SCIENTIFIC ABSTRACT SOPOV, N.P. - SOPRUNOV, F.F.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001652420007-4
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 26, 2000
• Sequence Number: 7
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

-some vew- al.tcyclic Isomers.of
A. A. Kt!qZd
h1lig. (Apin.
UIU-1-5(1932Wng . rsii-Jjtlon).-Sce@.A. 47, S17il
C, I t."Y L.

C,@njugs Lid 9Y-fAtc!rq.- xfv."Cond@rli; ation of Cqt-
with esiort; at mileic and furn&rIciteldi.
..nd it , IlArad 1"At, A At* ri-Itru.
IM74f; 49. &A.-rrittimclar inixt-ii. ri the dicries
alldifirc fii-t3 kO.1 molecich) %ere hratcd In 30 mi. b1c),li in
S'Med t4K-s 111-20 firs. to 1.1,040', DiAte iiwleate bm
it. t.1604, nV 1,44X.1; di-Pt vitrr, ji,o
bm IlVi-MV, do IMOO, XV 1.4110. DI-Mr furnamto
In. 1()1-21: di-M citer. tho 91-r@7-71, dts 1-0312, rtV 1.44Z,.
Th,ir irrze6mi w Jill bu t,@djmr, piperylene.
unl crude S-.xv,! clit faitti-Aing pruduct-i (the
at:41!i iscm, obt@tfi,c4 by hydroly-" of the "ters). Ds-Afe
4ym, 08-57?, b. 141.&-2'.
1.47;1:1; Ire a,id, M. 166 ; oan$ iso0w,
1A 1W. !..
di-Ale rorr, 1, 139 q.!i* (1,* 1.1 M_ ny, LVA2;
hcea,Lid, ill. IV) 70;;
clo LW:1, r" 1.47.12; trans i!.opmr, 59.470. b.
n As cir drid, tn. UYI-0;

4L CT
that of We ,jn3 furm, k1l. 165.3-6.5*. D: Are
1.1111, isil 1.4733; Irdyssform,
1.1010. xg 1.4704, free"id, difotm, Tn. ;,u-t
P,ssi, m. 183-40; dnhylrids of the ch n6f, m. W; Of-it of
Imsist fem, in. 141-2". bss@-Aft
dica,boxyt", , cil form, 5-4,5%, Is, 144-A', -r6 LWP, ni?
- , 40.7%. b. 14-1.5-40. 4% 1.6577. nV
V"; '@ -
: '372. cis
I
'Ppm, 631'(,. b. 167-4 .5': d@ OMPI, nll 1.4777a; i -'@y m,
M.1%. 1'. fri. AP; hoe C'CU 'CgIforon. ui@' 1776-
JIGOSIfirm, tn. 213-15', :mAspInVe, fit /"rm. m. 7A"
Oita of trvu form. m. 1*-7'. Di-Aft 3SlivirA *4, Y; 1@ -
A4r4n,-4 I-liumbiny0le, cis form, &13,2% b. (L4
- . - .. - - 16; trams forai, 52@/m *b. 1.50.5-1.6'. d.
IR-0.2, NIJ 1.4791. Di-Als 'Is 6-fvlarih y1sweyelther'ni-43.
cis f,tm. ski. 70-@0.64; frun; f,,rn,
29.670. 'ra. CInnJensatirA of alkoxyprenes
I malzic zjr futstati., add with :tlluiy-
prenes w-,-. ria" ia staled tube4 at 165-W lav.

The exterp mcm hydruly-u-1 to the ACHS in lwv@c..
I rcalinent of thp steri with 2,570 1450, pvc the P-Cvclo@-
herationed iriubox Oates. vren- obtamed: D;-Md I-
metbox' ciLqjorm. bl* 1731, dw
1.1781, vi@* 1.471M, Imms ijemer. ra, 07-S-, Ny
DAYS -# f-, ths
178-8.5". do 1.14-25, is)l 1.47,68; Immif"M. b. 17".5'.
dm 1.11F6, ml; 1.4735. M-El l-hvAovy@ycliAeur4i:,4,5-
-30. ti. 1.11 lp, mV 1.4704;
.1, MOM. n; 1.4679-
ellwzy ch f", ba 187-7,',-
d
g 1.07M, '14
o 1. 5, xV 1, IP4; Irani fa-,ft, h., 186% t6
IMZ4. Pi-Afg cis fan".
bm VMA-U--,-@ eft, 1.211h. .A; 1.4741); tracrfermt, m. 54.6-
r;.5*: tb,.:r J, in. IS9-0* atid 17-t-,,*. no.
IN-8I cisfolin 4.,
@5.5% du 1-M-1, 1.46-0* tru,ox fvrm

LLap N. P. and PETROV, A. A.
Studies of Loonjugated Systems. XLVI. Condensation of Alkoxprenes with
Esters of Maleic and Fumaric Acid,, page 860, Abornik statey po obshchey
khimii (Collection of Papers on General Chemistry),, Vol 11, MoEcow-
Leningrad, 1953) pages 1680-1686.
Chemistry Laboratory, Leningrad, Inst of A@iation Building

PSTROY, A.A.; SOPOV, N.P.
9--, @!' -- T. ,
Conjugated systems. Part 47. Condensation of butynone vith cyclic diene
hydrocarbons. Zhur.ob.khim. 23 no.6:1034-1038 '53. (KLM 6:6)
1. Khimicheakava laboratoriya, laningradekogo Instituta eviatelonaogo pri-
borostrayaniya. (Diane compounds) (Butynone)

US&M/Chomistry - Convrralon nrocenses
Gard 1/1 Pub. 151 - 21/38
Authqrs I Petrov, A. A., and Sopoy, N. P.
Title I Conversion of hydroaromatic aldehydes and ketones into aromatic hydrocarbons
during dehydration
Periodical I Zhur. ob. khim. 24/2., 298-302, Feb 1954
Astract I The dehydration of hydroaromatic substances having two double bonds and the
oxygen atom in the side chain in alpha-position relativeto the ring was in-
vestigated to determine the possibility of their conversion into aromatic hy-
drocarbons. It was found that during the distillation -Ath P205 or with Al-203
at 350-4000 the unsaturated hydroaromatic ketones and in the case Of P205 also
the aldehyde3p which form during the condensation of the diene hydrocarbons
and their derivatives with Alpha,beta-unsaturated aldehydes and ketones of the
fatty series, easily submit to dehydration forming various aronuitic compounds*
Fifteen references: 7-USSR; 4-1-ISA, 1-French and 3-German (1894-1953).
Institution : Institute of Aviation Instruments, Chemical Laboratory, Leningrad
Submitted : October 2, 1953

