SCIENTIFIC ABSTRACT VINITSKIY, V. - VINKMAN, M.K.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001859830004-3
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 1, 2001
• Sequence Number: 4
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

90-56-5-3/10
A Case of Breakdown in the Electric Power Lines of the Bashkir Oil Rayon
(Figure 4). The broken supports stood in places *ere 'he
line was perpendicular or nearly perpendicular to the wind.
The supports of the 6-kv lines were broken at the connection
of the upper and the middle section (PAIgure 5)- On a line
consisting of 160 supports, 78 were broken (Figure 6). In
the lines running parallel to the wind, the supi;orts re-
mained erect, but many wires broke due to the weiGht of
the ice. It is calculated that the twisting moment on the
upper section of the supports was 260,700 kgcm and on the
lower section 410,700 kgcm, which is 2.7 and 2.2 times
more than is admissible. Conclusions are that the hydro-
meteorological conditions were not fully known, that the
districts of Bashkiria have been classified as belonging
to the Second Climatic Area which is not the case, that-
the distribution of information on such breakdowns is not
satisfactory, that protective measures against glazed frost
are not being handled properly.
There are 6 figures.
AVAILABLEi Library of Congress
Card 2/2 1. Transmission lines-Maintenance 2. Electric cables-Climatic
factors

VINITSXIT# V.s latchik-isp7tatell; PAVLOV. Uu., inshener.
UrAl a helicopter in case of an engine failure. Grasbd.av. 13
no.9:14-15 6 156. (KM 9:11)
(Selteepters)
: . : ~ " " -~ ^;, , ; , : -, : . .~7 1 -- ,I- . .- w - . t -~ j -1 ~~71 - _ '
. - 4~, .; ! . , ~ Is. ;~r

L
ACC NR: AR6023291 SOURCE CODE: UR/0058/66/000/003/HD68/BD68
'~~
AUTHOR: Bershitskiy., A. A.; Vinitskiy., Ye. S.
_---i
TITLE: Ultrasonic signalling devices for levels of liquid media
SOURCE: Ref zh. Mika, Abs. 3Zh474
REF SOURCE: Tr. 1-y Mezhvuz. nauchn. konferentaii 32o primeneniyu molekul. akust. k
issled. veshcliestva I v nar. kh-ve. Tashkent) 1964, 293-294
TOPIC TAGS: liquid level instrument., ultrasonic equipment
ABSTRACT: The operation of the described instrument in based on the use of a degree
of attenuation of flexural ultrasonic oscillations in the wall of the vessel when the
liquid reaches a specified level in the vessel. The oscillations are excited with
the aid of two piezoelectric elements located horizontal3.y on the outer side of the
vessel, at the height of the monitored level. The accuracy with which the liquid lev-
el is determined Is 12 - 3 mm- The Instrument makes it possible to carry out remote
measurements and to monitor the level of corrosives toxic.. and similar liquids.
[Translation of abstract)
SUB CODE: 20
Cnrd

or
j-letin or' '~e orolo.rv-
0

GRASHCHRMOY, U.I.,profesoor; USSILI, G.M. (Hookya):(Po materialam S.P.
Yinitskovskoy, G.S. VorBa, S.H. arach, N.G. Grachenoy, M.B. Dunaylbvskoy
F.A. Rosinoy, T.-T.11"Stankevich. A.L. Sheakbuaw, A.A. Sbmidt)
Data on nasal reflex therapy in medical practice. Kliu. med. 33 no.
9:1Z-17 8 133. (KLRA 9:2)
1. Is terapavticheskogo, nerrnogo i fixioterapevtiaheakogo otdoloniy
Koskovskcgr ordena Lenina bolinitey iment S.P. Botkina i nauchno-
Iseledovatel'skoy gruppy pri otdolenii biologichookikh nauk
Akademil nauk SSSR, 2. Daystvitellnyy chlon AMI SSSR (for Grashchonkov)
(THXRAPIM ICS,
mass reflex ionogalvanic ther. technic)
(IlLaCTROTko~,
mass reflex ionogalvanic ther. technic)

VINJAS- V.
-7~-
"How our people accept and adapt foreign fish names." II
p. 270 (Morsko Ribarabvo) Vol. 9) no. 10, Oct. 1957
Rijeka, Yugoslavia
SO: Monthly Index of East European Accessions (EEAI) LC. Vol. 7, no. 4,
April 1958

VINK) B.; SDWHKOV, A.
No
OTurpentining in Tyumen' Province and practic#B of efficient
workers in this field" by G. Vartikovskii, V. Maksimov.
Rpyieved by B. Vink, A. Sezechkov. Gidroliz. i levokhim.
prom. 16 no.2132 163. (MIRA 16;6)
(Tyumen' Province-Turpentining)
(Vartikovskii, G.) (14akeimov, V.)

Vink, M. V.
M*V. Vink. Application of zirconium boride and molybdenum silicide
antiemission coatings.
Title: Seminar on refractory metalso conpounds, and alloys (Kiev,, April 1963).
Source: Atomnaya energiya,, v. 15, no. 3, 1963, 266-267

VELDRE, V.Ta.,, VINKATIZ, I.Zh.
Calculating the effective cross sections for the ionization of
hydrogen atoms by electron impact. Opt. i spektr. 18 no-5:902-
904 My 165. (MIRA -18:10)

VLWHEv V.r V-INYAALNSp 1.9 YARMs E.
------
*Ionization of hydrogen by ilectrons snowing for distortion of
incident and outgoing waves."
Report submitted to the Third Intl, Conf. on the Physics of Electronics
Ind Atomic ColUsionsp London, EWIwA 22-26 July 1963

VINKALNS, I.M.; Y,-AIUJIF,, E.M.; (jj'3'Yj-Z-Yjf()V, V.D.
Elastic scattering of electrons by lithium atom-- in the poltirl-
-.ation--exohange approximation. Opt. J spektr. 17 no.2:197-21),Z
Agt641, (MMA 17t8)

ACCESSION NR: AP501 ~G`f
AUTHORS: Veldre, V. Ya.; VinkaIns, I. Zh.
TITLE: Ca 1 c u 1 a 1; 10 n 0 fef ft, c t i ip c ro s.,,, ,,, o c t I o n.,~, frhLn. L z a t In
_12LqroFen atoms by electrun lmpa,'~
of
SOURCE: Optika I spektroskoptya, v. 18, no. 5, 1965, 902-1-t(A
.TOPIC TAGS: Impact Ionization, Ionization cross section, electron
polarization, hydrogen atom reaction
!ABSTRACT: To cheak on the capabilities of vaj.',Ious approx1mate r;.-'--tn-
.ods, of calculation, the authorg, unod an electron corripuLer t~, evntluate
numerically the effective cross s6ctLon,; for IonizatLen of atciidlc
hydrogen by elec",r, i, r- appr~~.z li--ia 1,
distorted-wave app,-.)xLm41tion ilth ii, ri.
effecis; '2 p ,r-y I ~T,, 11 , t!-,
Ionization are -I e 9 (2
Card 1/3

L 6449b-65
ACCESSION NR: AP9012626
change, and also with allowance frr '--h,- deformation of the Incident
wave. In all cases, an expan~-,.ion in partial waves !~-, u,-.(-J ani
f-tal f~ro,,~P, ne-ctior irt !-rIMS ~)f th,~I%,'I,
-1 tI P 0 M
-A 1 7~
Porn. approx1nat ton croc~fl 1
f ac t,~) rs ,,r -r- rr- I t,
discussed. The
since the curves dIff-r
in the distorted-wave approximati.)n I he pclarLzatiori
little influence on the total i,-jriLzal Ion cross section, and the Ioniz-
ation cross sections computed by ~he d is torted -wave iTP-thod agrees
better with the -Kp-rim-ntal data than "hooe
the other approximation~l. Cal culat Iot,5 In '~hf~
both the electrons after Ionization are d,-~ s c111'~~-d 1;y cr_)I_~' mi"
of the continuous spectrum y1eirl values that are 1'y
than the Born cross sectlon -.lose to the ionization thresnold. Allow-
ance for the deformatli~.n Of t~~o Inc! I-nl_ has practlcall,,.
P " fe c - riv. art. 1 r
Card 2/3

L 64496--65
ACCESSION NR:. AP5012626
ASSOCIATIM. None
SUBMITTED: 21may64 ENCL: 00
NR REP SOV: 003 OTHER: 006)
3 /7
Cord
SUB CODE: OP, NP

ACCESSION NR: AP4043005 S/0051/64/017/002/0197/0202
AUTHORSs, Vinkalns, I. Zh.; Karule, E. M.1 Ob"yedkove V. D.
TITLE: Elastic scattering of electrons by the lithium atom in the
exchange-polarization approximation
SOURCE: Optika i spektroskopiya, v. 17, no. 2, 1964, 197-202
TOPIC TAGS: elastic scattering, electron scattering, lithium,
exchange reaction, polarization
ABSTRACT: The exchange-polarization approximation developed by,
V. D. Ob"Yedkov (Opt. i spektr. v. 17, 189, 1964; Vestn- LGU, no.
22, 23, 1963) is used to calculate the total elastic-scattering
cross sections of electrons with energies 0-12 eV scattered from
lithium atoms. The calculations are also made by the distorted-
field method with exchange (Hartree-Fock approximation) and in an
approximation that takes polarization into account buit- not excbange.
The calculations are made for five angular momenta (from 0 to 4) in
the first variant and three angular momenta (from 0 to 2) in the
1/2

