SCIENTIFIC ABSTRACT MEZENTSEV, V. A. - MEZES, L.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001033730010-3
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: July 19, 2001
• Sequence Number: 10
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

PHASE I BOOK E,P11-ITATION SUV/4721
Mezentsev Vladimir Andreyevich
"Neobyknorven"ye" yavleniya v atmosfere ~Unusual" Phenomena in the Atmosphere)
(Moscow) Profizdat, 1959. 91 P. 30,000 copies printed.
Ed.: V.M. Pankova; Tech. Ed.: A.A. Golichenkova.
PURPOSE: This booklet is Intended for the general reader.
COVERAGE: The booklet presents In popular form explanations of unusual phenomena
occurring in the atmosphere. These include the apparent change in the shape
and color of the rising sun, the occurrence ot"airacalous" rains, the appear-
ance of "crosses of light", the green flash, etc. The booklet provides a sim-
plified scientific explanation of each phenomenon. No personalities are
mentioned. There are no references.
TABLE OF CONTENTS:
The Usual and the Unusual in Nature
C ar,1~3

KRITOPUST. V.1.-, PRESIITAKOV, I.R., Ger07 Sotsialisticheakogo Truda;
MIZM;TSSV. 7.A.; POPODIED, Te.Te
On the road of technical propress. Ilek.1 topl.tiaga 3 no.12:
3-9 D 159. (MIRA 13:4)
1. Nachallnik depo 14skI Yugo-Vostochuoy dorogi (for Krivopust).
2. Master avtomatnogo tsekha depo Liski Yugo-Vostochnoy dororl
(for Presurakov). 3. Master tsekha toplivuoy apparatury depo
Liski Yugo-Vostochnor dorogi (for Mezentsev). 4. Master teekha
bol'okhogo pariodicheekogo remonta Yugo-yostochnoy dorogl (for
Popod'ko).
04ski-Railroads-Repair shops)

MEZENTSEV, V., inzh.
Colored rain and snow, Stars~.-serzh. no.7:30-31 01 '~!
(YJR'~ 1:- - 9 )
1. Glavnyy redaktor zNrnala "Znaniye -
(Rain and rainfall) (Snow)

- MEMITM, V1441-k-ir-Andr9yevich; IVANOVp SJI., red.; KUDRYAVTSEVA,
O.V., tekhn. red.
[World of polymero)14ir polimarov. Foakva, Izd-vo "Znanie,"
1962. 55 P. (Novoe v zhizni, nauke, tekhnike. IV Seriia:
Tekhnika, no.22) (MIRA 15:11)
(Polymers)

-kZZENTSEV,. Visdimir Andreyevich; KANTER, A. I., red.; RAKITIN, I.T.,
tekhn. red.
[Our friend, chemistry) Nash drug - khimiia. Moskva, lzd-
vo "Znanie," 1963. 70 p. (NarodiWi universitet kulltury.
Tekhniko-eko mmicheskii fakulltets no.12) (MIRA 17:1)

WZONTSEV, V.
Sky eets riddles. Znanie-sila 38 no-1:45-47 Ja 163. (MIRA 160);
(Halos (Meteorology)) ,If*
1,
,e t

IIE-P. .,F'~ . . . .., 1 .:. I ! A . .
I I I.*- !., 1. 1 ~;
i 1~,i t I ~ ',,I I --,. :.
11; . - v Z! . - . , : ~
. I . .$
1 . " .- . :, -,.-;
'-i ~, .., '', 1. 1 1
. . . ~ i ~~ ~ . I ~ , - K,, - . :; ~ ',;I p1. 1 . . I!

