SCIENTIFIC ABSTRACT ZHELVAKOVA, E.G. - ZHEREBTSOV, N.A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R002203810008-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 1, 2001
• Sequence Number: 8
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

212 020 U-'vC L A S,S I F I ED PROCESSING f)ATE--0?0Cr7C
~:---CIRC 4 C C E15S It "W' NO-APOUZ413
~-,--ABSTRA~t--T.,4FEXTRACT--iU) GP-0- ABSTRACT. OF,
Zt 3, 4t,5,69 PENTA 1,0 q 3ENLYL, SYNv -MIYUt I NOS ITOL- WITH PliOPOCL WB2 AND
1,2,.ali~PALMI&TOYL,Si4,GLYCF:RDL tN C SU95 H.SU55 N-GAVE 32PERCENT
w,' -..,Lt~311.1,,2,DIPAL.41TOYLtS'liGLYCERYLi(P.HENYLt'6HOSPHOItYL),2,,I,4,5,
-6,PENT4,DtBENZYL,Slq,MYOtINOSITOLt M. 53-4PERCENT*.:* HYDROGENOLYSIS OVER
~MS PT CATALYST AND PO BLACK-.GAVE THC- IS9LATEG AS
PHOSPHORYL AN AL OG ,
-72PERCE -Y SIMILAR TO THOSE
-NH SUB4 - SAUT t. :M. 169. IN T.' TH11 S GAVE SPECTR~ VER
OF NATURAL .40NOPHOSMOINUSITIEDS.

~S.1-4/2 01.9 U NC?7A St F I E a PROCESSING DATE--IBSEP70
.~-TITLE-SYNTHESIS OF OPTICALLY ACTIVE PENTABENZYL ETHERS OF MYO INOSITOL.
TH RATURIAL STRUCTUR-E -U-
.,,:.T,3TAL SYNTHESIS OF PHOSPHATIDYL INDS I.TUL WIS
I 05).-KLY
-ASHCHITSKlYt B,A*l WUdAUYALJ.,nA~wf#* ;SHVEYSI V.I*t
~~-VEVSTMNEEVA, RiP., PREOBRALHENSKI.Y' A A
OP INFO--USSR
OURCE-TETRAHEDRON. LETT. 1970t, 1 8),"t 587-;-9P,_
AREAS--CHE41STRYi BIOLOGICAL AND MEDICAL SCIENCES
.-TOPIC TAGS--OPTIC ACTIVITYt POLYNUCLEAR HYDROCARBON, BENLENE DERIVATIVE,
-ORGANIC.PHOSPHORUS COMPOUND, ETHER, GLYCEROL, FATTY ACID, CHEMCIAL
_`.~'SYNTHESIS
~':~_cb";_TROL VARKING--NO, RESTRICTIONS
'DOCUMENT CLASS--UNCLASSIFIED
REEL/FRAME--1985/1509 STEP NO---UK/0000/70/0001006/0537/0590
.C PC ACCESSION NO--AP0101593
:77-

USSR UIC 616-9BB-73-036-2(47O!44)
RW.AI=VA Ye. V., ZHELYABOVSKAYAI, X. G.,, and' DRUMN., D. I.,. Saratovskaya
Oblast Sanitary EpidemkoleVVEL ,"Itrartoy Meacal Institute
"Ornithosis in Saratovskaya Oblast"
Yoscow, Sovetskaya Meditsina, No 9,, SeP 70., PP 150-151
Abstract: No case of laboratory-confirmad ornithosis in hurans was reported in
Saratov6kaya Oblast before 1967. As part of an epidexidological study conducted in
the oblast from October 1966 to June 19671 75 hospital patients Vhose symptoms sug-
gested ornithosis were given serological and skLu tests..Ihe T5 uubjects bad been
admitted with tentative diagnoses of,typhoid, paratyphoid' pneumcfaia, influenza,
and inflamation of the upper respiratolY tract,.: Eight wre dlA,-,,wsed as ha-ving
ornithosis (1 with the paeumonic fcx~, I with t1je. ialuetza typie). Four of the
eigbt had had occupational or other -contaotof ~dth,blxdsa~

