SCIENTIFIC ABSTRACT KILDISHEV, G. - KILESSO, S.I.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000722520013-9
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 14, 2000
• Sequence Number: 13
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

KIVDISREVJP G~; OVSIYF.'MO, V.
"Adjusting and, calculation of distribution aeries" b7 A. 1.
9zhov, V`op. ekon. no.12:114-117 D '62. (MIRA 16:.1)
(Mathemtical statistics)

";IL.VAA. ".1,, 1.L. and P--T;tjV, iP.
.?,--acti')n of ~alphatic Ou ides with Hydrogen FlurA tie, Coin ~unlcatlo:, 1, "hurnnl .
Obs!hc*-icy k imli, Vol. 1,1~, !4o.1, 194~j pp 95-100a

A
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Nov.
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00.3
1- a I IL.-L.
0
-,;i;c iw rs;w-ri wiT. -%.otT- -
Castom"O. V. V. gAta. 0V Wilishevot and N. A.
k~rvvbfuhcnskil. J. Cora. C". 1U.- S. S. A.) 11. 4n-8
0WO.-Previous rittempig to synthesise mroictics writ
110t vcry successful sond a new approach has been under -
t
asken: .11fic. CUl. Clio. Clio. CAI*; CCU: Of CO Air
tIX(Cl C).MgBr - RCII.1(011)(Ci 0.C(OI1)MrR (x
road'.'). k - %lr.C.Cll'.Cl11.Cli1.C)4C.CCli CIL
I C/1'.011. (716. ('11l. 01I)CtIo.obtainedbywid-
ins ! g. 2-methyk-yclobexanone In an equal vol. of
ether, to the Grignourd reagent (6.15 g. EtTIr. 1.5 g. Ms.
treated for 2V-24 Jim. with dry CoHi).,extg. after 3 days
%ith ether and seps.. crystals, m. 111-13'. The m-
sit-Wer was pf!pd. in thie same manner, crystals, tit. If"*.
INCMt(OH)CIII, obtained b adding 48 1. RCMC- o to
tile Griguard reagent (0 S. Ug. 27 g. Mr. treated for
W- 24 hors. with dry CsIll). wpg. the oily Uyer after l(likyu
and It act iQ"tiu# under 4 win., crrstals, in. IM- 10 *. (RC.
Alf.C111'. obtaitwd by the method developed by Kuhn
W.A.31.1371).. IRCIfc(O/I)CICI#,obtairicdi)yrarty-
ins out a one-tided rundenAtion of Coll, with RC%Ic.0
and X&Ntlo, crystals, too. 10D-10. The method of
Nicuwknd and others (C. A. 26, 78) was used in this
Perlin. Boris L. Rodziank
14boo.) -90 C-V oft
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0 0,0 ip-0 4, 4 ... 0 4 0 f 0 0
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of fluorine into Orgill com - A0
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a 0 a 0 0 0 6 0 0 0 0 0 0 0 * 0 ois 0 0 0 0 0 0 0 0
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KrLIDTSW7A. 0. V-
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Chaw jit-rT
1
am. T-CSR, 4 pp
Hy4rariuorlo Acid iu-,
OreAnic Cmy-.rtindn
'D,-)k kkad NattOr z~&SF. Nvi-a So-r` V '.VIJ, N
Nacribea n,!4w r^actlon 1.n se~Ars,. 1,in A'
oxIdes by hydroFNv flucri-Ir
17Norbydrin &nd &I-scusees
at.=a of ohlor!,r;e Into fluoride
PA 60%4
moo

* 61i W 0 -0 6,111,
0 0 0 0 0
slif x"..1 4141
ad d'&
lk isla.4 k__J ---
L. Knunrusts. 0. V. KII'dibva, sivid-1. P. Pillim. iNV POVOILM t'1 t I.Pt I
4' Zilar. MikkeiNhim. (1, Oft. Clit".1-14. WIOO(1040).- W.5 S. OcIlicl Oil and
iticini reacts with etii" wall 6 118 jI! tPUdS11-1,."citil"clif,
My It F under a varkty of cond V11blym= LiVe 415 he~. 81 l(kl-10* Jrwr 30% FC11,
a wilik (1) to give chaitis of polyctbykvt &"%. with will- MvOll.b.101-3'(J). 1(192g.) and 49S. riulysue(by, .00
ute Juills. of polyethylene fluorobydrin e-witent. P w". ene weiv $a
Id. with IICI.kt e" 'th agitation asict let stand
sucm.olully Intrtliluced by the UK of Elio als aisimt. -00
To NO cal. Milt) in a steel AuttICIAW Wait attkkd 20 g. dry 24 hn.-. the low" layrf ?-Ave .00
)L4 Ad'i"I it)
lip &Bid 20 S. 1. and aft" d lirs, lit Hall, the fulsil. was. bet 42-3% till !Aixt, air 1,411hi. .4. q OCHOW11,C11'r.
as'!, "ru"ind Vint a tantle of product% from whielk weft 20 g. JIL)CII#Cl J.4)Cjj#Cj lip ill ;N) ll1,j.AC%tjCA14Ma1tkd 14 1 1. -40
Atli Until
40-~,, 1JoCJJl('l IF. b. IL04% ill*, LIA -QV pyrdinc isth etaitilag. chess hmteij 0,
isolated ep the SO, flow ceand. lp- 24% (MIX110C11,01gir, b.
lj64 (j_ftapWkyjlreoax. in. 1254% 37 S. ESOCIAr 142-7', d;: 1.137, %V 1.4-70. Addn. o( 4.7 g. PhOll to -11114111
C11,011 and 21 6. noClio 01g) C11,4711s F. b. 1T24". 1.15 if. NA in 34 MI. NICIMI, then 11 g 4-?%lCCsHsS(1%- 411111411
Oe 4 11-. 1.1ifJ6. aV 1.41,ki. A imilsw prov"dure w- Used I' CII#ClilP, and beating 4 firs. on F straw ilalb gave 4 S.
the following Prepils. t-RvPrP-:-PW. --* 0
Pbot'll'allF. plates, IP, W.5" ths I (it)
00 a r4701 (M% tw"! CA 0
Iwapi'lesse Oxide), b. 1074,*, di: 1.112 4. *V 1.1=2 U- and 4.6 g. #Atd. a th IlCI at W and
in, 81-3 ). j,3-DVvar#4 ad stand 7-9 hm. gave 6b% C.Yl'OC1'11Cl11F)l. b. 1(321-4'.
(4(~% imm epiduarohydrin). he W. d:** IWO-v we*
d:: 1,1302, MV LIM'. Addn of 14.2 C. &-it to 40 g. I
0 '31 ij (Unst'll"d yield from and 15.9 g, dry CuSO. cm-Y 11; dall-s' standing tave 21,L
ilt1kne We - by-peciduct, tetr*mftb ldkx&w) I
MtCl'(OC'l,'C'1st)v, bill W. 11,1: 1,0914, aV lAr
b, M ill* 0 WIJ, sit 12913. ROMProk F611) in. b. W! (20ji.) W221r. Ns%(.NiA Vill]. water at -5*IoO'wcre
~:j 0.4', di- Vti~i -V 1.373, was Obtitil'Od in SO yield by
treated with C5 ail. c~1. 11C.; the upper lay" gave 40"
411110 Ar i Radius. ;Uu*d. Koji oVer ~Nl min, to 40 ;. (pCjjjCjjOjj
= nit'lik ' b ' fUd' dl- 1 MOR V
Maco.rre
In 150 mi. Elio and reflusting 3 hrs. with atiffing. (Cl--
00 43.5 g. pyn'diner in 91 nil. I't'
to vics treated
is* ~0916' 214 r
cjl')(FcjI')cIlOII (54) X.) and 75 g. N%#CrA In 43 mi. in 3 bra. at "* with 22.9 If PC4, Jet ;iand 2 lirs., and
11.0, slowly treated with W g. A.SO. in 23 nd. H.0. sarlif filtered: the filtrate pro an unstated yiehl 01 (FCIII~
I stirs~ 1&-I-o bell. rAve I-cWorv4-ftwor*-:-Jw*Mx~, h.
1414-3.5'. d:: I.M. %V 1.4235 (stiairarbasciat. M Ill- ClisMil'. Ill 114-16% ill: 1.2M, mV 1.417 (&"* a a
12-). Ileating 40 g. MIX31,011 and 19 It. 164 6; at dePresillsil Do The tralra) stomill system). 1 (23 C.) M,I a
170--W rAve an unstated yield of IlOCJlMioDCHjcjj2p. to 64 a. INXIA at Al-My". stiffed a lit$., slut Illown with
gave 33.4- FC11'CH.P(sC4, b. ICO-7'. d-.:
F Krusayants, 0. %'. KO'disbe", and H, Bykbov-
*mi A. Aid 101-13(1949).-ConversWaotUCifiA:HiOH a 1.4400. W11 (1-1.2 g.) in 20 tul. Cjfs below 3(), LO 0
t. F"Elf.ckisdil by KV toes in 2 stem with Initial lar. to 29 s. I Rod 39.3 g. pyridine in 4o ml. CJ1, wid
matiort Urthytirne ckWe. which thin wts with the result- too
itstit * tbe-.1k." %.pttift of XF AN VM PrO.OcOd to 0
dell.Wirmlillocination reactions in X~sscsal. Itelluxi"
Cd v, At;
_~-f - i -v A- -. -i'. -1- -7 q 1 66
1A is 19) M; , a, , I , I fW 13 - a ~ V.
U PIP & a it as As x Al 01 Is Or 9 An I I a 0 1 Of so a 0 3 - 4110i
0 0!0 0 0 0 0 0 0 -0 * *0 00 0 0 01a 0 0 ~*" 0 0 & 0 0 * 0 0 00 0 0 to 0 0 0 fillI
0 0 14,* 0 * 0 0 0 * 0 90 00 0 0 0 0 0 0,6 -0 -0- 0 6-0 0- 0 0000 0 0 * 0 a 0 02