~EzLtFISEVI V.F.- A.Yu.
Cancer of by-,a.,3t in man; ora obq~rvaticn. lvp. onk. li n~-.5:104-
10,6 165. (IMIRA 18:8)
1. 17, fakull"-Lskoy Kurskogo maditsinskogo
lnotltuta - orof. IMI.G.Ruditskly) .K:-,~7.--kcgo oblust-nogo
disparnira v-a-h - T.S.KwArashora).
.0

i1. UeSt't.rai tim ri!~ we T.!I

waIITSFV,jj-j.
The locomotive engiLeer called for a replacement locomotive ...
Elek. i tepl. tiaga 9 no.ll:;9-3C 11 165. (MIRA 19:1'1
1. Mash'-n.4st-InstrLkt,rr depo Kxshmurun Ya2,,alhskoy doroF,I.

tills
0
0. 0. R of
',a Z C; 'r as a 200 a o o0as
8T. 0. o4 0 u
a
0l
4t I'
f
o og
a 1 1. 1 * I z ", i -Slo- ;; 8
U-8 . p ~i 3 D. .1
Zoe* E-.
L --'atX a '
R
SOM

NNZNRSZV,V.S.. kandidat tekhnicheskikti nauk
Calculating water and heat predictions. Meteor.1 g1drol. no.4'
33-34 AP '53. (NLRA 8:9)
1. Sel'skokhosyaystvenrqy institut, Omsk.
(Weather forecasting)

-ry C- V V. S-,
AID P - 2510
Subject USSR/Meteorology
Card 1/1 Pub. 71-a - 20/26
Author Mezentsev, V. S. Kand. of Tech. Sci.
.r"P"W%6"GW"Ww.'0'
"'O'WO
Title P. S. Kuzin, Rezhim, rek yuzhngkh rayonov zapadnol Sibirl,
Severnogo, Tsentrallnogo Nazakhatana (Flow conditions or
ffl-ve-r-s"Tn- Southern Regions of West-Siberia, and Northern
and Central Kazakhstan) Gidrometeoizdat, Leningrad, 1953.
(Book Review)
Periodical : Met. i Oldro., 3, 58-6o, My-Je 1955
Abstract : The author of the article gives a very favorable review of
this new textbook for its exact presentation of factUal data
on flow, precipitation, climatic conditions and general
physico-geographical factors for different watersheds of the
analyzed areas.
Institution: None
Submitted : No date

AID P - 3178
Subject USSR/Meteorology
Card 1/1 Pub. 71-a - 5/23
Author : Mezentsev, V. S.
Title : Ono* more on the computation of the mean total evaporation
Periodical i Met. i. gidr.t 5# 24-26, SIO 1955
Abstract i A mathonatical analysis of the man annual evaporation in the
Central Asian watersheds, Tables indicating townst evaporatJon
and the radiation voluxiss are given. A mathematical analysis
of Bagrov's theory on possible computation of evaporation is
presented and criticized. five Russian references, 1911-1953.
Institution : Nora
Submitted : No date
r7P ?.I - -
- - /A 0 7

M-ZEI,r OP4 J 11 KJUZIN, P. -
_~. , V. 1. ASTWiffiUnIS V, G. V. 1. . TU a d
u -SC~vj, __y_, ---F 0.
Delivered a rep(~rt. or. questl,.ris -,f' nydr(Acgical
MPWt Prs"UW IM the 3rd AU-tblou *&*logical COugme, 7-17 Oct 1957,
MnjugrQ.
(rzv. Ak ft* gm. "r 90WIsf-, 3, PP3-9, '58)

V. S.: Doc 7/X,7V Sci (A-'ss) -- "A m--)tho~ of
computatiom und an tr apn1l, ti. tlir- tn~- -I ,)13a1 c Inos If
,west Siberian -plain 1,%zed on molBtui~~ Fire hoat supple,,".
uaco-,; crd-ir c' LF,,nin Stnt,~ V. Lumt,n,rjr~v, -,-wr
(min Fi6r~lf'r Educ Tisz~, v
Facui~.y), Y' coplr)n (n, IT~,

MEZENTSEV, V.S.
Average amiual runoff on the territory of Omsk Province.
Izv. Omsk. otd. Geog. ob-va no.5:11-15 163. (MIRA 17-5)

WZENTSEV, V.S.
Natural moistening balance of' tne West Siberian Plain and the
problem of the lower Obt Valley. Izv. AN SSSR. Ser. geog. no.5:
45-50 S-() 163. (AURA 16-10)
1. Sellskokhozyaystvennyy institut, g. Omsk.