USSR UDC 547.548.1
TSIVUNIN, V. S., ZHELYAGINA, L. V., and'KRUTSKIY, L..M., Kuzbassk Poly-
technical Ins titute:-"---
"Reaction of Triphenylphosphine with a,O-Unsaturated Acids"
Leningrad, Zhurnal Obshchey Khimii, Vol.43 (105), No 2, Feb 73, p 439
Abstract: Reaction of triphenylphosphine with acrylic, methacrylic, and
cinnamic acids yields phosphobetaines. Acrylic and methacrylic acids
react smoothly overnight in benzene with about a,30% yield. Cinnamic
acid reacts much slower, and the yield is poorer, The structure of the
products was confirmed by IR analysis and parallel s hthesis.
Y
A
WE MIKE1011MUSUMM"M 011MIRM RIM
MIN

AW;tractinA,Seivice, 'Ref. Code:
NUCLEAR SC~ . AJ~ST. /70 U kO All
37 TO THE THEORY, OF INTERACTION BETWEEN A
RELATIVISTIC ELECTRON BEAM AND PLAIMk. B20dazkevicb-
I Zbo-w4eml .L; RuldlAdze,.A.A. (Ltbetiev lost, .d
vChe it; 13:
I
The Interscilon betWi6n_ the It tied reIat1vlst1,t Wectron beam
of a small den~slty and p a 0M
.. plasma, eink Ln-A otrang 16ngitudinal iW-
netic fleld-Is. in~istlgited_ The, critical pl"MA d~nBity, above
"Ich the elL4--trokatic fnstabffitie~: mn~ be:deiejoped, Ili deter-
mined. in long enough ~jstems, tbe,critical dehiitk of pjasr~a is
tacrensedwith tb*gi-owth of itis density riachindisame halite de-
termbied,by the directid-ve~loclty 6f ilec tarons ifid the geometrical
dimensions of the skitern.. ioAe*stem6 limited in a longitudinal
direction, the. critical density of plasma may be de~ende4t also on
tho'systern length at~ Ij mgneti6 flit'd,inteasity. lit this ciao the
critical -density-In laiger. On ior- a long System,,
: : it foudws from
th&auslysla of the s ,tability,that tb~ ~maxlmum tu&rent of the elec-
tron beam, which msy 60 pisoe~ thi~ougb the "~i..gWde,'Increases
In the relAtIvistlo rqlan With'the I#'owth oif theelact ron:margy as
43 . DueIto this possibility. IM44 current& may pi!netraba tbLrougb
~~nse plas Ms. (auth)
RF E:'
IEL/FRAM
040M

UISSR UDC: 547.94
AMMOVA, B., ZHELYAZKOV L., DAIEVA, L., STEFANOVA, D., Scientific Research
Chemico Pharmh-c-RuTi-cal Institute, Sofia
stituted-4-Quinolo mi s. I."
'Biologically Active 1-Sub ni ne
'~Tashkent, ANhimiya Prirodnykh Soyed-tneniy, I-To 1, 1970) pp 98t.101
:.~--Abstract: Echinopsine-l-methyl-4-quinolone (I) and its structural analog echi-
sidine (II) both show physiologicalactivity, but in different -itays.
n
op
NK
(aY
OP,
CHI
G
It is assumed that the difference in the biological effects of these two compounds
...arp due to the structural. difference -- the substitutent in the fourth position
(zO or the 14H group). New 1-subatituted quinoionimines whiqh may 'be considered
:structural analoga of echinopoidine were synthesiied by a f6ur-stuge proceso similar
to that used for synthesis of echinopsine.,
li3

. _ '!I. I
J~' -' i"j- - ~_, Ii 1:i, . - . - - -
lj&l,~161 I
ii- 'I.I:iji :~ , " ii. i I I ;I I ii .1 - ,
~., Z ': 4 , . . - . ddAi . V U_M -

