaSe re-..erence is; 'A. L..E1I-Z'Xbba;:y,
"k
'ard 2.'3

S,/02YO'2/144/CD3/022/030
R~-diochemical 3yrthesis of ... B110 :3 10i
.1ndorson, j. -'C,. Che:.-. Soc. 430, 1737 (1958)-
institut i4-.,L. Ya.
(Phy3icocncmical institute iMen4 T.
larpov)
January 17,'190'2, by V. A. Kargin, "tcademician
Z TB.'--. TTED January 12, 1962
bard 3/13

ZININS A.V.; VMINA, A.D.; SIDOHOVA, L.F.; GUBANOVA., A.V.
Radiation-induced ciemical synthesis of organosilicon and
silicon fluoroorganic compounds. Dokl.AII SSSR 144 no-3:576-
578 My 062. OURA 15:5)
1. Fiziko-khimicheakiy institut im. L.YA.Karpova. Predstavleno
akademikom V.A.Karginym.
(Silicon organic compounds) (Radiochemistry)

L 19461-65 DJT(m)/W(t)/EWP(b)
IJP(c) JD
ACCESSION NR: AP4044671 S/OIZO/64/000/004/0084/0086
AUTHOR: Wang, Tolien-wa; Sidorov, A. X.; idorova. L. P.;
TITLE: Method of producing silicon spectrometric detectors with a broad region
of the sensitive layer ;o 12,7
SOURCE: Pribory* i tekhnika eksperimenta, no. 4, 1964, 84-86
TOPIC TAGS: spectrometric detector, silicon spectrometric detector
ABSTRACT: The development of detectors from Si compensated with Li and
having practically no dead layer it; reported. The detectors are based on a "new
phenomenon" observed by the authors in the course of their experiments with
drifting Li ions in Si. At a temperature of 125C and lower and at a voltage over
200 v. the entire high-resistance region had electron-type conductivity. This fact
facilitates bringing the space-charge layer to the surface. after removing a thin
p-region, a surface-barrier junction can be created by spraying gold. The
Card 1/2

L 19461-65
ACCESSION NR: AP4044671
resulting material has a very high resistivity. A theoretical explanation of the
phenomenon is offered. "The authors wish to thank B. M. Golovin, B. P.
Osipenko andj,_~VSlzov -for their interest*in the work, and also to thank other
workers of the Semiconductor Group of the Nuclear -Reaction Labo atorv. 11 Orig.
art. has: 4 figures and 7 formulas.
ASSOCIATION: Obl'yedinenny*y institut yaderny*kh issledovaniy (Joint Nuclear
Research Institute)
SUBAUTTEb: Z5Jul63 ENCL: 00
SUB CODE: EC, NP NO REF SOV: 003 OTHER: 006.
Card 2/2

1:S3.
T b 111 ---M
"1c c c

SIDOROVA, L.V.
Applicability of statistical generalizaticr, cLarts for the
calculation of the annual distribution of flow of mountain
,,idrol. no.4:72-70 164.
riverB. Sbor. rab. po F
(IMPA 19: 1)
1. Zakuvkazrjkiy nauchno-issledovatel'skiy gidi-oweteorologi-
cheskly institut.

CHANTLADZE, 7..1.; SIDOROVA,, L.V.
Annual change !n the mineralizaticn of water of the rivers
of Georgia. Sbor. rab. po gidrol. no.4:134-140 IE4.
(MIRA 19: 1)
1. Zalcavkazskiy nauchno-issledovatellskiy gidrometeorologi-
chaskly Institut.