IEZENTSEV, V.S. , prof.; PI'SINOV, I.F. , kand. tekhn. nauk
Pay more atte-tion to the ~,roblems of la-nd =elicration ~n Szr,--rla
and the Far Fast. Gidr. 16. no.6:61-62 Je 164.
(MIRA 17:9'
(,for Nezentsev).
~nyy institut
Omskiy sellskokhozyaystver.
2. Vsesovuznv%, naiie.,.no-isslgdc,,ra*,elt-liy inst-tLA ~Y`irotekhr-:ki
I
i mel-lorat--ii imeni A.N.',/os,~yakova (r,~r ~-,-sincIv"'.

i.V.; MEY,ENTSEV, V.,,.
. (i if;,, 1-! but4 or; c-l' ,, ta- evap-irat, Ion (.r., ! f.,! tf--,--: .. 1~ , --, .
J
Omsk Pr(Alnce. lzv. ftrzk. (Ad. Geog. r--)b-va fic.f :11-25 164.
1p:,))

MME"ITSEEV, V.S.
Hydr-oloFic and clirnatic cond, tions in the riorth an(;' in 'des %prn
Siberi-a as related thp plarmIng of larre revervoirs on ,he
Obl River. Dokl. Inst. geog. Sit). I Dlil'. Vont. 1 i)3.
(','I -,,A 12 : 1, )

e:. ia r-no,-c. s Fi:- r- r. a ::,e 1L f 7E: a 1. ar. I ,t
r I
,r, z.

MIZENTSEV V.Z.
'I
Moisture zonas and thermal reso4~s of the West Siberian Plain.
Trudy TGU 11+7:113-121 157. (MhA 16:5)
(West Siberian Plain-Climate)

L 57047-65 Ew-r(d)/FSS_2/EViT(j )/EPA (ss)-2/0,7 (M,)/EPF (0/F,',`P(f )/~')F (n)-2/9,T(0/EPR/
T7r--- -RPL WN/jIn-I
-ESSIO14 RM -H5014811
A
GO UR10209/65/0(*/006/0032/W35
AUMORI WMtjlv_s inevr)
~~tITLE 81 Powrful. siages
--So OV
1 2
kosm6navUM no. 6t, 1965s, 3 -35
7TAGGi c
J- T6pi :i;~a -.enaiii~~--liquid--rooketzfuel- -liquid
ent
liquiq--rocIMI
I--- roca-rocket thr
~~nt,, rocket propulsion
-tfid~ -bons rue---'
-ABSTRACT tX d Gf---the- -of
slir-ver- -IS- presents, -operatiowmid:
~with a-high-p6wer- Aght 060
--to-we ratio (40004
-resulting- from-thii- Antengity7of - the- thermal- processes, the'simplicity of
h
the,
c6nvers~I:on -of Afie- therml anergy -to mechanical, and the idnim
:Tbe liquid fuels-are burned in*thec
qu,
I of the natzle andicreate the-reactive thrust. Theor6tically' therG are ftuW dif-!~
ferent -fuel . possibilities# but. Iii practice tbe- choice -is limited by- the req a-'
ILlir
me
nts for reliabilit7 and the complete utilization of the fuel potential, The
eff otiv
0 eness of the ZHRD is judged by its specific thrust,,vhich is.the ratio of
-the
1/3

L 57047-65
ACCESSION NRj AP50U.811
characterized by:tbe Impulse acting on tbe-rocket from the combustion and dis-
charee of 1 14 of fuel, The specific thrust shows to what extent the rocket fuel
is effective and characterizes the completeness of utilization of the fuel's
theoretical possibilities. The latter is determined by the coefficient of com-
pleteness of the apocific thrust, the ratio of the actual specific thrust to that
which would be obtained in the same structure if there were no losses. Another
criterion used to judge ZHRD is the specific weight, the ratio of the weight to
thrust. All those characteristics enter in the analysis of the Tsiolkotskiy
equation. The construction of the combustion chamber presents problems, since
materials available are not able to stand the high temperatures generated. To
overcome this, the chamber Is cooled, eit1her by the flow of the fuels Inside the
wall of the chamber or by film cooling, in which the fuel flows along the combrus-
tion surface of the chamber. The thrust can be increased by increasing the pres-
sure, and the optimum pressure can be-calculated by complex methods. The fuels
are delivered to the combustion chamber by high-pressure, high-volume centrifugal
pumps. Stringent weight and size requirements of the pumps call for their opera-
tion at very high rpm. The pump power is furnIshed by a gas turbine, Rocket con-
trol can be effected by several means. The reliability requirements are extreme,
particularlv for manned launches. OrIg. art. bast 2 tables and 1 formula.
ASSOCIATIONt none
1-C,,d 213