ACCESSION NR: AP4043005
last two variants. The equations are solved by a non-iterative
method as used by Mariott (Proc. Phys. Soc. v. 72, 121, 1958).
The calculations confirm the importance of polarization in the cal-
culation of the cross sections for the scattering of slow electrons
by alkali metals. The observed minimum of the total scattering
cross sectiownear the threshold (Ramsauer effect) is interpreted.'
It is concluded that in elastic scattering by strongly polarizing
atoms, the polarization phenomena play a larger role than exchange
phenomena, and must therefore be taken ipto account-first. Orig.
art. has: 4 figures, 14 formulas, and 1 table.
;ASSOCIATION: None
,SUBMITTEDt 140ct63 ENCM 00
SUB CODEs NP# OP NR REP SM 004 OTHERt 014
.2/2

L 26521-66 EWT(1)/EWT(m)/T IJP(c) JD'Lq
ACC NRI AT6011777 SOURCE CODE: uWOOOO16510C)OI0001008710095
AUMIOR: Vink&lq0A_;_1_,~-
ORG:
TITLE: Ionization of the lwdrggIe atom by slow electrons
SOURCE: AN tut fizil~'..-.Z3.ektronno-atamnyve stolknoveniya; stomrWye
_JA=H*__1nAU ollisions), no. 2p Rigas Izd-vo
stolknoveniYa (Electron and atom collision; atom c
Zinatne, 1965p BT-95
TOPIC TAGS: electron scattering, hydrogen atom reaction,, impact ionization, wave
function) charge exchange, ionization cross section
ABSTRACT:~ The author calculates in various approximations the partial cross sections
of the iodization of hydrogen atoms by electron impact. By starting from the:Bon'l
approximation, the author investigates how allowance for exchange and/distortion of
the wave function of the scattered electron effects the accuracy of the results of
the Born approximation. lbe problem in solved in the representation of total orbital
angular momentum and projection. It is shown that allowance for exchange changes the
postiion and the total cross section of the ionization in the Geltman approximation
(Phys. Rev. vo 102p 171P 1956) more than In the Born-Oppenheimer approximation. If
exchange in disregarded, then replacement of the plane-wave component by the Coulomb
function of the continuous spectrum leads to an Increase in the partial cross sectio
and causes the total cross section to exceed the Bron cross section by approximately
Card 3/2

L 26621-66
ACC NRt A26o,11777
a factor of two. In most calculations the electron wave function Is approximated by
its plane-wave component. The integrals involved in the ck1culations vere evaluated
by means of a computer (BMM-2m). Me autbor thanks V. )La, Veldre for continuous
,,interest in the work. Orig. art. has: figures and 2C~~ lao*
SUB-CODE., 20/ SUEM DATE: 23jui65/ oRiG m. ooi/ om Rui oo6
71:

L.R�UL-66 EWT(1)/EWT(m)/T , UP(C) JD/G9
ACC NRs AT6011778 SOMM CODE: UIVOOO016~1-00
A-
AUMOR: Vinkalne, 1. Zh.
J"
ORG; :'C'
TITIZ: Influence of distortions of the incident wave on the partial cross sections
of the ionizatlon of the bXdMen
SOURCE: An IAUSR~ Institut Elektronno-atonWe stoknovenlys; atomrWye
stoDmoven1ya (Electron Ed-lit-omcollisions; atom collisions)) no* 2p Rlgap Ud-vo
Zinatne.. 1965j, 9T-103
TOPIC TAGS: hydrogen atom reaction.. ionization cross section,, impact ionizationp
wave functionp charge exchange., electron polarization
ABSTRACT: This is a continuation of a paper in the same source (pp. 8T-95., Ace.
A76011M) dealing with the behavior of the partial cross sections of bydrogen-atoui
ionization by electron impact by the Born-Oppenheimer and Geltman (fts. Rev. v, 102p
171P 1956) approximations. Whereas in the earlier paper the incident electron was
described by a plane wave, in the present paper the partial cross sections are cal-
culated with allowance for the distortion of the incident wave in the static'field
of the atom, and also with allowance for polarization effects. In other respects
the calculations were similar to those in the companion paper, and were made with an
electronic computer (BESA-2M). The results show that allovance for* polarization ef-
fects has little influence on the partial cross sections. on the other band,, allow-

L 26511-66
ACC NRs AT6011778
ance for the distortion of the incident wave in the study of the atom affects prin-
cipally only certain of the partial cross sections (QLOr)p vhich is decreased by the
allowance for the distortion. As a rematp the total cross section decreases to .
approximately one half and amounts to 70% of the excMage-free It6iii-c"Be section.
The wave distortion has a smaller effect in the Geltman approxiniiflo'n. The author
thank V, Ta. Veldre for guidance. CrIgs art a has: 5 figures and 15 forwaIas
mm cmz: 2D/ em wm.- 23ma5l opm Fm oo6/ oTH mw: 006
-2/2

ALT, Eduard; JAK0013I, Eduardt VINEELI A., retsenzent; A130, L.., red.;
117
LUMM, E., tekhn.
(How to handle a television set]Televiisori kasitsenine. Tallinn,
Eesti Riiklik Kirjastus, 1962. 138 P. (1-a-RA 15:12)
(Television-Vandbooks, manualo, etc.)

VIEKEVICH, Gavr1il Afanaslyevich; KOZYAV)lo', A., red.
[outstanding geographer and traveler) Vydaiushchiisia
geograf i Futeshestvennik. Minsk, Nauka i tekhnika,,
1965- 104 P. (MIRA 18:12)

VIRKUR, Ianos
1.
Ci:rrf~r-,, da~,a on the ident2..'Llcaticn -1.,--st of thymmol wilb nitric
Acta pharm. 141mr. 35 no.6:248-211 N 165.
1. Submitted June 17, 1965.

i2) 6 0

N nlv!

. 2'
Cl
117
i
-
Le
n
'

G 0l E
3- 61-1,1 zines ift -
10

r) y I rl 11

Y

No.
1960
J OA 3 P )

PJP.
(from aIC01101),
d i
r
nverte
(frel-i btmzene)) w-013 cO
"
(fl-om alcohol), ant
1 221-223'
rl -p -- -1 r Al
-dust and _,H (40C)H to t*-C a-111de
`
l
z
n
Cr,
_er-(j-UcOC1 lvj
l
169-170' ~r'rOm alco'lollp 11,
(III), m.p.
cool in the prescncc C"
0~ P H
ith
-6
was Cor'dell-90:1 w
5
Id to S_beriZrYl-11I-, n-P- 179-
-
e co
05H5n' " tl
' i0r
of
t
;
1800 (froln alcohol), CyciJ.zed by ac

coullity
GAMORY
ABS, joup. Rzyhimf~ no. 1 ig6o, No. 12to
tjITFOR
JPST.

l0KLc-. PUB.
;ABSTRACT 1101 in xy'lol to la, n, p. 3.89-1~,00 (fron alco-
c ont f". hol). &nr--logo-usly, from III find 3,LL-
c 6113 c 0!" 1 13-vuratroyl-Il l waa

1-111-1790 (froln alco
h01); CorlVerted to '7L.. -.r..
--)17-2180 (from n1cohol). To prepar-:~ 1c b-
',-rating 3,4 r, -1 CHO
-R12 6' (IV) with coric.