P-+ , I Id
- - I 77~ - 4, i 1, e y e ELI I C-yeq r 5 1 r, (1, 1 (
~, :. , " ~- - - - , - ~ , ~ " ~l ~: L. , ~t -,,~ , - ,-1, , L I
11 - - 4 . 'r b I 1NI
, -P -~,, - "Iltral. Crl,; Ccl ,~ U 5 01. -- I
--~ -~ Cr'le~; _,l -.1 - is; 10)
. ~,~ '44-34! 1 i,4,

SIDOROVA., 14.
Formation and plann'ng of public consumption funds on collective
farms. Vop. ekon. no.10.91-96 0 161. (UR-A 14:1C)
(Collective farms)

SHAUROV. N.I., polkoynik; SIDOROVA,,,M-A., starshiy nauchn" sotradnik;
a_
w
POPOV, V.A., redakcrto.,; j3wum&4jvjko M.F., -edaktor; ZMAKIR. 1.K.,
tokhnicheskiy radekt)r
[Aeronautics and aviation In Russia to 1907; a collection of
documents and paper@] Vosdukhoplavente I avistaits v lossil do 19D?
abornik dokumentov I materialov. Pod red. V.A.Popovs. Noskva,, Gas,
izd-vo obor. promyshl.. 1956. 951 P- (KMA 10-.23
1. Russia (1923- U.S.3.1.) MentralInyy gosudarstvennyy vqenno-
Istoricheskly arkhiv. Glavacys arkhlvnoye upftylenlye.
(Aeronautics---History)

MZHXR. T.G., doktor ekon.neuk. nauchuyy sotradnik; KOZLOOT, N.I., kand.
ekon.nuak. nauchn" sotrudaik; SOMOT, S.I., kand.sellskokhoz.
nauk, nauchnyy notiudnik; SIDOROTA, K.I.. kand.okon.nouk, nouchnyy
sotrudnik; BANNIKOT, N.A., red.; GUMICH, M.N., takhn.red.:
ZUBRILIVA, Z.P., teklm.red,
[Production e"nditures and the cost of products on collective
farms] lzdorzhki proizvodstva i sebestoimost' produktaii v kol-
khozakh. Koakva, Gos.izd-vo nallkhoz.lit-ry, 1960. 256 p.
OGRA 13:5)
1. Akademlya nauk MR. Institut ekonomiki. 2. Institut skonowd
Akademil nauk OSSRAfor Tenzher, Koz1ov, Samenov. Sidorovs).
(Callaztive farms--Costs)

LAFTEV.F I.D , staroMy nauelWy sotra; BUYANOV, F.S., staraMy nauchEyy
sotr.;-KASSIROV, L.M., starahly naucbnyy votr.; TEW~AYEVA,
A.P., starshiy nau(!hnyy sotr.; SUVO!"OVA, L.I., starshiy nauch-
nyy sotr.; SIDOROVA I E11 starshiy nauchnyy sotr.; =43N,
S.I., starnFly'nauchrWy sotr.; Prinimali uchastiye: ARYMPOV,
A.I., IlLladshly nauchnyy sotr.; VAZYUINA, P.F., raadshly na-
uchnyy sotr.; KARMUK, I.Ya., mladshiy nauchrqy sotr.;
KAXIAUKHOVA., Ye.I., mladshiy nauchrqy sotr.; 1GXLOVA, T.14.,
njudsMy nauchnyy sotr.; ROMOVSKAYA, L.S., mladshiy nauchnyy
sotr.; CHISrOV, G.N., m1adshiy nauchnyy sotr.; POTAPOV, Kh.Ye.,
red.; GEAASILOVA,'Ye.S., tekhn. red.
(Coux,,,unal funds of collective farms and the distribution of col-
lective farm incorel Obshchestvenywe fondy kolkhozov i raspre-
delenie kolkhozrqkh dokhodov. Mloskva, Izd-vo ekon. lit-ry,
1961. 386 p. (MIIA 15:3)
1. Akademiya nauk SSSR. Institut ekonomiki. 2. Sektor ekono-
niki sellskogo khc,zyaystva Instituta ekonomiki Alademii nauk
SM (for Laptev, Buyanov, Kassirov, Tex-,rayeva, S~uvorova,
Sidorova, Semin).
(Collective farms-Income distribution)