ACC NRs AP7009076 SOURCE CODE: uR/o4l3/67/000/003/0053/0053
:INVENTOR: Shtamberger, G. A.; Shullts, V. P.; Mezentseva, A. D.
ORG: None
!TITLE: A device for measuring the intensity ratio between two electric signals.
~Class 21, No. 190985 (announced by the Institution of Automation and Electrometry,
-.Siberian Department AN SSSR (Institut av-tomatiki i elektrometrii Sibirskogo otdelniya
AN SSSR)J
~SOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki, no. 3, 1967, 53
TOPIC TAGS: electronic measurement, electronic signal, signal analysis
[ABSTRACT: This Author's Certificate introduces a device for measuring the intensity
I atio between two electric signals. The unit contains two receiving elements for the
~first sign&l, a single receiving element for the second signal, an adding stage and a
Isubtracting stage. The input of the adder and that of the subtractor art each con-
ected to one of the receiving elements for the first signal, while the outputs of
hese stages are connected to a multiplier. The multiplier output is connected through
;
n averaging unit to the comparison result indic&ror. To improve accuracy in ratio
measurement when both the signals to be comp&red are subject to interference, the
nstallation is equipped with an extra receiving element for the second signal and two
1/2 uDc: 621-317-61-o82

ACC NRt AI~7009076
lintA-rlocked variable dividers vith identical transmission coefficients. The compari-
ison result indicator is made up of a control unit and a final registration device.
Phe receiving elements for the second signal are each connected through one of the di-
viders to the inputs of the adding and subtracting stages. The output of the averag-
l
ing unit is connected through the control unit to the controlling input of the di-
I
:viders. When mismatch reaches zero, the transmission coefficient of the dividers is
I
Ted to the final registration unit.
additional receiving element for the second signal; 2--dividers; 3-compaxison re-
t indicator; 4-servosystem; 5-fin&l registration unit; 6-receiving element for
second signal; 7-adding stage; 8-subtracting stage, 9--averaging unit; 10-mul-
lier; 11-receiving elements for the first signal -
CODE: 091 SUBM DATE: l4Jun65

MF2i,.NT:::',VA, A.G.
Ttjr.orli~.,i syndra-4 'r. Trudy 7,r. rej. lrs~. 111:53-56
163. (MIRA 1-8: 10)

A. i
Illiksov"i, F.D.; SJA,
of -,UF'~Aar -,e~ i-7~ brain
a~orling to Jata of Vc-rc)nezh pcly~-Iin'rs. T r AnST..
51: 38-4.2 163. (~'.FA ls:lrj)

POLILOV, M.I.; KEZEUTSIVA, G.L.; VXTROVA, A.A.
Boric acid solutions for treating seborrhea of the scalp. Vest.van.
i derm. 30 no.4:56 il-Ag '56. (KIRA 9:10)
1. Is Karskogo oblastnogo kozhno-venerologicheakogo dispansera.
(BORIC ACID)
(SIBACIOUS GIANDS-DISEASZS)
(SCALP--DISEASES)

POLIWV, IfJ.; HEZENTSEVA# G.L.
1
Occupational nickel dermatitis. Test.derm.i veno 35 no,,3854-
57 gr 161, (mm 14841
1. Is Kurpkogo, oblaqtn~go kozhno-venerologicheakogo dispowera
(glavuyy vrach - zasluthenmyy vrach RSM N.P. Vagayev).
(SKIE-DISIMES) (NIMIL-TWOMMY)
I C.

N 7 V A A
USSR / Cultivated Flants6 Cereals.
Abs Jour : Ref Zhur 195", :o 34'~2'-,
Author : Hezentseva N.
'- -'-L- ~icultviral Institute
Inst :-HHI-;~FaT 9~
Title : - n .., -ect -.' -oco w Cronq n ','ap I,, r t
'. ield in Cie iight Chestnvt Soi-is of Stali,wrads;-ay-
0 bl,- -q t
Orig Pub : Sb. nauch. rabot stud. StalirLgr. s. kh. ln-ta,
1956, vyp. 2, 23-27.
Abstract : 'lo abstract.
Ca rd I/ I

L-5U5-66

MEZENTSEVA, N.L.; PETRIN, A.I.; KUROV, G.A.
Epitaxy of germanium films on germanium during vaporizat"on ander vacuum.
Fiz. tver. tela, 6 no.7:2026-2031 Jl 164. (MIRA 17:10)
1. Institut kristallografii AN SSSR, Moskva.