i-, 4
loaf -a
Tr"
intO at' 24
I P. J. Car: Hui.
anti N

.kConjugated Istasm, LVII. Condemdom of
agidehia Ith p rrylane and immism6.
N. F.. , pov ( "at. Aylittion lnxtr., nin 4 457: CHI
@I.W
LOW; J.
4 Otftitil. tmirtlatlon); d. C.A. 50, 233b.-
Cut on IIC,CCIIO with pisterylvie wW taupesin
occuris fit the directlon ex"eti (mm rWrolde Whirlion
.of tile metants. Ileating 0.2 L IICICCIIO am I -if.
Oterylvise NO!. Pure) in 30 fill. ellb 5 hit. at 1,101"'Ji
1% :-mdh 4.54ibydrokmIdAyde. hat W U, a
2 P
1.0.9810. xV 1.110114; semicarbarome. in. 1117';
2 4-d
Phem)Aydrazone in. IW-70% $@-xftroph""Xwh
re
.183-6'. The sWhytle hvuW with 8 gave 0- cC It
.lid W yUl while Irculmsent with McMgl pvc V
rl-mells 2,5-JihyJropAexyk4rbixal, Its 104.5". - at
=-. xV @zmr% which diAd. with 1076 (COJI Pat
78 ;:Mc1RLCqIIj, itlentific
% A by ossialation to Phtha, a"
When the pitteryk-ne for the ubuvc reaction W" obtained by
Aehydrittion of methylpropenylcurbfuu! with 1111r. the re-
timalting altichyde w4s able to react with nuiltic' anhydride
&ad with S. but in Um latter cam Pu toksaltichyda coasts be
,1906ted front tile tarry poiluct. IN"bly sonte kqxnLd=-
tion of lpe t1ouble botuls in she dihydra comixf. took Ithm.
Sin ffir h 17.5 x. IICICCIIO with 11.5 9. CIft:CMc-
C
70 -,.dkyW.(;-ddjydiabexzu1&kYde (1). W
105. W13. X17 1.51al; semicar&WOxe. in A&W.
q
j)@-xijropktxy(Aydrawms, sit. ltrl-.3*;
drawne. in. 214-15% Heated with S It gave Me
@CIIO ia,110@@t ykLI. I with McMgI gave
m,rskyl-3.0-4ohydrophexyicarbiprot, bia 1164-0.5% die 0.11111M.'
@sV IZAM. which with (CO@Ilh dehydrutost tol@NfelitClIll.
G. M. KOfAJAPVL_

5,6 p 0 \J
Con4enzation *fth usethaulUte.
1
ds b b
d
"
l..
y
1.1-A,,i Tilstruments
I Leningrad).
Vt. I sons. .49, ms.
The lenwing cmdensol no- Im le prelem
fol
brkvquinout in usupuls at 140-M* 12 hrs. (Pmpd4, %
VW . and =, b. ji, 40, %V given)r I 3-B*Wdkme
.
h
f
. .
It
C14
emm. % Afir
b, 78.".6% 1.0130, fal me
&
cycl-ke"r 1 1 - I a
. 0. IA
M% AM* 4-ow
O@ , 1AW6- A 64 1
mdAyl4-cydoAexrxt-I bw W7', 0 ELM.,
diioop:Tm I-ca

.439% Ate 3,
05
ate. b. 105. .5*, O.OM, 1.4722; tadiene. 79% e
.
4-corli-yiste, b. W6.5'.

=_
=71M _
M
3

k
3
1 3204 Afe 2A4mApdhykxe4-ry-
,y
,..
k
h
1o
now I-carboxylak. bw 10".5 1 MM, 1.4870; chloro-
preme -eydeAcum&I-corboxylak, bw I 15-
16#, j.40% A(* 44kloroj
16M, 1.4898. These esters (0-1 wole) were trfttcd'
with MeMclimmol6g.-Alow mgIn utjo.yier6
the followfug corresponding tertiary aks. Mes (R,
. dn. and xV g1m): JcydoAcxt*-l_ -60, 0.9-M.
fl
V-eyckhemem-1-yi, 10" , 0."%, 1.4107;
JASM; S-md!
'
10-11
. 0.0344, 1.4822; :."i-
I
-
*
112-13
, 0.9301. 3.4840. J.4-di-.

Irv, -,y
4
0.9554, 1.422 =PS-OWA
OS493 is
-OM75:'i!4%; J.Z
0.8m, IM76; 2
71-3. , 0.917p, IAM.
i. In thb reactim ww save cuume.
dehydromated ovti Pt-C at U&
bms )42-3* OAM I 48M- o4st
osm. 1!665; Q 17&-
0j"
.4932; 1,4-,
G. u.K.

SOPOV, N. P.
Preparation of hydroaromatic compounds on the basis of products of
the diene synthesis. Part 4: The action of organomagnesium compounds
on esters of cyclohexone-4-dicarboxylic acids. Zhur.ob.khim. 26 no.6:
1602-1609 Je 156. (MIRA 11:1)
l.Institut aviatsionnogo priborostroyeniya.
Ocaters) (magnesium organic compounds)

i op the baSIS a
crai-ilon -of
Iction of organo-
e dim syntaeus.co
produits of tb -c
I osterl of 4 yc
m4poslum compounds witt
J. Gen. Mon.
...... C.A. 51, P6AL
M.-R-

d
-k. Khi I
divin , d6skek. Khi I foll).-Cood"Umm 01
lwvnm di in with dimethyl of
Actty rbozyUc acid
in
d1hydrophthalle acid. @ Fmm esters of
am and homr4opes; the Corr 0" ids and ash 0108
dedvW. Prep. of dibydmphvtb.Uue Wand Its "MA
@4#m
teMed mom satidictorily Rom etters of &cetykaedkodxkiyUv kM'
than imm the add, " (a the latter Cabo 40cubmiatioa 11jid other:
take Va. The easiest esters to sarally wwo those of
-*A' C- "@ dri 6 1Its,
most dif kult those of 3 : 11-1
All acids wen white crystals:
gh
@fli wat, In twasene, others, CIM, and
d boiling water. A. 1. B.

PETRGV, A.A. ;-@@
Research in the field of conjugate systems. Part 67. Condensation
of propargylic aldehyde with 2-halo- and 2-alkozybutadienes. Zhur.
ob.khim. 26 no.9:2452-2457 S 156. (MLRA 9:11)
1. Leningradskiy institut aviatsionnogo priborostroyeniya.
(Propiolic aldehyde) (Butadiene)

Ided IYASIM. Th aider of sdifidou aC

,
O T.
I
-A. A. Petrov. a.
1. Serneov.
to vf*9192W
N.
a(lob cf. CA. St.
15394b.-Addn. o f 00 g. Ur in CjHCJ$ to vinylwtykne,
i at - 260 gave on (tactionation of (M products inostly 1,4-
dibronio-I,Z-butadlaw, bw 6DA-70.5*, and a lesser wnt.,
of 1.2-ilibroino-1,3-butAdiene, bw 43-60. The result at,
.-10* was sindlarto that dercribed earlia (C.4.44,7751c). t
.Thew products wen characterhmd by Infrared spears.
Authentic was prepti. from 1.4-
:dibmmo-24mtoseeWpowd.XOII,bmgl-1.3*,*VI.5160,' I@L YV"
Addn. of HBr to vinylacetykae In the ce of CuBr
o S-bronto-ks-"iew. bw 42* *V r4W. 'M Imc- -
gi
:,v
tr n
ba 43-6 , above treued 4 irs. ;9 cold, KOI1 In
Meof I gave pure bw 43-3.6'. *V
I.MN. Vinylacety and NCI ve 44kkr#-Jj4wkJi-@
cue
!
Wth
e Above substances
limm 87-6-8% s
V 1.4779. @
svere characterized by Infrared spectra, Rxawn. of lufm-;
ied spectra of the products of brominstion of vinylacetylem
ihowred that in adda. to 1.2- wd 2.4-dibromobatadienes
ritegi above. the revetion abo ykHs BrCUjCHBrCjCH
wbich contandnates both the
b
L
in
f th fractions described.
s-
vors th
for
f
ower
a
ove.
e
g o
f 1
di
i
4
l
1
24A
d a
e
m
f
d
t
-
rowo-
t
on o
i
a
,
.
d I rare
*c
m
ene.
'
d
g
.
of the jzQoducts an discusse
n 4eta
hro
-.
ectraaltud, zeactivity of vioylacotylqAby@rocar5
1107-74; 0. C.A. 31 'shmrn-
I
-jT
-HC
CWCC
CC
CH
j7
j
(
S
]iC?CCM~:CH,.HCiCCMe:CHMi.Cffs:%Cbfe*)CiCH.,
r
Cp
H
C
CE
H
H
C
C
:-
-:
H
IC:C
CI
r,
HSC:CHCiCMe' Hi
t'
1
S
CHCjCBu. and I-hexen4-ync. To this group the vlayli
Is characterized by frequencies of 3110
3030
IOA
rou
,
,
g
p
an -11 the Cff:CH group by 3W,.1620,j
. 4 gWcr@.
Distri 4E4jAE20(j)/4E3d