UPM, I.D.; TSHYAYEVA, A.F.; WILINIKOV, N.G.; CHENTSOV, R.Ye.
(deceased]; SEFF, Ya.F.; SUVOROVA, L.I.; ZASLAVSKAYA, T.I.;
GREKOVA, A.I.; TOUNUICH, V.S.; IBRAGIMOVI A.I.; KOTa-UBA,
T.Ya.; KUFaLEV, V.11A.; KOVAMSKIY, G.T.; KAJIUS11,A.A.
[Kalnins, A.]; SIDO;,OVAj N.I.; MALISHAUSKAS, V.I.
[E.alisauskas,V.j; r"ISEC12-ay, P.P.; BUGAREIVICH, V.S.;
KlUtNAUKHOVA, Ye.l.; Al!~~FIYEV, T.I.; KAZAKOV, I.G.;
W14OVSKIY, I.A.; red.; LIUKUTA, N.I., red.;
TSITEO, I.A., red.; VOLIUNA, V.V., tekhn. red.
[Material incentivfts for developing the collective farm produc-
tion] Materiallnoe stimullrovanie razvitiia kolkhoznogo pro-
izvodstva. Moskva, Izd-vo Z SSSR, 1963. 326 p.
(FILRA 16:12)
1. Akademiya nauk SSSR. Institut ekonomiki. 2. Institut eko-
nomiki AN SSSR (for Laptev, Teryayeva, Suvorova, Zaslavskaya,
Sidorova, Karmukchova). 3. Sredneaziatskiy gosudarstvemyy uni-
vercitet (for SapU'nikov). 4. Komi filial AN 999R (for Chentsov).
5 Insiitut ekonomiki Ado' Estonskoy SSIR (for sepp). 6 i3as1ikirFkiy
filial All SSSH (for Grekova). 7. Institut ekonomiki All Belo-
russkoy SSR (for Torkovich, Kovalevskiy). S. In:Aitut ekonomiki
A14 Uzbekskoy SS2~ (_Por II)r-li;imov)
(Continued on next card)

LAFTEV, I.D.-- (continued). Card 2.
0.. Institut, ekonomiki P11 Ukr.SSR (for Kotsyuba, Pasechnik).
10. Belorusskiy institut, ekonomiki i organizatsii sel'sko-
khw~raystvennogo, proizvodstva (for Bugarevich). 11. Vsesayuz-
rj-1 in-stitut, sakharnoy svekly (for Areftyev). 12. Institut
ekonomiki All Kirgizskoy SSR (for Kazakov). 13. Rabotnik TSent-
ral Inopo )-on, itata KorwiuniAicheskoy partii Poldavskoy SSR (for Gu_
r.ov,,~,'-iy'..14.::u;y'oyshovskiy planovyy institut (for Kurylev).
(collective farms--Incore distribition)

68229
0 0 S/0-18/60/005/02/020/045
AUTHORSt Ambrozhiy. 11. N.,t- B004/BW
Luchnikova, Ye._F., Sidorova, M. 1.
_-----------
TITLE: The Thermal Decompcsition of Carbonates of Rare Eartbj'z),.' the
Ceriur~lSubGroup
PERIODICAL: Zhurnal neo.-Canicheokoy k-himii, !960, Vol 5, Er 2, pp 366-371
(USSR)
ABSTRACT: The authors investi-ated the thermal behavior of "he carbonates
of Lap Cc-, Pr, lfdp and Sm. The analyses of these substances
are Given in table 1. L. S. Shrayber took the thericex tl~
(FiCs 1-5) by means of the Kurnakov pyroneter. Table 2 presents
the data of thermal dissociation of the carbonates, and table 3
the temperatures, at which the decompocition is completed.
The dec;r-position proceeds according to the following scheme:
a) Dischz*rCe of the crystal water, b) formation of inter-
mediates, except for Sm 2(CO3)31 c) formation of the oxide.
Ao far az the thernal stability is concernedp, the compounds
Card 1/2 investir-.11ted may be arranGed in the follovinG orders

68229
The Ther,.,z-.l Decomposition of Carbonates of S/071i/60/005/02/020/045
Rare Earths of the Cerium Subgroup Boo4/Bo16
Pr (CO Ce Sm La (CO
2 3 3 2(CO3 3 2(CO3 3 < Nd2(CO3 3 2 3)3*
There are 5 figures, 3 tables, and 11 references, 7 of which
are Soviet.
ASSOCIATION; Saratovskiy -osiidarqtvennyy univer3jtet im. 11. G. Cherny-
shevokogo (Saratov State Univer.-Aty imeni-11. G.Chernythevrkiy)
SUBMITTED: September 26, 1958
Card 2/2