USSR
AVRAMOVAJ. B., et al. Tarhkent, raiimiya Prirodnykh Soyedineniy, No 1, 19-(0, pp 98-
::,*.,The reaction was carried out with boiling 4-aminoqu,inoline together with an excess
of the appropriate alkyli~ting agent in, a suitable solvent. Reaction time varies
:from 6 to 25 hours. All the resultant quinolonimines were found to be biologically
active with respect to the central nervous Oystem,~ -most of
them having centrally
~.stimulating and antidepressant properties. The stronk;est --antidepressant action Is
shown by echinopsidine, the firBt member of the homologic a~~ries (P = CH3). As
the carbon chain associated vith the nitrogen atom-increases in length to four
at-oms, the antidepressant property decreases,'andIthere is an. increa3e in non-
-specific stimulation of the central nervous system. Tim arcm3tic derivatives showed
elemento of antidepressant activlty,, though vreaker than in echinopsidine, and the
double bond in the substitutent seems to lead to a tranquilizing c-11'ect. Larger
doses of the compounds produce a curare-like myorelaxant effect which increases
,in strength when the methyl group as5oeiated vith the nitrogen atqta is replaced by
heavier radicals. Carbonyl groups in the molecule reduce the
myorelaxant effect.
With respect to antichGlinesterase activity, quinolonimines are much more active
-than echinopsine, but less active than gaJant4amine., The qu~nolonAmines are more
biologiaAly, active:and more toxic than..,echinopsibe..
3/3

USSR UDC: 669.884/.88'.053.4.068
BARER, R. S., MUN, A. I., 711ELYDKOVA, G.._~_ V.
"Study of Sorption of Lithium and Rubidium by the'Hydroxides of Various Metals"
Tr. In-ta Khim. Nauk. AN KazSSR [Works of Institute of Chemical Sciences,
Academy of Sciences KazSSR], 1973, No 361 pp 82-86 (Translated from Referativnyy
Zhurnal Metallurgiya, No 8, 1973, Abstract No.8G200, by the authors).
3 4+
Translation: The absorption of Li and Rb by the hydroxides of Fe , Al, Sn
Ti4 + and MnO2 is studied. The influence-of the pH.of the solution, various
electrolytes, the nature of the sorbent and conditions Iof its production on
the process is determined. The absorption of Li and Rb+ is strongly influenced
by the acid-base properties of the hydroxides. The mechanism of capture of Li+
Rb* by various hydroxides is studied. The influence of the salt background
on the sorption of Li and Rb, MnOV Al(OH) 3 is studied,~and it is shown that
the effects of*secondary cations are determined by the'nature'of the electro-
ly-tes and the nature of absorption of the microcomponents. 3 figures, 14
biblio. refs.

7 `T;lp'l - ~ ., 1. 1 - ~~ ~ . , t," V-=
, , . - hdiiii;aliiiii, ;146WH414 honim w! 616 -, - ; -1-
!; ;~ t;~ -,-. ; : 7 . - ~: ; 1 la. : ~ ;; ~l I ~ 1-
:; l lij;4 It ]IN T-1 iL IMNItIA lliw IN in , ; IL I 1 7 ll-~T I I fIll, 141. it I ;li

2k2 016 UNCLASSI.FIED. 0A,r,,---,-,4DE_c7c
IRCACCESSION NO-AP0133003
9STRACT/EXTRACT-JU) GP-0- ABSTRACT. FOR THE EXPTL. ii'l A GLilST
,'.FURNACEt A CHARGE: C01,4TG. 10PERCENT BRIQUETTED C E -AS' 'J"SED. 1"HE
SHOWED-!4ECH. STRENGTHS, 14 SU5,40 EQUALS 85-~93PER~Ll~ifj ".1 S0310
~3,4--~MPFRCENTt AiNID CONTAUNEO 5 1e .25-1.809 .ASH 5.810-10.6, A,,,ji) vE~,LSFt.;j~E
~3,8-_10.6PERCENT. THE'PROCESS PARAMETFR~~ OBTAINED WERE COAPARED W 1 11-1
THOSE OBTAIN' J D
ED WITH THE USE OF THE.USUAL COKE, p IG pjZrjojjrF
;'SH014ED NORMAL 14N AND S A140 SOME-1,14
AT HIGHFR: ;S1 CONC11S. 0.0401 AN0
'-0#92PERCENT, RESP). THE BPIQUETTED COKE ON,CHARGING SHOWED SUFFICIENT
STRENGTH AND DID NOT FORM A BREEZE* THE LENGTH Of-THE OXIDIIING ZONIE:
JN'THE FURNACE WAS 1000 MMt AND CO DISAPPEARED AT 250-50-) MM FROM TH-1-
__MOU-TH OF TUYERE. MAX. TEMPS. IN THE HEART+l AND 30SH WERE 1845 AND
-,L3-..80DEGREESt RESP.v AND THOSE OF THE PIG IRON AND SLAG AT THEIR TAP
-HOLES WERE 1515 AND 1580DEGREESt RE SP. A CHARGE CONTG. 50PERCENT
BRIQUETTEE COKE DOES NOT CAUSE ANY COMPL11CATIONS M.'~THE ORERATEON Of: THE
';FURNACE..-
___UNr LASS-IF IEO