'
at -00, 6-nitro-pvma r.,i.F,- ~J:)
synthesiz-3d,
960 (fron alcolhol), oxid izod allkrilin~--
t 4/6

il'.~.3. RIM, PM Irl.) 1110. 1 1960Y I'lo. 1260
~TIJST.
T T7,~
JAPSnIACT so2,ution of FalnC4 to 6-nitro-3,),,-R2'-b,~,r--o-!c
1 ont noid, m;p. 142-L,-131 (from bon7ene),
j - j
0'0
or ho t C,'
OV in r-1 a ol -P")
benz o c acid, m.p. 3-35-1360 (ducamp. f-,~
thlosalie,-ylic -v~td
collno I) ,from whIch 41,5-R21-4-
(V), m.p. 202-2030 "'T-oln ajeohfoj), -.4tt'i 0*1 '-"l
Lill,
by tho diazo methorl; by the maLhod
above, V was convertod to
-4 RD: 5/6
G-33

Yr
T.
F! Z Kh, LM r,, 960
kJ
r
t ve Of -""r el r
na'

L 33619-66 Ewp RH
ACC NR, AP502501 =-1-9- - C__0_D_E ___T~_jo_oo5_j6 5-10- _71'16iij(Y~81 /o8q
AUrHCR: Xlivenyl, Ferenc; Vinklers-Flemer; LazarL_Janon
ORG: T-natitute of Pharmaceutical ChemistKy, College of Medicine, SzeSRd (Szegedi
Orvostudomanyi Ogfetem Gyog5rsz8rosz1 Vegytani Intezete)
TITIL: Further studies on the reduction of sulfo-~hlorides and thiolsulfonic acid
SOURCE: 11agyar kandai folyoirat, v. n, no. 31, 1965, 481-489
TOPIC TAGSt ostor, chemical reduction, oulfonic acid, mercaptan
kBSTRACT.- Reduction of aliphatic and
alicyclic sulfo~hlorldoi proceeds, at *room temperature, through the'
sulfinic-acid and probably sulfonic acid, yielding mercaptan. The process
tak93 place parallel to the formation of disulfide, which results from
-the-reaction of oulfinic acid and mercaptan. 1-then the reduction is carried
,gut at the boiling point, a part of the aulfinic acid is converted into
Sulfonic acid and thiolaulfonic acid aster. In the case of the reduction of
!6romatic sulfochlorides with zinc and acid the aulfinio acid formed at
room temperature further reaots to give thiolsulfonic acid *steps At the
*i1ine poi4. the yield of thiolsulfonic agId_pister Inore&Apso ./Orig; iA*' hast
5 tables. LBased on authors' German abstj/ LJMSt 33,90_67
SUB CODE: 07 / SUEM DATE, 1911ar63 / CHIG REFt 007 1 SOV RUS, On / OTH RM 008
C.M III L5 . - ~ .,T.:eii*

SZABO, Janos; VINXLER, Elemer
Rearrangement mechanism of N-(3,4-dialkoxy~-phonyl-mrcapto-
methyl)-benzamide derivatives to benzo-roa-10-thiazine deriva-
tives. Magy kem folyoir 68 no.7t279-283 Jl 162.
1. Szegedi Orvostudomanji Egyetem Gyogyazereazi Vegytani Inte-
zete.

TI11M, Alois, kandeblol,nauk, doktor
- -t'~ - I ,Information on the Journal Veopiasmo~ Voponke 4 nool:375-376 138
(KIRA 11:8)
1. SpetaiRlInyy redaktor zhurnala ONeopInsma-0 Adres nvtora
g. BratieInva. looledovatellaki7 onkologicheskiy inatitut. ul.
ChokhoRlovatakoy arati, del7e
(CZBCHOSLOVAIIA-ONCOJMY--PMRIODICALS)

-A mj~'-T of th~ E'~
Id. rt't" I, 'f !)t 2
fornif o! qn! j I ji r i d F "'i, A id A f '~ ~ ) ; It
C&cfj ,ttjcr wl 1~,,N A 11,C) 14 c., Ttcri f the i,Ul-
ralt, ard 1. .-It 1 1, of 1101. c-tild ~1-~ ~Xplatn the
J I g~'- M 'C .1i'SC i~ S 4 ; in 3c
tnt IKIr ett'.Ct With 156) 1:111 :1 4,~ -4i,L ~An "~e Kvll~
14 ~j i I '~~TV 11 T4 c.
11 in ('14C1. bv vJ~!tng a CHC1, .41l nf BzChli
ti,d cillowing 111all t' stand U,r 24 firs gwing tbe r" -
';( (), )S i~~ in 76 7'. ~21 ~' !&1 4 ' arl'; -
live k, liso
Slailluly tile Wele WUM'd ITm.
tile c,Irr"ponding &sWfidn: from (p-ONPhS)i. m. 152-4'
(VIU; (1,2-CJC,1i,S~_ in. 109' (dcco[ripn-) (VIR); (p-
CIIC~ii's h. m 87 9'. ~ I nt 9-3 * Ru-ther RX0111
arid ioxiclation gave The :hi-ulf-c-te cif V11, it ISO* and of
V111. m. 151 2', R XV. LX=-- Y,

VINKLER., E.- KLIVENII, F.
Confirmation of the identity of the alleged sulfenic anhydrides arvi thiosul-
fonates. In German.
P. 15, (Acta Chiiica) Vol. 11, no. 1/2, 1957,, aWapest, Hurx,-ary
SO: Monthly Index of East Europem Acession3 (WAI) Vol. 6, No. 11 November 1957

Prepim.ti n cf aryl-benzo thiazire 11 A raiacti,-,n c-)~
a rmatlc imi!v t!dceti,.:!r t h fo e I-,.; de
P. 99 L, in G~!man
'S'C: I,.',nthL-.* ln~lex of Sast Evro e--an Accessions (;~:-Al) W. VC--- 7. !'o.
K-.,rch

TR-ei~GX ~Rf-W-U.T- i~ Ed
d
ad Ect
esters of sul enic acid;j (1) have been proven to be atractur-
ally Identical with the alleged "sullenic acid anhydrides"
(1), The hydrolysis of sulfenyl chlorides and the ro0ing
prodticts (1) are discuised in the light of theu f1mWigs.

N.
170S61 (The Norfuclic of nmit
inkm
I-r "L tKAwn ot hullo-
FAt"t "4 of MuMitt L Of u
~.-Tdcs- ) Areimia ~.4 &srulfidok
a=lfakl"Wok bimplAmbe rrdukci+~&L
k , &-.d Frrew, Kbv~i. Magyar Ke'mtai
Im-l"U4.19A. P.
Devekipmerit of a strapte, gene-rat synthesis. Themetkd ece,
siderittiom; and practical rmults Structural formillal. 21 ref

VTNXLUjr Go -Yei
Unusual course of hemrrhagic vasculities. Vracb. delo no.S:
.U7-119 Ag 163. (MIRL 16:9)
1
it Terapevtichaskoye otdoloniye Aktyubinskoy gorodokoy boll-
nitaye (PURPURA (PATHOLOGY))

fvi W&A"WhImanovsk)
Increasing the output power of the Ollodinaw radio recei'vere
RMio no.1:23 J& 155. OMU 8:3)
(Radlo-Receivers and raception)

USMI/Electrodes
Nrd 1/1 Pub. 89 11/27
Authors I Vink6vich, Go
"War
Title i Increasing the output power of the OBodinab radio receiver
Periodical i Radio 1, page 23, Tan 1955
Abstrikot I The author states, that the use of the 2ZhM tubes Instead of the
IN3S on his 'RodinaO radio set, as suggested by 'Radio" in No. 11,
19.53, gave very satisfactory results. Circuit diagram.
Institution t ..........
Submitted I ...........

VINKLER, F.,
V. BRUCKNER, Acta Lit. Scio ReZias Univ. Hung. Frsnf--Iaco-
C3
Joaephinae, Sect. Chem. Ifilincral. Ptiys. 6p 145-59 (1938)

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kv it 0 It If
.
0 :10 0 0 a 0 6 0 0 q 0 0 did 0 0 0 0 1# 0 0 0 0 0 0 0 9 0 0 0 6 6 a a a a 0 0
1
of 0 0 0 e * 0 0 0 a 0 * 0 0 0-9--vLO 0-0 0 * a 0 a 0 0 0 0 0 * 000

C140
Light -bowpdm by N-lt"Ithiodkylpild"vAide dodys.
fives. Arpm Ki'o. K04YA11. Alto$ H. Cw1im-kr. JJAO
2. , I 4SM49) (in Ganunf.
unit, Suled., (Awm: I ir.
-Tlw extinctim curvvs d 0 dtfi%,. td N-Wylth~.1kyll-
pilthahmide. and #4
PhthAllunde. Aud Y-vwthyIphthjIimide were drul. and
ducunt.d. h1vill Fluily