Se Yn e. A-,,:, 1,
70=WA acctyknk'VoupDy33DDaW2115. the same group
wkWn tbe thain by about. 2250 cm.-I Conjugatiatu di*-
Placest!w ban& towardlongerwaire-lengths. Thelotensity
Of the absorption caused by the unsatd. links agrees with the
expected lewla of electron dispkeement caused by the sub.
stituent radicals. LXX'4. Reaction of pro"I bromide
,so
With a4l flcad1deh deMmder the conditions a RA(Ormat-
am reaction. etrov, Vu. 1. Forfir'cva. and G. L'
a= a.
Semenov. Ibid. 117".-Reaction of proper I broraide.
Ivith Zis and Aleh bx,
(C' ydes wAs run as descn earlier by
Henbesto d al. A. 44, -1934j), but ussing HtjO *3 solvent.
Reactions with AcH and EtCHO give a mixt. of I-Pcnty*-
I" and J,:-pesdadk#:-4-V1, bi4 45-W, N 01-2'. No 76,11
dp O.DWO, PoV 1.4384; the former was
yield from propylene oxide and HCICNa FrCEqqdjjn N'011's'.
72.5-3.5*, dto 0.8018. xV 1.436& Propatgyl bro-
.mkic nold pr(jutgyTahlvhyda similarly gave 14myn-4-ol
cnnwm:n;ttc4l with 1.2-hexattlen-1-ol, bm 64-5% bso 71-2'.
to kl,@'
tolutuftulfonntes which were converted to unsaid. hydfo-
Carboni: I-pcntyn-"l gave J-penten-1-yne, b. 40.5-7.5%
dw 0.72293, uIr while 14w-xyti-4-ol gavc J-hexen-1.
yne.b.7-9-4*.ds.0.7425.xl?1.43SI. 'Infraredspcctruotall
products are shown. G. Al. Kosolapoff

Distri
4E4j/4E20SjYqX.7
Pr ?aratlaa of hydmaromatic hydrombons by Prd7d4
WaftedTfam
of a 10
Viatica
an tZkow,
ale'
'T'r
___@27. @IiWt@
FO@94187,.-Tfit followiag car-
27. li 5- .4
b1nols weire prepd. reviously dw.Abcd technique ( C-A
ly
47. 2735h): withy 34yclaiaps-1-yi). ba -93-34', dn'
O.QM, "V IAM2* bw 104-4-8%
0,0503,1.4932; 73 5-14',
.0,9310.1.4woj-63.370flo o J-C lowra-1-yo, bit 306-
7* 0 0463 14830; 53-7. Abolyro-c Wom-l-ill b"
F", ($06
0:92i@, 1.4 ell
ba 1214-2.5', O.Ml, 1.4775; makyl(MAVS.,
I-A. ba 101-1.150, O."M, 1.4822; 881 k6-OsAyt-s-
1.1."49:
T
k"Os I bo 102-2.5-, 0.9492.
1=011,14), ba 111.6-12'
b.1061-.0:9423,
1. 830; 4-w lokexrn-Z-yl)
.1.48341 #1 yt("= bv 116.5-17
1.4828; omzols "4WiQAsxv#-l
110.5-11.5% O.W49 - 'N% othylMS4
1, IAM .796 @ 14*r
34yclohaex-l-A, big ll"*, O.9.,W5,1.4951; -74.7% *wtb
bio IM-7' 0
.1.4970; wejkyl(j.S-exdv"kylw ;-cydokenm-1,;4 bo*91.5-
2.5', 1.0012, IAW5; AbAlS-et.
ff eke. were
yl), ba 109-100, 0.9M, I.M. The precedlu
acetYlated with ActO In preseactol a drop of HSo4, Yielding
7.
LID.

rA ov,
WOW. O&M. 1.46M.
09W.
Iltj,4 @@t9 -Og6i .,!Z;, @jj@. IIA%t

6 6&-72*, 0.8W, 1,4779; 42@2
%@ POWAYI-1424-
r
A
diMWW4-CYdOAeUX4-y
,
)d
r", ba 83 r OSM. 1.4921
JJ,"ixdW-$-4cloh4xcx-1-yi)dkew, bis 704-1.11'.
69-2a

4795,
.
OM - 64.2%1@mdk -(J."iwdhylJ-cyckk*t**-
0.84, 1.482D; 42
54nda.
3% (1
.
,
4-70edo". b. 71-4. 0.9254. 1-5050.
ysis of methyl(IIA
carblayl acetate Pvt an WWMSIOUA result. yiddial mixed
acetates of crotonyl and 'methylviny1carbinyl acet".
50'
h
P
l
l
f
C
e acetates over Pt-
s o
at 3
yro
t
save ownly the
yw
expected aranutic hydroestbous.
Sea coudenut1w 61 woklo wilb'Pl' "taLe
Pe
7!
imesic ddehydtp with W- .
-. slular

e
c
l
e %) the p4sotner,
r
a
ti
w
ly
ol
iZ
h
l
s
fs
u
@the fact that (2-Metbyl-a-cyclobeled-I..
T
lg
e@dr
yl)etbeneoudeh
CAM with somtk43asutr, as evidenced by oxidation maw
l
to FhtL2lk acid Lad uuH mt. of lswhthalk add. Sim
IJAF'rs dehydrtvtniktion of (4-methyl-3-cyclobezen-1-y!).
ethene, dwribed above, gave a McC4H.Et which oxidiud,
h
thafic scid with 0 Null amt. Of isoplithallo
tnainly to terep
rasolapoff-

T IT Ui. th,@ :4crw
.@n L
late. jyntberir, of i@ydrcaromat-,- i.1corO2--' (@.onden-
sats!;-ra dienovyki, icyc-dincriiy s ;i.-,*e.- gidroaro-
matIchesbrik!) spivvw i
FrIUMCAL: @humal Obshcliey Khi.:%Ii, L'j"7, Vol- '27, :.r 1), 291,6-291.1 (03R).
I I - -
A:M11ACT: in earlier Fubli3hed papers in @ne (S Lf,t- of this arm
t1cle particij%ated .1t vas Jmrest!@,at,@@d ivLeUcr is -x,33ible to ob-
Lairl U-1,valen', hydroaronatic alcohcls ind hydrccar@,oiis [!,? from
products of mhe c@),Ovrisatlon cf 1,3--.Urene with mo-',@Yl
i..etacrylatc- ni-th tlve ai-,', of orj:,a[ViC Mal,;N@-IiIJM In this cons
m e ure
"eCti-.)!1 it, Yla-- :7!!(-,W11 thM. mIxturts xu!nsive te F rat
are cutained n-n O.C, cf u,-.,n the methyl
acidc. Tv 0@.f, -@nt@ work the
:.tut,loor,i -ra+@ it the mix-
Lures forminC i.-, t-tl @,,n c@-11"-1,'.1@',,il. -to ::-Xtures Of
alcch@@!S a@ld kt!troN@S cieve)-@:p i.-- ""e- @rr OJLF .1-methyl-
ScLd and witn W,:i] J, reaction
vt-locity ane rvla,,ive. yi@A,:- -)f t"fl` depen=
Card 112 ltwt, or, th,,., th@- 7,f tw'iv @Irl the ring