ZOZULTA, A.P.; MEZMSWA, N.H.. PISHKOVA. V.H.; YURIYYIVI Tu.K.
Some characteristics of methyl selonaphenyl ketome &M
bensoylacetone. Zhur.anal.khim. 14 no.1:1?-21 Je.-F '59.
(MIRA 12:4)
11, N.V-Lononosov Moscow State University.
(Butanedione) (Ketone)

'C
I 4ZMTTSEWA, N. P.
"CAtal.7tic Isomprization of linsnturate-I Hydrocarbons (Alkoent-s. Cy(!la-
alkpjips. j--ne Sub IB May 51. ;-kisrow ~',re.--r of Lr-P.1-i
Statc U Iment 14. V. Lopnn,)sov.
DlqsprtELtionA preonntod for volpn~7n wil Pn,,.inmrtn,, lArrec-s in Aon,-riw
Jurine 1051.
SO: Sum. 110 - 1-80, ') '~~! 55

HENOTSEVA, N.I.; MOGILEVSKAYA, O.Ya. (Moskva)
"Collections of scientific works by the labor safety institutes
of the All-Union Central Council of Trade Unions". Reviewed by
N.V. Mezentseva,, O.IA. Mogilevskaia. Gig. truda i prof. zab.
4 no.12:53-54 D 160. OCRA 15:3)
(TRADE UNIONS)

GM." At"NA NoN 474-
(1956).-In productinn of WievNII the conen. of tho vapor
ratles from 0.004 to 0.05 ing./I. (if air. Toxicity to white
mice apMn to be: ab&nlutfly NIhal 16, ntin;i,ial Irthal .5,
mu. tolt-rabic da-~z I -F) mg .;T At Ir vd the e
produm, Irrivaliall of re.--illilutory or-pliq and vp~, tkmlesl;
at 6 dwagL t6r flnw Is prxluct,l. alld 10-18 111g./1. do:~--tge
cyanGgi-, convulslon3, and cle.Mb (Yotmr. A Fmin. conract
with 6kin prodtweB point at Imiger cOntatz
mumn.lifica tion ul tkc-ic5 ;wvm-ri, concur iN
T end. at 0 '(16 fu n1r. G. M. KagalapxAT

137- 58-4-8705 D
Translation from: Referativnyy zhurnal, Metallurglya, 1958, Nr 4. p 341 (USSR)
A UTHOR: Mezentseva
TITLE- Data for a Medical Classification of Tungsten aud Titanium
Compound Dusts Used in Powder Metallurgy (Materialy k
gigiyenicheskoy kl.arakteristike pyli soyedineniyvol'frama i
titana, ispol'zuyemykh v proizvodstve poroshkovoy metal-
lurgii)
ABSTRACT: Bibliographic entry on the author's dissertation for the de-
Free of Candidate of Medical Sciences, presented to the f-y
Mosk. med. in-t (First Moscow Medical Institute), Moscow
1,?57
ASSOCIATION: 1-y Mosk. med. in-t (First Moscow Medical Institute),
Moscow
1 Tungsten dust--Medical research--Bibilography
2. Titanium dust--Medical research--Bibliograp~iy
3. Medical research--Thesis
Card 1/1

"Wenic Charseteristles of the Aerosols of IndustrIal TOnsaten
and Solm of Its Compounds Utilized to Powder K&WIWW,' by
J. V. Mezentseva, Chair of Hygiene of Labor, First Moscow Order
of Lenin Medi-cal Institute imeni I. M. Sechenov, Gigiyena i
Sanitariya, Vol 22, No 4, Apr 57, pp 25-29
Investigations of hygienic conditions in plants which utilize tungsten
and its compounds in the production of hard metal alloys and the production
of electric light bulbs revealed a high concentration of metallic tungsten,
tungsten carbide, and tungsten trioxide dusts in the air, with particles
up to 4 microns in size. Medical examinations of the workers in these
plants disclosed a number of cases of diffused pneumoconiosis. The
experiments coDducted on white ratg to determine the toxicity of these dusts
established that tungsten trioxide was the most toxic of the three sub-
staw ma on ten aerosol*
so.. Pro hylactic measures to prevent the for ti of t
P
awd periodical wedical examinations of the workers are uripd.