0
0 0
0 0

slir"d I hr. at 65' NAw fwl% (PCHICHM.P0. th, lea'. 0*
4;: 1 J651 a V I*W1. 1 (01A it.) addtd to 23 it. 90,01
iftl to tko'
At U-40
wa
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i
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f 6
7
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.
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I FCHWIGOk~V
79 XV
4198
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.
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, mV lZINK). AI
ba M-W. ill: 1-9aft
-
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.
.
.
is
.
,
.
;
The ow tif c -mimolAr aints. of rrAqents and warming 24 t
U
OCI and warming 3 hr%. to I
p
10 CICII#L
xV 1,31111,
143-6'
441M
1: 1
d
b
0
0C0Cjj
V
'~

O .
.
.
.
,
.
pC
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,
kirs. to 00-70 gAvv an unstated yield of (FCUClfs
)#-
02-4 411*13191 $1$*
1 4(")
So
b
10 mokm) and I (ki~rrlikaf)- Wil'COUT mmil-Illy gAve W; F(71147111-
*
* I
Vilt)
AIA)
10 1 9
h
.
,
l,
i
rook 4-Mr~%Il w:~r irrAted %ith agitatim at
#l-10' with 30% NANI Witil
`nLU%MlIV AM
stictod
W .
.
, *I,
r, his S7-w
. ill: J
OCOCI[s
he cr Caw 44
6"mj&wAt luth i %"p
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him
filterr~
and wiNtird
giving KS-Wj% 4-
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AP
l
l 00
.
4
4
.
.
,
'
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ar
y gATT
(1wimaw). AcCl simi
.
VAC14CHIF (U), bit 174-S
: 1.291). mV 1.5111).
. d. b. 115-16'. ill.: LOW). AV I .:0C. Addu. of 51.4 g. Wilt- Al 0
Eta.NH (7-7 g-) and 2k) g. H heated in a scaled tube 3 kn.
to IN)"
coolcif
and treated with %'&Oil gave (PCHIC111) COCI to 2n g. MWIll-WHI And wArming to
W11-4 '
ill:
(*jj
b
p) 1fr
Cjj
C
Cjj 00
0, ,
,
:
EhN. b. 107-13 * dl* O-R.-, 5 mV 1.44 -A
~T; jivrek. m. 134
i;
()
tl
l1
Vt
1;
;4
) i
F
f
O .
.
l.
Ch
(
j
gave 60% j
j
W), Thi. (30 X.). 41 g. I1cF,. 4n4
*V 1.4918 (skin i"ild
"
" 00
,
.
r
n
rom Ft
ll).
h
r (
g. Ph
it
(
g
And re-
H in CK) ml
HW let btand owirni
ht
And 21
9
.KAw 411
21 lin. At 144
o
16 KF,aftrr"hr%.A' I
1%,
ltvl-H* d" I :N),!
AV 1

o
.
.
g.
,
g
-
Ruled 3 hrs. gave 31% PhCU,C11*F. It. 157-A)", th, -
.
.
1j. tPCjI,),CHOII an,]
Addit. of 38.5 g. ICII.COC1 to 2 so

0 874W, d.11 1164. aV 1.4965. 1 (21) g.) addtd to 1W) I.E.

S'
COCI
d l
d 24 h
8F
0% .
niu~ to 40-W' saw A)% ( 04)'Cllococll't. b.
w
'Mi
l`
)
41
T
00
to
an
et stan
rs. gave
, at
Al
' g.
s (
3 d.*: Mg. ~V 1.518 (ifyiM41).
IS
1
PCIfiC1110COC7. b. M-31 *. d,': 130). oj* IAC30 (ski
4
i
i
hi
3
d 32
24 l
1410
6
)
1
f littated 6 hr*. to Im' ith So g. IISF, mixed with 51) g.
'
*
ll
414
1 00
-
rr
.
An
ter
irs. at
kat); t
. a
s (
C.
g.
o
*
93-8'
01
ove 457
(FC11
CV
h
d
O)
I
=
W% .
110(l)CIIJ, b, 121
. i
.
.:
KIF pve 157. VC1101(
2
Off
%1
KOSWA
0 00
.
,
it
,
s
.
.
.
g
0
.
j,
V I zw. I (is X.) in 1k) C. water treated uItane- .
.
P
.05.
aV 1.4 00
ousl In small portions with 20 X. k-Jiful(li and 3D ml.

d with Il
011
filt
d
t
li
SO
d
a
IOT N
00
ere
ra
. neu
ze
.
i. evap
l
.
.,
mud distd. with lIpS(l,. gave FC11jLW1. b. 130A1 00
(after repeated drying with CuWA) (ykq,l under 10%).
' 00
The No soft of The above, heal--I with
!j mote M to
00 1 VtVt*. nve FC11,010. b. 72-6"1 d1l: 1.3813, cV 1.411t). 00
00 00
00 00
00 eo
00 00

III
~

L 0000000000000000000000000000000000000*0000:
0 9 0 0 0 0 0 0 0 0 * 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 * 0 0 0 0 0 0 0 0 0 * 0 0 0

MM/Obamistry Itydrogen rluoride Jan 49
Cbemiatry Fluorine Compounds
c0 "Uteractivity of Aliphatic Oxides With Hydrogen
Fluoride, n'" 1. L. Xhunyants, 0. V. Killdisheva,
1. P. Petrov, lust of Org Chem, Acad Scl USSR,
Moscow, I.X, pp
"Zh= Obshch Mim" Vol XIX, No 1
Ylucrobqdrins may be formed by direct subst"";t,-
tiau of Cl in two steps, first involving qumt
ti" formation of etlWlene oxide from ethylene
chlorobydrin under the action of EF. Then, upon
ellaination of EC1 f~rom the chlorobydrins, EY is
%Ami
MM/Chemistry - Aydrogen Fluoride (Contd) Jan 49
potiverted into ID1, liberating EF, which.reacts
according to EF + 37400F. Under pressure - tlils,
reaction gives a 35 - 4o% theoretical yield. of
0"TIene f lucrabydrin. In addition, f lucrine-
sabstituted acetals, acids, ethers, etc, weris yre-
W164, and a list of 38 fluorine compounds with
-theIr physical constanto and methods of preparation'
to SIven. Fluorobydrins reacted with acid halldes,
Including those of phosphoric, nitrous and sultonic
acids, giving 2-fluoroetbTl esters. Eaters of
"Ifonic qplds are characterized by. a pronounced
alk,ylating ability. Phenol, diethylamine, etc.,
wwo f lucroathylated. Submitted 10 Yhy 47.
Aft 58/49T31

