SCIENTIFIC ABSTRACT G.N. DERIM-OGLU - G.I. DERKACH

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000310210014-9
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: January 3, 2017
• Document Release Date: July 27, 2000
• Sequence Number: 14
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

DERIM-OGLU2_G.IL., iiazh.; PISAREV, A.L., kajad.teklin.nauk
Series of autput-type a.c. magnetic amplifiers for contactleas
control systems. Vest. elcktroprom. 34 no.1:26-31 Ja 163.
(NIRA 10:1)
(Magnetic amplifiers)

IMMIF, A.
-- _
Fluid relays, On tokh. 3 no,9;45 -9 '58. (MIPA 1-1;10)
illectric relays)

DERING, A.
The low-freque:.-icy selective amplifier.
P. III. (LACZHOSC) (Poznan, Polandi) No. 1, 1956
1
30: Monthly Index of East European Accession (EEAI) LC Vol. 7, 110~ 5, 1958

L 34453-66
ACC NRt AP6026191 SOURCE CODE: P0100-2-27V310-007001 di-M&
AUTHOR:_ N rinL, _Mw,(Haster engineer)
01G: none
TITLO: Matched filters
SOURCE: Przeglad elektrotechniczny, no. 1. 1965, 13-16
TOPIC TAGS: electric filter, pulse signal
ABSTRACT: The article defines a matched filter as a linear filter
Which maximizes the ratio of peak signal power to mean noise power.
This aspect.is analyzed mathematically. In addition, several import-
ant characteristics of such a filter are discussed, i.e. its fre-
,quency spectrum, its impulse transfer function (response to the
;DIRAC delta) and others. This type of filter is viewed as the opti-
'MUM system for detecting pulse signals against background noise, its!
performance is compared to that of -the inversion filter, It is also
viewed in-terms of "encoding" and "decoding"s It is pointed cut in
,conclusion that the matched filter can serve as a model or standard
tor the performaace of other filters but that it itself can lie reQl-'
only in "prbximationa Origo arte has: 2 figares and 24 form)2aso ZJTR_s7
SUB CODE: 09 / SUBM DATEi none / OTH REF: 003
3 UDC:

DERING A,)),.,, glav. red.; TUROV, M.G., zam. glav. red.; BERZON,
E.M., red.; BUCHKIN, N.A., red.; KOZIOV, V.K., red.;
NAYMhRK, I.I., red.; NIKOLAIEV, K.N., red.; SUSHCHEV,
N.N., red.; TERESHCHEMO, Ts.I., red.; YUNMEYSTER, A.B.9
red.; PULIKINA, Ye.A., otv. za vyp.
(RepDrts on the technical level of the manufacture of
reinforced concrete productB] Sbornik dokladov ob urovne
tekhniki proizvodstva zholemobetonnyl:h isdelii; informa-
tsionnyi material. Leningvid, Otdol tekhn. informatsii.
No.3- 1959. 81 p. (MIRA 16:11)
1. Leningrad. Vaesoyusnyy nauchno-issledovatel'skiy in-
stitut po mashinam d1ya promyshlennoati stroitellnykh
materialov,
(Reinforced curcrete products)

IWATHTS, Ye.V'.; MMKO, L.D.j MUSIMOV., A.I.- G)ROVMO, L.I.; WRING,
Aj. 1, DRAKE, L. V.
Treatment of pulmonary tuberculosis vith phthivaxide inhalationso
Vracb.delo no.1laUl-142 14 162., (MI31A l6s2)
1. Otlastnoy protivotubefk~leznyy dispanser g. Nikolayeva,
perveya bollnitea g. Vikolaye7a, tuberkuleznoys otdeleniye
detskiy tuberkulmanyy sanatc-riya No.1 g. Rikolayevao
(TUBERCUMSIS) (PHTRIVAMDE)

'174-111CA 12 1101. 12/8 Ophth. Aug. 58
1.183. ROENTGEN DIAGNOSIS OF AFFECTIONS OF THE LACRIMAL PASSAGES
(Russian text) - De.Kipg A. S. - 14EDGIZ (Moskva) 1956 (63D pages)
In- the general part ana-to-rfiy-ii-nT-pli-y-grdlog5,, clinical examination molthods and
roentlgcnography of the lacrimal passages are outlined. Bismuth nitrate is recom-
mended as a contrast medium which will give et suffic.iently good shadow, which is
siable in vaseline paste, and whKch is practically non-irritant to the lacrimal ducts.
To prepare the emulsion the finest bismuth nitrate powder is thoroughly stirred
with vaseline until a consistency of a thick cream Is obtained. It Is best to prepare
it immediately before use. Roentgenography is done immediately after introduction
of the paste. To obtain a frontal view the pa tient lies down in a chin-nose Position.
A lateral view Is taken only to make the roentgenologic picture more exact. In the
special part of the book various roentgenologically demonstrable changes in all
parts of the. lacrimal passages are discussed. Roentgenologic changes are related
to clinical manifistations of the pathological process. The book is illustrated with
73 roentgenogramni References 42. (S)
W I

LZRING, B. Ye
"Arterial Blood Supply of the Kidnvy in the Direct and Indirect Circulation
of a Rabbit. Experimental and MorphologLcal Research on Rabbits." Cand Hed, Sci,
L'vov State Medical Inst, Chair of Anatomy, L'vov, 1954,- (KL, No 1, Jan 55)
Survey of Saientific and Technical Dissertations Wfended at USSR Higher
Educational Institutions (12)
SO: Sum. No. 556, 24 Jun 55

USSR Hun, an and Animal 1~,:oi:phology,(Normal and. Pptj~olo,-j_c,~111.S
CardiovaseDlar System.
Abs Jour Ref ~hur -' Biol., ITc, 21; 1,058, No 971o6
Author Derin&,_B.Y&v---
Inst Lvov Obl,-st Scientific Sociotir of Anatomists,
Histolor4ists and EmbryoloFists
Title Arteries of Lymph Nodes of the ?elvic 3xtrenity and
Their '-articipction in Collateral Blood Circulation
(-."kni!tomo-'~':~-,Pcrizie,ntal Investigation).
Orig -Pub Sb. nauchn. rebor Lfvovsk. obl. nauch. o-vo anstamov,
gistol. i ernbriol... 1958, vyp. 1.. 52-56
Abstrcet It was shown in 20 rabbits at the ages of 6 nonth-s-2
years., that lymph nodes (LIT) of the hiind extremity are
supplied 13- 1-3 arteries of the necrest trunks; besides,
the supplying arteries, approaching the LN, -nastamose
bet-ween themselves, In experiments with e-Cclusicn of the
externol ilice nrt4)ry, it was determined thpt in the develop-
ment of collaterol circulation, the bi-,nches which suppler LIT

SOV/1.24-58-3-2834D
Translation from: Referativnyy zhurnal, Mekhanika, 1958, Nr 3, p 41 (USSR)
AUTHOR: Dering, 1. S.
TIT LE: A Study of Ash-precipitating Devices Operating With the Introduc-
tion of a Water Spray Into a Gas Stream (Issledovaniye zolo-
ulavlivayushchikh apparatov, rabotayushchikh v usloviyakll
vvedeniya v potok gazov raspylennoll vody)
ABSTRACT: Bibliographic entry on the author's dissertation for the degree
of Doctor of Technical Sciences. presented to the Odessk.
politekhn. in-t (Odessa Polytechnic Institute), 1957.
ASSOCIATION: Odessk. politekhn. in-t (Odessa Polytechnic Institute).
Card 1/1

VIKOLIM., V.Ya..-, Prim'-gli uchastiye: MSH, L.J.;
Preparation of higWLy dispersed silicon dioxide. Kh1m.prome nool:
48-52 Jla 162. (MIRA 15:1)
1. Nauchno-isoledovatellskiy institut otinovnoy klWui:L.
(Silicon ootide)

NIKOLINL, V.Ya.; KNYSH, L.I.; DERING, N.A.
Preparation of highly dispersed silicon dioxide by va~or-phase
hydrolysis. [T~rudyj NIOKH114 35:64-75 163.
(MIRA 18:2)
I

DERING., S. A. Cand. Med. Sal..
"Optico-Ciliary Reseetion and Its Influence on Intxa-Ocular ]Iressure,,"
Vest. Oftalmol... No.l. 1949
ODtical Dtseaseis Clinic, Bashkir Med. Inst,

WWDM" ~n' c - BRLOSTOTSKIY, Ye.M., radaktor; BELICHIZOVI,
yt, 1:1: 1 416r
kete'a- i6isk radaktor
[1-ray diagnosis of diseases of the lacrywl ducts) Rentgeno-
diagnostike zabolevanil slazootvodiashchl.kh puteis Hoolkwa, Go@.
izd-vo mad. lit-ry, 1956. 58 pe (?LIRA 10:3)
(IACRTMAL ORGABB-DISICASES) (DIAGNOSIS, RADIOSGOPIC)

DERING, S-ALL kcund.med.nauk
Cuse of retrobnlbar axial neuritia following the Intra-EXterial
administration of penicillin. Oft.zhw. 14 no.4:245-24-8 1159.
(KIRA -(2: 10'.)
1. 1z U-skogo Voyenno-Morskogo gospitu'Lya.
(CP21C IMRVB--DISMS3S) (PHNICULIN-TOXICOLOGY)
(INJUTIOITS, INTRk-ARTERIAL)

DEMG, S.A., kand.med.nauk; SHEKHAM,O.V., vrach (g.Nikolayev)
Stable spasm of accommodation in diseases of the central nervous system.
Oftozhure 15 no.7;426-431 160. 11MIU 13:11)
(NERVOUS SYSM-DISPEASE15)
(EM-ACCOMMATION AND REFRACTION)

DEENGAS, L.N.
~-'
Some organizational suggestions to improve the work of for~-,nsic
medicine experts, Bud.-med, ekspert, 8 nool:50-51 Ja~'Ar 165.
(MIRA 18:5)
1. ShELulyaskiy mezhrayonnyy sudabnomaditsinskiy eksFert.