cra
WDT
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Ott 'tio 00
01. 4,009, rA e -lite
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IS. AS Vr% 0 e Of
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SPA~ Or ~qevOscl
'rolls, -ID e,01~11 Of ,tax,
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,tbe jo ee oxos V4 .'s
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Ae ties .08.1c ,re froz ?v
01 CV06 93A
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&*,P,Vvs
40, . -,n

UPLUN, Z.S., kand.med.nuiik; WAMEMNYA. N.Y.. kund.Tied.nauk
_ienic evaluation of aerosols forned in the prodnetion of
lutrd alloys. Gig. i %an. 24 no.6:16-22 Je '5q.
(14IRA 12:8)
1. Iz kutretry gigiyany truda I Moskovskogo ordena Lenina
meditsinekogro instWita iment I.K.Sechenova.
~DUST
hyg. evaluation of aerosols formed in prod.
of hard alloys (Rus))
(INDUSTRIAL HYGME
same)

?rofC33or
(,oo:,__co'ogy of
?6iya ru
!963. 335 P. 1500 CoPie printed.
Knamlidullin; Tech. Ed.: Yu. S. Bel chikova.
;Z~ provide information on the toxic effects of rarQ
and i:,L".zrial applications o" raro
'_:'ro 31B ~:,a Tca clinical pictura ar.,
poizonlnSs is also givin. Th.re ai
t' _'7rfoct on an Or-nim 0:
&_ L'_ A.
,.-C, Di3pczsc, and Other .:atals Used In Industa-1 Lnd
)-air Compourds.
0. Ya. -11e
!bdenum. "1:1 7_
-II'C ~' e V Et
V . al
Zirconium. 0. Xa. mo-Ilewk--ya
5. Vanadium, 1. V. Roshchin
6. Tant-alum. Y,, L. Yegorov
Niobium. Yu. L. Yasor-
T B. i17
Z-4.-

I,, Frofeszor
-adk*i-kh notallov
z)lc (~,Oxjcojoa of Rart, Meta1z)
`6
6
9 3 335 P. 1500 co,:ic- printed.
S. Khamid4111n; Tech. Ed.: Yu. S. B 11chikova.
zl: 'Jo orovide information on the toxic effects of rare meta-,s.
and :_.-:Lu-,_Aial applications of rare met
--Qrc_o1:j zLre d4LL-cu_,3:,,c_,. The clinical picture and
Vr r-,re-metal poi3onings is also given. There are -"),)7
'I"Icct on an Or!!oanllsm of
v &D ~_ "_ ~.L ~ Q.
Dispersed, and Other Metals Used in Industry and
i_~Ir Compounds.
-."-denum, 0. Ya. Mogilevskaya. 20'
117.
"Sten. N. ri'lezentseva 4-
V. Mazentseva et al 58
'rconium, 0. Xa. Plog'levskaya 71-
5. 'J-.radium.. I'.' V. Roshchin 82
60 ~,"ntalum. 'Yu. L. YeSorov 95
7. ',;;.obiuTa, Yu. L. Yegorov
8. S. E. Sar."=-atskaya
q.- ~_d ;.ta S. Vorob.1yeva