4~ t
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Pit"'
f4i-,
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t4
v,
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I

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V-(, \ ;, -t) I I ~, i i c 4 el i-if I
LINIKOVA,M.G.; ZILIDISEUIVA.O.V.; XNMAETS,I.L.
ts-thiolactones. Izv.AN SSSR. Otd.khim.nauk n0.3:569-570
my-je 155. (NLBA 8:9)
1. Institut elementoorganicheakikh soyedineniy Akademii nauk
SSSR (Thiolactones)

KNMANTS, I.L.;KILIDISHBYA, O.V.;PMVOVA,Ye.Ta.
Convernion of mercaptoamizo acids. Report no.10.New method for
the eyuthesis of polypeptidan. Izv.AN SSSR.Ot4.khiw.x&uk no.4,.
696-704 ji-Ag 155. (Miak 911)
I.Institut orgazicheskey khisil imeni N.D.Zelisakege Akademii
nauk SSSR.
(Peptides) (Amino acids)

5-V-7-
""Luz
V'N
AN

1 3 .
~ 021'~210WIKI Y, Rel-RIAM V"I'llp,
i,
T
U.
I " , . . ~ I - .

KILIDISHEVA, O.V.; LINIXGVA, N.G.; MOWOLrNSXATA, I.L,
Conversions of morcapto amino molds. Part II.Ce-,P-dlsubstltutsd-
-K-acylaminocarboVIia acids. I%v.AN SSSR Otd.khim.nauk n0-7:834-
842 ji 156. (MM 9110)
1.Institut s1em*nt*orgRnlch#skikh soytdineniy Akadomii nauk SSSR.
(Acids, Fatty)

USSR/organic Chemistryp Syiithetic Organic Chemistry. E-2
Abs Jour: Ref Zhur-Kbimiya iio, 6p 1957, 19o69
Author 1dl1disb#W-,QitVAp Gambaryan N.P., 7'alonskaya M.M..,
Inst
Title Problem of Decarboxylation of -acylamino - -haloido-
substituted Carbonic Acids.
Oria Pub: Izv. All SSSR, Otd. 1-1im. H., 1956p 140 7t 850-854.
Abstracto: cilp -Diebloro-,,~-benzoylaminolsovaleric acid (1) and
(,,, -oxy-g - chloro- C%.- bentoylaminoisovaleric acid (11) by
beating vith (CH3100)OD or at the action of ketene
(III) form 2 h 1-4-acetoxy-4-(2-chloroioopropyl)-
oxazolone Q.- t Is ahcxim that II at the action
of a solution IIAHCO~ is easily transformed into iso-
butyrylbenzimide (V7) apparently.. through the formation
stage of ~-lactone- Eleven g. ofl-benzoylamino
Card 1/3
Card. 2/3

KILIDISHEVA, O.V., Doc Chem Sci -- (diss) 11,143 -disubstitu ted-
-Ck-aminocarboxylic acids". Mos, 1957, 19 PP (Acad Sci USSRj
D
Inst of Element,-Organic Compounds), 100 copies. (KL, 1-56, 114)

r,q
V"Y.
Vi, tr~
,gANS5,
1-73,
to
11"M -,Rf
Ay
13
0 N-0
An,
Nlft

ji
i-4t,

p*g,
7~ "All

KNUEY TS, I.L.; PIRVOVA, Ye.Ta.; LINIKOVA, M.G.; KILIDISHIVAO Dove
.- - - -
P -Thiolaotones, their polyc'ondensation and polymrization, Xhim,
nauku iprom. 3 no.2:278-279L.156, (MIRA 11W
1. In.9titut alementoorganicheakikh soyedinenly AN SSSR.
(Iactones)

50)
AUTHORS: Lin1kova, M. G.p SOV/62-56-11-12/26
Savosina, V. M., Knunyants, 1. L.
TITLE: 06,A-Disubstituted. &,-Aoylamino Carboxylic Acids
(0("A -Dizameshchennyye-ct,-atsilaminokarbonovyye kisloty)
Communication II. A New Method of Forming
Oxazole-4-Carboxylic Acids (Soobshcheniye 2. Novyy sposob
obrazove.niya oksazol-4-karbonovykh kislot)
PERIODICAL: Izvestiya Akademii nauk SSSR- Otdeleniye khimicheskikh nauk,
1958, Nr 11, pp 1348-1353 (USSR)
ABSTRACT: It has been communicated (Ref 1) that o6, ~-dihalogen-
Of--acylamino propionic acids easily react with water,
alcohols,and amines and that they form c6-substituted
06-acylamino-A-halogen carboxylic acids (I) - Purther
investigations have demonstrated that c/,t/-~-dihalogen-o6-
acylamino propionic acids easily react with mercaptans and
according to the halogen (chlorine or bromine) mono- or
dialkthio acids are obtained. In this paper a new reaation
for the formation of oxazole carboxylic acids from
a6 -acyl amino- /1-halogen acrylic acids is demonstrated.
Card 1/3 oC-substituted 06 -acyl amino - /1-halogen propionic acids

&,',/3-Disubstituted o6-Acylamino Carbox'ylic Acids. SOV/62-58-11-12/26
Communication II. A New Ifethod of Forming
Oxazole-4-Chrboxyl.ic Acids
transform into oxazoline carboxylic acids under the action
of alkali. They form according to the conditions either
a.cyloxy-pyroracemic acids or oxazole, carboxylic acids.
The mechanism of formation of acyloxy pyroracemic acid from
o6-substituted oC-acylamino- A-halogen carboxylic acids
has been described already earlier (Ref 3). In this paper
a mechanism of formation of oxazole carboxylic acids from
c4-acylamino-/I-halogen acrylic acids was suggested. It was
shown that the formation of oxazole carboxylic acid from
C6-substituted c4-acylamino-/I-halogen rxopionic acids takes
place over a stage of formation of 2-aryl (or alkaryl)-4-
substituted oxazoline-4-carboxylic acids without preceding-
transition into the corresponding o6-acylamino-ja-halogen
acrylic acids. There are 7 references, 3 of which are Soviet.
ASSOCIATION: Institut elerqentoorganicheakikh soyedineniy Akademii nauk sSSR
(Institute of Rlezmta3 rg&ut Compounds of the Academy of
Card 2/3 Sciences,USSR)

xr,
50) scv/6 2 - 5 5 --l. 2 - 9 1/2 2
AUTHORS: Killdisheva, 0. V., Sh,~kina, V. V., Knunyants, i. L.
TITLE: a , 3Di ,:u1 1.~ ,, t J" tu tt- e d a -- A cy 1 am --' n o Ca rb 0 x y I -_i r, ' d SD
,,&.m(,-:31ichenz-.yye..ct-ats-'lam4i,,okarbono,.,yyc.e kislcty) Communication
3: Propionic Acids (Scobshcheniye 3.
a,a-Dia-L.a-.'-,~anino-P-gaic4.doprop-'Lono-iy,ye kis1c.--,y)
PERIODICAL: I-zveztiya Akademii- nauk SSSRO Otdeleniye khimicheskikh nauk,
1-158, N-r 12, PP 1461-1467 (USSR)
ABSTRACT: Some tllm~! ag-~~ `,!, was proved (Ref J thitt a,P-.dihalogen--a-.qcvl-
amino acidi (1) easily react with water, alcohols,
amines and me-l-captans, forming the corresponding a-subst-ituted
ct---PcvlsLmino-P-ha,'ogPn carbuxylic acids (11). Unsuccessful
atte:ipt~j xers~ made '.o obtain the a,a-diacylaminc-p-halogen
propinnic acids (III), whore X = NHCOR, by a reaction of a,P-
dihalog2zl-a-acy.latr.-*-nc prop4cnio. acids with the ~!orrespondiing
am.ldc,-- Further invealtf-gations z;ho-eied, ho7;ever, that a,a-di-
acyluminc P-halogen propionic acids car. easily be obtained by
,X 4
!h--: of hal"gell pyroracemic acids .-Lh the cor-
.rt~sponolne ir the presence of concentrated sulfuric
0 a r, i i-ii th,,3 same way ab in. the produuti,--n of u,a-diacyl-