Trs' j i7
C.;D
0 c 1 Z'cl 0 t1-
31 'RO-.-.)rO due tions Ac 00 WOi!.'ht and tha I.Lino
L 'a I
Case of tho IT'-- ::a' Brood*
in
C)
U 7Z;
_aTE'? 7"~~ 3u c

DERIN-OG U. G.N.,, inzh.; PISAREV, A.A. kand.teklm.nauk
P
Magnetic amplifiers vrith a.c. output fc-r noncontact control
systems. Vest.elektroprom. 33 no.6:47-51 Je 162. (MIRA .15:7)
(~~gnetia- amplifters) (Automatie control)

DERIPASKA M V
Combination elie of sinple design. Kuz.-shtam.proizv. 4 no.123
45-46 D 162. (MM 1681)
(Dies (Metalworking))

SILKAY A.N.; DERIPASKO, N.N.
Constant level regulator of a dephenolization system. Koks i khim,
no.2:39 162. (MM 15:3)
1. Makeyevskiy koksokbi-icheekly zavod.
(Separators (14a.chinery))

DERIPASKO P.G.; KOVALEV, G.V. ve-berinarnyy vrach; GRIGORIYEV, N.n,.
9
Reducing echinococcus in sheep. Veterinarila 42 no.9:45-46
s 165, (MIRA 18-.1-1)
1. Nachallnik voterinarnogo otdola Nauchno-isi3ledovatell-
okoy veterinarnoy stantaii Cheaheno-In1jushokoy ASSR (for
Deripdako). 2. Veterinarn;ry otdol Nau,chno-isoledovatell-
okoy voterinarnoy stantaii Ghoclieno-Ingrushskoy ASSR (far
Kovalev)., .3. Zaveduyushchiy otdolom pixazitologii Nauchno-
issledovatellskoy veterina:moy stantsiJ. Checheno-Inguahskoy
ASSR (for Grigorlyev).

qK0, P.G.: DKITRIUMIT. L.K.;
Rjin ICHO P.Ye.. prof.: Jyq;~, -n&T=V, G,,DA;
SUKWI V.akj.; P.O. Yetvraoh.
Poisoning of cattle by oorn silage contia6minated by pathogenic fungi.
Yeterinarita 35 no,4:79-81 Ap 158. (KIR& MY)
1. reesoyasnyy Institut eksperimentallnoy veterinarii (for Radkevitsh).
2, 11achallnikvatotdels, (for Daripasko). 3. Starshiy vetvrach vet-
otdola, Groanenskogo oblaellkhompravlowkya (for Dmitriyevokly).
4. Dir*ktor oblyst7baklaboratoril (for %,vydov), 5. Zaveduyushohiy
khimicheskim otdolom (for Saakyan). 6. GIavnyy vetvrach Groananskolgo
rayonEL (for Fink). 7. Irolkhoz iment I-ga May& (for Atoyan).
Wattle-,Diseases and paste)

DEMIDOV, 14N., kand.veterinarnykh nauk,- DIWFASJiQ,,__F._Q., r arnyy vrach;
__rte . in
ROVALEVY G.V., vaterinarnyy irrach
Application of difluorotetrachloroetbame in cattle fascioliasis.
Trudy VIGIS 6:216-220 159. (MIRA 15:5)
1. Gromeaskoye-bblutne" upravleniye sel'skogo khozyaystva.
(Liver flukes) (Parasites-Cattle)
(Anthelmintics)

DEFJPASKOP POG6
- ---. .- -, 7- .-- ~- -. . I I-
Epizoc.~io-iogy of leptoopirosis ilL cattle. Veterinrlia 41 no.W"~-
28 Ag 164, (MIRA 18i.4)
1, NEtaluillnik veterinarnogo otdela Miniaterstva proizvodstva i-
zagotovok sellskokhozyaystvannykh produktov Cliecheno-Ingushakoy
ASSR, '

1. DERISHCHEV, M. G.
2. USSR (600)
4. Peanuts
7. Ciliation of gynophore and pod of the peanut. Bot. zhur., 37 no. 6,
1952.
9. Monthly List of Russian Accessions, Library of Congress, Mardh 1953.
Unclassified.

USSR / Cultivated Plants. Commercial, Oleaceous,
Sugar Bearing.
Abs Jour :Ref i'%ur - Biologiya, No 2, 1959, No. 6347
Author :Derishchev, It.
Inst - 0 c ent. R a. Inst. of Oleaceous and
Essential Oil Crops
Title Selection and Seed Cultivation of Sunflowers
In the Altay Krey
Orig Pub :V ab.: Kratkiy otchet o nauchno-izsled. rabote
Vaes. n.-i., in-ta maslichn. i efiro-maslichn.
kul'tur za 1956 g. Krasnodar, "Sov. Kuban"',
1957, 31-35
Abstract :The selection experiments wi-.h sunflowers
started in 1956 In the arid zone of the Altay
Kray (Kulundinakaya Steppe). The 8392 variety
of VNIIMK (All-Union Scient. Res. Inst. Oleac.
Card 112

USSR / Cultivated Plants, Commercial, Oleaceous, m-4
Sugar Bearing.
Abs Jour Ref Zhur - Biologlya, No 2, 1959, No. 6347
Crops) which took the first place because
~7
of its yield of seeds ~,.2 cwt/ha) and oil
(2.47 cwt/ha), showed itself as a good
prospect for the steppe part cf Altay in
the competitive variety tests in 1956. Many
numbers with a shorter vegetation period
than the 8883 variety were found In the nursery
dedicated to the eva3luation of the descendants
of the 8883 variety. Amon3 them, No 291
which has a vegetation period, shorter by 12
days than the 8883 variety, surpassed the
latter by 25% In yield. -- 0. P. Plyusnina
Card 2/2
94

R17_waA Pharmacology, Toxicology, Analeptics U-3
,,.Xbs Jour i Referat Zh.-Biol., No 1, 1968, No 3388
Tanas6scu, Gh., Costesou G., Ionesou G., Tanase
Author RqZrLiv,
I., Dimitriv M., Manesou M., Carp, N., Neasouf C,,'
Grigorescu-Simionesou G., loneou C., Nitulesou, F.,, Sib-
ioeanu Gh, Voioitu., Al.
Inst i Not given.
Title 2 A Study of Sulfur-Containing Amino Acids (Methionine,
Cysteine, Cystine), Cyclic and Haterosyclic Amino Acids
(Tyrosine, Tryptoph&n, and Histidine), Nucleic Acids (RNA
and D14k), Proteases (Trypsin, Cathepsin, Dipeptidase and
Carboxypeptidase) and of Nucleases (Ribo-and Desoxy-ri-
bonuclease) in the,Cerebral Cortex of Itts Under the In-
fluence of Luminal and Benzedrine.
Orig Pub t Bul. Stiint. acad. RPR. Sec. Mod., 1955, 7, No 4, 1193-1208.
Abstract a A study was made of protein and nuoleio acid metabolism in
Card : 1/2

M.M.&MA / Pharmacology, Toxicology, Analeptics U-3
Abs Jour : Referat Zh.-Biol., No 1, 1958, No 3388
Abstract : the cerebral cortex of rats during a state of luminal-
induoed depression and of benzedrine-induced excitement. It
was shown that under the influence of benzedrine there was a
decrease in the amounts of oysteine and cathepsin; there
was no change in the tyrosine and tryptophan contents When
luminal was administered, the amount of cathepsin was in-
creased and that of tyrosine and tryptophan remained un-
changed. No alterations in the activity of desoxy-and of
ribo-nuclease were noted during excitement. During a statet
of inhibition, an increase in the activity of both nuoleases
was observed, whereas there was no change in the amount
of RNA and D1,Lk. The authora conjecture that during sleep
anabolic processes predominate over catabolic processes,
Card 2/2
I-

1 .
Piece of wquiplaent for climbing trees. Le--. khoz. 5, .:o M`~ 1952.