Receivers and Transi;itters
USSR UDC 62 1. 3 9 1: 5 19, 2
144
ZHENCHUGOV, V. N.
"Study of the Allo~,zZble Pot,~er oil: FM Noise at the Input of Hie Freqtzency Con-
verters of an FM Signal Receiver"
Materialv naluenno-cekiin. konferentsii. Leningr. elektrotiA11n. in-t svvazi.
Vvp. 2 (Materials ofthe Scientific and Technical,Coafetence. Leningrad
Electrotechnical Communications Institutei.Vyp, 2), Leningrad, 1970, pp
161-1.67 (from RZh-Radiotekhnika, No 8, Aug 70,'.t*Vbs tract No 8.1160)
Translation: This article contains an investigation of transfornations of the
Fist signal and FMI noise in a system consisting~ of a superhigh frequency Pon-
verter of an intermediate frequency amplifier and a frequency detector. The
equation and spectrum of the noise power at the output of the frequency de-
obtained. The allowable intensity of FM,interference at the input
Lector are
of the frequency converter of the radio relay line~recetver is calculated
for transmission of 600 and 2,700 telephone.-channels.

USSR UDC 632.95
BLIZNYUK, N. K., KHOKHLOV, P. S., KVASHA, Z. N., WRKOVA,_L__L, LEVSKAYA,
fATYUKRINA, Y6. N., VARSHAVSKIY,
-G. So, PROTASOVA, L. El., SOLNTSEVA, -L. b
S. A., BARMOV,Yu. I., LIBIMAN, B. Y.a., ZHEMCRUIZHIN, S. G.
"Method of Production of Dichlorides. or Dibromides of Thl'ophosphonic Acids
or Their Bis Analog"
USSR Authots Certificate No 332095, filed 19/08/69, published 17/04/72
(Translated from Referativnyy Zhurnal Khimiya, No 24(11);, 1972, Abstract No
20591, by T. A. Belyayeva)
Translation: Compounds of the formula RP(v-)X2 (I) (R=alkyl, aryl, aralkyl;
k--Cl or Br) and X2P(S)A(S)PX2 (II) (A-bivalent hydrocarbon radical) were pro-
duced by the reaction of mono- or dihalo hydrocarbons with S,: P -and PX3 with
heating to 250-400' in an autoclave of stainless steel, or nickel in the
presence of catalytic quantities of 12 or its-compounds , Example. A mix-
ture. of 0.24 mole PhCl, 0.24 g-atom S, 0. 16 gnatom white P, 35 ml PC13 and
0:05 9 T2 is heated at 290-330' for seven.hours in an autoclave oE stainlesp.
steel, the PC13 is distilled, then vaCUL101 distillation Is used to separate
I (R=Ph, X=Cl), yield 6011., B. T. 109-1120/3, n^OD 1.6241. Similarly, I
were produced (given R , X, yield in B.,P. in *C/mm, n20L)): 4-Clc6H4,