SOV/62-L,6-1 2-9/'22
a,P-D-isubstituted a--Acylam~~rlo Carboxylir. Acids. Communi:;ation 3:
amino--P-Ha-'.~gen P:~-piriiio A-,'da
a minc-, --irLoxylic. acids; (Ref 2). Ace-.rjin(7 to this method th--,
-x, a -, -I-' ~..-y lam' no-B --halogen propionic acids mentioned in table
L
The dehydratien of apa-diacylamino-p-halogen
acids ci,. heatfxq led to the gaturated
(VII) The Lhtziin;~(! Ycr,-~ ~,zs-,ially crystall-
liz;~d froam an'-y~rjde as stable, color'COES, crystalline
On Lhe act-ion of mc-thy.. alcohol, -Al 2-1.70thyl-4-
oxa,!olune-5 1,i tht.~ absence of
tile new propionJc acid
V' I w.'-t'pi .'ht- melting p,,)-int ',3j0 was ea-n-4iy formed.
7-hpre are 2 tal,-,Ies and 7 -afezi:nces, 3 3f which are, Soviet.
4
c-heski'-vi soyea`nen-v Akad-F-m-*i -,auk SSSR
ASSOCIATION: ln5cj
7,,
\1-4t:'.4-at~ L;f Elem-in-.organic Coi,,ipoundj, Aoadem,,- Cf Sciences,
USSR),
SUBMITTED: M--c'i 29, 1957
Card 2/2

2o-11 .0-1 -22/52
AUTHORS: Golube7a, N. Ye., Killdisheva, 0. V., Knunyants, I. L.,
Member of Academy of Sciences
TITLE: Cancerolytic Pei,,tides ( Kantseroliticheskiye peptidy)
PERIODICAL: Doklady Akade,-,ii Nauk SSSR, 1958, Vol. 119, Nr 1,
pp. 83 - 86 (USSR)
ABSTRACT: Cancerolytic, sarcolysin-containino dipeptides (table 1)
were produceA hv condensation of the N-formyl-derivative of
p-dL-(13 -ethyl chloride-)-amino-DL-plionylalanin (sarcolysin)
with ethers of various amino acids. By the interaction of the
sarcolysin-ethyl-ether with p-di(,6-ethyl. chloride)~amino-
phenyl-acetic-acid the othyl ettior of p-di-(P-ethyl chloride)-
aminoplienacetyl-sarcol.ysin was obtained. Further p-di-
(P-ethyl chloride)-aminophonacetyl- andK -L/p-di-(/~- ethyl
chloride)-amino-7-plionylbiityryl-derivates of various amino
acids were produced whose -cneral formula is Civen ( table 2).
By the interaction of p-di-QI-ethyl chloride)-aminophenyl-
Card 1/3 acetic-acid ands /p-di-(jS-othy1 cliloride)-a!rino/phenylbutyric-
"lo-119-1-22/52
Cancerolytic Peptides
acid with anilin in the presence of 1,3-dicyclo-hexyl-carbo-
diimide the corresponding anilides were obtained; it is true
that in the case of the interaction of these acides with
2-metl,Yl-5-ethoxymethylene-o'-am~ino-pyrimidin or with p-di-
((i-ethyl chloride)-aminopli,-~nyl-acetic-acid with cyclohexal-
amine only N-acyl-derivativen of 1,3-dicyclohexyl-urea were
isolated. Preliminary samples on the cancerolytic action of
the sarcolysin-containing peptides were performed in the
Institute for Experimental Pathology and Cancer T',erapy of the
Academy of Medical Sciences of the USSR (Institut eksperi-
mentallnoy patologii i terapii raka Akademii meditsinskikh
nauk SSSR). It became evident that the sarcolys-in-peptides
possess marked properties close to those of sarcolysin which
act against tumors and which at the same time are not toxic
and have a high selectivity of the action upon some tumors.
Finally the general method of production of anrcolysin-con-
taining peptide3 and that of the individual peptides is given
Card 2/3 in a kind of experimental part.

KNUNYANTS, I.L.; GOLUBEVA, N.E.; KILIDISIEWA, 03. (Moskva)
Principles underlying the production of specific carci-nolytic
preparations. Usp. soov. biol. no.2tl67-173 S-0 160.
WIf-A 13:11)
(CYTOTOXIC DRUGS)

KNMANTS, I.L., Akademik: GOLUDITA, N.Ye.:-XILIDISILrVA, O.Y.
Cancerol.vtic peptides of directional activit7- Dokl.AH SSSR 132
no.4:836-838 -Te '60. (MA 13:5)
(Peptides)

K-ARPAVICHUS, K.I.; GOLUIjEVA, II.Ye.; KILIDISHEVA, O.V.; KFUNYANTS, I.L.
Cancerolytic peptides having specific action. Report No.2:
p-Di-(chloroethyl)amino-DpL-phanylalanyl-D,L-valine. Izv.
All ISSSR. Otd.khim.nauk no.7:1297-1299 JI 161. (NIMIA 14: It )
1. Inatitut elementoorganicheakikh soyedinaniy AN SSSR.
(V&line)

KARPAVICHUS, K.I.; GOLIJBZVA, N.Ye.; KIL~DISH~VA,_O.V.; KNIJITYANTS, I.L.
Guncerolytic peptides having spocific action, Report No,3:
N-[p-di(2-chloroethyl)-aminoplienacetyl] and N-(p-di(2-chloroethyl)
-aminophenylbutyl] amino acids. Izv. A14 SSSR. Otd.khim.nauk
no.7:12Q,9-1303 JI 161. (MIRA 14:7)
1. Institut elementoorganiclie8kikh soyedineniy AN SSSR.
(Amino acids)

KNUNYANTS, I.L., akademik; KILIDISHEVA, O.V.; GOLUBEVA, II.Ye.;
ZURABYAII, S.
Diethyleneiraido,Tphosphor7l and diethyleneimidothiophosphoryl
derivatives of amino acids and peptides. Dokl. AN SSSR
W no.2:37C-373 Ja 162. (MIRA 15:2)
1. institut elementoorganicheskikh soyedineniy AR SSSR.
(Amino acids)
(Peptides)
(Phophorus organic compounds)

KKUNYANTS, I.L.; GOLUBEVA, N.Ye.; KARPAVICHUS, K.I.; KILIDISHEVA, O.V
Cancerolytic peptides having specific action. Zhur.TKIO 7 no.2:
238 162, (MIRA 15W
1. Institut elementoor anioheskikh soyedineniy AN SSSil.
fPeptides) (Cytotoxic drugs)

KNLTNYANTS, I.L.; KARPAVICHUS, K.I. (Karpavicius, K.I.); XIL VA 0. V.
~F,E~
Cancerolytic peptides with specific action. Report No.4; New
derivatives of sarcolysine and their use for the synthesis of
peptides with different position of sarcolysisne in the peptide
chain. Izv.AN SSSR.Otd.khim.nauk no.6:1024-1031 162.
(KRA 15:8)
1. Institut elementoor anicheskikh soyedineniy AN SSSR.
Mptides) (Sarcolysine)