DYKHANOV. M.N.; SIDCROVA. M-1.
"at ...... -,
Syntheois of 2,4-dichlorobenzoic said. *Bd.prom. 10 no*4:11-14
O-D 156. (NLRA 10:2)
1. TSentrallnaya laboratorlys Moskovskogo khimiko-farmatsovtichaskogo
savoda *Akrikhlng.
(BUZOID ACID)

- i - -, . ( - I - V- ,
I - !: -, ."I!'-. i , .: . , I - ~ ... I _-; . - 0
~: ~," , - 1. , ~ e :, I I -r- j Z * 4 L; 7~4::n Tn ~- e " ~ :~ * r ,, , ~. t~n -, - a I
, _) _~ _ ~ L
. . - C:~,7 f I
f r " , ~ "": , c -
, . t , ~ - , t1, 71-,- : , i.cl 1'' r.*)*- .- , r-4 I
. ; .- ~ - ( M 1 RA 18.- )

FRIM11GIM.M. D.A.
Relationship between tLe phenomenon of induced polarization and
the electrokinetic projerties of capUlary.systems. Vest.LGU 16
no.407-69 f6l. (MIRA 143)
(Polarization (Electricity))
(Carillarity)

i(AMMANI B., kand.tekhn.nauk,-. LINLVSKIY, Ya., inzh.; GUTI14A, ~Lq inzh.;.$ID,GRGVA,
No, Anzh.
Insulating miaterials for layered e*Wrior elements of buildingab
Zhil. stroi. no.ItIO-12 163. (MIRA 16:~)
(Ininilating materials)

LAZARESICH, S.K., kand.tekhn.niuk; REHT,iii, Ya.A., starshiy n;,uAnyy sotrud-
nik, kand.pkonomicheski.kh nauk; DOHLEVA, N.M., inzb.; 6 lwitc)Vi~, N..n.j
ekonomist
Comparative economic efficiency of various wall materials u5ed in
large-panel construction. Stroi. Pot. 7 no.9-.6-9 S 161.
(Hi1tti 14.11)
1. Rukovoditel' sektora ekonomiki proyektnykh resheniy hauchno-issle-
dovatel'skogo institut.i ekongimiki stroitel'stva Akademii stroitel'stva,
i arkhitektury _'SSR (f.)r Lazairevich). 2. 14auchno-issledovatellskiy
institut ekonomiki strAtel'stva (for Rekitar),
(Building materials) (Walls)

- SIDOROVA, R.B., uchitellnitwi
Forest festival in a ischool. Biol. v shkole no.3:62 S-0 161.
(MM "
1. Srednyaya shkola I'lo.173, Leningrad.
(Natural resources)

USSR/Hedicine - Meningitis Jan/Fbb 50
Streptomycin
Treatment of Tubercular Meningitis in Children
With Streptomycin," N. D. Sidorova, Asst, Chair
of Children's Diseases, KharIkov Ned Inst
Yop Ped i Okhran Mater i Det" No 1, PP 39-42
Discusses results in 58 cases of course of treat-
sent involving suboccipital andlater endolumbsir
injection of streptomycin. Treatment produced
changes in course of-diseaf;e for most part in-di-
rection of progressive improvement. Found early
treatment sharply decreases mortality rate,
USSR/Medicine - Meningitis Jan/Feb 50-
(ConLa)
before 10th day of disease 36 $, and thereafter
86 %. Found treatment considembly less effec-
t.ive on very young children. Chief, Chair of
Children's Diseases: Prof Ye. Ye. Granat.
tn
163T46