ij 41 Ad 6 1.'*
j? ,a ?1; 1. it villao 1161 *11041,11
16 IF Is is b4 tir- A
A Al -A-A--L A 2 2 0 -A I I AA 11 (A
A
like 0-ani"Islijillop
00 lu systhwS of WwAslytic 11"quisfilism bes". treat_
*0 C Awfie sew revolifilmo N (I ocyl advall"c Ple"A Intill ef IV gave 41- ,4,,tk- 14 Itw 'j.
ir"alraylaninvo
66 Wit ItOll Ifidliffe I.J Y'Savr 4",:41Y IN,.111.1 ."m~lsqq 4 Illo, j i
*0 $Mr ill fit pirtubtle wilb MCI awl vorope. IllornylavIvidimm 44a jkl. jVIi 1, ..'611119 VI m 14".. .
the iijbirl rile. A she Irmillitist elyst. nIAW4 PVV 9 SM111-11 I-k with IWI, and 4.1,1011d A.ah"ll, N,J)ll I', fj,~
uil Identified as -43.44methroypbe 0~4mrnt"Itrlly- WAAAI gave While Fle"lk- with Iky ju,le, hwh
00 'p-dilrovortnanor (11). The r-ikm 017its pyridine with Inat their water of crytIn. at tLj, when h"(1,I la 1w. a
in
fleatim CJICII fit. ell the -it! kl,-ntid,,l a. *00
soptifiao chkiride and puril IA the JIM * and we
ptridtiort led t- an (4ivr-Fmn oil reonsialing ril the n-
Treating I In pyrWine with im4jng it)
fin W7 IF 4mikle, a CIICI, cit. and the wills. The etystalline nja- irmwe. miller (Itorific. 4 .00
Iffoobly plepol. vetalloyl ch while lxmdrr mrs"t '219"1 Na
ftfs Is toil emskiing 4
Ihm r"Pil. this rzt. save a a d-dti-Pilf(IfthiltY4 IVID. VII ill CIICI. vu-tmnsumi *at
0 the .-wralnuyl,my emilixi. I IV I. lloi.~Ovinjj I in a mOtt. Irrat"I with IUCI in CIICI.. After filleting ilk- Initil,
i tAf pirtkilitn' aful CIICh Rl"l Mill-lie'll jr-bly ifisid. PUCIII. Nacl unil evaloa, The filigair K 1hk
00 C( )CI I. C111cl.. liters larl1j, a ClICIA 1-%t, Awl rvnpg. it fit
'ily
so IN Who Save Is YTIU,w tat v'"14i.1611.4 the-lbetwvt ivilb we,% litlAill"I. the victit-Ota. redticil"ll -4 Vill
As "nsl. IV). vk~mttvlylkl t"luctit" -9 the I ming 14i tin-l- **
00 incAwtel alul the ale. *An. col lrall to '""IC 1:1. 1 ~14IFVI 11'11 1`111ITIM I - d-IWn 141V [All zoo
electrodes III z)% ll,$A), to -43,4- elhant4 (EKI. IX in il4urtor ome,t timril with PtK:I, arul
'.., '~.,Iylr) xi~ "k-11- ell a
the rt]Mfkt. I heated. then nmit"I, Aaken mt mrith Ill. lICl atut ntle 40
in. elk. with NaOll elth I-4itig. Nll~l ;~1rifvskx th~ -l,,
-IJW fkItq4yIi4- .4 Ill I'A loo,141011. t
PkIk. me-i'l wet I.$ Imoll oh'. III. fair. m. ,1 1.
fit
t:0 0
SLA A4?AkLU#rKAI. tsTINOW CL43SIFKAIICN %o9
iL &*a 0
11, vd4ollo -16-, T-. _i dA I
W-v x- tw- -o--a
an A
0 &1 10 Is I
is 0,9 0" It 49 9 * o o 0 0 0 4 0 0 a 0 & 0 0 0 0 0
go 00 0 9 0 9 0 Is 0 0 Is 00 0 0 0'# 0 0 0 111 0 0 0 0 0 0 0 0 4 0

C J
_

alitoxy groups in oryl. jai

t itk
Na. ;!, [)it.
tit-
I-111hlyine 111'rh a e4
I Prif). the
vnitilm mi tim not,, haml

delh
-1111%v4 %hile thev Ivetts f
ito An smansloigiarmp anonewr on the other
For ,
1111, Intl"r WIFIK"I 41.7-41itilkoxy derivistiv"a Obtained frorn
6-11it m-v.-Tsli fir 4141 Ktruritir" of Which Wnis provm
I-A-lear ns"I Mismutonno. wnm cooveriml into 8-arayl- i
Ijjj,'.aIi,-yIin nini-In dorivativea anti tIm latter woro mulm.
!. opsi-iolly ryt-lianivil to 4-oxo-bnoanthiazine derivativea accord.
i'lK its 114111no onol Minvidl. Tho Comimunds thtio pn,lmmd
I.MV041 141 IN# 41411100111 With ilia OXkJAIiGI1 PrAfmtn Of 11110-
minxinc, Immm. '11se asu4juivarmol klaittity nr the protluelto
elstainiA by imiumbiguoum mynthovix and by oxidation, ex-
ellpiim tim poomeimmy or a-Ficaftion of sba alkoxy jr4up
iu
ma
j

Cowltry G
G2.t('-..Dr'Y Organic Chemistry. Synthetic Organic Chemistry
~,bs. Jour ilef Zhur - Xhiu-, No 5, 1959, so. 15375
Author Vinkler E.; K-Livanyi, P.; Klivenyi, K.

Tltlc :on Reactions of Aromatic Ethers of Wosulfini

Acids with Grignard Boa ents. On the Prepa P_
f
l
Aromatic Sulfonic
tion of Certain Salts o
Or 13 Pub. :Acta ehim. Acad. scient. hung., 1958, 16,
No 2, 247-249
Ab3tracL :It was established that ArS(O)SAr (I) (where
Ar=4-03C6~~ (Ia) orcK-naphthyl) with C6H5-
CH2149C1 (!I) forms ArSOCH2061'5 (III) and ArS-
MgCl, and that Ia or I (Ar =C05) reacts with
MigBr (where R =C3H7 or C6H5) with the forma-
tion of RSAr and ArSOMgBr (IV). Hydrolysis of
IV takes place according.to the fomula:
2 IV+2H 0-+2HOMgBr+2ArS(=O)H;t2HOSAr-qo2 I+
?~
e reaction of IV with II, III and
IT20. By
Acids. Preliminary Report
Card: 112

Counti-
i G
,*..)r,, .1yLutr Ref Zhur Wn., No 1959,
No. 15375
6 ho r
Inati'Llut.
Titlo
Or i.- Pub.
At~stract :MgGlBr are obtalned. Analogously, III and
cont'd. HOMgBr are formed from IV and C6H5Cff2OH.-- V.
Skorodumov
Card: 2/2

VINKLER., Elemer; KLIVENYI, Ferenc
Mechanism of the hydrolysis of aromatic sulfenyl chlorides.
Magy kem, folyoir 65 no. 11:44-452 N'59-
1. Szegedi Orvostudomanyi Egyetem Gyogyszereszi Vegytani
Intezete.

VINKLER, Elemerp Doz.9 dr. (Szeged); KLIVENYlo Ferenc, dr. (Szeged)
Contribution to the mechanism of hydrolysis of aromatic sulfenyl
chlorides; a new contribution to the chemistry of thlosulfinic-acid
ester. Acta chimica Hung 22 no-3:345-358 160. (EEAI 9;11)
1, Institute of Pharmaceutical Chemistry, Medial University,
Szeged. -
(Fqdrolysis)
(Aromatic compounds)
(Sulfanyl chlorides)
(Thiosulfinic acids)
(Esters)

0
VINKLFR, Klemer; LAZAR, Janos; KLIVVrfI, Ferenc
~- ~-_ ~~ . -,- -41 - -
Proving the composition rf the so-called "aystine disulfoxidew
by synthesis. Plagy kem fol3roir 67 no.7:303-306 Jl 161.
1. Szegedi Orvostudomanvi Egvetem Cyogyazereazi Vegytani
Intezete.

FEMICZY# Lajos (Szeged 428, Hungary); ZSOLT, Janos (Szeged 428p Hungary);
VINKM, Elmer (Szegedj, Beloiannisz ter 9 Hngary) KLIVEM,
j Beloiannioz ter 9, Hun
11ff#2-(5zeged- gary~
Antimicrobial activity of aromatic thiolmaphonates and thioloul-
phinates. Acts. biole Hung 12 no.2:121, 126 161.
1. Institute for Plant Physiology,, University of Szeged (Head:
I. Szalai) and Institute for Pharmaceutical Chemistryo Medical
University, Szeged (Headt D. Roszegi).

VTNKT.P,'J,M_,-jner.dr..,.doz. (Szeged, Ebtvos u.2); LAZAR, Janos, d r. (Sze-ed, Fotvos U.2);
KLIVMI,Ferer~c-,d-r.-(Szeged,-Eotvos u.2)
Data on the constitution of the so-calledIcystine disulphoxide.11
Acta chimica. Hung 30 no.2:233-238 162
1. Pharmazeutisch-Chemisches Institut der Kedizinischen Universi-
tat.