Con0ensation of the ",'@iene ("n
k4 Wi.U _'et@yl 75-11-6/56
2P-2
'Synthesis of i@drcarcmatic .,kc@:UF and 'j..yd.-rcarbonso
(3ce table 1).
Thus qttite a niviber of Lrlval@,-nt alrc@hrols and keturte5 Wac p:-oduced
fro- 1#., @acryl t ,
I mproducts of tlc -cndurz,'ktI:@n cf ro-,-tI)yIx @ la @, nith divinyl..)
piperylone-, isoprere-, dipz@@-.penyl_, dij,3opropenyl-, cyUopentadiene
-1,3 anrl cyclohex8daivne-10 -Odt!) the aid of .7.iaL;w2!;hLn@i:ethyI iodide
and inaenesiurr. ethyl icidide. Ey dehydration of fi-;e the corm
responding hydroaromatic hydrocarbons were o@)tained. i,:-,J.-c,!arbors of
the type 1,11-ai-.rw-tYyl-l-i-soprcpc-rylcyclc)hexciie-3 co-tij not be dehydra-
ted with platiniLli.
There are 14 talAes, anl 'If references.
@c oo Alreraft Equ:iXv-at Construction @Lenincrads-
Z.SOCIATICAI!: jeningmd Institu+
j,@j,r iiiititut a-viatsio iya).
nfio-o pr:Lr)-)rnsLroyen
SUbLI'MD: November Ij 1956.
AVAIL101U.". 41, . -,,i !t , @; -_.% @ r
1. Diene compounds-Condensation rez,.-tions 2. @@droanomvt%.Ac
Card 2/2 alcohol"Ynthesis 3. Hydroc@rbons-Synthesiz
4. M,,-thylnetacrylate-Co.-idensa'~ion reactlons

Y
oi* @-Trocrriicn? ith
of .,lcoiiolu, cetnten roid
uglevoljorodov - korichn, 'rm alldegidom.
tset
Ante@ 3pirtov, a UtOV
"iurnul '101. 23, 6,
u @;,:,A
--ing -ir previou.-? inve:Aigsition -icf 9
unt-, n.. thc
au6hors investimitcd the condensation of (Iiv;nt!Iq Pirerviene,
iaoi)rene, eyclonentaijiune, cnd cy-clohmidienE
-.,ith cinnamaLd-:.-!iyJe. -'rom thp aldeh,,Aes thu:-, ob"iAnA, "ec-
ondary alcoholj, their-rcet.!ttes, -ind, by P-vrol.,-,.As of thc
11,Ater, 'i-Mrocurb@,nc ne;-e
c ozu t arits, w.1 vieldz- of
befizv1dehyde i.,n,i J.ts houolot-rucfj ,re in t:-ble 1. The
ccndenu@@tion o' c.,,c1o7,vnt&d4.ene-1,I -.O.th i@-Jinnmiic "Zid could
not be effecte;-1. @-'he Vig-
o.!orlc:iq, 1:quid-, -!,!.,ich ...Vi! u'ajil..-
1/5 --oluule in t-ther, luenzene, and alcohol. -or all @11eh.w1ei,

'79
6a.1-Cri.-ation o Diene-.H.-irucarbono '-ith Cimintm III ehyl e. .,yi,thesiz of hydro-
ILCetates iml !@,f-!Poci,rbonq
rnd ~,4-flinitroo~ieriyln-tjr;;,.,.oiit., *erL,
obtoillvA. -, -o'-)YOnry 111coh9li, fl-3m th@.- oi,
un 2 - ijhcnv It e tr,,hy(:ro 1,1,.! hvttc
ioli!"e
-.,nd its homol@jpwitt-. They crr- u-ven more vitcoiis than the alle.-
hyleo. From the alcohol olotnined from thia nI-Jch-.,Jc;. t-.,o
-)luc- o;;, c:-- t, llin,@ -rpi ow.- J@qqid (tvall., nri -! i : ?
t, 0 'ile
ii, t,.blc the-ic
At V.-, Cleir
t joili ir bovp
u
tho!:v ot' the letter; have the @!..mc e!.eeLfic p, rz, v,'- t i
--cr ::-fr-,.cLivc -iccc ne h,.jro-t.--*c-,:natc
citt eon @rribl.. -.o.
1-bons .)I' t -
t',;e baoi- of -,ot,,@blis'nQd on i f@,.-rlivr occar:iuli
t!i-i rosulting rxrc. Given the formul,x. 1 ir.
@,--hle 5 t':'lefs 11-1-1 .rc-. I taoic., nn! 17@ r-ferc,,,,,:,
9 )f -A-ich tire Sov4,-t.
I

n- it!, Cinn-mal ti@liyl--,. e!: of H.rjro-
Acetater fin!
I Lon.Jnr--od lrinti tiit - vint7lonno:-o -ribnrovtrn-:'n@-.-;
in:-til-, .of Aircraft lostromas a t)
nd.

S/079/61/031/()04/CO2/,'o6
ID 2, @,201, IS72-11407 B118/B208
AUTHORS: Petrov, A.A., Sopov, N.P., and Savich, I.G.
TITLE.- Studies in the field of conjugate systems-.
CXXXI'V. "Co-dimerization" of divinyl with diisopropenyl
(Diene compounds. LXXIX) -
PERIODICALt Zhurnal obahchey khimii, v. 31) no. 4P 19619 1140 - 1143
TEXTt Taking into account the paper by A*F. Plate and co-workere on the
"co-dimerization of divinyl with cyclopentadiene (Ref- 51 Izv. AN SSSRP
OM, 1958, 1279) which indicated a dependence of the reaction direction
on the structure of dieneB and on temperaturet the authors of this paper
studied the "co-dimerization" of divinyl with diisopropenyls The reasons
were the following: The structure of the "co-dimers" of divinyl with its
homologs was determined by dehydrogenation to benzal homologep and by oxi-
dation of the latter with permanganate to corresponding aromatic acids. In
this connection, errors were possible in the determination of the compo-
vition of the initial hydrocarbon mixture because of incomplete dehydro-
Genation of the individual components of the mixture, and because o-, m-t
Card 1/6

3/079J61/031/004/002/006
Studies in the field of conjugate B118/B208
and p-dialkyl benzenes give aromatic acids with different yields (eepeciL
ally, in the prouenoe of an o-isomer). Dienes were selected on the follow-
ing anpectst According to the scheme
-Clio Clio CHOH-C113
+
C113
&OCW13 CHwCH*
O_C(OH)-CH3
r_@ J_Cooft O-Coon C-Clis
&3
the' formation of only two dimers (I) and (II) is to be expected owing to
the symmetry of dienes, which considerably facilitates the analysis of the
mixture. The method previously used to confirm the structure of the re-
Card 2/6

20948
sj"P, 7 9/61 /0 100410012,101@5
St-adile3 in the field of -,onjugate B 9 / B
high quanti1-1E;.-,, this p,@Iymer :ontains thc- t! . rl 41
The reaction pre9umably proreeds v.1a a oix-memberel irans4ti@n c-mplere
The previous assumptions on the prevailing directicr. -@-f ":,,j-d1mer1'zat!.c-n."
of divlnyl with diisoprcpenyl were thus confirmed and defined. There ar-
I figure and 6 Soviet-b!-00 T,@fererxee.
ASSOCIATION* Leningradskly tekhncl:)gicheek-,j instL.--t
(Le-ningrad Technological Inst4it-,te imer,: Len@v@-'.'
SUBMITTED% April 2@, 1960
Card 4/6

SOFGVP N.F.; KOVNERI M.L.
Preparation of hydroaromatie hydrocarbons by the pyrolysis of
acetates of secondary @dcohols obtained on the basis of the
conden+ion product of Isoprene with crotonaldehyde. Zhur.ob.khim.
33 no.411142--U45 Ap 163. (WRA 160)
1, loningradakiy Institut aviatsionnogo priborootroyeniya,
(Hydrocarbons) (Isoprene) (Crotonaldebyde)

SOPOV, N.?.; KOTI"R, M.L.
Preparation of 1.3-butadlene di@@rivatlves by pyrolysi5
of secondarj alcohol ricetntps cbtqined on the basir of
the condensation prodiiets, o!' ioprone and piperyleno with
iinsat-irated al,lahy les. Zhur. ob. khim. 34 no. 5:1,,92-1496
I@y 164.
Ibid.sI496-
1499 (MIRA 170)
1, LenjWs"y JnWtut aviatsionnogo priborostroyeniya,,@,,.
1. -CA _. 1@

SOPOV, N.P.
Production of hydroaromatic hydrocarbons by the pyrolysis of
acetates of secondary alcohols obtained on the basis of the
condensation product of bivinyl with crotonaldehyde. Zhur,org,
khim. I no.22233-236 F 165# (MIRA 18:4)
1. Leningradakiy inatitut aviatsionnogo priborostroyanlya.