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After tire ether, *&. cvthf hill nmfl,.%,,, X1,
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USSR/Cbemlstry - A23172atIon lob 49
Chemistry - Benzate
"Alkylation of Benzene in ther-pr9sence of R9OjjAj0l2,-
IF. G. Sidorom, Te. A. Vdortsara, lab Org Chem, Can
Asia State U, pp
"Zhur Obahcb Xhim" Vol X.M. No -2
Studied alkylation of benzene by olefins, halogen
derivatives, and 9,1:ohola in presence of ES04AID12.
Showed that condenspticr. proceeds well with oWlas
fyield of alkylation prod-,;.-ts -8 - 86% of theoretical)
and bmlogen aerivati-7es kyield of 60 - 83% of '- %
tbooretical; . Reaction with alzohols 3s poor: PriaLT
46/49T15
ITSSR/Chemistry - Allkyln~t; or- ~Contd) Feb 4.9
alcohols do not yield to allcylation, sezondary opee
yield poorly, I'%, yieldi, whil-3 tertiary produce up
to " of the Tiel! of alkylbenzenes. ?axa-isciisrs
f o= during el*lat4 on ir. presence of ESOLAM
-2-
USOiAIC12 ~auaes paxtial iocmerizatiof. of raUcals.
-it G-t
S
u Etted 29 0,
46P.49T15

USSR/Miewletry - ADWIstion may 51
"Cycl&lkylation of Armatic Compounds. IV. CmA*n.
sation of 1-Methylcyclobexanol-1 With Benzene,
Toluene, and Phenol," N. G. Sidorova, Lab of Org
Chen, Cen Asia State U
"Zhur Obahch Khim" Vol XXI, No 5, pp 869-874
Condensation of 1-metbylcyclohexanol-I vithC
and C H CH in presence of AIC13 yielded 1-r;Q1 ;f
1-pbeGicyhohexane (I), vth C6H5 OR in presence
H3PO4 yielded 61% p-(l-methylcycl6hexyl)-pheno1 (n)
afid 18% 1-methylcyclobexyl ester of phenol (III
182T36
USSR/Chemistry - Alkylation (Cont~d) may 51
fully isomerizes into II on distn). Products cbar-
acterized by prepn of derivs. Identity of II vith
product of diazotization of p-(l-methylcycloh&xyl)-
aniline shovn.
182T36'
to

0 y A
Chemical Abst.
Vol. 48 No. 5
.-ibldornoft. Jr. S.
Mar. 10, 1954 32, 1
CA
-.47
orgoTdo G homistry
own

SrDOROVA, N. Q.; GREBETIM, A. D.
Hexane
Cycloakylation of aromatic compounds. Part 5. Synthesis of trans-l-methYl-4phenylcylo-
hexane. Zhur. ob. khIm. 22 no. 9, 1952
Monthly List of Russian Accessions, Litrary of Congress, December 1952. Unclassified.

U SS R
1934, NO. Ittwa.-CoweUNMUOM of a
moalkyls with CJI# and PhUe In the
gave 47-81% monoolkylated produo
quired 0.01 C.-atont Al as freshly
Wo compd. Aftlation was =Y
erizatiort of primary Into se-adary
appitrently proceeds through the tom
medIatessuLhPsRAICI&&ndP4A1CI.
Chlora- mid bro-
cc of metallk At
lit reaction re-
r mole of
=by Isom.
. The reaction
of Al org. Inter-
----j23,AlO.3.&W
BuBr (pad of It added Initially and the balance dropwtu
after the start of the rtaction) 30 g. heated for 2 his. at 70',
gve 51;q BuPh (1). bw 170-1*, ag 1.4920, do OS631, wW*
% Cs Mut, b. 178-240*. BaCl 24. C.H, 00. and At 0.31
min. &OD-WI produced 81.2%1. Nltmttwol;
641/g P-nitro-smAntylbennue, bs 132-4% *1
W11 - this Ith S. and HCI produced
butylanillue ~. U4-, V LWW, d. O.QnO; #-m-butyt-,
acetaullide. m. M. 8*; and P-m-butylbens:aallide. m. 1310i
(ftma1c.). BuBr3O, PhMe3o, and A10.3 g. heated forii
Isrs. at 700 gave 04.3% BuC4HMe (11). bnt IW-3'. mT
LOW, do JAM. DuCt 12, PhMe 15, and At 0.15 C.!
heated for 1.5 bri. at 70-801 give 62.517# 11. b. 1004M)".
AmCIII-5,CJItQO and A10.1 C. heated for2 hrm. &00-80'
V a mfxt. of MV. Aillylboneem, bm IW30, xV 1.49M,
~esm. x-qIf11rCI 27, CoHe 23, and At 0.3 g. produced
47ci itc-octylbentene, b. 242-6'. ag 1.4850, dw OMOI-
Pli
C HiCl 35, CWs I!%rd JAI .0j,15g. heated to 701 and the - -
reaction continued I produced Ph:CH#. bw
250-W. m. 20'. A cooled soln. of EtCl in 75 S. of Qffa
added over a period of 2 hrz. at 404 to 0.3 g. of A] produced
73.75c PhItt Ittz 134-60 V 1 49M d 0.8M, wul a m1a.
of 14k' iW.Rt.. b. I aft;~ !repeated di-An. bra
SG
I
-W, m*J I ZM, do SM. M. Hosth