V c, ~ ~ j
AUTHOR:
, _~- L
Deriy, I.G.p (Belaya TBerkovl, Ukrainian SSR) 26-12-25-49
TITLE:
The "Aleksandriyall Dendrological Park at Belaya Tserkovl (Belo-
tserkovskiy dendrologicheskiy park "Aleksandriyall)
PERIODICAL: Priroda, 1957, No 12, pp 96-97 (USSR)
ABSTIRACT- The author gives a detailed description of the "Aleksandriyall
park, now in the possession of the AN of the Ukrainian SSR.
It was laid out in the XVIII century and covers an area of
201.48 ha. The park contains 420 varieties of trees and bushes,
among them century old oaks and valuable exotic trees, such as
a tulip*tree, a black pine, ash trees, weeping oaks and others.
Over 150 different kinds of fruit trees and berry bushes grow
in a separate garden. On the slopes of the Paliyeva mountain,
in the park's south-western corner, many varieties of herbs
can be found which are characteristic of the steppe vegetation,
albng with hundreds of other plants and grasses all over the
park.
AVAILABLE: Library of Congress
Card 1/1

3ZILIY, I.G.
Trees in the "Aleksandriya" Arboretum of the Botanical Garden
of the Academy of Sciences of the Ukrainian S*S.R. Trwiy Bot.
aada. AN URM 5:110-132 158. (MIRA 12:2)
(Kiev--Arboretums)

The Aleksandriya Arboretum. Biul. GlLav. bot. sad& no-30:10-15
158. (MIRk 11:6)
lol)ar&-opark "Alalwandriya" go Belaye, TSsrkov' .
(Belays. TSorkovl--Arbo,.-stums)

DERIY, I. G.
-
- - -------- -.-.
Cand Biol Sci - (diss) "Trees and shrubs of the Belotserkov den-
drological park "Alexandria" and their utilization for land-
Bcaping the Ukrainian SSR.11 Kiev, 1961. 26 pp; (Dnepropetrovsk
State Univ imeni 300th Reut&on of the Ukraine with Russia, Chair
of Geobotany and Higher Plants); 200 copies; free; list of author's
works at end of text (12 entries); (KL,, 5-61 sup, 183)

:DERIY, i.G.
Introduction of Securinega suffru.ticosa (Pall.) Rehd., in the
Ukraine. Biul. Glav. bot. sada no.53rlO-17 164.
(MIRA 17~6)
1. Dnepropetrovskiy gosudarstvennyy universitet.

i I ~F,
- I- - . - ~ \~ i`' ..~_

U ss~
new phalo-purlic lbelbW 014kiemloh~N- lim rvbcLav
1~ 1),may (Glim A-( "fa-milm, I I,5,19J4)~ Tbedi,cclo,~!coinnaiioo
of Ox ofavicily ir.DJ'UIIi pf Shim 1~s dill'a-uh for -1 l,;m)Nl t "i,
of
lmc)ha~ in which Ell'"il sRj~JflWfv alc Lml~,
of thc i~ mois~.ired by poi
i;j the sp.%-ir~~-a ,,ic iwczaLzml by rrWL,-c!"~; -mai; Ddi t X~ I
to"

DEKYEVA., G.M.
Experience in the treatment of glaucoma pati 'ents with DtArsonval
ourrento under ambulatory conditions. Irest,,oft,74 no.lt23-24 161.
(MIRA 14:3).
(GIAUCOMA) (DIATHERMY)

DERMaILYA, V.; MURSALIMOV, A.
---
Problems in the improvement of planning, financing, and
calculating operational costs of grain receiving enter-,
prises. Muk,--elev. prom. 29 no.8:4-5 Ag 163.
(MIRA 17:1)
1. Planovo-ekonomicheskoye upravleniye Yazakhskogo ob*~t-
dineniya khleboproduktov.

IRRIMAN A,; SANV, St.; VELIGIIMVA, D.
Experiences with hypothermia in surgery of congenital cardiac defects.
Miirurgiia, Sofia 11 no.5-6:449-452 1958.
1. Iz Xhirurgichnata klinika. pri ISLTU
(CA'RDIOVASCUTAR DIVACTS, COIIGXNITL4 surgery,
hypothermia (Bul))
(HYPOTHZRMIA,
in caraiovasc. defects, congen. iturg. (Bul))

E R -T A,
Mod ul Mortild humonts upon pullmi)uary neuro-dystrophy I",
by Tagattim1% A, Ti;,,yl, U, VqsAlc~ r~ndj - lii~ Ar~a t
to). Acad- Sci, Atmpi 19M, 0. c~&1144121411111.,. of
tolliculoid, tvgtohl. glyco- and mincrohi-cm tic oid horinvoc-q
Aftrr studied on tht dekTen of long. infiltra,:ion and !-,uFvIvaI time.
follnwing bilateral ccrvical vagotomy fit rati.. The quotictit wt. (if
lui.p (mg.) over b(xiv wt. (g.) was thu measure of lung infiltratimi,
',%1i accortlcolA * (DO",) . slightly inhit;its ir-hitrati,.m and
conAderAbIvrolo"13 survival Linio. Lutvids inhildt devoinjiment. of
;lung I iout all effect oil survivoolAiM4 Folliculineand
tL-3tosterone slightly, corfis,)ne more so, increzim infiltrationand have
Offmt oil survival tim-!. It is bugj,,ri,tcd thit there is a paralleliEnit
twern inhibitory r1fect of lung infiltTaUrn xnd atimsthctic activity
of the lutoids. A. B. L. Bcz--

IERKACa, A.
-......
Relays. Takh.mol. 22 no.5t32-33.40,3 of covor.My 154. MRA 7:6)
1. Student Novochartmeskogo politakhnicbmakego institute.
Mectric relays)

VAVILOV, L.; USHAKOV, L.-,,- PE'RUCH, A.; AKOLIZIN, L.; YUISOV, L., agronom;
YEVMENENKO, L.
Successes of chemicalization. Zaahch. rast. ot vred. i bol, 10
no.1:4-8 165. (MIRA 18:3)
1. Nachallnik Primorskoy stantsii zashchity rasteniy, VJILdivostok
(for Vavilov). 2. Nachallnilc Brestskoy stantsii zaahchil,,v. rasteniy
(for Ushakov). 3. Glavnyy agronom Brestskoy stantsil zanhehity
rasteniy (for Derkach). 4. liachallnik Pskovskoy stantsi,L zaahchity
rasteniy (for Akollzin). 5. Mogilevskiy otryad po zashchite rastenly
(for Yutsov). 6. Nachallnik Gomellskoy stantaii z&shchity rasteniy
(for Yevmenenko).

X-RT.'Acill, A.A., cand Tk-a., 141 -('(U-'C- selection of
ers 1f:T,-;7T7.-: Al:
("in nf Al-jr 71-r.-io-i-ii c~ d f r -I r.; i co-
7)ic'17 (711., 30-!-,c 1120)

..' DIUACH, A.A., inzh. (Kiyev); SIITIKOV, V.M., kand.tek-lin.nauk, dotsent
Iffect of economic factors on the parameters of networlai of
districts with distributed loads. Zlektrichestvo no.5:3.5-
22 my l6o. (MIRA 13:9)
(ZLectric power distribution)

USSR/ Engineering - Glass furnaces'
Card 1/1 Pub. 104. 10/12
Authors Derkach, A.D.
TAle Multi-duct muffle furnace of continuous action
Niriodieal Stek. i ker. 5, 29-30p May 15154
Abstract A description is presented ok a multi-durt muffle furnace employed at the
Ceramic Product Factory in Tashkent, for baking tiles, Drawings depicting
tile above mentioned furnace are presented, together with technical
specifications.
Institution: .....
Submitted:

14-57-6-12695
Translation from: Referativny zhurnal, Geografiya, 1957, Nr 6,
P 130 (US T
AUTHORS: Fasulatin, K. K., Derkach A. D.
TITLE: Composition and Distribution of Coccinellinae in
Trans-Carpathian Region (Nekotory-ye=annyye o sostave
i kharaktere raspredeleniya koktsinellid Zakarpatlya)
PERIODICAL: Nauch. zap. UzhgorQd5k, un-ta, 1956, 'Vol 16, PP 147-166
ABSTRACT: The authors discuss Coccinellinae found in the
trans-Carpathian Region (two species from the-subgroup
Subcocciflellinae and 61 species from the subgroup
Coccinellinae The art-cle describes their distri-
bution thriTu-ghout the area, which is related to the
distribution of fauna anti flora upon -which they feed.
The authors distinguish t,,,be types which are peculiar to
plains, deciduous and conifer forests, meadows, fields
Card 1/1 orchards, and gardens. L. D.