CC NR-'z7,~16033879 ?5cy!A 5A )46.1001, P3
SOURCE, GODE: lfu/,
AUTHOR4 Khvanyl --j
Fcrenc--FHv(:ni, F. (Doctor; ~`zowed -j--!L~q1rjj
(Dontor; Szeged), Eletux Profonoor; Doct,or; Szoged)
ORG: Institute for Pharmaceutical Chemistry, Medical University, Szeged
TITLE,: Further Investigations on the reduction of oulfochloridos and thionul.'Lonic
acid esters
SOURCE: AcAdemia scientiarum hungar-.'ca(. Acta chfiftica, v. 46, no. 4, 19AJ5, 357-372
TOPIC TAGS: sulfur compound, organic sulfur compound
ABSTRACT: A great number of vulfochlorides and thiosulfonic acid estercl wac r,--,-;uced
with zinc and acid under various experimental conditions and the products of the
reaction were determined. The results -re presented in full detail. Fur~,her
reactiors between the reaction products -nd/or the initial reaction campor,ents
wr.,r(,, ~,lI~o dis cussed. This paper provides further daLa on the findings reporteci by
the authors Ibid., vol. 1, 19151, p. 319 and vol. 5, 19/54, P. 159- Mrni. Doctca,
E..Rozs,a carried out the experiment. Orig. art. has: 2- table3. [Ori6. art. -in
Ge rnian I[JPRS: 34, 165 1
SUB CODE: 07 SUBM DATE: 1814ay65 / ORIG REF- : 006- / SJOV REF: W1
OTH IREF: 010
Card 1/1

Distr: 4E2
A"DiTatigationg In th a U
And
Acaj;. 0. Uwe. 13,
AM
Of &Tom& 5
JO The meebaulsin of the reduction tic Ullonyl el.
of Ul
tam
rides was reviewed and the struc c Sulicnic Ruby-
1/1 drjdcs Investigated. Millard MalentA&L-

VINKLETI, E.
SCIENCE
PMIODICALS: ACTA Cli-,~,JCA. Vol. 17, No. 2, 1958
Vinkler, E. Data on the prep-wation of arylbenzo 1:3 thia'zine derivatives.
1U . Verification of the position of the alkoxy groups in-aryl-benzo. 1:3
thiazine derivatives by synthesis. In German. pa 201
1
Monthly 14-st of East European Accessions (EEAl) LC, Vol. 8., No. 2
February 1c,59, Uncli~:-3s.

r,~z
thetic
Sin 140 8) 19581 25219
or oomnic- I%ivi'P ?
Sze;bo y 50
A,bs 7
ielloeS
Of, So 3 ~~ehjde
Natholl Plead of wbeu7jo' yo
0,, DOrilvativeS tbioe+,erg
pregarat,410-a f psorati.0 IPOTIO 12; 140 11 99.100
Tjt3-e ~a, J~OOtl-ou 0 1 lIvn6of 1,951)
So atr
W CIAj
Ot tbiovholl' tajo- R,'R j.C JI 3
the whe '1 3 4-(CR30
the
-57 ere IL
C11 v I VLzM33 ides
06trE6C,t JeS ~ scw)-,~, J',(C 113 -1
44,O),LCA, !,-(.M3 Of C.%CeGs
33 R,CH3) Rl~:31 the forl~.) Vj:M 8611
-S C
J!
e (30 vlo)~tcs
IVX2-140 6 1,
186) 9 0
(Clecojo_
card 2/z car& -103-104. 7; jet
see RZtla,,, 1956., 2.57224 xg li-I

MR, KLIVENTI. F.
Data on the react4~on of sulf-nanhydrides; a preliminai-y communicaticn.
P. 95
Vol. 60, no. 3, Mar. 195"
MAGY U',KEMILI IFOLYOIR,"A.T
Budapest
Source: Monthly list of East European Accessions, (EEAL), LC,
Vol. 5, no. 3, March 1956

VINFLER, E.; KLIVENYI, F.
VINKIE7, E.; FLIMM, F. Bimolecular reduction of aromatic sulfanyl chlorides
as a mechanism of the formation of thiophenols. TI.
Synthesis of thiophenols. TI. Synthesis of thiol-
sulfonic adic esters by condensation from anthralitione-
1-sulfenic acid and aromatic sulfinte acids. In
German. P. 307.
Vol. 7, no. 3A, 1955
ACTA CHIMICA
SCIENCE
HUNGARY
So: East Europeon Accessions, Vol. 5, No. 9, Sept. 1956

VINKI-17R, E.; SZABO, -J.
Production of aryl-benzo-(e)-1,3,thiazine derivatives; a new rearrangement reaction
of aromatic acid amide sulphides. In German. P. 323. Vol 6, No 3/4, 1955.
ACTA CHIMICA. Budapest, Hungary.
So: Eastern European Accession. Vol 5, No 4, April 1956

T7.-~ 7
23. 01moltrular rc,hictioll of aryl I'll
lid file Mer In I
Vnfhtslg A MW still,,IffnAty! by III# tondens:31ion of
;
finthraquinotle- I -out Ms , Acid aRd xtoma(ic tOphinic
Oddl -- , I , ii 1 1,
lated atlumilt of Zille qII.1 hy(huchintic. acht
sulphinic acid If (81 11, theor.). Thi- rt-actioll provei /7
that durillh, tile rvdu.~tloll tit comIK)mIll I .00t1hig Aj
thini'llellol III Im end product tile filterilloliate forint'd
in the first stage of the reaction k undoubtedly comiximitl
St. In an analogo" manner 2-indItyl-twmem., mit-
phonyl chloride was reduced to 2.1211-th I-Imlizelle
tile
sulpl;Jnle acid with a )-IcI4I of 746,a 'Orl nnd tile
compound 4-chloro-Iltnicne sulpliony~ chloride to 4.
chloro-benzene sulphinic acid (yield 750jo theor.). Tile
condensation reaction betwecn compound 11 and
anthraquinone-i-sulyhenic acid In aqueous acetone
yielded I-anthraqu nonyl benzene thiol-aulphonate
(60.501 theor.). This reaction confimia the assumption
that t, e aryl sulphenic acid produced during thesecond
stage of the reaction sequence I ~ III condenses
with the sulphinic acid derivatives present to the corres-
ponding thlopherull con,
t,,,).ounds. TPese experimen,
provide further data oil I reaction ruechaufstu of till?
auction process of compound I to coinpouud Ill.
-49

The bimoloivWreductka of beiYanesulfanyl chloride
fsllw!2!~n for J!Mbaa. 1. 9km(jVinklrt
land
Sri. Hung. I. Y14-24(Iq5lxW 'er=a).-Fl,SrhCI (1)
!(14.12 0. 100 ml. MO. and 11.4 g. Zn dtt,-t (88.76% ptrre~
Za in all cases), treated In 45 Min. wit)i W m,. concd. 110,
'I n di3-1
;with stirring, the Mist. stirred and refluxed un ItheZ
!appeaxtd, the Rtj0 phase sepd., vrashed with Na;C0j sotn,'
:an H&O, dried, and the Et.0 ei-apd.. gave 9.0 g, (80%).
'Cry3t. PAJ5015A (11). needirs (flora MC01-1-1110), TTI. 38-
40*, Similarly, 1.7 $. PhSO31f, 30 Jul. RIO, 0.66 g' zw
Idust, and 10 ml. cottrA. IfCl rave 0.4 g. crude It.
jlooed~apwlse with stirring to25,7 ml. coned. HIS04 and
142 g. crushed ke below -51, the mixt; tritated gradually!
with 23.78 ff. Za dust below 0 , ltined I- hr. more, warmed
I gradually to room temp., heated to boiling. rcfluxtd 30 ruln.;
till the Zn disappeared, some PhSH steam distd.. the rcsiduc
extd, with C4H#~,: the ext. washol with HO dried. and the
Cjfs evapd. e 9.42-3184-11TV P/hSi (11.1). m. and mixed
M.P. 80-
1 (2.0 g.), 60 mi. WOH, and
1.62 g, Za dust. treated with 16 nil. comed. HCI at 01 with.
stirring, the auxt. gradwalty heated to ouifing, refluxed until:
the ZJJ disappeared, steam distd..' and worked up as above,
gave 1.7 g. M. Accordiaf to the method of Schiller and;
Otto 11ler.9,15MI976% .7g, PhSO611 and IA15g, PhS11;
reAuxed 30 min. with stIrTing % ith 6.4 MI. coned. 11404 in
!~.;35ml HsO the muresoed PhSH steam dIstd., the resid tic
'extd. kith Uo, the ext. dried. and the C*H# evapil. gave 1.0
(46%) crude 117. Thereductionollisj*stulatedto "go
throtgn the stcps 1 -4 MOX U -4 M --4 PhSH.
Richard 1. Akawj4a

FEJENCZY, Lajoe (Szeged (1,228), Pfungary.); ZSULT, Janot; (Sznged (422),
JJungar.-j.);_Yj1R444,_B1emer Szeged, Beloiannioz ter u, lh~.);
KLITLI-M , Elemer (Szegodp Bololanninz ter 9, Hungary.)
Antimicrobial activity of aromatic thiolaulphonates and
thiolsulphinates. Acta biol Hung 12 no.2:121-126 161.
1. Institute for Plant Physiology, University of Szeged
(Head: I. Szalai) and Institute for Pharnacautical. Chemistry.,
Medical University, Szeged (Head: D. Koszegi).