"o I-! P~s~~46~"9) 0, v.
GOFMAN, A.; FREY, A.I.; RUTSHYW4N, I.; OTT, Kh.; SHEMIAKIN, M.M.; KIS11FALUDI,
L.; KOGHENOV, N.K.; DEREVITSKAYA, V.A.; PHOKOFIYEV, M.A.;
SHABAROVA, Z.A.; FILIPPOVA, L.A.; SHANKMAN, S.; XHAYGA, S.;
LIV, F.; ROBERTS, M.Ye.1 GAVRILOVI N.I.; AKIW)VA, L.N.; KHLUDOVA,
M.S.; MAKSIWIV, V.I.; IZELIN, B.M.; SHEPPAHDj R.K.; SHKODINSKAYA,
Ye.N.; VASINA, O.S.; BFRLIN, A.Ya.; SOFIINA, Z.P.; LARIONOV, L.F.;
KNUNYANTS, I.L.j GOLUBEVA, N.Ye.; KARPAVICIPJS, K.I.; KILI-DISHEVA
===p
,; WDZIGRADSKIY, K.; KAFTARO M.; LEV, M.; KORENSKI, F.;
Q,V
BUASSONAI R.A.; GUTTYXIO St.; KHOYGENIN, R.L.; ZHAKENO, P.A.;
BAZ11US, S.; LENARD, K.1 DUALISKI, S.; SHREDER, Ye.; SHMIKHEN, R.;
KHOKHLOV, A.S.
Results of the Fourth European Symposium on the cbemistry of
peptides. Abstracts of reports. Zhur. VKHO 7 no.4:46S-476
162. (MIRA 15-8)
1~" Aktsionernoys obahchestvo "Sandos", Basel', Shveytsariya (for.
Wman, Frey, Ott, Rutshminn), 2. Famateevticheakaya fabrika
"G.Rikhter", Budapesht, Vengriya (for Kishfaludi, Korenski,
Dualakt). 3. Institut khimii prirodnykh sojedineniy AN SSSRI
Moakva (for Kochetkov, Derevitskaq&,,ShuVakin, Khokhlov).
4. Laboratoriya khimii belka Moskovsk6go goeudarstvennogo
universitsta (for Prokoflyev, Shabarova, Filippova, Gavrilov,
kkimova, Khludova). 5. Fond meditainakikh isoledov&niy, Paseadena,
Kaliforniya, Sev.Soled.Shtaty Ameriki (for Shankman, Khayga, Liv,
Roberts). 6. Laboratoriya khimii belka Instituta organicheskoy
(Continued on next card)

Go-4han, A.,-(Continued) Card 2,
khimii AN SSSR, Moskva (for Maksimov). 7. Aktsionernoye
obahchostvo Mibaff, Basel', Shvey-tsariya (for Izelin).
8. Liverpul'skiy universitet, Angliya (for Sheppard). 9. Institut
eksperimentalinoy i klinicheskoy onkolofii AMN SSSR, Moskva (for
Shkodinskaya, Vasina, Berlin, Soflina, Larionov). 10. Institut
alementoorganicheakikh soyedineniy AN SSSR, Moskva (for
Knun,fants, Golubeva, Karpavichus, Killdisheva). 11. Institut
organicheskoy khimii Budapeshtskogo universitota, Vengriya
(for Madzigradskiy, Kaftar, Lev). 12. Farmatsevticheskiv 6td'31
Aktsionernogo obshchestva "Sandos", Bazell, Shve ts iya (for
Buassona, Guttman, Kho7gonin, Zhakeno, Rutshmann~, ar13. Issledovatell-
skiy institut farmatsevtichaskof promyBhlennosti, Budapesht,
Vengriya (for Bazhus, Lenard). 14. Aktaionernoye obshchestvo
"Shoring", Zapadnyy Berlin (for Shreder, Shmikhen).
(Paptides--Congresses)

XNUfWTS, I.L.; GOLUBEVA, N.E.; KARPAVICHYUS, K.I.; KILIDISTIEVA O'V
I--------,.-------.?- r
Cancerolytic peptides or directed action. Coll Cz Chem 27 no.9:
2253-2254 S 162.
1. Institute of Organoelementary compounds, Academy of Sciences of
the U.S.S.R., Moscow (for Golubeva and Ki-I'dishova).

KAZIMA, N.B.;.KILIDISHEVA, O-V-; KNUNYANTS, I.L.
Canceroly-tic peatides of specific action. Report No.5: Some amino
acids and peptides containing a N-di-(/3-chloroethyl)aminophosphoryl
group. Izv.AN SSSR. Ser.khim. no.1:117-131 Ja 164. (MIRA 17:4)
1. Institut elemetitoorganicheskikh soyedineniy AN SSSR.

KAZIMINA, N. B.; KILIDISHFVA, 0. V.; OUNYANTS, 1. L.
Acylation of serine, cyatine, and cystamine with p-d i
(2-chloroutbyl) apiinophenylalkanic acid chlorides. Izv AN
SSSR Ser Khim no. 4:755-756 Ap 164. (MIRA 17:5)
1. InsLit,ut elementoorganicheakikh soy-odineniy AN SSSR.

ZtJ,Q-'BYAN. S.E., RASTEYKM, L.P.'! KILIDISHEVA, O.V.- KNUNYANTS, I.L.
y - - ~,-: - P
No&.acyl derivatives of arginine containing c/,di(2-chloroethyl)
amino group. 1-.v. AN SSSR. Ser. khim. no.10.-1899-1901 0 164.
(MIRA 17:12)
2. lnntit-tzl. clementoorganichoskikh noyedIneMy AN SSSR.

DAGENE, M.I. (Dagiene, M.); RASTEYKENE, L.P. (Rasteikiene, L.1;
KIL.'~_kklLAI_O.V.j KNUNUNITS, I.L.
Noc-acyl derivatives of histidine bearing di-(2-chloroe"uhyl)
amino group. Izv. AN SSSR. Ser. khim. no.5017-919 165. (MIRA 18j5)
1. Institut elementoorganicheskikh soyedinenly AN SSSR i Institut
khimii i khimich6skoy tekhnologii AN Litovskoy SSR.

1T

ACC NR, A26024023 RCE CODE: UR 0062/66)000/006-flll--S,/-11-1*6--!
ITHOR: Knunyants, lo L.; ruzerauskas, A. P.; KWdinheva. 0. V.;
rervova, Ye, Ya.
ORG: Institute of lieteroorlyanic Compounds, Academy of Sciencen.,SSSR
(Inatitu*t clementoorganicheakikh soyedineniy Akademii nauk SSSR)
TITLE: Symmetrical diethyl di-p-nitroplienyl 1,2-ethylenediphoophonate
SOURCEt AN SSSR, Izv. ser khim, no. 6, 1966, 1115-1116
TOPIC TAGS: nntitumorigenic compound, alky1nitrophenyl diphonphonate
OeV 0-09 A/ I C- t5c' IV 7He'rl (L pl? 0 0 F- SS E/ "72POVA.,/). .9
4 t c -r-Y V .1 r VX-) 1PA15,V 4 C1
A B ~ OT 'It- ~ E-T
'Previous studies showed that some bisethyleneimines possess antitumorigenic
'properties; in this connection, preparation of symmetrical diethyl di-p-nitro-
.phenyl.1,27etliylenediphosplionate (11).was studied. At 68-700C. tetraethyl.
1,2-ethylenediphusphonate reacts with PC1, to form chloride I., which reacts.
,with p-nitrophenol in the presence of triethylamine at -10*C to yield (72X)
II, mp 96-1040C:
Card
AP
UDC: 542.95+661.*718.1
Go I OCIII,
(C11jjOhPC,11jC11jP(OC6111):1
C1 0 C1
OC,116 N04 C11110 0 0
PCHICHIP PCHIC1111 -OC4116
(11/8 -8\C1 0
No,. NO,
11 is a bifunctional phosphorylating agent. The reaction of I and 11
.with cyclohexyainine yields symmetrical diethyl dicyclohexylamido-1,2-
ethylenediphosphonate, mp 211-214*C:

'-Acc- -62-46273
NR,
Oell,
PCII,cillp
SUB CODEi 071 SUP11 DATE: 2SJan661 'ORIG REF:
(W.A, 50; CBE No. 101
0011

AiSM/Cheini"t -16action
I ry
1/1 Pub. ~151~- 4/36
Authors I
oreskov G., X.; Jniri' 6
onov, V V.; Ozerov, R. P.; and Killdishevai, E. V.
Title Gherdcal reactions-ih V -KOO :and V2P5-K
295 4 O~07 systems
Nri.odical zhur. ob. khim., 24/1, -23729 Jan.1954
Them- ographic and x-raj investigations of V205-K004 and V205-K2S~D systems
were carried out to determine their reaction characteristics. The Zormation.,
in the first of.'theAwo-Systems of:'a.. compound close in its composition to
V20 K2S04 with a melting point of about 5000 was discovered. The eutectic
point between this compound and K2~04 was established at below 4300 which
inds to an approximat V dntent of 0.4 mol/frac'tions The fusions
correspc 20 c
&d systems
With larger * osulfate:,contentsln-the second of the investiga
Pyr
vm re., f ound to have low melting.points and easily convert into glass when sub-
jected ic, cooling, :Avi exothermal effect during the heating of this system
was ob9orved.at 2750,,and i-thisle, explained by the formation-of a V~05
K25207 compound. -Elevon r~eferences: -3-USSR; 4-German;2-Italian and I-
Scandiwvrlan (1905-1950Y. Tables'; graphs. Also 1--Zinglish reference.
In3titiition Scient.iric Institute of.Fertilizers and Insecticides
Submitted I lay '110, 1()!03

q i

. I . . I . . . . I -I -
i . I. j . ..I . . . . . I I . - . : . . I . I , . I . I . ..-1 * ,
. I . . i

AUTHORS: Illarionov, V& Vop Ozerov, R. F. and
Killdisheva. Ye. V.
TITLE: Phase Diagram Of V205- K20 in the Region K205 KVU3-
(0 Diagramme sostoyaniya V205 - K20 v oblasti
K2015 - KV03)
PERIODICAL: Zhurnal Neorganicheskoy Khimii, 1957, Vol.II, Nr-3s
p-0 701. (USSR)
ABSTRACT: Differences and similarities between the author,42
communication on this system and other relevant data are
briefly discussed, with special reference to an article
by F. Holzberg, A. Reisman, M. Berry and M.
Berkenblitl- There are 4 references, 1 of which is
Slavic.
SUBMITTED: November 26, 1956.
AVAILABLE: Library ofCongress.
Card 1/1

S/078/60/005/012/012/'016
BO17/B064
AUTHORS. Illarionov, V. V., Ozerov, R. P., Killdisheva.
TITLE: The Phase Diagram of the System)l 0 - KPO
PERIODICAL: Zhurnal neorganicheskoy Khimii, 1960, Vol, 5, No. 12,
pp. 2802-2803
TEXT: The section of the three-component phase diagram of the system
V205 - K20 - P 205 along the KPO 3 - V205 line was investigated. The system
was thermographically investigated as well as by X-ray analysis, and on
the basis of the results obtained the phase diagram was drawn. The forma-
tion of the two compounds KPO 3'V205 (1) and 4KPO 3*V205 (11) was found in v/
the reaction of the solid phases KPO 3 and V2 05at 300 and 380 C. The
first compound is brown, and melts at 350 0C. The mQlt of this compound be-
comes vitreous when cooling down. The second compound is light-green, and
melts at 8460C. In contrast to the former, this compound shows no tendency
to vitrification. The X-ray pictures of these compounds are compiled in
a table. There are 1 fi-ro. 1 table, and 5 Soviet references.
Card 1/2

The Phase Diagram of the System V 205 - KPO3 S/078/60/005/012/012/016
B017/BOG4
SUBMITTED:
August 28, 1-958
/ .
Card 2/2

ILLARIONOV, V.V.; SOKLAKOV, A.I.; KILlDjSHEVA_s.-Xe-.-V,
Phase diagrams of the systems V205- X3PO4 and V205- 1,4P2-07.
Zhur.neorg.khim. ~*-"*A:1355-1360 'Je '61. (MIRA 14:11)
1. Nauchnyy institut udobreniy i insektofungisidov im. Ya.V.
Samoylova.
(Systems (Chemistry))

. r

1UNTUROVA, I.M.; kIL'DYAYEVA).V.F., kand.biologicheskikh naxlk
Virus diaeases of potatoes in the Far North. Zashch. rast.
ot vrod. i bol, 7 no.1:35-36 16-1. (141RA 15:6)
1. Nauchno-issledovateliskiy institut seltskogo khozyayBtva
Kraynego Severa, g. Norillsk,, Krasnoyarskogo kraya.
(Russia, Northein-Potatoos-DiBeases ard pasts)
(Virus diseases of plants)

ACC W; SOURCE COME.:
AUT~:C'R; Kildys-1 (Prosiden', AN iSSR, Academician AN SSSR);
(Chief scientific sacretaxy Presiditmi Ali SSSR,
Corr0s-)oix11n,-, member AN SSSPO
os~'Z: -110nC,
TITLF": N1---, clections In tha acadc-my of sc~cnco,5: SSSR
SOUaC7: 1:.vcstjy,-., no. 156, 5 Jul 66, p. 3, col. 1-5
ZOPIC aciencific personnel, scientific organization
A -I S T:!A. 'I --': I
On -13 A.P-il 1966, the Acade-,y of Scionces USSR announced that it wo~~Id
consl,,c: no.-minations for election of new members. In response to the
various scientific and L(~UCational Institutes nominated 247
caadid:.Le-- for full member~,h.-;p (academicicn) and 491 for correspondn.-,
i,-. e m b e rslh 1 p .Of these, 46 were elected to full membership and 76 were
elected to corresnonding membership. Thc: names and.affiliations of the
new membc~-s are listed below:
1. Full Me-mbers
A. N. Tikhonov
eral c.--d 'N. G. B-sov, L. F. Vereshch,~~--'*-.-,,
S. V. Vonsovskiy, V. L...Ginzburg, A. N. Prokhorov
Card 1/5

ACC NR: L~,7011025
c;* L'ur-lear Phyc~cc. M. A. Markov, A. B, Migdal
D,*v-*j-*o,,: of the Physical and TechnEcal Problems of En.rqcI,,ic,,,. V. I. Pop'--ov
Earth Sa-Zences. V. V'. Menner, .14. A. Sadovskiy, A. V. Sidoren-ko
D , i v i ci a no-F' M-3chm-,ics ard Control Proccoscs. V. P. Barmin, P. D. Grushin,
V. 11. Mi!3hin, V. V. Novozhilov, N. A. Pilyugin, M. K. Angel'
D-ivision of G-~reral and Technical Chemistrv. I. V. Petryanov-Sokolov,
G. A. 'Aazuvayev, N. M. Emanuel'
DiDision of tke PhysicaZ Chemistry anf:! Teoknology of Inor~ganic A.4a -,-aria Ic.
I. P. Alimarin, S. T. Kishkin, A. Ml. Sa-ma-.:in
D`Vieic, c~f -,;i,3 Biocherrish-~, Biophysics, and Chemistry of
Activc ,'Or,7_:?ou?~---?s. N. D. Iyerusalimskiy, Ya. V. Peyve, G. M. Frank
of' PhusioZoqu. P. K. Anokhi-,i, Ye. M. Kreps, V. V. Parin,
B. V. Petrovakiy
D,,~*vLsioy: of General Biology. B. L. As taurov, N. P. Dubinin
Div-,~7icn of Histom. A. A. Guber
Card 215