1-COUNTRY
CAII-EfYMY ZooloirJcFil Psraaitolo~-y. Acarldp, An'4, Inspetn I
C Asp:asq VRotors. lnsectB.
A R5 . J D, TR RZUiol., No. 14,1958, No. '526B6.
v Fk no v , K . A Z4-41
T11ST, Astrasihftn Anti.!Plagug Station.
TTTIU, MEArIbution and Dynestalc,.Ei of ULL- NuimberB of
RoO ontzi ' Plans In One o f' the Lo c al I tl ~qs o f the
Slit suhzone In the Northwestern Re~-Ion of*
PT! I
CFIG
Sb. tr. Astrakhanslit, rxotIvochLLrn. Lit., 39~,~,,
. vyp. 1, 289-301.
A qSTL 1,', 01 111L a typinal section for the i-Alt suh7.nqe in
the northweFtern rpaien of the Crispinn Sea
dwell rodents of 13 speciev ; the., most nkinerOUS
ime the "emuranchik," crested and mledsy ger-
bils and the domestic mouse. 3234 flans wero
collected. 11 flea aracles were n~,tild on tho
lIttle beasts, 6 In the bcrrows' entrpncea &TiO
4 In the neats or the "amursnehih." On the
average for 3 years (1951-1953), the highent
abundance Indices of the floss (1) were ob-
served In March-Arril; the lowest (0.3),

fips. JOUR. RzhBicl., Nc. 14, 191:8) ros 62686.
A~: i
T tJ,(,T,
i T T TLE
ORT%G. PUB.:
APST11ACT ! in July. On the midday gerbits, I 14~pt at n
o14-0.4). On the "emursnehilkB," I
low level (0
were the highent (3-5) In the rarlod of manp
awakenins (March) and Fradually diminished
until the state of hib~rnRtion (0-3 In October-
November). In the burrows' entranceej were,
hiphest In March (3-0), t1ien dimiIn1shed towards
su=er and apain IncreaGerl towards autuinn. It
waB noted that the fleas' exabAnqa procoads
CARD: 2/3

C :*" NT C, 0 11 Y
FZhfziol., Vo. 14, 19-54 No.
AUTHOR
RIST.
TITLE
Orin-,
pr"eminently nccnrdln.~ to the dosi;zn - sual."lk -
'~emursnchik' - gerbils - domestiv mouse, form-
inr,, as It were, a chain fron the stal-pe to the
Subantrople rod6n4,B.--R. 13. KOSMInS~,'ly
3/3

DERKACH, A.S... inzb.; SHTETOJ, V.I., irzb.
Characteriotice of the perfornance of automatic alectronic
compensators in electralysia shops. Priborostroenle no.6:26-27
Je 165. (MIP& 1817)

DAMCH,B.; DZRrACE.V.
Self-bralrivC winch. Mast. U91. 3 no.12:19-20 D 154.
(KIRA 8: 6)
1. GlaviWy makhanik shakhty no.4 kombinata Molotovugoll (for
Darkach 3. ) 2. Nachallnik makhanichookogo teekha (for
Darkach,V.)
(Mine hoisting)

IMPTACH B, a
Id _4 --- f
Anniversary of N.K. Gudzii, active member of the Acad zW of Sciences
of the Ukrainian S.S.R. Tienyk AN uRsR'28 no.6t-48-5i is 957. ~
(Gudzii, Nikolai KallinikOTIchl 1887-) (Km 10.-S)

----------------
. P ~ /' h, "i C ty, i~ ~~
USSR/Pharmacology. Pharmacognosy. Toxicology - T-9
Chemotherapeutic Preparations.
Abs Jour : Referat Zhur - Biologiya, no 16, 1957, 71877
Author : Derkach) B.N.
Inst
Title : The Study of the Antitoxic Properties of Antibiotics on
the Detoxification and Desintoxification of Antibiotics
in Relation to the Botulism Toxin.,
Orig Pub : Tr. Kharkovsk. N.I. In,-ta Vakein i Syyorotok, 1956, 23,
25-33
Abstract : The effect of Biomycin (I), s-zine (II) and levomycetine
(III) on botulism intoxication was investigated. To 1-2
DLm (in 0.1 ml of physiological solution) of botulism to-
zin I was added in 0.1-0.8 mg doses, II in 0.1-0.4 mg,
M 0.4-0.8 mg and put into the incubator for 1-6 hrs.
at 37 C, and then injected intravenously into mice. It
vas found that I, TI Euid III have a detoxifying effect
Card 1/2 - 8o -

USSR/Pharmacology. Pharmacogaosy. Toxicology - T-9
Chemotherapeutic Prepwrations.
Abs Jour : Referat Zhur - Biologi.M, No 16, 1957, 71877
on the botulinic toxin; I vas the most effective.
The combined use of II and III, and also of TI and
1, or III and I heightens the desintoxifying effect
on the botulism intoxication.
Card 2/2 - 81 1.

DERKACH, Dentyan Ivanovich; VANCHUK, L., red.; STEPANOVA, N.p tekhn,
[Analysis of the economic opgrations of an industrial enterprise;
in charts with explanationej Analiz khoziaistvennoi deiatell-
nosti promyshlennogo predpriiatiia (v skhemakh s poiasneniiami).
Minsk., Gos.izd-vo BSSR. REd. nauchno-takhn.lit-ry., 1961. 298 PO
(Accoimting) (Industrial management) (IOU 15:5)

DERNACEp D.7a.
Mechmization of the packaging of plastic goods. Plast.massy no.2:71-
72 161. (MIRA 142)
(Plastics-ftakaging)

MMMACH, P.A.; OTCHINNIOVA, A.I., student; 13RXACH, N.A., student.
'JI0~1WHOOMW
Iauk.%tp.L'viv.un.
Corrosion resistance of cadmium-sine alloys.
21:110-120 152. (KL2A 10:7)
1. Kafedra neorganichnoi. khivii.
(Codmium-41ac alloys-Corrosion)

0 _06 i -s-ive-94 a _W__ M_vw
a
ru I 1
A a 41-SLI. J-1 ~"O M.-A-MA J_A_ S_A
T
A

00 a OWWWaullifto Onletuft ia Abuslathim-Ohvit ADM. - (I. J. IN-t-liko &at
0o4 ~A (Mmin. Skim. Mar. (J, VAim. Vkrvipw), 10314. M M. (10-79 t
~
f
h
i
.
t
menta
111% W-fln t7knabditnt.) 71pa purpme o
e expre
t
W
d
h
i
i
inamatten, atruc
um
was to c
ne, l
Orm
ke limits of Uke existence of the
i
in thp silrel-aluminium system. and also the thermal ronditlomi for itit exist.
~
wr1" upM forthrrmitlankilyLlik. while the mat were
riliv. Ithat of1hvftmIAi
ii44vil in air after heeling. Tlwrmal t"Unt-M w&4 v#irtk%f out in a tubular
13
*lectrictuntsixt. ToobviMeikxid&VA^ the sLinploswrto vorreed with active
ewbon and swid. The tymUd samples wore etchttl -with alkali; thtw rieh
In Llumlnlum wrm tmW In Im-drefluoric add. Th~ 'XiA manstatten Imt tent

under Whirb thin structure ApIguit depend on flij- &-priv of saturation of Ow

solid sitlution. In samples w th a mckmatration, of aluntivitau. thia
It a
pattern Is formed at ordinsil ottotivig after cryttidlizat ion from the liquid state
arid dam not require special heatW'ta hiCh temlulinThe solid solution
I.I. " . highr
of thw conotintmilow Is "W&W with y 'r
Aluininium coponntrittim give a 1171tim"WUtten patte-W only after [Wrliminary
livatinit at a high terappraturp fors, long time. Soll,loolutiorworthewoon.
contrationx w not coinviletriv maturatml vilth the v Ishkite.
7;;09
00
see,
-00
0
goo
too
so*
ire 0
Gee,
see
gee
goo
tie*
use
wool 41134110 .11 0MV got 131411194" L11
U a AV el F I Oak
I p tp K a U 9 " 11 tr
0 0 0
40 000 0 0-00

iiliftut RuDai&n scientist and patriott Dmitrii Ivanovich Mendeleev.
Nauk. zap. Vviv. un. 13:27-34 149. (MIRA 12: 10)
lolafedra, obahchey neorganichookoy khimJ.i LIvovokogo goeudarstvannogo
universitata imeni I. Yranko.
(Mendetleov, Dmitril. Ivanovich, 1834-1907)

MIKAGH, F.A. -~
....................
Corrosion of zinc-tin alloys in hydrochloric acid with hydrogen
depolarization. Nauk. zap. Llviv. un. 13,01-102 t4q.
(NIRA 12:10)
1.Kafedra neorganicheekoy Ithimil Llvovskogo gosudarstvannogo
universiteta imeni I* Tranko.
(zinc-tin anove --Gorr o9 ion)

ISRUCHI ~?~ ~ VARSKIY, A.F. (Areivaralkyi, A.P.], student IV kurse.
The chemistry laboratory of M.V. Iomonocov. flauk. zap. LIvive un.
13:137-145 149. (KM 1-.:10)
1.1afedra, naorganichaskoy khimii Llvovsl,,oro gosudaretvannogo
universitate, imeni I. Franko.
(Lomonosov, Mikhail Irasilevich, 1111-1765)