IV
'3071
Z & zz.
T-.)ksikolo~;iya radkilth metallov (To:f._coloMr of Rare Vletals)
1963. 335 P. 1500 er~rlcs printed,
1. S. Khamiciullin; Tech. Ed.: Yu. S. Bellchikova.
P`,rAPOSZ: 2o provide information on the toxic ef fects of rai.-~
c~'-Ic7aiatry and industrial applicationB of rare
t" ~6c;rooolz are discussed. r1he clinical pictuzz-u and
or rare-metal poisonin-z is also given, There are
Effects on an OrSanisr-
of t.
VU -
Industrial Dust of,nixed composition Cor,,~Iaining Rare
and OtherMetals and their Compounds,
industrial dust from ore concentrates. 0. Ya.
gy plantq.(hard
r-la7 austs at powder-matallur
;.;!1Ojz). ez. S. Kaplun (DeceLsed) and N V.
rrast of metallurgical (Beszer;jar) slags. I V. Ro3hoh_f
4., Industrial dust from copper ores* Kim Tai:in 24:-
Industrial du3t from luminop' n ores. E. 1. GOlldman at %]
.- I -magnes-lum and
DuLt of ra,.,r the.rMorezi4sto 'h-"Ome
'_-1. A,
z

VOROBIYEVA, R.S.; ZHILOVA, N.A.; KASPAROV, A.A.; MEZENMEVA, N.V.
Comparing the toxicity of mereaptobenzimidazole and
N-phenyl-N-isopropylparaphanylenamine. Kauch.i res. 22
no.2:18-19 F 163. (KIRA 16:2)
1. Kafedra gigiyeny truda 1-go Moskovskogo ordena, Lenina
meditsinBkogo instituta imeni I.M. Sechenova.
(BEIrZI]KIDAZOLETHIOL-TOXICOLOGY) (PHENYLENEDIMINE-TOXICOLOGY)
(RUBBER INDUSTRY WORKERS-DISEASES AND HYGIENE)

VOROBIYEVA, R.S.; MEZENTSEVA, N.V.
Toxicological evaluation of the vulcanization accelerator
N,N- di-isopropyl-2-bensothiasole aulfenamide and of the vulcanizing
substance paraquinone dioxime. Kauch. i rez. 22 no.5:27 My 163.
(KRA 16:7)
1. Kafedra gigiyany truda. 1-go Moskovakogo meditsinskogo inatituta
im. I.M.Sechenova.
(Rubber industry workers--Diseases and hygiene)

VOKE I YEW , R. S. , kand. mod. nauk ; ALZENTSEVA , 11. V.
Disorders of the. ",ver fwiction under tne Influence r,," some new
accelerators rf vulcanization cn the rrganism. Trady i-go 1411 28:
- (MIRA 1-::_
1, 1?-222 'i~4.
A. Kafedra gigiyony truaa (zav. - 1,ruf. Z.1. lzraellsori) -go
Moskovskogo ordena Lenina mpdits-.rskogo instituta imeni Sechenova.

TUESINA, I.L.-, MEZENTSViA, S,K
Changes In ~ s~- - I n ph! I tri v. fk w j ir, am, grjin ~, timors fif
the ov&ries in tne vr-o-t-ss --f T:'p. Onk~ 11
no. 8 -, 38-4,1 1 t,5 (MIRA 18til)
1. 1z III khJ y& P,-Lf~ Vj.
Tobilevich), aborawrii kzav, --
dotsent I.F.,Jraim lr~-i 1 1 tu t~a onKu ~ ~~g, I AMN SSSR idirek tor
doystvitel(ayy 41isn AMN SSSH pr-,J, A,l,,S"rebrov) L
gln#jku'logl,-fjeqk,-,pr,- zav, '!J,Mz6ntq,3va)
lengoronkndi,zpans-ra v.,avr,,7.- v:-a-ri ~ , S. Y 8 t- I t6yn,

ASNER, B.T,I. MEZENTSEVAs V.V., insh.
Experience in the manufleture of boalery cut from knit cloth.
Teket. pros. 25 no.M41-44 0 165. (ICRA M10)
1. Naoh&llnik eksperlmen"Allnoy laborstoril Odesakoy trikotazhnoy
fabriki iseni Knipskoy (for Asner). 2. EksperimentalInays
laboratorlya Odeaskoy trikotashnoy fabriki Imeni Krupskoy (for
Mezentseva).

ICUMSMA, Ye.l. (Tashkoat)
Same remarks on T.B.Pelarkey's review of Kh.M.AbdLullsev's book
'Gazette relation of mineralization to graaltold latrustoas.0
ZsV.V~ss.uIa.*b-. 85 ao.1:227-126 056. (MM 9:7)
1.8rodus"tatakly gosud&rstvQAR" Ualversitet.
(Ore deposits ) (Amull"v. Kh.M.)