vi ~i
_
/An ittempied sycth"
J
I I I ... za
dvAlAv" k %
"
"
sl
'
,
&n J. ,
~

cri, 5f,
tfrlg.) Afagy
fl
,:t~ssflll afirmpl. w,r,! rjALI, I ~t 'I?'.
th i4 I ine ta," ftom
4r,l
A
r-i-_
fal ion k,
Distr : 4E'd

phides bj the bintulecula; reductkatt
fin GtIma-l'
r
Icla Chi;f -ca
5, 1~114, N,,. 1-1. pp. M-11;6i
werc obtainv! by 9.c r-doction nf
bewme vilphol-,il ch!,,Tide to pwnyl lom-ne fhiol-Q
1 '11,1 at- and oillitityl c~r-,vrtjvt-!y, I,y
!j'.t'?rlllired ul"ourif"; of J"jac (tu... ullel '6rl Oc
Ft~PT' wpatimls' TO determine th'~ qclikullty
of the tesx1loll '-)~t'm.6vr inve%tie.Wmn wi-ic wAvrt;tktn
and thf, succci4kil ppanfilill 0 R gn'.1f nolubvt 'j(
lonlaly purf; thi,I*ufp?"m%te (fi'matim -- vith, pt-Ith,
rarigliq, from 51 0 100'~', - wctc rn .rr]Ltl. lims nivVi(A
P.-,)vrxl to Ir- n~lrmor t.1 othel pt,mlut,m ilticribtd in
litesl?llte~ -liv cumpo'mund--
fffod Ith lields "f 75 to I )mq'fvan("j:f-5 of
the mctflod are th-tt Only . pure Itomfic sulpNo'lyl ll'y
thlotidr~ am 5uit'llh iv, s'lirfin -rizli. awl, tt.:~t
the J-112CtiOll conditiar" pmscribcd tru3t b- Muctly
adherrd t(.

i5l'
HUN G
ialphCm.: '1J4 'hi 1 -!'1%
.1.1 di L11~111111~1, J~y Ot'! L;1a~1.1QCUL1T fCi1';' 1k)TI U1 1111-
r~'Iiulllc 'vi~ i"it'li"p-ar
.7 z j.,, 2
I I t'I go"! I -, i-H by I ke C.11. ~ hu" I allmullt
(1) ;OA i z' ~ iuto 010 cor-
t1l) w driulphi(Its
11CF. Of ','M:-5 Mill'!M1
'111.0
It,
hlif-11 Ar-%-'.-Ar f VoC1,4 111~0
lit
(w,
ow,
M-1-naplithyl thtinillillimmit; Of dil(tllphide J1 pCeparcd
ill analogy by 111C It( liclioll of
acid clijuride. Tli[,; litoceduro proved to be mure advanta-
gemis for the prepaiatioli of t1ii,walplionates I.e. disul-
phide!; 114an other m..-thLKJi dcicribed ill literature.,

v/ MAL

UN G
Production of aromWo thioctIthank tileft ad disitiphides by
binioleculu rejuction of sulphoWorldes. -J,.V Ittkier and U. IVI'v-
-
MULT i-
f. tita olam. Autog., 1934, 5, 159-- W j. -'I Ic %,qll-.I;i MX 1. 2 77
3 and 2f(-!SOCJ+5Zn+
iyjk-ar to lk, t,,vnerjI cxprvi~ioni
i
c
ffw the Convudion of orwit-tti~ sufphon~l thlufkdu~, iWo ~%rmtiat
thiusulphortic tstuvi nud di~ulphidtri rc-ipedi%ely. Fwimin~~ lZi

and Zn dust at 0' which k then %varmcd until disiolution of the
Rictal is con'Pitte. The 01"Creal layeT is ficed fruill Sutphonic

u-tulyl )-tuluv
acid, driud tnd distilled givin- ncthitnulphunate,
m.p. 95-9,7*. in 571~ yield. Tht following com1p),ands are jimlared
similarly -. f-tolyl p-toluencthiusulpfumate, tup. 76-77', p.
nuthasyphen-0 Cl,lf,,OiS'. m.p.
38'
3 - 4-ji
-I 3 :
tells
x
~
j
h
86
-
n
o
,
t
.
)
yp
aa, C, p11,,O.S, (7501.), in.pi. 110-112'. P-aCLtamidGpknYl P.
acttarmdobejizentthiosull)hoti;tte, in.p. 225' (decomp.), m-Carbazy.
phtnVI m.p.
216-217'
,y), r-Woruphonyl P-thlorcjl)tnsenetlii(riulpli(in-
34'
1' 3
1 -
-na
htil I na thAlene I
ate (8401)
rt
,
,
,
p.
jo
p
118-1201 (lit
14-40)
When reacticit i;
n4
ate (IW%)
.
,,
,
F.
of a lar
i
l
t
ith u
er
r
rti
b
n
f Z
th
i
t
i
d
w
io
ou
c
m
aT
u
o
o
carr
e
n
e
opo
g
y
V
-W
89-
di-
l
di
83
3"
d
t
ll
-c-
ucts ar-s
pro
j.), in,p.
.
)
p
y
(
(
o~
'
'
92*
44~494:
4"7*
i
th
4i
h
m
t
)
-
me
cny
.p.
oxy
tn~p.
.
.
,
. pp
(
p
3 -. 4 - 3' : C-tetramethoxydipbtrtyl, in.p. 94% Pp'-diacetamido-
*
182*
2
1
1
180
i
f
l
-
0-
,
2
% and
respect
ve
/.), forms m.p. 1
diphenyl (7
y.
'
239-240' (decom
pp'.
m
asbo
di
hcrt
di
l (100%)
)
-
"Im
c
p.
,
,
xy
.p.
y
p
1
%), m.p. 70-71 . and di-l-uaphthyl di;dpbM,
dichlorod'Ptenyl (73
000%)' M'P. 85-tld'. H. WRx.-ti-)

VINKLER, Z.; KLIVENYI, F.
Verification of the stivueture of aromatic thiosul-fonic acid esters bv the chan-;Cal
method. I. p.13. (Magyar Kemiai Folyoirat, Budapest, Vol. 60, no. 1, Jan. 1954)
SO: Monthly list of East European Accessions (EEAL). LC Vol 4, No. 6, June 1955, Uncl

N,

:c'-- VI),termliantion by a chemicsi method of the structure of
R; vinklLr-
Aromstic thlostillonji: esters
nd F
X11
1 to ~.ve the oily (11S)t. All products were Iden4ed 6
'
-
a
.
,
, d. m.p. with autbentk samples. R, R
, virt. umd (I
lit If '.4, onts I I per mole I dtirittlort =f reartiort (min.). r. Zn, ml.
t, Ensilih sifninta~y).-Decbhnl

betwren the structurts RS(00511' (I)wul -id 11), and m.p. are given! Ph, Ph, 1.1-5,
11C), prNhiclo, yie
' O
I'f%
44' iLnd (M~
0
43
2
5
S
M
O
M
W;
(R and Wbotharonwic) tot thiointiotliC Ott 175 IL.15 Rot Pit- .
.
.
,
.
,
i
,
,
,
,
Ph, Pli, 1-15. 4, 15, 133. 5, (PhS~, 0.9; P-~ I e~
vlotisly liveix inade by chem. methods, and only recently b

l
f
d
C
6
z
C,11,, 1.19, 4, 15. 1,59, 5. (P-McC.11,S)ir, 0.9. 46'. P-Me-
rare
a
spectruscapy (
yinertnan anti W,
1)
, C.A.- 4 0C.H., p-TNItOCjII,, 1.6, 4, 30, OX3, 10, Q-MeOCJI.'~.
8354e). Htpetition of earlicr reductions be III and N.A- 1.2, 40% I-C,,11, I-CUj. 1.7.5. 4
45
1.0
10
Q-Ci*lli,S~

IISO, (NIffler and Smiles, C.A. 19, 1133; Hinsberg, C.A .
,
,
,
,
; P-CICJ(i, P-C[C~Ilj, 1.6, 4, 30, 0.83, 5. (p-ClC,-
1.4, 85
3, 650) lit general substantiated the previous rinutts. SiTni. H.S)j, .2, 70' und p-CICJ14SOlH, 0.10, 93'; (IV) Ph, P-
i
laraddrd. reductions werecarried ont. on I (ot U) (R R 1.32
Ph.50,1f, 0.15, 80* and ujs-
NTCC.11,
2
30
0.42, 5
P-CJC#JW and (R - p-CIC.Ho, RI - Ph) to give "l"w"c ,
,
.
,
,
clungtd. IV, 0.75, 62* and OZ; (V)P-CICJI,,
P-CIC4H*SChH and (PhS)i. Since the mol. was split it% all
ass!-
such reductions
no decision betwc,!rx land 11 was
a Pit 2.8 2 30, 2.69 10, ii-ClCaLSOJI, 0.6. 93 * and (PhS~,

*
,
p
p
' 0.4 and V. 0.6 80
and MIT, 0.3; Ph, a-MeC.H,, 4, 4, 45,
ble. By using Za and IICI (C.A. 49,23-10h
, in anit". cguiv, 4.85, to, 2, 35' and o-MeC.HSH, 0.5 213d
to2and4 flg.-~itc;mspcrmrtel,resp.,decis:an Tnight finally
be niade, The given wt. vf I was dissolved in 5() tril
Etjo PhSO-11, 12, O-Niecli" Pit, 2.64, 4, 30, 3.19, 10, o-NeC,
'
.
.
the Zn dust added, the fuming RCI drapped in ditring IG-20 lf~iWl, 0.6, 54
and (PhS).. 0.7; Ph, jb,-McC.II., 2.04, 4,
44' and
30, 3~10, 10, M50111, 0.1 and (P-AleC4HSN
1.7
inin. under stirring and ice-cooling, the rnb,t. refluxed until ,
,
p-McC.H.S11, 0.7; p-McC.H., Ph, 2.64, 4, 30, 3.19, 10, p-
all Zu had dissolved, cooled, the Et,O layer (A) washed with 0.7 ind PhSH
MCC.1140,11, and RhS~
0.7:~ P,%