:Ar-cor
Legwninous fodder plants. Skopje (Zemjodelsko izdavatel-no predprijatije)
1950. 59 P.
4SB-205

SOPOV, S.A.
We are using a now method for ethylating gasoline. Reftianik 2
no.8:23-24 Ag 157, (MIRA 10:10)
1.0perator stilosmesitelluoy ustanovki Khabarovskogo nefteparera-
,bat7v&yushche o savoda.
fithylation) (Gasoline)

SOPOV, 3. 1.
Paralysis
Bilateral paresis of the recurrent nerves. Vast. oto-rins, 14, No. 3, 1952.
Mon&hly LjMt QL Russian Accagsions, Library of Congress, Octo@" 1952. UNCLASSIFIED.

SOPOV, S.I. (Smolensk).
@-- -,4j
Anesthetic techniques in tonsillectomy (contrast anesthesia).
Vest.oto-rin. 16 no.1:83-84 Ja-Y '54. (MLRA 7:3)
(Anesthesia) (Tonsils-Surgery)

LUKIYANGII, V.L., deputat Vorkhovnogo Soveta SSSR, mastt3r blokEL MartanoVskikh
pochey; GOLIKOV, I.N.; BITp B.I.; 1ZPatSKIY, V.V.; A=r-T--,
Gwroy 3otalaliBtichou)-ogo Truda) vajtsov:j'ic,%ik; MARM;V,
C;I,'RllOV, V.D., stalovar
Wo -m-to carrying out the deoisionn of tho 22d Congrous of the
Corzitinlat Party of t'..,! joviot Union. LetaIJurg 7 no#7:2-6
il t 62.. .(MDA 15:7)
1. hichne-Tagillskiy metallurgichookiy kombinat (for Luklyanov).
2. Direktor Toentrallnogo nmichno-insledovatallskogo Inutituta
chornoy matallurgii, (for Golikov). 3. Sakretarl partiynogo
hudVAa llak@jyevskogo matallurgicheskogo zavoda (for Buy).
4. Direktor zavoda "Azovi3tall" (for Loporskiy). 5, l4agnitogoroldy
motallurgicheakiy kombinat (for Sopov). 6. Direktor GomidarstvonnoSo
soyuznogo instituta po proyektirovzLqi.,,,u agregatov ataleliteynogo
i prokatnogo proizvodstva dlya charnoy (for Mantsev).
7. Cholyabinskiy mutaUurgichooldy z--vod (for Chernov).
(fletal-lurgy)

. -SOFQI. Ye.
Ifew aspects in the commercial activities of "Saverportfilm-0
Vnesh. torg. 30 no.10:38-39 160. (MIRA 13:10)
(Motion-picture festivals)

SOPOV) Too
The Second Moscow International Motion Piature YePtiVal.
Vnesh. torg. 41 no.6:33-35 161. (KM 3427)
(Novgorod-Demoription) (Novgorod-To=ism)

SOPOVA, A.A.; RUNKOVA, N.V.
- W-Oww
Problems relative to production cost. Koks i khim. no.5:59-60 '56,
(Coke industry--Costs) mu 9: 10)

C ZEC IT
1,44141413 61 lflNf% of cubfmd bow,
dies With Ulu@dgfm C40 , " - 4:! TPP short.
kyPOP-M, 99* Temam.
fma Nis F UVI I FAROW-77-
-IIOG-2(1953).-Treatment of Me ether of crystal viale
carbinol base with MeUgT (23% excm) gave crystal
violet Ili Ult; SJMII&fly He tlhef Of ffiRlechite gWft
catbinol ban and PoteMlit pys sualachite goet HI salt;
Me ether of crystal violet carbinol base with BtMgBr Vive
crystal violet HBr salt. while Me ether of inslackite gma
carbiW base and 1306flift pve malachite grem HBr Wt.
The reactions were run 16 Itts. at to= temp., after which
the mists. wei quenched Is H80 and AcOH added. To
boiling Wo. of 2 Z. crystal vlolet cublool ban Ue ether to
RUO-CXi was. slowly added 60 mt. of 940 solo. of M*U9l
(torn 3.54 S. Mel; the addit. made om 4.6 hm, Wowed
n
by heati 12 bra. gave after sq. treatment 0.81 g. (
14 CUO, W. 200-10* (from WON). SmIlAwtv
rl Ci
IWI
flulachit, ffrcXVmG -bi(nol bam Me ether wW MeMS1
larly gave UftNCsff4)mCPhMe, m. 134* (in= MeOfl)t
,,(froma WOW.
" W--j ---a

I "el 1-1
'Lene ano
With CO"To"mcls Co*, St-Ite ical
it Sci,
"'Reactions 0 GrouPS. C' C c-
ly,
Actil),ate(l
91C,
last,
c and -ec"Inical DissertatiOns Defended
SO: Stui. llo. 70h, 2 55 surve, 0' sc'e."lt'f@
ia Us,'@a Ilic,her I-Aucational Iristit-utions (16).

USER/ Chemistry - Reaction processes
Card V1 t Pub. 151 - 23/37
Authors : Porekalin, V, V., and Sopova, A. S.
Title t Reaction of nitrostyrene with certain compounds containing methylens
groups activated by carbonyl and carbo.V1 groups
Periodical t Zhur. ob. khim. 24/-
513-516, Mar 1954
Abstract t The reaction of omega-nitrostyrenes with substances having mobile hydrogen
atoms in methylene and methyl groups,, was investigated. The hydrogen atom
were activated by electronophilio (carboxylp carbonyl) groups oriented in
alpha-position or in conjugationwith the methylene or methyl groups. The
affect of basic catalysts on the reaction of nitrostyrene vith various
compounds possessing methylene groups activated by carbonyl. and carbo3yl
groups is explained. A now method for the synthesis of gama-amino acid
derivatives was introduced. Eight referencest 5-USAI 2-.Ger=n and 1-USSR
(1879-1949).
Institution z The A. I. Gertsen Pedagogical Institute., Leningrad
Submitted z October 23, 1953

,-'Rvsct" of "Itt" I with pernt. C7v1pjltn;u w6mill. ep
In? mrth )IM7 ac mited by casimmA and carbosvf/,'
xroum. V. V. Pm,kolht -rul A. S,. @3-vr,. . r@;.
I .,

ASI

U S S R

;O0,19yattests of derivatives at -V-fiwna -1gle. %0. V.'Pen@
Namk Si.S.R.
-
903-5( 4-Oold tion of PhCH:CHN% with
W
-
51
ht
Iter
CITAC
H
11 2 b
W
81
4
1
d
d
N I
-
,
.
t
n
e
rs. at
.
m
gave
r3
%
PACH(C1tsNOs)CJ1(MFJh;tp.G4*. Th6(6g.)in),fA
was added to 5 g. Ni catalyst (Adkins and Billim. C.4. 42
.1328c) In WWI presatd. with 11 at town wrip. and hyd;:
"*
i
ti
d 5 h
7
k
t
-
on con
rs. at
nue
1renat
give 0
% J-p
esy
132*
44
b
h
lidi
hf
O
Thb
f
S
- ro
ar
et
axy-
gam, m.
rom
e
H).
(
A