ACC NR: AN70110425
Dfviofon o"' and Law. B. M. Nedrov
Di;nsior of -E-Conc-mico. A. M. Rumyantsev, T. S. Michaturov
Divisiom of and !bangua2c, V. 1q. Zhirmunskiy, M. B. Khrapchcnkc
Sibcric,: D-I* s ior. G. K. Boreskov, N. 'N. Vorozlitsov, A. B. Zilukov, Yu. 1"~.
Kuznetsov, L. A. Melentlyev, A. V. Nikolayev, V. V. Struminskiy
II. 'Corresponding Members
o" N. P. Buslenko, V. Ya. Kozlov, S. P. Nivilt-lov,
Yu. V. ?rokliorov, A. A. Samarskiy
Ipplied Phyoic~7.. 1. D. i3akhrakh, A. F, BoF-,amolov,
V. S. Borovilk-Romanov, L. A. Vaynshtcyn, L. P. Cor'kov, Ye. M. Lif!;Iiit!;,
R. V. Khoklilov, 1. S. Shklovskiy
7' 'v~c *r?' ~, , -
o-; -'car PhT e-'cq. V. P. D.-helepov, L. B. Okun', Ye. L. Fcynbcrij,
L. P. Fcoktistov, A. Ye. Chudakov
Cord

ACC NR;
Lr-*Vio--'O~-' ~f :;kc llh;'~~3ical ard Technical Problems of Ercrgetic3. N. S.
Ear-h Sciences. Yu. D. Bulanzhe, P. N. Kropotkin, V. V.
Rzl,-,e-,,s"--,*),, B. Ronov, Ye. F. Savarenskiy, Ye. M. Sergeyev, A. I.
Tugarinov, V. Ye. Khain
of '~L-Uhanics and ControZ Proccese;,- G. S. Bvushgens, S. V.
Vallander, S. S. Lavrov, N. N. Moiseyev, I. F. Obraztsov, G. S. Pospelov,
V. S. Pugachev, B. V. Raushenbakh, G. P. Svishchev
Division of' General mid Technical C;?crnst!-i. N. S. Yenikolopov, Ya. it.
Kolotyrkin, A. A. Petrov, A. S. Sadykov
7 ~a a s
5.~~z,,isicn of the Physical Chemstz-j and Te-6:wZog I of Inort anic A tem Z
R. S. Ambartstmyan, V. V. Kafarov, B. N. Laskorin, Ye. M. Savitskiy
of the Biochemisti~i, Biophysics, and Chcrristr4 of PhysiologiccZ
A-,"iVe C'-.--71oa:ds. M. V. Vol'kenshtcyn, M. N. Kolosov, M. A. Prokof'yev,
t.. S. Spirin, A. A. Shlyk
:~iviaian of PhycioZogy. 0. G. Gazenko, P. G. Kostyuk, A. M. Ugolev
of Cencral BiOZO,7'11. A. P. Andriyashev, M. S. Gilyarov, A. L.
Takhtadzhyzp, S. S. Shvarts
co'd 41/5
ACC NR: AN-7011025
Yu. V. Bromley, Ya. S. Grosul, Yu. A. Polyakov,
V. L. Yanin
Of and Law.- C. A. Ak~Lnenok, D. A. Kerimov, T. T.
Oizerman
V. A. Vinogradov, A. C. Nilcykovskiy, T. V.
Ryabuslikin, G. Solodovnikov, T. T. Tii-..o;.'cycv
L,'-terature Languare M. N. Bogolyubov, D F. ',ar v
q Ico
A. A. Bor'ovkov, G. S. Gorshkov, M. I. KarFapolov,
N. N. Fuzyn;v, m. c. Slin"&O, V. P. Solone-nico, L. V. Tauson, N. N. Yancnkc)
~A:-, D Pr e s s :5012-fv
SUB CODE: 05 / SUBBM DATE: none
Card

j."I
.' A 1.
LUIDYUSHEV, H.M.; SIBGATULL114) Kh,A.
Perforation of the stomach by a second ulcer after suturing the first,
Kaz. mod. zhur. no.6157 N-D 761. (Mliv~ 15:2)
1. Shugurovskaya bol-aitsa (glavnyy vrach - Kh.A. Sibgatullin)
Leninogor,gkogo rayona Tatarskoy ASSR.
(STOMCH-ULMS)

KILIDYUSIIEVSKIY, P. F.
Ehysics-Study and Teaching
Development of the thinking of students in physics classes. B.F. Killdyushevskiy. Fiz.
v shkole no. 5,1952
Mont List of Russian Accessions, Library of Congress, December 1052. Unclassified.

KILIDYUSHEVSKIY, I,D.-
~
Pollen in the arctic atmosphere. Bot.zhur.40 no.6:657-860
N-D 155. (MLRA 9:4)
(Artic regions--Pollen)

XIL-'DTU.51W-VSJaT, I.D.
Mosses of the Polar Urals. Trudy Bot.inst.Ber.2 no.11:313-33 156.
.,2
(Ural Mountain region--Xosoes) (MLRA 10:2)

KILIDTUSHEVSKIY, I.D.
-1, . , I , . " -C, ,
Development of some species of the flora of Malyy Yamal under
the snow. Bot.khur. 41 no.11:1641-1646 N 156* (MRA 10:1)
1. Botanicheekly inatitut imeni V.L. Komarova Akademii nauk SSSR.
Lenin.-rad.
(Yamal-Venets National Area-Plants-Frost resistance)
(Snow)

KILIDYUSHNSKIY, I.D.
Conference on Alpine flora and vagetntion. Bot.Ehur. 43 no.10:
1519-1523 0 158. (MMA 11:11)
1. Botnnicheskly institut imeni V.L. Komarova AN SSSR, Leningrad.
(Alpine flora-Congresace)

-KILIDYUMVSKIY, I.D.
Recent data on the relation between the vegetation of tundran and
the Alpine mountain belt. Bort. zhur. 44 no.2:235-239 F 159.
(MIRA 12:6)
(Alpine flora) (Tundras)

KILIDYUSHEVSKIT, I.D.
Some structural features of vegetation on the eastern slope of the
subarctic Urals. Bot. zhur. 44 no.7:929-942 Jl '59.
(MIRA 12:12)
I.Botanichoskiy institut im. V.L. Komarova AN SSSR, Leningrad.
(Ural Mountaino--Phytogeography)

POSTNUOT, Ivan Hatvayevich; KIM, X.I., red.; MUTHIKOVA, O.S.,
takhn.red. -------
fxectric machinery; brief course) Blektrichaskie mehiny;
tratkii kurs. Moskva, Gos.energ.isd-vo, 1960. ~24 p.
(XIU 14:4)
(Ilectric machinery)

4IL-II)YUSHMKIL I.D.-
Formation of vegetation in the southeastern part of the Verkhovansk
Hango under different environmental conditions. Probl. bot. 5:62-71
16o. (MIRA 13:10)
1. Botanicheskiy Institut AN SSSR, Leningrad.
(Tomponskir District-Mountain ecolog7)

KILIDY[ISIEEVSKIY,- i.D.
Some results of research bi~ Qw North; a conference on.the'jproble=s
of researchp utilization and protection of the vegetative cover
of the Far 'North of the U.S.S.R. Bot. zhur. 47 no.7:1067-lMO
i1 162. (I-Imp lf,:g)
1. Botanicheskiy insfitut imeni, V.L. Komarova All SSSR, Leningrad.
(Russia; Northern-Botanical reset,.r,ih--Congresses)

c~ V,. I

I.D.
Cmpllng a field guldo to mos5eB and liverwurta. But.zhur. "49 no,11~
N 164. (MIRA 2821)
1. Bctan1ch6skiy institut imeni V.1..Komarovu AN S~SR, laningrad.