I% N11,01-1, the alk. solu. acidified with cc ncd. HCI, and 3 ,
,
,
P-Mol-14, 2,84, 4, 30, 3.19, 15, Q-CIC.1,104, 1.1, 71 - ard
C. FeCts added to give the orange-red Fc(O?SR)s (M),-
's reduction mtOod (loc
cit
The
11intber
id
tifi
d b
) PhSOJI,tracc;
'
I
.
.
.
en
e
y
g NICC.H" c,-Nre_
tl.SOH, 0.2, VV and (Phsh, 0.8.1; P-
H"
f filtrate trota IH was washed with Et,O and (lie dIM 2 78 4 30, 3,19, 15, f-?,TtC.11.SOiH, 0.221, and (o-MeC,,
Elio layer evapd. to leave the RSIL A was washed te-
ffS)i, 0.05; IV, 1.32, 2, 120, 0.42, 6, M031f, 0.09 aild (P-
peatedly with ITO, dried over CaClj, and the ZtjO evapd.
i4 R')
-NfeCsH#Sh, 0.0 and IV. 0.3. The prectcling
11 (R
,
.

C~~7. '2_

VINMER, E.; SZ-00, J.
Attempt to synthesize 4~aryl-l, 3-benzothiazirie derivatives. P. 55. (MaUar Kemiai
Folyoirat, Budapest, Vol. 60, no. 2, Feb. 1954)
SO: Monthly list of East European Accessions (F-FAL), LC Vol 4, No. 6, June 1955, Uncl

Country ; Hungary
Or-tagory : CmCaulo nheTUstry. SWhatio orgttnic Chemictry
Abs, jour. Raf. zhur.-z-aimiya No. 6, 1959 19418
Author Vinkler E * - Klivenyi -P.; Szabo, j.
Institut. iffirgAiall cademy of 9ciences
T it Investigations in the Field of Organic Sulfur
Compounds. Short Communication.
orig-atb. Acta chin. Acad. scient. hung., 1958, 15)
No 4t 385-388
Abstr-,.ct Reduction of A.802CI LIs wherein Ar, - C6H51
P-CH3C6F.jJ 10CH C HU p CH OC H 3j1i--(CH30)2C6H3j P-U113-
P166H, 42
CONEC041 ) with Zn in acid medium takes
lace over the stages ArS021f t1I) , ArS023hr (III) and ArS&kr
fiv) to ArSH. By action Of C12 on III were obtained 1 and
ArSCi M which excludes the possibility of the structure
ArS(0)8(03Ar in lieu of III. The product obtained by Zincke
(Zincke Th., Farr F. Liebigs Ann. Chem., 1912, 391, 55), to
which the structure ArSOSAr wus ascribed, has actually the
structure ArS(=O)SAr (VI) and was obtained by oxidation of
IV with CjH COOOH (VII). By action of VII on VI there was
obtained ii, which negates the possibility of a structure
Cards 1/3

Country
catcgory
I
Hungary
G-2
19418
Ab3. Jour.
Author
I-.18titut.
Titlo
0111g, Pulb.
Abstr-,,ct
Card: 3/3
of VIIIa with VIII or with V results in V1.
a. IOffe.

4F

. a
&

Bommam M--- - W-1 -
.;7ZI, -- I-IM -
I . ~.!- 1---,--.,J,l --

-W -- / .-- - - - - --- I . -- I I I ~
I I ; fl-
i
I
V- "

"I fj( Zil ;iIia
Iludlictioll nf thiolsul(I'll.iteg In ;);) m)"m
t'jilivalt-nt In two at-mis to
Tables. 1-2 ref.

CA
Aftmpl*4 avemawas rose-
,,.. t Vtk yt%=;. Elm4r Vinkler suit
jinut StalWo (Univ. lacW. Ifung.). Aila- Mm. flust. 1.
i IW-7(1951XIil Rtjnj&n).-v-Cj 14CO~N CH,Br and N&Cll-
(Milth pys O-CA(coh-N.Va, Cif ICif JCOoRt~jg, and
Na at butrail at im Impleted Pcj ud)vc loci I x4sth.
The reaction drAcribed by Sue (C.A. 41 34460 ~ vm re-
lAted to this reactim. aince ip-Cjt.(Cbh'S'CJlrOll with
4wed. 111M)i In the presetace tit CIIXCOsFi It gi4ve dilkjW-
iWidOWAGMe, Ill. =1-3', 41111 11CIM. WvMt Fissily

r 1 9 to to v 13 14 n11 to a is a zi A'A is a A A~ 0 v
A_
AA 24 CC $0 1141

OGA

00
Ch1welide of sualic ads, 1111'"+ ~ vilikIrl ~SIAI Vind
38J. A,14 CAria. ft Nys. I.N.S1 1. 'It
dcrin. weft Aults"I 44 lite 0114M.111-10 (1) 14 1IL411'. w-61.
008 perild. IfOln 1311111C AWW And fIrf VISUM114 W-411111114 W
r
thrill
t
tin
Ch
193
420878)) b
h
w
dl
A
em.
r
a
i
ac
loo.
,
y
g
(
at a hiSh temp. in a rkwA41 tutw. The c"whie o( 41-1

o6a Ut
~ eviniloant cif anuw-wbile vrywlal~, wil, in ether antl Calh anis
iforconips. qnickly In the air. Estert sit di-1: bIr, Cilly.
o tht.1'. V.Aotk~ Iffi4oll'. 11, -'J 3% 1;1, 1., TO 7';
"
,
0
: ; M-1,40, m. liki
; 4?
Ph, twillon, fit. 1:01
1
; thysityl. m. 107-11% Itoot Fv~Fvm.,[ 616.
m, 70-7
w
-Cofer). cooll"Owm M. IN,$': Itnu [WHIcurtfivil. Ill.

eel 11.0-61 AmMe CJW.,Iicf,. n( di-1, too, 104% -Ikthyl-
iunilif fit. VJ-J -4141414nrl

aa 'M C.IIAN. ilmil" xfo*snp to.Will, in, 1141% Acotrriv
cneedles, at. 1434". A - 2 - Nsplithyl - 41 - n6dituilli.
needlis, us. 197-S'. Ar detiv.. nerdim, in. 1641. 1.
Bensoyla-&4actic acid clikwalide, Cnit.0tCls. in. 140'.
Istvin Finkly
dr
__0o
:-os
-00
j-66
0 0
009
tie*
Ala s L a-ItALLUNCKA& W994TURf CLAISOKATIC
ZA 11.
-As T.- - -
I a Ott war fxa wit ytctn u4s"Oft ot.4AA I I I It 12 '1 4 0
I ,
o 00 o 4111a 4110 0 0 4111 Mi * 0to 0 4111.
111110 0 o 0 e of 0 0 0 0 0 *J * 0 see 00 00 Os * 0 0,

C.lig jpVI 168,
~Ncjlsclt von".
tA 41 I= m-
Ow mctim 4ftw6bsd by Ilew Ual by bla Its
letted to Ibif Ob--t"- The I clfr
rA vAds
Utp CAAN
IWOM to 17 l" is
'CO"" I C110.
..d. 11 ykbkd obe Nor owl
ly am"d muska I- F"ll
nabil. (=o

The resectim of S.(bromeemethyPplithallwAdo with so-
dium meeletak cater. RICUS& 1,41kirr A fill lancM.S'i'Alm. I I'llit
NrIC011, liolusay), '114 1 Aim so, ~Xvto III
IW.Wo). - NILM.Of (1) "oh NACII(C(11,1.14 its
.. ~.OhN
".114 IAVC C1,111k: Ill( (lipi'l Ms. 441.1 %Alto
I-co,stal J else rs,pected
the romoian dowribed by Due (C.A. 41, 344tV) i.* uut re-
tell lot ibis otnervaticon. The pratilum ublititird by lalm iot
et"1414110416,11 oil 1 (11, 41141 cll,
'I h plovett Its 1k. I*-C.IUV(fhN T, flitiff,
kOhl..
'wried.11A),vielcletill andlICHI), 'Flarnpolorrmliuni,o
ptubablycolusedliy else BrAud
N dinues in I - (Protliminary cumulutticAtion )1. Finily