SIDOROVA, If.-G.; DMIZOVA. Ye.A.
Gycloalkylation of aromatic compounds. Part 6. Condensation of 1-methyl-
cyclopentanol and 1-chlor-l-methylcyclopentane with benzeno. Zhur.ob.khim.
23 no.8:1399-1401 Ag '53. (KI-EIA 6:8)
1. SredneFLziatskiy Gosudarstvennyy universitet-
(Condensation products (Chemistr7)) (Aromatic compounds)
(GA 47 no.22:12268 151)

C'l
"i
0
USSR/chemistry - Alkylation Sep 53
"CYclOalkYlation of Aromatic Compounds. VII. Con-
densation of Cyclohexanol with Chlorobenzene,*~N.G.
Sidorova and.1I.S. Lapovok,- Lab of Org Chem, Central
Asiatic State Univ
Zhur Obshch Xhim, Voll 23, No 9, PP 1509-1512
It has been shown that the alkyllation of aromatic
hydrocarbons by cyclic alcohols, in the presence of
AlCl 31 gives good yields of monoalkylated products.
This method was tested on halogenated benzenes,
especially chlorobenzene (I). The condensation of
26M"
I with cycloh"anol (II) in the presence of AlCl
was studied, and the conditions which give yieia
of cyclohexyl chlorobenzene up to 85$ of the theo-
retical were determined. It was shovn that con-
deneation conducted'under heat results in n-cycla-
hexyl chlorobenzene, whereas at 00-200, a mixture
of o-cyclohexyl chlorobenzene and p-cyclohexyl
chlorobenzene is obtained, with the latter pre-
dominating. The condensation of I with II in the
presence of phosphoric acid (III) could not be
achieved. III acts as a dehydrating and poly-
nerlzing agent.
26ST29

S'180ROVA I N.a.
US.".R/Chemistry - Alkylatinn
Card 1/1 Pub. 151 - 17/36
Authors s Sidorova, N. G.; T5ukervanikj 1. P.; and Pak, E.
Title t Alkylation of aromatic hydrocarbons with olefines in the presence of metal-
lic Al and halogen derivatives
Periodical i Zhur, ob. Idtim. 24/1, 94-96, Jan 1954
Abstraot I The possibilit7 of alkylation of aromatic hydrocarbons (benzene) with ole-
fines (ethylene, propylene,, iaobutylene, isoamylene and cyclohexene) in the
presence of metallic aluminun and additions of halogen derivatives, is ex-
plained. The amount of Al used for the alkylation was found to be of no
great importance since only a small part of it enters into reaction. Room
temperature was found to be the most favorable condition for the reaction
with low-molecular olefines; high temperature was required for olefines with
higher molecular weight. The results obtained from such alkylation are list-
ed. Five references: 3-USSR and 2--Cerman (1895-1953). Tables.
Institution % Central Asiatic State University, Laboratory of Organic Chemistry
Submitted i July 1,, 1953