3 0 refluxed,
hn. with 301) ML 18 lICI pvt 75.6%
1
NCJ1
209' R
9
CffPAC11
CO
1f
l
R
O
)
rIam di
.
,
. m.
t
*
s
s
.
boiled In AtsO 3 bra. t1ils pvt the N-Ae ax*)A
70.4
Y
tn. CS' (Irmn hexane). 0. M. XONVIAPO

Subject t USSR/Chomietry
Card 1A Pub. 3.19 - 6/8
Authors S Perekallus V, Ve and A* So Sopova (Leningrad)
Title t Nitroblefins
AID F - 3171
Periodical s Usp. khim*# 24# 5t 613-634t 1955
Abstract : The preparation of nitro6lefine by nitration of aliphatic olefins
and by condensation of aldebydoo with primary saturated nitro
compounds is reviewed. The phypical and chemical properties of
nitro6lefirw ftv discussed In some detail, Your tables,, 158 ref-
ences, 7 Russian (lV3-1952).
Institution i None
Submitted : No date

AUTHORS: Pprokatir.. V V.
TITLE: The Synthesis of v Aminketonei
(Sintez P - amin--k@etoaov)
PERIODICAL: Zhurnal Ob4h.,hey Kh'.mii '958, Vol 28 fir 3 675-679
(USSR)
ABSTRACT: The effectively rea'Lized reaction of nitroolefines with
acetic ester succes3fully realized by the authors offered
-ty to make uge f th-is reaction for the elaboration
the possib�lli.
of a new synzhes:..s of,;-amin:4e-.ones These ketones have
,nv
hitherto not been . estigated as there seemed to be no
possitle ways for the'r 3ynthes,-s as wr@'All as vi-@) possibilities
of heterosyclllzat@on form-ing mult-ipti pyzo:jne derlvatives
of intereat for chemistat it wae oz' interesT xo find the
dependence on their structure of the ^apqbi1tty af condensation
of unsat@)rat--d with a,;Pt,c enter. The 'reaction
of nitrostyrene with acezl:@ ,,ster or a catalytic contact
with triethylamine a,-,,d pyr-4,iine "Le_d tD the formation of the
ethylester of the 2, acetyl - 3 - phenyl - 4 - nitrobutyric
Card 1/3 N
azid (il (go-.82 %).. The reduc-.ior, of this ester

The Synthesis oil J' A=iln@k'eto--@eq
-" :@ '?"I. ," 't I '@' .
resulted @.n two prcdu@zi Jecend?.ng on th,:- react@@:. pez-,.@d.
j ftc. ni tr-@Cr,@up and
the hydration fo:7 10 ho-.i-rs on'y
le-d to the formation of ethylesters cf th-,;! 2@acetyl-3-
pheny1-4---&r.:.nobLtyric. ac-ld (II) @ that for 48 hour,.. h,.@Wever;
was accozpaniei by the saporification of the eiter and the
forma@jiori of 2-v@oty! -3. 4 -onan-,butyric a,.',d (III) The
vatur A tile am"noketi.,)IO ' n@@id (11) wat) aublei:ted to different
chemica' reactiona, 1. Th-@ saturation of a tenze-ne
so'Lut.'.or. with dry hydroch1cr--ine furni shed the hydr@@chloric
sa.'-, ((IV) 2 @ re acti.cn of EtcetyAchloride ga-ve the
acetyldii:r., vative kV", 'I.- 2-e heatingr with a 10 @ bydrc-.-
chloric acl-- le-d to th@.- se-)Iut: on of the basio. problem:
As a cons,@tq-@@ence of thf,- ketone cleavage the go aminoketone-
@..amino-2,pheny'pentanon-4 (M in form of 11@drochioric salt
resulted with a y-,e-d of 45
% The aminoacid. in heating above
the mel'@ing point, easily converted to the pyroltdine
derivative by h4--tero:y,-,1:zation.-, th;.s agair. was converted
to the hydrochlorl@- salt L-f 3 phenyl, - 4 ., acetylpyz-olidin-
5 (VlI) by dry hydrk@shlcrine, Special attention was paid
to the structure of the ionacnqa':ion produvt (I) which was
to be detormin@-!d. It formed In an. alcohol medium with phenyl-
Card 2/3 hydrazine in the pr,?6erc@- c4 h-@drochlcrine u,,,id the phenyl-

The Synthesis ofr-Amincketones
79-28 3-24/61
methylpyrazolone derivative (VIII), which is identical
to the reaction product of nitrostyrene with phenylmethyl-
pyrazolone; hydrazone (IX) synthetized from (I) was converted
to pyrazolone (VIII) by heating in benzene in the presence
of phosphorus pentoxide, Thus the structure of the
condensation product of nitrostyrene with acetic ester is
clearly proved..
There are 3 references, which are Soviet
ASSOCIATION: Leningradskiy pedagogicheskiy institut imeni Gertsena
(Leninerad Pedagogical Institute imeni Gertsen)
SUBMITTED: January 21., 1957
Card 3/3

ZHUR,AVLEVA, L.Ye.; SOPOVA, A.S. (Leningrad)
Laboratory experiments In the preparation and study of some proper-
ties of polymers. Ehim. v shkole 14 no-1:54 Ja-F 159.
(MIRA 12:2)
(Polymers)

100BOVICH, Ya,S.; PZIZKALIH, V.V.; SOPOVA, A.S.
Determination of the structure of some dihydrofuran derivatives by
means of Raman spectra. Dokl. AN SSSR 134 no.5:1083-1084 0 l6o.
(MIRA 13:10)
1. I-eningradskiy gosudaretvennyy pedagogicheakiy institut im. A.I.
Gertsena. Predstexleno akademikom A.Mereninym.
(Furan--spectra)

SuPOVA. A.S.; PL-REKALIN, V.V.; BOBOVICH, YA.S*
Synthesis of dihydrofuran derivatives. Zhw.ob.khim. 31 no*5:
1528-1532 My 1619 (KIRA 14:5)
1, Loeningr@Ldskiy pedagogicheskiy institut imerii A.I.Gertsenaa,
(Furan)

SOPOVA, AiS.4 TEI.T;'- LA.
Reaction of acetoacetic eater with 14-nitrostyrenes. Zhw.ob.khim.
31 no.5sl532-1534 My 161, (MM 14:5)
1, Loningradakiy pedagogicheskiy institut imeni A.I.Gorteena,
(Acetoacetio acid) (Styrene)

OSOKIN, Aleksandr Stepanovich; BESKOV, S.D., prof., doktor khim.
nauk, retBenzent; kand. khim. nauk,
retaenzent; POLYANSKAYA, A.S., kand. khIm. nauk, retsenzent;
ALAVERDOV, Ya.G., red.; VORDNINA, R.K., tekhn. red.
(PrincipOB of general chemical technology] Osnovy obBhchei
khimicheskoi tekhnologil. Moskva, Vysshaia shkola, 1963. 390 p.
(MIRA 16:7)
1. Laningradakiy pedagogicheskiy institut im. A.I.GertBena
(for Sopova, Polyanskaya).
(Chemistry, Technical)

SOPOVAP A..S.; PEREKALIN, V.V.; rURGHENKC, 0.1.
Interaction of 1-brcmo-l-nitro-lpentene and -bromo- -nitrootyrone
with some compounds containing active methylene groups. Zhur.ob.khim.
33 no.7:2140-2143 JI 163. (MIRA 16A)
1. Leningradskiy gosudarstvennyy pedagogicheskiy institut imeni
A.I.Gertsena.
(Pentene) (Styrene) (Methylene group)

SOPOVA, A.S.; PEREEKALIN, V.V.; LEBEDNOVA, VA
Interaction of 1-bromo-l-nitro-l-pentene andA -bromo4-nitroatyrene
Uritj active cyclic methylene components. Zhur4,ob.khim. 33 no.7:
2143-2145 Jl 163. (" 160)
1. Leningradski,7 pedagogichaskiy institut imeni A.I.Gertsena.
(Pentene) (Styrene) (Mathylene group)

SOJIOVA) A.S.; P-'-'!@;KALIN, V.V.; L.". "IHEDLIOVA, V.iM.
Interaction of --,.-(p-niti-opiienyl)-fl-bromo-fi-nitroethvlene
with some active cyclic methine and methylene components. Zcur.
ob. khim. 34 no.8:2638-2641 Ag 164. (MIRA 17:9)
1. Leningradakiy gosudarstvennyy pedagogicheskiy institut im.
Gertsena.