C.401
RA?ZOO! an the oximstloa of 3.44metholtyphisnyl 1,
devy do HicnAr Vinkler and Kjonill Anilk-twil.
AfAd Vais. Swil,'Mos. it Pkyi. 2, 10.1-M!"SPin Oer-
nian).-ToO.I. C, Na its 6 mi. abs. RtOll wits ad,led WS~
C. the mereaptitle ppt4l. after 14s.
miss. by addst. of 2t? mi. sAlse. ether Its sin.ill porti,ons. fil.
ttred, waJtcd with abs. ether, athictl to 1.1 CrAnt dc%yl
chloride in 7 ml. atn. MOIL Ouken I A min, warr added,
And the product rccrnt-'. from C41(t. giving V'-c light
ycilawi,h needles tA .4#o)~-
PAtexylacetoPhrosext. tn. 103% 1 mot. in PtOll treated
with 3 mots. 11ON11,11cl and 9 mots. KOll in watvt for
I hr. at the b-p.. the salts. cooled in ice and nrutrAlized,
and the product recrystd. from EtOll gave
CJI.Sl,, m. 97-41". l.tV'Afj Finily

- -V -R, , kr- Jui tMoriinyok dr)ktora
jt4r.L1 _Pdomor, ~ rd
An account of the LibliCO 3YMPOSfWa on tho alwmintry of nrganlc
sulphur compounds. Kerl tud kozl 14TA 22 no.3/41462 164.
1. Institute of Pharmaceutical Chepdstry, S2riged Medical
University, S2eged.

cm

V.~
1,/17. The spatial structure at Alasulphorift acid eltitra
determined ~y_chemlcal me
ISUIVIlkinic prIv'__Vjw and Sul I it
chlorine. (lit Gelman) V. K 1 11
k It, 10.55, Nil. 3 4, 1.1s.
Aromatic t1dolstilpItfaile acid esters are split by
tile actiall of Chlorine I to -it * 5 'ding sulphollfc
c1dorides and sisiplicnic chorldes. Ski plielli- acidit, nil.
hydrides are decomposed under identical conditions I lito
tile Corresponding stilphilliv midle cill.rides and stil.
plicnic chlorides. Thus the !tructimil lis)-tinnetry of the
thtolsulphollic UcfL] rsters, wits verified by Cheillizal
reactions. However thtse leactious ljIlvd to ftinjWi
4ny furtlicr Information co-werning the real structure
oftheconilkotitula i. -, whfcl%,~Ithe
bonterides corr,::,jx)iidti to tLe votitp,mids pripaitti.

VINKIER, R. (Winkler, R.1; TAZAREVA, M.V. [translater]
Chemistry of tetracyanoethylene. Usp.khim 32 no.12:1525-1536 0 163.
(141RA 17:2)

NARZML4DV, M.Ne.
NOV-speoies of the ge~ Ipbldiera HRL (R=opteras. Aphididae)
from-Tajikistan. Dokl. AN Tafth. SSR 3 to.5:49-54 160.
(MM 16:2)
1, Institut zoologii i parasitologii ims akademika Y9.N* Pay-
lovokogo AN Tadzhikokoy SSR. 2. Chlon-korreopandent AN Tadsbikokoy
SSR (for Narx Ikulov) ?TaJlkistan-Flant lice)

VINKIM,N., luzhener
Unification and standard technology for consumers' goods. Prom.
koop. n0-7:11-13 J1155- (Ml.RA 8:11)
(Russia--Kanufacturers)

Radioblology
CZECHOSLOVAKIA
ZADUBAN, Milan; HUTOVSKYj Milan; LIPTAKOVA, Gizela; VINK
Institute of Exper mental Bi-
Olga- Department of Radiobiolo", i
0 Slovak Academy of Sciences, and Chair of Biology, Faculty
'of atural Sciences, P.J, Safarik University( Oddelenie Radiobio-
logic 'Ustnvu Exporimentalnej Biologic Slovenalcej Akademie Vied a
Katedra Biologic Prirodovedeckej Fakulty Univerzity Pavla Jozefa
Safarika), Kosice#
"Determination of Radioactive Iodine in Plants."
Bratislava, Biologia, Vol 21, No 8, 1966, pp 578 - 588
Abstract: The authors describe a method of measuring - the ac-
tivity Il 31 in plant materials either directly or after
chemical treatment* 1131 is detected by means of scintillation de-
tectors using beta or pamma radiation. When 1131 is the only radio-
active eleyient present) chemical treatment of the sample is not
needed; when other active elements are present.I ma be determined
spectrometrically or after a chemical treatment. IT31 is extracted
from plant materials by NaOH at 10000; the extraction can be im-
proved by ultrasonic devices* Separation-oonoentration methods re-
commended are: extract ion-pree ipitation, ion exchange by a solid and
J'
liquid anion exchanger; chemical sorption. 7 Figures, 3 Tables, 3
i/1 Westernt 5 Czech, 2 Russian references# (Ms. ree , 5 frov 65).

Stratigraphic column of pre-CambrIan and lower Paleozoic
sediments in the GorW Altai. Kat.po geol.Zap.Sib. no.61:
5-25 '58. (MIRA 12:8)
(Altai Mmmtaina-Geology, Stratigraphic)

421C9 1'. - struktura
,-r,c o;
linallyuCc vystupana severncm-alta-~. Tr-,Ay ;~-o, m-ta(akad naul-
2 ~m~, . .1 --
zap. sib. j'i 5
SO: Letopic-I Zhurnaltnykh Statey, Vol. '.7, 1~94F-

VINI(PAI-1, M. K.
26978 VINKMAN, M. K. - Novyye dannyye 1 vezraste giperbazitcv adtaya. Dcklady akad. -'%auk
SSSR, novaya seriya, t. MIII, N'o 1, lrb9, S. 135-36
SO: leptopis' ghurnallnykh Statey) Vol. 36, 1949

VI WAN, N. K.
UNOR/0061W J%d 48
Stiitif icatim
Orography
*Stratigrapb.v of the Earliest Deposits of Northeast-
am Part of the Altay Mountains," H. K. Vlnkmn,
3 3/4 pp
"Pok Ala Nauk SSSR" Vol LXI., No 1
Vinkman's investigaticns In the subject area olarl*
existing Ideas of the stratigraphy of Cambrian and
Pro-Cambrian strata. He conducted them alcng the
lover course of the ratun River, where the Katun
horst-anticline ledge and the Anay depression most.
aubmitted 6 Apr 1948.
8A9rrT

vilaml, m.K.
Stratirraph7 e- Proterozo1c.31nIan, and Corbrian sed'=Pntx in the
Gorn.vy Altai. Trudy SNIUMMS no.5:4-50 159. (MIU. 11:6)
(Altai Mountains-Geoloff, Stratigraphic)

SZMTIKOV, V.M.; VINMAN, H.K.; K0901TOV, A.R.
Cambrian-Ordovician and Ordovician in the Gorny7 Altai. Trud7
81JUGGINS no.5:51-66 '59. (MIRA 13:6)
(Altai Mountains--Geology, Stratigraphic)

-I __ --- - --- --- - - __ __ --- - - --- -
VINKMAN, M.K.; GINTSINGER, A.B.; POSPELOV, A.G.; POLETAYEVA, O.K.;
YEGOROVA, L.I.; ROMANENKO, M.F.; FEDYANINA, Ye.S.; ASTASHKIN, V.A.;
CHMYSHEVA, S.V.; ROMANEWKOp Ye.V.; ASKARINA, N.A.; BOYARINOV, A.S.;
NADLER, Yu.S.; GORELOV, G.F.
Scheme of the stratigraphy of Lower Cambrian and the lower part of
Middle Cambrian sediments in the Altai-Sayan fold area. Trudy -
SNIIGGIMS no.2023-34 162. (MIRA 16:10)

vi RA&A-~; GINTSINGER, A.B.; YEGCROVA, L.I.
Key sections of the Lower Cambrian and Sina in Gornaya Shoriya
and the Gornyy Altai. Sov.geol. 5 no.12.-44,56 D 162. (MIRA 16:2)
1. Sibirskiy nauchno-issledovatellskiy institut geologii,
geofiziki(i minerallnogo syrlya.
(Gornaya Shoriya-Geology, Stratigraphic)
(Altai Mountains--Goologyj, Stratigraphic)

1~1.--.1- -1
VIKKMANI__M.~~; GINTSINGER, AN.
Correlation of Cambrian sediments in the western part of the Alta-1-
Sayan fold area. Trudy SMIGGIMS no.24:38-78 162. (MIRA 16:10)

. !! ~', z,, -Z, "- -
GINTSINGER, A.B.; VINKMAN,,M.K. .
- ---- ----
Stratigraphic position of phosphorite and manganese occurrencos
in Gormaya Shoriya and in the Kuznetsk Ala-Tau. Trudy SNIIGGIMS
no.24t107-115 162. (MIRA 1611O)

VIMIAN M.K.; ASTASHKIN, V.A.; i'-,J~Y~VS)Y'Iy' B.G.
;'r
ratigraphic sch' 3t' of Pre-Cambriart 4]
St Alai au
the Kuznetsk , Gol-naya Shoriya 9 the
Gornyy A:Ltai. Trudy SNIIGGDIS no.29:34-49
- , 1, -%
rar.1 ' ': "; -, - -
". I -,inefi, ~Ir.A "
%lair '.~- h;~I
164.
U,URA 18:3)