sl~okov
USCR/ Chemistry - Condensation
Card 1/1 Pub. 151 - 13138
Authors Sidorova, 11. G.
Title Cycloalkylation o? aromatic compounds. Part B.- Condensation of 2-methylcyc3D-
heyanol aril 3-mthyl.cyclo Nntanol with benzene
Periodical Zhur. ob. khim. 24/2, 255-259, Feb 1954
Abstract i The condensation of 2-methylcyclohexanol. and 3-nethylcyclopentanol, with ben-
zene in the nresence of AlC13, was investigated at different conditions. The
two reaction tendencies observed in the case of 2-methylcyclohexanol are ex-
plained. The products obtained during smooth and rigid reaction conditions
arc listed. It was observed that the condensation of 3-mthyloyclopentanol
with bonzene is not accompanied by any noticeable isomerization of the alcohol
radical. The stereoisoiw-ric product obtained in the latter cane is described.
Ten references: 5-USSR; 2-USA and 3-German (1924-1953).
Institution: Central Asiatic State University, Laboratory of Organic Chemistnr
Submitted t Jul-.v 1, 1953

** ~ 111~_'j(_ ':11111/! , :IV, ,__ -
USSR/Organic Chemistry - Synthetic Organic Chemistry, E-2
Abst Journal: Referat Zhur - Khlmiya, No 19, 1956, 61468
Authort Sidorova N. G.., Feyershteyn, N. M., Kochetkova, E. A.
Institution: None
Title: Cycloalkylation of Aromatic Compounds. IK. Reaction of 1-p
cyclohexanol with Benzene
Original
Periodical: Zh. obahch. khimii, 1956, 26,, No 1, 191-197
Abstract: On condensation of 1-phenylcyclohexanol (I) with C6H6 in presence
of AlCl takes place primarily reduction of I to phenylcyclohexane
(TI). 8ondeneatiou products consist of l13-02I) and i,,4-(iv) di-
phenylcyclohexanes (14-22%). Addition to AlCl3 of: water, HCl,
Cu2C12 and SnC14 has no effect on course of-reaction. With FeCl
is obtain-101I and phenylcyclobexane (V); with AlBr3 yield of III
and IV 26-47% that of 11 30-37%- Reduction of I to II by action
of AIC13 takes place also in abstice of C6H6 in iso-octane (800,
11 hours), yield 25%. From CJD25 mol 1, 0-037 mol A1C13 in 100 ml
Card 112

USSR/Organic Chemistry - Synthetic Organic Chemistry, E-2
Abst Journal: Referat Zhur - Xhimiya, No 19, 1956, 61468
Abstract: AMAJA n gradual Mating to 800 in 3 hours is obtained IIp yield
a:d mixture of III and IV (22%). Dehydrogenation of IV with
Se (340-3800., 2 hours) yields p-terphenyl, while III gives m-
terphenyl. 0-05 1101 1 and 0-05 mol AlBr3 in 100 ml CA are left
standing for -12 hours, heated for 7 hours gradually increasing
temperature to 80(l, produces II, yield 17-5% and mixture of NEI
and IV., yield 36.!P%. On increasing amount of AlBr 3 to 15 e ui-
valents yield of XI is 30%, yield of mixture III abd IV, 45%.
0-05 mol V in 10 ul C6H are slowly added to mixture of 0.025 mol
A'Cl3 in 10 ml C61 . lez stand for 24 hours, heated 4 hours to
800, produces 13-4 yield of mixture III and IV. Communication
VIII, see Referat Zhur - Khimiya, 1954, 34125.
Card 2/2