,Wl@ll, i"! I hil , ;@,:Pl t.@ 1 ly ic-i I. Al @lv @l , ;,', "', ;
11 A 1@ , I ,, k ? 'T Kh .I.I reli . ; "", (;,@' t . ,
,, e J, . r e, J .
@l 1". cl. @
c-in be obtained fror. 1.4. luch-tilA i;,- r,@jLza.
;,e ri i n g r ti d , Ned ra . 1965. 17 50 1) . 18:5)

@iIXIOVA7 A.S.; YURGIIIAKOP 0.1.; PEEMKALIN, V.V.
Syntheols of nitrocyclopropanes. Zhur. org. kh-'m. I no.9:
1707-1708 S 165. (MIRA 18:12)
1. Loningradskly pedagogicheskiy institut imeni A.I. Gertsena.
SubmItted May 12, 1965.

PEREKkUllp Veevolod Vasillyevich; Prinimali uchastiye: SOPOVAv A.V.; MIUMt
O.M.; ZONISp E.S.; ZOBACBEVAl M.M.; KVITKOI S.MX;MLSKOV-#-Tu-.V-.; KAP-
LINt S.V.; POLYANSKAYAv A.S.; PADVAv G.D.; ZONIS9 S.A.9 red.; FOMXINAv
T.A., tekhn. red.
[Unsaturated nitxo compounds) Nepredellnys nitrosoodineniia. lanin-
gradt Gos. nauchno-tekhn. izd-vo khizr.. lit-ryt 1961. 335 p.
(MIRA 14:7)
(Nitro compounds)

7h
USSR/Medicize - TrAberoulosts, Sep/oat
@anatoriums
Medicine - Psychologyp Ibdicine
and Psychology
"The Cause of Iatrogenic Conditions in Patients
In Tuberculosis Sanatoriums," G. N. Sopoya,
4i pp
"ProbleaW Tubarkulaza" No 5
Discusses psychology of doctor-patient relation-
ship.
21/NnTh

S,QPOVA, G. 11.
Personnel of the Feodosiya Sanatorium of the Ministry of Defen36
compete. Voen.-med. zhur. no.12:43-44 D 161.
(MIRA 15t7)
(FEODOSIYA-SMIATORIUMS)

sePOVA, 0. -1.
Sopovaj 0. 1.
"Pigment paper
its quality)."
Moscow) 1955.
Science.)
(a @tudy of its basic properties and methods of improving
Min Higher Education USSR. Moscow Polygraphic Inst.
(Dissertation for the Degree of Candidate in Technical
Knizhn3y-a letonis'
No. 15; 1956. Moscow.

nn;4L)v and (J. 1.
S S R 103 .914, Svp! r !I-,c rd
graphit p.q.:-r k,lr ov w PnI111,19,
StallifiMd I)MVT, OIC Phr"OR' iifiVC - b-
t hC -NIU16if.; qu
morr rv@idily dislr@)Ivrd fruni the'unexpCI&Ad arl M.11#
Ind file 11rilltmg i. improv'A by tmating the
I J's 2' Vnvl@

BERE 71 t,i. rt:.(A, ITSKI-17 L. A. . red. -. i-ILLNFTEV,
FOYOV,' ; A. L.,, rt2-i. P.A. . red.
re-j.i IIIUVA@j 0.1., red,
[lr@msa,@tlons of the Conference on the Sclentifll,, Basis
r--f Lhe I@rc-csstes @)f ;r,.r,',Ang and Methods for T',ioir
Impr,)vementj Trudy Ko--ferentsii po nauchrym canovam prc-.
tocrol-v I ikh soverrhenstvovaniia, Mo-
sk-;n.- -i il---aLellstv. No.l.
19 (" 1 4 p 41111A 18:5)
pc osnovam protsessov pechata-
nlyl, puya,:@ lm-@ s,@vershenst-vovaniya,. @'osccw,,

A111CHKOV, N.N.,; M&BOTINSLIL Yu.H.,; ZAYKO, SOPOVA, T.L.o;
TySyACHIrM, S.J.,; XUOPDU, I.D.(Loningrad)
Tiss4o changes following disorders of Innervation. Arkh. Pat. 18
no.1 3-14 156, (KLRA 9:6)
1. Iz otdala patologicheskoy anatomii (zav.uak&d. N.N. Anichkov)
Instituta, skeparimentallnoy meditsiny AMI SSSR.
(laRVOUS SYSTIM, physiology,
off. of denervation on surrounding tissue (Rum))

KRUGLOVj B.I. (Kruhlov, B.I.); SOFOVAp, Z..Vej KUSMARENKO, G.J,
(Nushnaranko., H.I.)
Ferromolybdenum catalypts for the oxidation of methanol in
formaldehyde. Khim. prom. [Ukr.] no-3:3-8 J1-S 163.
(MIRA l7t8)

301T, Lm)?@lo, dr., tu@lo--ijulyos fontuikatnre
Dark percentage of the poplar. Erdo 14 no.2:66-70 F 165.
1. Scientific Inatitute of Forestry, Sopron.

1@@ Kuco
kUTHORS: T:@ r h,
I T LE'
PERIODTCAL: A4ademiya
S Ole), /I 591100i'10' 7
b' 0 3 1B 2 @-'O
A a6 em; : -,ar ., A! ar ; -ia P@ . and S.Dprar.,,' V. A.
and syrtheols j@ fu ryl n 4. t ro - y I e r, e
nq@;k SSSR Dck.` ady 96' "06,
TEXT; When 9-.udy-lng the @r@,tiem of, ob-mining -,ompolurdo of
the hetero:y:!i3 series :crtaining n,. *r@@ grours In Polymer. -,ha-.r, the
withors pr,@d,.-.ced a..Ifury' e-@hyl-ne and
:r- *:he -P-_r.'.rn o" '@hr@ ew@'-r,,rs, '@hs- :rg :tt:-hods urf:-
-_j -a -. @.n'er.3a*. icncr,@ J@.; ribel ir. r I', li,,@ s m r 1; s
.r, tile R
B, P@ ; b . r
e and r. i I
ml e n ha n n "h V.- i; r. cf
L e A nn 11r;0 sy!:.-,h-@sis. @41 a- t -,n
n i@a raf f i r L R
A@ S S,,,. - Kh_m, v""',@rs
a. fury'. 'i." 'f fu! -.r. *,he
C,qr--, * /I

Ph
5/020/61/139/002/014/017
Polymerization capacity and synthesis ... B103/B220

and with the use of 5c,4 of catalyst (related to the monomer). The polymers J.
obtained are thermally stable, infusible, and unsoluble in conventional
solvents. [Abstracter's note: Essentially complete translation.]
There are 2 figures and 3 references: 2 Soviet-bloc ana 1 non-Soviet-bloc.