0 0 0 0
0 0 0 40 omoto
V11 I u 10 11 32nid Buys *4 41 Q a a ait o. AT
0 c 0 U 6 is x L a 0 To 4 yl, A F a
e t1 lot ..0
..Do. ... ... . 00
ijAAOP *I PUIA 'p-ta 1H 9v Sq pnwiaw -" auut qd
MlAfp 1-% ---oid op p 03'"
6 ~_
ImrA)dmme ju aanappm M 91 All-p!Aa q*jqA I S + (jj0ftZ + qa
son' :uOjpw eqj JO UD!WUM ap 01 F ive
:va lunlom U"tS 1 11 .~A JO agumul -91fu M Ignv4 "PoOdWWO IM-0 at 90%) ViSTBA JO Ocvwmq GA13" v IV ! -
womm OU
"'Pooi'StYd jo -od-d -j pa= oq a= m". mWaga, U, WADq~ SaIr ITYC" joj jLL= ~UjIlluo,
;9 uolmum 30 Cnvl QU -@MY H IX -amqdmowj% on tit SIpt us jKnu mpuaw q,jZY)q *bK jWL-9
of* f . I it
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-q1 u! flum-V dnojz.qll, qU pmq p"p- -g at&-i2Uq attt jCq piwar-1 (M-w of Pau
P.. p,,,q 'T."m J, "f
MIT = IlHa+ Nuwrio + 2voi *- W991 Of Ima
0!2 vwagjul aql zpY,& torld 1q412K W#X -01raff p, .=V-b
gjjW mplu 9 U, Wnwo wpmo
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91 IPPA pop"Goo I J14M Ing 'ajdmvv wU sqj im ruoll!puaa mee jqj A"n Ile*
Go= go ",004 UUI*Ulw Qp ja ah" 'lug OR4 JO WDP~jdW0
03 Soffe VM jaj a (V, L46 -p- ia. on patq1jou -.nu 4 ul 09
Rl'j' P41M.1 aq AV- ln%L OR$ - 14 SM WPWO0 PUI WUUAM n" A[qLWPPUDQ I nq
V0q*=ftD PM .3 0 0
-M.0 qnjWA IVON%Mtp M UVRI AW
iaq*.Ilq '(W-0 w Sluo.(q MwqMns jnq -rng sum
A411% GWIN QU -jQpAOtj *Mp V MAD; crt
'YO 142ma JO ulvS 'AARTIQ I 'lap, uotworit M mpm rmAAC :gIP go
NK %,:-1; q11A -COUT 941 v"Romo M UO ijppfw ijDA 0ja
01POIna 4ql Sq uollp0qu! 01 91qAO.Cjqt-d 1661.0 1 1" *M- ' vfOunV mv ul Suptusoo tmV gun3on."s ruwd 0 a
lw!14x)Qql otti jo p I . At pav -dm" enpinbil oql "oqv -0 j"
WINU. 01-0 APO "A lufaa UO" -4m 01 PK- I
vqi sw (qj jo wa3re) SH %gj, na Zng tzyvs -r Ima 9 -Nu M-
L%WPjYDjtj1YQA~ IM91 IV F tylov (11 uij--(tm too
AO p
=1 Vqv a t top-ML *(a) 'it 101mc-mm vxm jaw)
P.4
Go- 1, r
I VIPWAS"m "M 79 IT" 15V11WU T _~A 'tqRrwW"0 -8 -A wee
v4sm pw "" "Mommo am"Mam so p OWN
_777
I Ir
0 it to a OF It it 14 a of e1 a R a of a a u a 44 A q% it ti ft it 0 6 1 1 f I I t I no
~I.K1,2'. 4Imwe .11. 9 -
4D a 0 000 0 0 0 * 9 0 1*0 to 0 0

nUKAGH, F.J.
--F
Corrosion of alloys of the cadmium-bismith system In hydrochloric
acid. 11suk.zap.L'viv.un. 21:89-97 '52. (MIR& 10:7)
1. Kafedra neorganlohnoy kh1vii.
(Bismuth-Aadmium alloym-Gorrosion)

MUCH, P.A.; OVCHIINIKOVA, A.I., student; IMRXACH, N.A., student.
__1111111
11111thm
Corrosion resistance of cadmium-sine alloys. Iauk.sap.L'vIv.un.
21:110-120 '52. (KLRA 10:7)
1. Isfedra neorganiobnoi khtaii.
Oadmium-4ine alloys--Corrosion)

RMUCH, P.A.; MOVALEM, V.I., stu&entka.
Corrosion of lead-sine alloys in an alksline mvdl= .Nark.sap.
Llviv.un. 21:121-124 152. (MLRA 10:7)
1. Kafedra neorg&nichnoi kh1m1i.
(Lead--Zinc alloys--Corrosion)

USSR/Pbysical Chemistry Thermodynamics. Thermochemistry, Equilibrium. Physico-
chemical Analysis. Phase Transitions, B-8
Abst Journal: Referat Zhur - Xhimiya, No 1, 1957, 366
Author. Derkach, F. A.., Kolisnichenko, U. M., and Kullbik, 0. G.
Institution: Lvov University
Title: On the question of the Existence of a Limit for the Chemical Sta-
bility of Alloys of the Mg-Cd System
Original
Periodical: Nauk. zap. LIvivalk. un-tu, 1955, Vol 34, 72-78 (publislutd in
Ukrainian with a si ary in Russian)
Abstract: The dependence of the chemical activity of Mg-Cd alloys on the compo-
sition has been investigated over the concentration range from pure
Mg to 60 atom percent Cd in solutions of 0-1 N H2S04 and, in an acetic
buffer of the composition 0-25 X CH3 COOH t 0.25 N CH C )Na The
volume of hydrogen liberated was measured at 100 in C %S'04 solution
and at 250 in the buffer. It is shown that the chemical activity of
the alloys gradually increases from pure Mg to a coneev&ration of

USSR/Ppysical Memistry - Thermodynamics. Thermochemistry. Hquilibrium. Pbysico-
chemical Analysis. Phase Transitions, B-8
Abet Journal: Referat Zhur - Kbimiya, No 1, 1957, 366
Abstract: 5-10 atom percent Cd, after which it decreases fairly rapidly and
becomes insignificant in the region of higIL Cd content. Under the
conditions investigated pure Cd does not dissolve. Notwithstanding
the results of previous investigations (V. V. Skorchelletti and A. I.
Shultin, Khimicheskoye razrusheniye met,ll(!Yi ONTI, 1934). not one of
the theoretically possible stability limita could be established.

2K~ ~AC -ZA,- GOLOVATYY, R.M.[Holovatyl, R.M.), dots., otv. red.;
KVITKO, I.S., red.; SARANYUK, T.V., tekba. red.
(Laboratory work in inorganic chemistry] Praktykum z neor,-
ganichnoi khimii. L'viv, Vyd-vo L'jivalkaho univ., 1962
447 P. (MIRA 16:5~
(Ghemistry, Inorganic-Laboratory manuals)

Trtchlogt~! ~OsasNorfflNodrmwotyl and JI-phosphoryl chloride of
trichloroiminoacetyl Shur.ab.khIn. 26 nooll:2009-2014 J1 1,56,
wai gilo)
1. Dhopropstrovskly metallurgicheslkly Institut.
(Acetyl chloride) (Phosphorus empatmda)

KURSANDV, A.V.-, DERXACH, G.I.
Eaters of /V-phosphoric acid, trichlor-Diminoacetic acid, amd
trioxy-phosphazotrichloroacetyl enter. Zbur.ob.kbim. 26 no.9:
2631-2638 S '56. (MIRA 9:11)
1. Dnepropetrovskiy metallurgichaskiy inetitut.
(Esters)

-4-
--."~'6 -;:7

tv
C
-3d

and tdd -&-Y~~-
g, n 1 Mw
Z~Eur. OblAxhel c C-A 51, 1&21b
Ae I
-Too. 45 -g M, '
atom Na in 0.415
ed 0.015 moic C'C6CON-PCj in :6,40, aftel:
stirring'W miu. the'traxt. wig briz-BY ivkxed a rid hittme
of 7'.5"f" U-I
Uorn AN~M; cooling lidded u ppt
;r
erl,
NCOC71M.M.134-18 (Pct. it is0owl"
by HtO tftycm cw tx Oijug, Ir-jr mplilly ID;t3 one '.q D poup '41
hot 2q. 31c, Roll. To OXO snole 1-C"B'ON3 i3 M 1131-
FO was nddM witb ke voolLax 0.03 mole --C%0 )NUM03
In Mir-), after etyling to 0" the tolu. vn-- rav! Hy syashrd

M. OD-I*. WfuXing 0.04
mole 1-'CjH-O'Xa ln'ft-O -with 0.02 m:)U CCJjC ONWIP06:
10 min., Ritz-6-ag, and e~taj)g. in =cuo gave 6,53% Mr
COJVHFCJ~OC,,1174~ (Mt ri. 13D-41- (Et,01;). ;~~bicb is
%ydml)7,cd ritb rarre diPikulty *.hnn :he walog-Gus 1%
ester. ReAuxiar G.C911 mol', I in 39 rnl. ),'ION nd 2 ml. N:
N5011 Until a 3"In. formej (I hr.), conrg. i.' rcuo, and
adding dil. NAZI nnd eorL-1;: gave 60.9% HL I iydru')Ysis n]

i soln.-whicb on at-Adifientiop
PVC U 1;rtti
jave US% U$L1o;g'Oj1Sly w the, yllpm 0- 1 there

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I!Ut,D), vift); warm&l
)AICC11,
lb W70 Rioll pva ?4.V%a Won. l9q,24.