MSR
BLIZNYUK, N. K., et al., USSR Author's Certificate No.332095, filed 10/08/69,
published 17/04/72
C1, 53.5; 124-3/1.5-2, 1.6229; p-MeC Hz Cl 54.5, 125-7/1, 1.6120; 4FC6H4,
C1, 72.2, 95-7/0.5, 1.6028; Ph, Br,'91,'~127,'-130/2, 1.6850; 4-FC6114, Br, 55,
135-8/1, 1.6758; PhC'12, Cl, 76.4, 120-3/2, 1.6150; 3-yr~04, Cl, 108-110/1-5,
1.5908; 4-MeC04CI12, Cl, 53.3, 126-9/2,;1.6035; 4-CIC6iVI12, Cl, 61.6, 129-
133.2, m. p. 74-6', --; 2-FC61140ii, C1, 61.6, 129-133.2, m. p. 48-90,
2.4-Me2C6113CH2, Cl, *47.5, 140-1.6615; 2.4-CI2C6H3C112, Cl, 43.4, 147-9/2,
m, p. 100-111, ~--. Also produced were 11' (X-Cl, &-'CH2CIt2), yield 61.5%,
m. p. 92-3*. 1 and II are intermediate products for the production of
insecticides, acarocides, fungicides7-and,herbicides.
2/2
41

:::1:41UA:~; III:
USSR UDC 632.rD
KHOKHLOV, P. S., MAFKOVA, L. I., ZHEMCHUZHIN, S. G.
"Preparation of Dithiophosphonates"
USSR Author's Certificate No 329184, filed 4/08/70, published 30/03/72
(Translated from Referativny Imiy
y Zhurnal Kh' a, No 24(11), 1972, Abstract No
24N592, by T. A. Belyayeva)
Translation: Dithiophosphonates of the formula RP(S)(SR")OC(Me)=CIICOGRI (1)
(R=alkyl or aryal; R' and R"= alkyl), which can be used'as physiologically
actIve substances, are produced by the reaction of the anhydride of the cor-
responding dithiophosphonic acid with acetoacetic ester in an inert organic
solvent in the presence of a tertiary base with subsequent alkylation of
the salt formed with an alkyl halide. Eyample. Taking a mixture of 0.03
mole.benz-yldithiophosphonic acid and 0.03 mole Et3N in~,30 ml C6H6, add with
-25* a solution of 0.03 mole AcC112COOEt in,.10 ml C6 , heat to
mixing at 20 H6
70-80' for 15 hours until the precipitate.dipsolves completely, cool, filter,
prioducing Et3N-salt I (R~--PhCH2, RI=Et, R!'=~H) (II), yield 71.8%, m. p. 149-150".
Take 0.02 mole 11 in 20 ml C6116, add.0.02 mole HtI, hea:t 3 hours with agita-
tion at 60-70% cool, filter, wash the filtrate with water, dry over M.*S04,
evaporate, producing I (R=PhCH2p R'=FV=Et), yield 81.2t, after chromatography
1/2
- i ! 1
L 11 i, 1i 11 iii iii 1i d ..6 i
V
i 17 MI"I", !,;-Z, i k, till ~ffl, 11;10113k ;Hr~illl

2/2
40
i IM ~R ll;rf~VS I IflifflAt Ail I liI IJI
AW.,

USSR UDC 632.95
BLIZNYUK' 11. K., KALUMM, L. A.,
lip
rocedure for obtaining O-Chloralkyl AiaidAhidl~h0s~h4tesll
USSR.Author's Certificate No 296773 filed -28, No,~ 69 bliihed 15 Jun 71 (fron
pu s
RZIi-K-hizilya, No 6 (11), Jun 72, Abs tract No ~6N610)
Translation: Substances with the general formula ClR.OP(Sq1)(0)~j,,Z2R3 baving
high fungicidal acti ity (I; R = alkylene; RI ~ alkyl, :aryl, ar-11kyl; R 2 ant',
R3 11, alkyl or It2PN = a ring radical)-arti obtained.by the reaction of r:yclic
alkyleneglysol i-Illorophosphites vith sulfonamides -wit ~>
h heati-r- of an equimolar
mixture of reagents to 60-100'. A solution of 0.025 moles of ethyleneglycol-
chlorophosphite in 10 mk of C 6116 1,-, added to in .9olution. of 0,025 nioles of plienyl-
sulphenmorpholite in 5 vO. of C (reaction temperaturo. of the ww~ri