HUHN, A. (;.
35525. Razviti yo GritOlroy Ehirurgii Na ". kra I ~ e. V 5b: Voprosy Gru~;noy
Kllirurgii. T. 111 . 1'., 191.1), c. 1V-21.
Letirisl Zhumallry~-h Sltite~,, Vol. 4~1~, 1 osl:va,

K I LEIfuI
"Bibliograpkv of t"ne ~iungarl-m geoloa and related sciences in 1)52.11
. .11 i
(FOLDTANI K07L-jjjy. 'PLI.ETIN OF THE TFIGAHUI U-,.OWjICAL 30CL~,Tf, Vol. 83, No. 113,
Jan/Mlar. 1953, budapest, Hungary)
,30: .1 Vol. 2 'k). 7, July 1)~3, Uncl.
ilonthly List of Ea.3t Lkropewi Accessions, L.r,.,,

ADAM, Oszknr,; KII.;.NYI., E.Va
Determination of approximate velocity functions by means of
refraction travel time curves. Geofiz ko-.1 12 no.3/4:67-78
16-1.

YJUNYI 1 1.
Bibliography of Hungarian geology and related sciences in 1954, p. 260,
FOLDTANI KOZLONY., BULLETIN OF THE HUNGARIAN G"LOLOGICAL SOCIETY) (Mj'p-yar
Foldtani Tarsulat) Budapest, Vol. 85, No. 2. Apr./June.. 1955
SOURCE: East European Accessions Lii~ (EEAL) Library of Congress,
Vol. 4. No. 12, December 195D

NM3WOVj, G,, gornyy dispatcher; KITS UO A.; DEMA, A.
Mine,ro and theSz lodging house. Say.shakht. 10 no.8:34-35
Ag 16le (MMA 14:8)
1. Shpkhta No.8 k=binata Primorskugoll (for Nekrasov).
2. Komendant obahchezhitiya shakhtoprokbodehookogo upiavienija
No.29 Popasnyanskiy rayon,, Ieganskaya oblaot' (for Demina).
3, Hashinist vodootliva. shakhty imeni StAlina v Iugans,koy
oblabt (for Kilepu). (coal miners)

Ka---R, K.
New type of a circulating pump for an all-glaBB apparatus. p-849.
CqEMICKE LISTY (Cheskoslovenska akademic ved. Cheskaslovensks
spotlcn,Dst chemicks) Paraha, Czechoslovakis. Vol-53, No.8, Aug. 1959.
Monthly List of East European Accensions (EEAI) W , Vol.9, No.1, Jan. 1960
Uncl.

I. KILER, Mirko, strojar
Regulating the Sulzer single-tube steam boiler installation
with cupercritioal steam prosoure. Pogon 2 no.11/121179-186
N-D 161.

ZELEPUYdIA, Sof Iya 1vanoTna; KILERQG,_ILJL [Kilieroh, N.M. I I red.;
BEREZOVSKAYA, D.N.tNerezovs1ka, D.N.1, tekhn. red.
[Antimicrobial properties of edible plants) Antymikrobni
vlastyvosti, istivnykh roslyn. Kyiv, Vyd-vo AN URSR, 1963.
51 p. (MIRA 170)

KOLCHYNSKIY, Illya Grigorlyevich[Koichynalkyi,, I.H.1; NILEROG, N.M.
(Kilieroh, N.M.], red.; DAKHNO, Yu.M., tekhn. red.----------
(Observatories in space]Observatorij v Kosmosi. YViv, Vyd-
vo Akad. nauk URSR, 1962. 46 p. (MIRA 16:3)
(Outer space-Exploration)

NEKRYACH, Yevgeniy Fedorovich;_Kll&RQG
,_ _NM. [Xileroh, N.M.), red.
AaA-va; DAKHNO, Yu.B., tekhn. red.
[Polymers in technology and everyday life]Polimery v tekh-
nitsi i poveiakdennomu zhytti. Kyiv, Vyd-vo Akad. nauk
URSR, 1962. 63 P. (MIRA 16:3)
(Polymers)

FIDOFLICHRO, Ivan Grigorlyevich[pidoplichko, I.H.1 PUSHBA,
Yakov.1cvnn[Ruw1,ba O.IA.1; KILF'POG, L.M. ~ Kilo rcl-,# I, ] ,
p , .
red.
[Origin and developont of life on the earthl Pokhod-zhen-
nia i rozvvtck Aryttin na --emli. Kyiv, Na"..va dumka,
1964. 73 p. (11111,iA 18:2)

KIL!-~!&X, A., Y'VXylr:-lV, D., hUR?AKOVA) V.9
'l ;;., ;.:TKk"Ll'IY!Vz;-,~l," U.
I;T~;F, ?IT u v ) - .. I -
Cir-.'.77,11, -'T.
'7A? -~"T
KILF3,~C A. 'f.,
r,T~l X-EV, F. I KOL.'Xi V K 1"':
V.
Nestprc,~--, V. "".
7oreno-;t forester of tlie c,~"Untr~,. lrs i.
ste )' 11 10. 5, 1952.
Lil,rar.- of Con-ress '.11
.ontlily L, A of Russlan ,iccessions,

KIT !M0, A. T.
Sovremennve desantnye sida. CModern landing crafts2. Yoskva, Upr. voen.-ziorskogo
izd-va NK~T Soluza SSR,1945- 117 P. (Biblioteka ofitsera
NN I IN C DLC: V895-K5
SO: Soviet Transportation and Communications, A Bibliography, Library of Congrassil
TefTte-nce Department, Was-hIngton, 19-52, Unclassified.

JUIESSO, A.
Powerful Icebreaker-barees. Mloahey Flet (Merchant
Fleet). Issues Nos. 5 an& 6, 194r).

KILICSSO, Avks*ut.4_jUjch; MOROIZOVSKIT, N.G., kentr-admiral, redaktor;
'RItM3ViCH, G.I., rodaktor; IrCINTOROVICH, A*I.. tikbmichookiy
redakt*r.
(Auxiliary vessels of the imperialist povers' Vapenegatellayl flot
j
imperialistichookikh gesudarsty. Pod rodik.N.G.Morozovskogs. LaziR-
grad. Go*. setuzzoe Izd-ve sudestrolt. pronyahl., 1955. 503 p.
(Ships) (KLRA 9:5)

KIISSSO. Avkaoniy Illich; VASILIYEVt I.V., red.; ZUDINA, M.P., tekha.red.
ps- a,nd-vessels of thn navy] Korabli i suda voenno-morskoro flota.
Moskva, Voen.12d-vo H-va obor. SSR, 1957- 193 P. (MIRA 11:2)
(Sbipa) (RuBsia--Navy)

A.I.; KUZIMINA. V.S., red.; KISINA. Ye.l., tekhn.red.
Equipment for raising and lowering fishing boats] Ostroistva
dlia pod"ema i spiska na vodu malykh rvbolovnvkh sudov. Moskva,
Piolichepromiedat, 1957. 154 P. (NIRA 11:2)
(yishing boats)

KILESSQ,..A..I.; FAW4,AZYAN, R.A.; KONONYUK, B.Z.; VARTINSEN, Z.A.;
ANDREYEV, N.V.; SLAVIN, S.V.p- RUSETSKIY, S.B.; GLUSHKOV,
V.P., otv. red.; PLISKINA, Ye.M., red.; TIKHOMIROVA, S.G.,
tekhn. red.
(The shipbuilding industry of capitnlist countries) Sudo-
stroitelInala promyshlennost' kapitalistichaskikh stran.
Moskva, Izd-vo AN SSSR, 1963. 471 p. (MIRA 16:10)
1. Akademiyn nauk SSSR. InstJtut mirovoy ekonomiki i mezh-
dunarodnykh otnosheniy.
(Shipbuilding)

-,_ .,'!vksontiy Illich; , ilLZII., retconumt;
YINDI~:*I-%Ii!~V, N.I., nsu,21iri. red.; red.
[i-.odern i~.acfiitic shop shipsj' Sovreii,eririye
l.eningrad, llouaostraenie," 1964. 2/~') p. 17:8)

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mmutwit;W91 mavesite brick and saw methods fat its U" in metalluW
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Mauch.-Tokh. Isdatelst" C hernoi 1, Tsvetnoi Metallurgii, Moscow,
1933. p. 81-108.-A detailed analysis of various magnesite and
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