AUTHORS: Kirsanov, A. V., Derkaoh, G. 1. 79-12-16/43
TITLE: Trichlorphosphazoaciles, Trichloroisopliosphazoaciles
and Their Derivatives
(Trikhlorfosfazoatsily, trichlorizofosfazoatsily i ikh
proizvodnyye).
PERIODICAL: Zhurnal Obshchey Khimii 1957, Val. 27, Nr 129 pp. 3248-3254
(USSR)
ABSTRACT: As it has been shown before trichlorophosphazoaciles of the
RCON = PC1~ type are obtained by the action Of pEintachloride
on the ami es of the carboxylic acids, which on the occasion
of partial hydrolisis form dichloroanhydrides of the acil-
amidophosphoric acids. Up to now only a trichlorcisophosphazo-
acile was known i' e. tricliloroisophospliazotricli.-LoracetyI and
some corresponding triaroxyisopboi3phazoaciles. It is of inter-
est whether also from other carboxylic acids tri,.,hloroiso-
phosphazoaciles and triaroxyisciphosphazoaciles occur or
whether the trichloroisophosphtizoe.ciles occur only in the case
of triohloroacetic acid and ita arialogs. Trichlorophosphazo-
aciles were produced for the diphenylahloracetic acid, tri-
phenylacetic acid and p - nitrobenzoic acid and their thermal
Card 1/2 stability was investigated. It waa demonstrated that

Trichlorphosphazoaciles, Trichloroisophosphazoaciles
and Their Derivatives.
79-12-16/43
i;richloroisophoaphazoaciles occur not only for trichlor-
acetio acid and its analogs but also for diphonylehloracetic
acid and p - nitrobenzoic acid. T3!ichloroisophos;phazotriphenyl-
acetyl could not be obtained, since dichloroanhydride of the
triphenylacetylamidophosphoric acid when thermated has no
durability. The authors obtainod -the di- and t ri. - 0( - napht-
oxyderivatives from the corresponding .3ynthes-zod trichloro-
phosphazo- and trichloroisophosphazo compounds. The syn-
thesized Tri -of- naphtoxyisophosphazo - p - nitrobenzoyl is
the first derivative of trichloroisophosphazoaciles obtained
from crystals.
There are 6 references, 4 of which are Slavic.
ASSOCIATION: Dnepropetrovsk Meta.Uturgical Insilitute
(Dnepropetrovskiy metallurgich.esk:iy institut).
SUBMITTED: October 16, 1956
AVAILABLE: Library of Congress
1. Trichlorophosphazoacile:3 - Chemical analysis
Card 2/2 2. Trichloroisopbosphazoactles - Chemical analysis

D7RUCH, 0. 1., ~r-ml choni Sci-( 5(1 c -, d s
A
and their derivative-c." r:iev, 1915C . 13 pp (Xc-nd Scd In":t
U J* 1--,7,1
of U--cmic ), 120 copies ( ;':L , ") - - r, Q

1 79-28-4-52/60
AUTHORSt Shevchenko, V. 1. , Derkach, 0. 1.
TITLEt Dimethyl Eaters From Aryl Sulfozi-N-Methyl-Amidophosphoric
Acids (Dimetilovyye efiry arilaullfon-N-metilamidofoafornykh
kislot)
PERIODICALs Zhurnal Obshchey Xhimii,.1958,VOI.28, Nr 4,PP-1085-iO87OSSR)
ABSTRAM In recent times a great number of' diesters of aryl sulfonami-
dophosphoric acids were produced (Ref 1). It is, however,
probably not proved that they have amido-like structure
(formula I). However, it is not excluded either that the
compounds of type M are in equilibrium with a phosphor-
azo form (formula Il .
ArSO 2NH-PO(OR)2 ArSO,,,N-P(OR)2(OH)
M (II)
The structure of these diester8 can hardly be explained by
chemical methods. Also for the explanation by physical meth-
ods compounds of structures M and (II) as Samples are ne-
Card 1/4 cessary in any case, A great number of compounds of structure

79-26-4-52/60
Dimothyl Esters From Aryl Sulfon.-11--14cthyl-Am.idopboophoric Acids
11 are known (Refs 1, 2), while compounds of the structure
are unknown. Therefore, it was of interest to alkylate
M
the silver and sodium rialts of the diesters ofaryl sulfon-
amidophosphorio acids. It could be expected in this case that
either phosphorazo compounds or esters of the N-alkylated
aryl sulfonaniidophosphoric acids would form because some
cases ivere known in which alkylation of silver and sodium
salts took place in ono case with nitrogen and in the other
with oxygen.
The authors investigated methylation of silver and sodium
salts of aryl sulfonamidophosphoric, acid and dimetbyl 'esters.
Methylation of sodium salts was unsuccessful. The sodium
salts remained unchanged after long heating with im thyl
iodide on a boiling water batli, while they were converted
into ill-smelling compounds with dimethyl sulfate. On the
other hand, silver salts easily react with methyl iodide under
formation of dimethyl esters of the aryl-sulfon-.N-methylamido-
phosphoric acides
ArSO2NAg.-PO(OCH 3)2 +CH3J -i~ AgJ+ArSO2N(CH3)-PO(OCH 3)2
Card 2/4

79-26-4-52/6o
Dimethyl Esters From Aryl Sulfon-N-Methyl-Amidcophosphoric Acids
By this method compounds of the formula III were produced for
Ar- o-toluylp o4.-naphthyl and P-naphthyl. These compounds re-
act neutrally and are insoluble in alkalies. If boilt for
a long time in aqueous alcoholic hydrochloric acid the com-
pounds of formula III are lWdrolized under fornation of the
corresponding N-methyl-aryl-sulfonamides which proves their
structure.
ArSO 11(CH )-PO(OCH H __> ArSO 1111CH
21 3 3)2 + H20 2 3
The 14--methyl derivatives easily solve in methyl iodide, acetone,
benzene, and boiling alcohol while they are difficultly
soluble in petroleum ethei, and insoluble in water. The com-
pounds of formula III with Ar a %_- and (Z-napbth;l are 0
crystallized compounds with meltinf; points at 91 and 82
respectively. The melSing point3 I the isomeric trimethyl
Pctti,rn are at 84 85 , reapectively (Ref 1).
and 93 - 94
The compound (III) with Ar - o-toluyl could not be obtained
in pure form. The reaction product formed a thic*k, oily
liquid which cannot be distilled without decomposition.
Card 3/4 The mentioned reactions as well as the crystalline form and

79-28--4-52/,50
. Dinethyl Esters From Aryl Sulfon--Iq-Methyl.-Amidciphosphoric Acids
solubility of the formed compounds are described in detail
in an experimental part. There are 5 references, 4 of which
are Soviet.
ASSOCIATION: Dnepropetrovskiy metallurgicheskiy institut
(Dnepropetrovsk Metallurgical Institute)
SUBMITTED3 March 18, 1957
Card 4/4

AUTHORS: lCirsanov, A. V., Derkach, G., 1.; 79-28-5-21/69
Makitra, R. 0.
TITLE: Triaroxyphosphazoacyl (Triaroksifosfazoatsily)
PERIODICAL: Zhurnal Obshchey Khimii, 1958, Vol-. 28, Nr 5i
pp-_~ 1227-1232 (USSR)
ABSTRACT: The similarity of triaroxyphosphazoacyls and triaroxy-
phosphazosulfone-compounds (II) shows up in a number of
common chemical properties so ihat their reactions of for-
mations are in common:
RSO 211 = PC1 3+3NaOR 31JaCl+RS02 11 - P(ORI)3
RCON - PC1 3+31Ta0R I 311laCl+RCON = P (OR I )3
Between them, however, also specific chemical differences
with re-ard to heating and hydrolysis, The compounds M
sDlit off rather easily (depending on the radical) from
tie corresponding triesters of phosphoric acid and produce
nitriles according to the scheme RCOTT = P(ORt)3 ---> OP (OR Q,
Card 1/3 +RCN (III). The compounds (II) are very much stable agai4.t

Triaroxyphosphazoacyl
79-28-5-21/69
heating so that until now there has been no case of
splitting according to scheme (III). They saponify
easily with alkali liquors under the formation of salts
of the diesters of the corresponding alkyl- or aryl-
-sul.fonamidophosphoric acids, but they do not saponify
with water in neutral solutions. Therefore -the synthesis
and the separation of the products (II) do not meet
with any difficulties because of the easy saponifiability~
All compounds (I) saponify on boiling practically quan-
titatively to the diesters of the acylamidophosphoric
acids for which reason the synthesis, separation and pu..
rification of the triaroxyphospha7oacyls takes place so
difficulty; for the same reason in. the experiments care
must be taken that they do not come into contact with
atmospheric humidity. This difference can apparently be
explained by the fact that in the saponification of the.
compounds (I) in alkali solutions the carbon- and oxygen
atoms of the carboxyl-group take par' in the hyCrglysis
and increase the positive charge of the phosphorus -atom
according to the given scheme 1. In the saponification of
Card 2/3 the compounds M) mainly only the nitrogen- and phospho-
j U - -

Triaroxyphosphazoacyl
rus atoms take part
There are 2 tables
Soviet.
79..28-5..2!/69
in the hyarolysis (see scheme 2).
and 7 references, 6 of whi2h axe
ASSOCIATION: Institut organicheskoy khimii AN Ukrainskoy SSR
(institute for Organic Chemistry7AS Ukra-inian SSR)
SUBMITTED: February 22, 1957
Card 3/3