SUBMITTED: March 30, 1961
Yield in polymer of*a-furyl nitro-ethylene in the presence of
sodium methylate as catalyst, dependent on temperature.(A), quantity of
catalyst at optimum temperature -100C (6), and time of polymerization.
Legend: (1) quantity of catalyst; (2) time of @)olymerization.

Card 3/4

Tannin-
1', 19'12.
o,.j L-- ai; c@' itij'-1-1-11 for
7. W, 11
9. Eont.hl: Li--:t of RusAin A,--ctisslons Lp Unclassif led.
y c Ccnz,.--e!::-, March 1953.
f

SOPRIKO. A.Te., in2hener.
; - -a I - I @ I . I
1mproving the quality of a mixed, oak and willow bark extract, Log, rou,
14 no.2:31-34 7 154. (KLRA 7 1
(Tanning)

BARBARICH, Andrey Ivanovich,- GONCHARCVp Stepan Valentinovioh (Hopcharovp
S.V.]; KATINA, Zcya Fedorovna; SOPRIKO,-Alek.swWr Yomollyanovich
[Sopryko, 0,0,]; XOTOVO M,I,p &Oa6i biologenaukp profop otv*r9d;j
DAKHNOj Yu.M., takhnred.
(Wild tannin plants of the Ukraine] Dykorostuchi dubylini
rosIM Ukraimy. Kyiv., Vyd-vo Akad.nauk URSR., 1961 142 P.
NIRA 15:5)
(Ukraine-Taming materials)

LIVYY, G.V.; GALOPUtOVIL11, M.G.; VASIUUK., N.Z.,-
KAZARINA, N.I.; CHURINA,, V.I.; GILIW,, B.A.; 'YEGOROV) X.A.;
GOICHAR, Ye.G.
14Dthod of refining the skin aide of fur articles made with low
grade peltry; Soviet Certificate of Inventions No.11,7290, Kozb*-
obuv.prom.. 4 no.8:43 Ag 162. OffAk 15:8)
(Fur industry-Technological irmovations)

SOPRIKO, X.
Improvement of thr quality of food must be the prime objective.
Obahchastv.pit. no.4:48 Ap 160. (MIRA 13:6)
1. liachallnik otdola obahchestvannogo pitaniya Kuybyahevakogo
gorodskogo Uprevlenlya torgovli.
(Kuybyshev--Restaurants, lunchrooms, etc.)

CHAYKIN, P.I.; SOPHINOVS&M., T.K.
Effect of thoron on the determination of radium e-nation. Inform.
abor.TSEGEI no.51:131-3,33 161. (MIRA 15:8)
(Radlum) (Thoron)

SOPP=IP Gaspar, dr.
Angiotensin skin test in the treatment of hypertension at the
d1strict physicianle offices Orvo hetil. 106 no#25tll66
20 Je 165.
1. Tlszafoldvari IT& Korzatorvosi Randeloe

1*0PRONIP JoZsc.f 31 dr. (Ndapeit)
Let us fight those who a" dairaging rciilroad InEtallatI.rnbj
Munka 14 no.10;9-10 0 164.

.. . : - . 11. .
, ; : *@ne !: -,@ - @, " - - " @@:, "I' '- 11 . , -k@,
.,@ rl o . @ : @ 1 11; V 16, .

SOPRON, Jozsef, dr.
Railroad workers have fulfilled the plans of the national
economy. Magy vaeut 7 no.19:1 0 163.
1. Szakazervezeti titkar,

SOPRONI, Jozsef, dr.
When doas a railroad work well? Magy vasut 8 no.70 3 Ap 164.
1. Vasutas Szakgzarvezat titkara.

Sollil.0"li-joucf, dr.
I I
Five days in Fmice ; 11 @ , al?-xiioni congress of
railroaders. Pt. 2. , 7 11o.13:5 2 J1 163.

SOPRMT, Jozstjf, dr.
Report or. a -@tady tow- t,-j cvcder. Ilacaul 1.3 rio.11W-30
v u
N 163.
1. 7auut-asok titKarsi.

SOPRONIP Jozsef, dr.
Some methods for economical work in railroading. Munka 14
no. 6:12-13 Je 164.

WIN, A. (UD5PB) (Cherkassy); SOPRUN, N. (UB5fE) (Cherkassy)
Shortwave anteana stages, Radio no.4t23 Ap 165. (MIRA 18: 5)

SOPRLJIIMXOI A. N. (Moscow)
"On the Stability of a Liquid Layer."
report presented at the First All-Union Congress on Theoretical and Applied
Mechanics, Moscow, 27 Jan - 3 Feb 106o.

I.T..
SUibility of the flow of a fluld layar. lz,;. @ZSSI'I. Otd. takh.
nauk.Hokh, i m3himair. no. 1:142-W Ja-r- tal. (IURA 14-:2)
OAmitiar flow)

S/179/62/000/002/011/012
E031/E435
AUTHOR: Soprunenko.. T
-,P, (Moscow)
TITLE: The boundary layer on a slightly wavy wall
PERIODICAL: Akademiya nauk SSSP. Izvestiya. Otdeleniye
tekhnicheskikh nauk. Plehhanika i mashinostroyeniye,
no.2, 1962, 131-133
TEXT: The case of the flow of gas along a wall whose surface
has the shape of a sine wave in which the amplitude of the wave
is very small by comparison with the wavelength is considered.
The approximate pressure distribution is taken to be that for the
potential flow of an incompressible flutd past a wavy wall.
The stream function is sought in the form of a series in powers
of x/X (X is the wavelength) with coefficients which are
functions of the similarity parameter n. The boundary value
problem is replaced by an initial value problem and solved by
the Runge-Kutta method on the Strela computer. From the results
it is oasy to calculate the local fr-iction at the wall, the drag
and the stream function. The result for the friction at the wall
was compare*d with the solution obtained when second order terms
Card 1/2
------- rnan
Value Of to Of the present pap Itude at which
CO/6 or and also a
Of the boundary layer (co in the a
1@mPlitudo rid smaller
than that ob 6 is the thickness
"'ath. Mech., ",.25/.7 (1947), t4ined by H. G@rtjer (Z. angew.
There are 3 fi,,es. 233-244; jM0.28 (1948)t 13-22).
SUBMITTED; December 18, 196.1
Card 2/2

ACCESSION NR: AT4006711 S/3043/63/000/002/0117/0122
AUTHOR: Paskonov, V. M.; Soprunenko, 1. P.
4"
TITLE: Boundary layer along a slightly rippled wall
SOURCE: Moscow. Universitet. V)rArchislitelIny*y tsentr. Sbornik rabot, no. 2.
1963- Chislenny-trye metody* v gazovoy dinamike, 117-122
TOPIC TAGS: rippled surface boundary layer, boundary layer separation, boundary
layer, boundary layer flow, flow surface structure, pressure fluctuation, laminar
boundary layer, boundary layer equation, flow problem solution programing, In-
compressible gas flow, flow along rippled surface
ABSTRACT: The method of differences was employed to determine the values of the
wave amplitude a* at which separation of the boundary layer occurs for the first
and second waves. All calculations were carried out by means of a standard com-
puter program for solving boundary layer problems. Reference is made to a
criterion for separation of a )aminar boundary layer, as giveat ay G. M. Bam-
Zelikovich (Raschet otry*va pogranichnogo sloya. Izv. AN SSSR, otd. tekhn. nauk,
No. 12, 1954). Calculation variants for this study included amplitude values of
mi, o.W, mo65, 0.005. 0.003, 0.002 and 0.00). The results obtained show
that separation occurs within the range of 0.006