U. Reaction
con) ds.
'is"On
kw. ~ Y r M, TV, w
A7
201- r
Gr=ne
J
1j1
U
S
S
R
26 -0(10561
(10
.
.
.
.
.
.
.
'
(Ene; tniuslation); 'J.. C-4. 49, of 6.7
to 8.8 g. I-phtityleydohexanal (1), and200 ml. cif4l,
folloi md by 4 days at rwas -tettip. and 30 hrs. -ut 40-50',
finall r reflusitig Ltrktil- MI evolution ---d. gave 60%
and 14.4% 1wineric diphellylCyclohal-
'
~
~
-"
It Ow reaction juixt. was directly efluxed 3 bra. the
ants t
.
! ~
: '
I'
ykielk w"c 371%, ouil IBQof, Mp. Under [be latter tech-
nique, 4.4 C. 1. 6 g. J10s, anti 100 ral. Calla iiave 40%nnd
'Flit diphenylattA
22% y1elds of the alitive protlucts, tv!qi.
prod tict yielded soine. in. 108', and
wiaotner. which wos iduitified 4fttr dehy,lrogenation W
the.
m-lisplicayl, Dry Wtwispaued for 2

drd)ivL;e with 4.4 g, I in 80 tul. Cella anit the M41t, rauxed
4 It i. on a stcain tmth, yielding 36% arwl 26%, rt5p., of the
alit it products., If the nat.ofl, AICII, and C41(sis Mated
wit k a few drops of 1130, then tefluxed, the yields am 42% and
Adda. of sinall anits. of CuC.or SnCt4 zave situllat
-
2
111;1
: Rcl, gave 18.6% phertylekelollexane and fime,
1
dif hell~lattfl product. However, heatici; 8 8 E. 1, 8.1 g.
Fc Cis, and 75 ujl. Call. 4 hr,,. at 75' gavs! 40% phenylcyclo-
he cane unly. (8-8 S.), 13.5 g. Miles, and 100 uA. CJ14

cy:10hexane and 30.WD J,4-4iph"yIVycIuhcx;Ane mixed with
sove 1.3-isomer; the we of LS ecluivs. of AIDr, gave
3(%aitd43%.resp..
Oftyly a4ded,8 Jr. p6myleyclob"eae in It) ml. Ctf-L and,

'
at r 'A hri,. the ruixt. brated 4-hts. at W. y-l-lding 60%,
!l
r
ttng hydrivirbon aild wilefl
s1
a,jes. 111.~ttlur, 4.4 g, I in 6tkoatic with 3.35 g. AIC14 11

44
77 1
vi xr~
4~

a1
firs. at Poo
fi
M-I,Y,~Yclohex4deapi 04h44nidcnfi__
ed pr ucts. X.

nd
hlorocyclobi ondenzAtion ofA;4-c!~lohoxAAAdiol

,
' G" Sidurova
ot with benzevc
N
can

and Yu.

Yglobel
_ _
_
,
, V. Zha r.
4 It Obrkhel Xhim. 76 510-W
ffk-
dW
d
d
n
V
i
,
(jUZA?.
To .5.8 g. I
yclohc.%%ut
suspen
e
o m
.
i
C*Hs %was added 20 i t. AICJ, mid the mitt. heated 4 firs. at
700; aftcr aq. treuti %ent wiLli.1-ICI them was obtaincd, 10%
mixt. (I) of-1,3- anti 1,4-diphcnykyclohexanesj bit 1607-200'-
(ticbydrogenation ta in. and p-terphenyl).- 81[inilarmadjon

of 4-chlurocycloliLM3
M gave: some fifienAcyclolietine (can-.
"
7
tarninated with, phei ~lcycluliexcric) and I.. Pure 1,4-cyclo-... .
hexanediolm.1i" The ttw uf AM. gave 43.5%pheuyl-
cyclohexame and 2.15INVOI. 1,4-Isriuc:rof.lotiried.inC.116,.
with AIC13 gave phi aylcyclobexone and I., Thus the reuc-
tion results in'alkyl stiou with lotm tiou of I and in forma-
tion (of phenylCyclol igatic contandrtated, with oleft; The
yields are mi-Kicri cel r affected by rtnomat propo-ttions-
-7

SIDOROVA. NA.: VALIBIKOV. Tu.V.
Cycloalkylation of aromatic compounds. Part 10. Condensation of
1,4-cyclohexanediol and 4-chlorcyclohexanol with benzene. Zhur.
ob.khim. 26 no.2:SlS-520 F 156. (NLRA 9:8)
1. Sredneazlatskiy gosudarstvennyy universitot.
(Cyclohexanediol)(Cycloheianol) (Benzene)