Kirsanov, A. Y., Derl-ach, G. 1. 9--28-7 -36116 A
TTTI,F,: Trichlorioophoophazoacyls of the -.*..rouintic Leriet! (Tri-
khlorizofoc-fazoat9i1,,, nromatiche3kogo ryadi)
.-iP',!)!CAL: Zhurnal obshchey Ithii-Ai, 195-R, Vol. ?V, yr 7, Pr. 18e7-*:'l"--'
OSSO
AB'~-TRACT: Renently obt!-,ined according IV,
the reactions (1), (2) and (3). It %Yn~t of import,-,nne to the
authors to find out whether the reaction (3)
.RCONIIPOCI2 + PC1 5 -> POC1 3 + was of gene.!-!
character or whether it holds only for carboxyl-ic t,cids with
a clearly electronegative character. Itturned out that th-4--,
reaction (3) ir (if general character for acids of the aronz.t.ic
series. The authors obtained trichloraphosphazoncylo of the
type Ecel NPOCI in almost quantitative yields, in which
2
R is of the olectronegative ch.,~racter just mentioned (Tqble 1).
This reaction takas place considerably more slonly r;nd at
higher temperature than (1), and it reminded the nuthors of
Card 1/2 the reaction of 13hosphorus-pentachloride with the N,N-diilkyl-

Trichlorisophosphazoacyls of the Aromatic Series S 011 //7 r! -2- 8 - 7 - 1116 /6,~,
AISSOCIAT ION
SUBMITTED:
amides ofearboxylic acids (Ref 5). The t:7ich1oroisophcsr.-azc-
acyls of the aromatic series are liquid and low melting ery,,7tal-
line products and cleave-off' POC13 on herating ondev the forl-m-i-
tion of nitriles according to the scheme:
RM____NF0C1 2 > POC1 + RCN (4). They are stable in t.-.o
absence of humidity and gan be well stored in closed containc--r~:
at room temnerature. Some trichlorophosphazoacyls and di-
chloranhydrides of acylamidophosphoric acids af; viell as the
co.rreaponding acylamidophosphoric acids, which were dynthe.7izE!d
by the authors and had been unknown before, zzerved ns initial
products. There nre 2 tables and 7 referencess, 6 of -.,.-hich
are Soviet.
In.,jt4tut organ ic hc c':o,, I:himii A~.aderiii nauk Mr-rainskoy ')SR
(Institute of Organic Cheniotryj AS UkrSSR)
Iday 10, 1957
1. Cyclic compounds--Synthesis 2. Cyclic compounds--Properties
3. Acids--Chemical reactions
Card 2/2

AUTHORS: Kirsanov, A. V.,,,,D kach, G. I. SOM79-2b-B-51/66
TITLE: Triaroxyisophos,.Iioazoacyls of the Aroma.ic Series (Triarokaiizo-
fosfazoataily aronaticties.kogo ryada)
PERIODICAL: Zhurnal obalichey khimii, 1958, Vol. '28, Hr 8,
pp. 2247 - 2252 (USSR)
ABSTRACT: Until now only five triaroxyisophosphoazoacyle of the type
RC(ORI) - NPO(ORI )211,tve been synthesized according to
Lhe reaction RCCl ~NPOCl 2+3NaOR' -4 3NaC:1+.RC(OR-)-NPO(ORI )2'
Reaction I, with the notat.ion R and RI). Only one of --Iese
compounds is crystalline. On the basis of the few facts known
the reaction (I) may be considered a Ceneral reaction, or a
conception of the general propcr-~ies of the triaroxyiLlo-
phosphcazo compounds may be formed. In the previous paper
the authorsworked out a general method for synthesizing
the trichloroisophosphoazoacyls of the aromatic series (Ref 3),
which offered the possibility to determine,the limits within
which the reaction might be used in re,,,-ard to the triaroxyiso-
phosphoazoacyls. It was found that this reaction can be used
Card 1/3 in all cases for the aromatic aeries. 22 triaroxyisophospho-

Triaroxyisophosphoazoacyls of the Aromatic Series SOV/79-28-8-51/066
azoacyls and 1-trimei;I-Loxyinoplius.phoazoacy1 ware obtained
in good yield (see the experimental section and table 1).
The properties of these compounds differed sharply from
those of their isomexic triaroxyphosphoazoacyls (Ref 4), as did
those of the triarox.,risophosplIOILZOaCY18 from the properties
of the trichloroacetic acid aeries (Refs 1,2). The triaroxy-
isophosphoazoacyls of the arom-atic series are crystals of low
meltina point and which can be distilled in a hiC;h vacuum
without decomposition. With heating under atmospheric
pressure or at reduced vacuum they carbonize gradually, and
the for,.-iation of triarylphosphates does not occur (this is
a difference from thtn isomeric triaroxyphosphoazoacyls). This
shows that the reaction
.-ieat
ArC(OR) -ITHPO(OR) 2 "' OP(OR) doe3 not occur. The tri-
aroxyisophosphoazoac.Yls of the aLmatic series do not hydrolyse
in boiling water and they saponify easily and quantitatively
only by boiling a-Veous al.',-ali alcohol solutions according
to dicigr_m (II)(sce table 2). There are 2 tables and 7 refer-
Card 2/3 ences, Alich are Soviet.

Triaroxyii3ophosphoazoacyla of the Aromatic Series SOV/79-28-8-51/66
ASSOCIATION: Institut organicheskoy khimii Akademii nauk USSR (Institute
of Organic Chemistry 113 UkrSSR)
SUBMITTED: June 5, 1957
Card 3/3

AUTHOR: Derkach, G. 1. SOV/79-29-1-51/74
TITLE: C-Chloro-P, P-Dimethoxy- and C-Chloro-P, P-Diaroxy Iso-
phosphazo Acyls (C-khlor-P,P-di7,etok0i- i C-I:hlor-P,P-diaroksi-
izofosfazoatsily)
PERIODICAL: Zhurnal obshchey Ichimii, 1959, Vol 29, Nr 1,
pp 241 - 245 (USSR)
ABSTRACT: Recently (Ref 1 ) the authors and collaborators obtained tri-
chloro isophosphazo acyls accoreing to the scheme
RCONHPOCl2+PCI 5 --~ HCl+P0C13+RC(;l = NPOM IV in connection
with the reaction of phosphorus pentachloTide with dichloric
acid anhydrides of aryl amido phosphoric acids. It was only
natural to extend this reaction also to the diesters of acyl
amido phosphoric acids and thus to obtain C-.chloro-P,P-di-
alkoxy- and C-chloro.-P,P-diaroxy isophosphazo acyls (I)
according to the scheme RCONHPQ (OR' )2+PC'5 -~ HCl +PCCl 3+
. 41
RCC1 = NPO (0R1)2 . The compounds (1) are according to their
chemical nature chloric acid anhydrides of diesters of
Card 1/3 N-phosphoric acids of imino acids and are therefore bound to

C-Chloro-P,P-Dimethoxy- and C-Chloro-P,P-Diaroxy SOV/79-29-1-51/74
Isophosphazo Acyls
have on the one hand the properties of chloric acid an-
hydrides of imino carboxylic acids and on the other hand
those of amido phosphoric acids. The synthesis of the com-
pound (I) is of interest as it has hitherto been unl~novrn
and because it is used as a basis for a new type of phos-
phoric acid derivatives. The second reaction proceeds much
easier than the first. In the case of mixing to.-ether e.,-.
Pcl5 and dimethyl ester of acyl amido pho:3ph:)ric acid the
reaction takes place very vehemently already at roqln temper-
ature under separation of 80-9%~,o of hydrogen chloride and 010;6
of the theoretical quantity of phosphorus oxychloride. The
reaction can also proceed without a solvent (benzene, chloro
benzene). The separation of phosphorus oxychloride entails
great losses in the compound (I). C-chloro-F,P-dirniethoxy
isophosphazo acyls are thick, oily liquids cr low-melting
crystalline products so that in contrast to C-chloro-P,P-
diaroxy isophosphazo acyls they cannot easily be separated
in form of crystals. All of them are reactive compounds
Card 2/3 and rather stable in the absence of mointuro. In the case of

C-Chloro-P,P-Dimethoxy- and C-Chloro-P,P-Diaroxy SOV/79-29-1-51/74
Isophosphazo Acyls
thermal separation they form in almost quantitative yields
acid nitriles and chloric acid anhydrides of the correspond-
ing phosphates according to the scheme
RCC1 - NPO(ORI ) 2 RCN + ClPO (OR') 2. There are 1 table
and 4 references, 2 of which are Soviet.
ASSOCIATION: Institut organichankoy khimii Akademii nauk Ukrainskoy SSR
(Institute of Organic Chemistry of the Academy Of SCIAM-aer
Ukr SSR)
SUBMITTED: September 18, 1957
Card 3/3

AUTHORS: Kirsanov, A. V., Derkach, G. I,
SOV/79-29-2-52/71
TITLEs C-Aroxy-P IP-dimethoxyisophosphazoacyl.9 and Mixed Triaroxyisophos-
phazoacyls (C-Aroksi-P,P-dimetoksiizcifoafazoataily i Bmeshannyye
triarokeiizofosfazostsily)
PERIODICAL: Zhurnal obahchey khimii,. 1959, Vol 2(),, Nr 2, pri 600-605 (USSR)
ABSTRACT; In the preceding paper (Ref 1) the aixtho-rs synthesized C-chloro-P,
P-dimethoxyioophosphazoacyle and C..c,aloro-PiP-diaroxyisophosphazo-
acyle (I) according to the scheme
RCONHPO(OR') 2 + Pol 5 POC13 + HC1 + RCCl-=:WPO(O11.)2- (1)
The problem was whether the C-aroxy-P,P-dimethoxyisophospbaz-3acyi.B
and the mixed triaroxyisophosphazoacyls of the type (11), which
have hitherto been unknown, may be obtained by aroxylation
of these compounds (1) according to the so-heme
RCCl- NPO(OR'.) 2+R"ONa. ) NaCI+R(,'(OR") NFO(ORI )2'
Other syntheses are connected with great difficulties~ Synthesiz(Il~
Card 1/"! takes place without difficulties. In mixing equivalent amounts of

SOV179-29 - &-52/71
C-Aroxy-P,P-dimethoxyisophosphazoacyls and Mixed Tzj.aroxYis.)phQsVhaz-)a-,ylS
n-chlorophenolate and C-ohloro-P,P-d:Lmethoxyisophosphazoacyls in
benzene solution the synthesis takea place under a strong develop.,
ment of heat within 5-10 minUtes,, in the case of othe:-, derivatives
only within 2-3 hours, All mixed triarDxyisophosphazoacyls are ob-
tained in crystalline fo--m after the distillation of the solvent.
The C-aroxy-P,P-dime4.-hovisophosphazoac;yls form first as o--'lv,
which soon adulpt a crystalline shape. Compounds (11) do not hzidro-
lyze with water if they are boiled, they hyd:volyze difficultly in
boiling alkali 1 e and eaeaily in aqueous alcoholi-:! solutions of
alkali (Scheme T Some of the initial compo-ands were synthesized
anew according to scheme ', describee. above, The mixed 4,riar~xyico-
phosphazoacyls are no insecticides, In this respect C-n-nitr-_-
phenoxy -P, P- dime thoxyi sophosphs z oben 7,,%yl is very active,.- There are
3 Soviet references.
ASSOCIATIOP: Institut organicheakoy khim-'j Akademii nauk Ukrainskoy SSR
(Institute of Organic Chemistry of the Academy of Soi-ences, UkrSSFI)
SUBMITTED: December 16,. 1957
Card 212

4.
AUTHORS: Derkach, G. I., Kirsanov, A. V.' SOV/79-29-6-9/72
TITLE: C-Pbosphinyl-P,P-Diaroxy-Isophosphazo-Aroyls (C-Fosfinil-
PvP-diarokaiizofosfazoaroily)
PERIODICAL: Zhurnal obahchey khi,mii, 1959, Vol 29, Er 6, PP 1815-1818
(USSR)
ABSTRACT: The C-ohloro-P,P-diaroxy-isophosphazo-at.,yls of the
type yield under the influence of water
ArCCl-JPO(OAr' )
2
the diaryl esters of the acyl-amido-phosphoric acids (Ref 1)s,
under the inf3uence of sodium alcoholates and sodium arylates
the corresponding esters (Ref 2). They reactreadily with
ammomia and amines and are its acylating agents'analogs of
the acid chlorides of the carboxylic acids. It was of interest
to find out whether this analogy also holds for the reaction
of A. Ye. Arbu4ov, i.e. whether the above-mentioned acyls
also react witfi the esters of the phosphorous acid like the
acid chlorides of the carboxylic acids. This was confirmed
by the. experiments. These acyle react already at -150 under
considerable heat evolution according -to Arbuzov and yield
Card 1/2 the corresponding (!-phosphiiiyl-P,P-dia:roxy-isophosphazo-axoy:Ls

C-Phosphinyl-P,P-Diaroxy-Isophosphtizo-Aroyls SOV/79-29-6-9/72
according to the acheme:
ArCCI-NPO(OArl) 2 + F(OAlk)RR1 - AlkC1 + Ar,-,-NPO(OArt )2 M.
OPARI
Among the 9 compounds synthesized (I) only -two have a
crystalline nature, the remaining ones are dense liquids or
vitreous products. Analytical data, apl?earance, solubility,
and melting points of' theae compoundn are given in the tablet.
By shaking with 90 0jo alcohol they hydrolyze quantitatively
within 4-6 hours yielding the diesters of the acyl-amido-
phosphoric acida and the corresponding acid esters of the
phosphorous acid, phosphinic acid or also ol the free
diphenyl-phosphinic acid, according to scheme 2. On the
hydrolysis of the compounds (IV) and (VIII) (Table) it was
possible to separate nearly quantitatively -the diphenyl-
phosphinic acid. There are 1 table, and 5 references, 3 of
which are Soviet.
ASSOCIATION: Institut organicheakoy khimii AkademiJ. nauk Ukrainskoy SSR
(Institute of Organic Chemistry of the Academy of Sciences,
Ukrainskaya SSR)
SUBMITTED: May 27, 1958
Card 2/2

ACC NRi
SOURCE CODE:
AUTHOR: Derkacb. G. I ;_�l
ju renkq, Ye I,~.L ~ ~1 an, B. - Ya.: LLPtu la , IL I.
ORG: Ins itute of Organic Chemistry. AN UkrSSR (Institut origanicheakoy khim'.1
AN UkrS,)R)
TITLE: Sii8ocyanates and diisothiocyanates of alkylphosphonic acid3
SOURCE: Zhurnal obshchey khimii, v. 35, no. 10, 1965, 1881-1882
TOPIC TAGS: cyanate, phosphonic acid, thermal decomposition, chemical decomposition,
phosphoric atid, thermal decomposition, chemical decomposition, phosphoric acid,
I
4-hiocyanate, potassium compound, reaction rate, urea
V, t . i A4.
ABSTRACT: . It was shown earlier that the thermal elooom isitionlos..
esters of dlaryloxy(dialkoxy)ohlorophosphazoeargo3rliolactids and
-ale ;rs of urethanephosphoric aoidj"
Ste iyields diesters of lsocyanato-.~
phosphoric aoldi AlkOCONHPO(OWS
AlkOCON-P(OR),C) (110),PONCO
Unaer similar conditions, dlearbethoxy diamides of alkylphosphonio.
a?'~,ds form dilsocyanates of alkylphosphonle acidss
11P0(NHC00A1k)2 ~ fi1'0(NC0)2+A1k011
Dilsothlooywiates of alkylphosphonlo aolds are obtained in good-
yields by the reaction of alkylphosphonle acid dichlorldes with
potauslum,thlooyariates KNCS
RPOCI, 11ro(NCS),
UDC: SL,7.2,L]

ACC NRt A-P6027089
D11cocyanates and diiaothlocyanates of alkylphosphonle acids react
ivigorously 'with aloohols, phenols, and amines to form the oor-
responding phosphorylated urethanes and ureasi
A
Roll 0 11PO(NOC00,I)s
111'0(NCO)s RNII,
HPO(MIGON111%
Orig. art. has: 1 table. 1JPRS: 36,3281
SUB CODE: 07 SUBM DATE: 06MaY65 ORIG REF: 003

m NP(j) ROAT
SOURC9 COffE1 UR700-7-916W(Yf&/00:[/OI62JOiZj
AMOR: Ivanova, Zhe Me; M2tuga, N. L; Stukalo, Ye. A&; Derkach, G.; 1.
ORGt Ingtitute of Organic cherls!.M, AN TjkrSSR (Institut organiches1my khimii
AN uia~s-sT
TITIZ: Isothioganates of allwl esters of mthylphosphonic aoidland their derivative-i
SOURCE: Z.hmial obahchay khimii, v., 36, no# 1, 1966, 162-163
TOPIC TAGSz eater. phosp1mte, Viosplioryl&tion, chlordnation reaction rate,
aboadcal synthesis
MISTUCT: Chlorides of a1171 esters of mtby1phosphor6c acid,, lilm cliallwl chloro-
phosphates, "act with potassium thiocyanate to form isothiopyamates of a1171 estars;
of mthylphosphonic acids. These isothiocyanates mV be chIca-Inated to yield dichlo-
ridoa of' monoa2kylmonomothylphoop-honyliminocarbonic aoid. Both series of reaction
product4 react vigormoly with alcohols, phenols, a=)]A& ardL AMiMB 'to form the
eorrespcnding phosphorylated derivatives of thioureas and iWmocarboxylic acid.
Four iscithiocyanateu amd tuo dichl W a uero eynthouizod andl dharacterizodo Orige
art* hass I table. fJP1tS1 3.5,;;j
SUB CM-t!;: 07 / SMI DATS: lWu165 ORIG RMFt 002

DKIKACH, G.I.; LEPESA.. A.M.; -KIRSANOV, A.V.
Alkyl esters of N-dialkoxy- and N-diaroxyphosphinyliminocarboxylic
161. I'NnA 14:10)
acids. Zhur.ob..khim. 31 no.10:3424-3433 0
1. Institut organicheskoy kbbdi AN Ukrainskoy SSR.
(Esters) (Acids, Organic)

DERKAGH, G.I.; SHOKOL, V.A.; KIRSANOV, A.V,
Diesters of acylamidophosphoric acids. Zlmroob.khim. 30 no.10:
3393-3397 0 "61. (MM 14:4)
lo Institut organicheakoy khimii Akademii nauk Ukrainskoy SSR.
(Phosphoramidic acid)