ACCESSION NR: AR40257"* S/0299/64/000/003/PO64/PO"
SOURCE: RM Blologlya, Abs- 3P421
AUTHOR: Mezentsev, A. I .; Mezentseva, Z. 0.
TITLE: (3P421) The effect of ascorbic acid on the course of acute radiation sick-
ness In relation to Its time of administration
CITED SOURCE: Sb. tr. Sverdl. mad. in-t, vy*p- 39, 1963, 117-125
TOPIC TAGS: radiation, radiation sickness, ascorbic acid
ABSTRACT: The affect of ascorbic acid and of its time of administration on the
course of acute radiation sickness was studied in 157 white rats receiving 700 r
of X-ray. Ascorbic acid was administered as a 5% solution I.m. 15-20 minutes be-
fore or within I hour after Irradiation. at doses of 50-100 mg/kg. The survival
of irradiAted animals receiving ascorbic acid was 10.4-33.4% for pretreated animals.
55.6% for those treated after Irradiation, and 33% for controls. The symptoms of
acute radiation sickness were qualitatively equal In all groups of animals, but
there were quantitative differences. The most marked symptoms were observed In
rats receiving ascorbic acid before Irradiation and In controls. Ascorbic acid is
ry~~mmended as a prophylactic ogent against acute radiation sickness.

!~ ACCESSION NR: -AR4025766
:V. Kozlov
IDATE ACQ: 27Feb64
I
I
i
I
i
.~crd - 2/2
- - -- I ,
SUB CODE: LS ENCL: 00
I
1)
1 0
I
q
0

LVIIINAP R. YA. , I-IEZENTSOVA, N. -N.
Hydrocarbons
Synthesis of hydrocarbons. Part 14. Synthesis of cyclic hydrocarbons with double
bond outside the ring.
Uch. zap. Mosk. un., No. 132, 1950.
9. Moathly List of Russian Accessions, Library of Congress, October 1952. UNCLASSIFIED.

LIVINA, R.Ya.; TAIITSYRNVA, T.I.; PAYNZII'BMO. A.A.; MXZZHTSOVA, R.N.
Synthesis of hydrocarbons; symthesle of isoolkaneg. Izv.Ak ~--'
ad. nauk
SSSR; Khim.otd. no.2:161-165 Mar-APr 51. (CIJQ 20-7)
1. Laboratory of Organic Chemlstrv imeni N.D. Zelinaki7 of Moscow
State University.

LI;YIXA.R.YA.- YMENSOVA, N.Y.: AKISHIN. P.A.
Alkycyclohexene
Contact isomerization of unsAturated hydrocarbons. XVII. Isomerization of alkycyclo-
pentane and alkylcyclohexene in chrome oxide on aluminum oxide. Vest. Moak. un., 7,
No. 2. 1952.
9. Monthly List of Russian Accessions, Library of Congress, October, 1952., . Unclassified.

"~-~T~7 -.bQ.Ae
M 44. N T 5 OV A. 11. 1,.
tall
a
'bdt. -Nosh No. a. 4' vv I
-4 d. '1 41.
Yelobeunit. Cul:cjl,,. P=""1 "it MW
Vol. Ito. a AIA (11111011 45cm.. diasq. IA Call.) at am rate
0.08
APr- 25t 19% gor" 811-0% -L-oute -m"Wim (by va-
ftm
fill an -
R =wc
Orge"s modstry am
Ydkkxem (11) and pm IRMU atilt. of
y am ie, In a 9&,*- 1 and It
awk knClune + PhAtc. to 111V
It of 7 on I'm
`9~%- ~ww--Gi
Nf.
A/ Z>.
me

lurt

"
IZ
S.2-

MAISI.Wacri
47, *9
b
bmd Awng fro
~eena miagatths-C atom
1.49Y. ttnm
-dAy-dAmal -aria- mmw
7tV6) jl.Sj6jhjO
( '~121 -ab6at I
A
~250-~.& th bw
..A (d RAHIM,
R=rE
16
With 1qyjCYdWmtaDe tbfte.WXB"; 13 0 Pethyl-:gg~e (IM31, 3~b HtPh (IUM), and
do beddke I e. 1.
rtene, - a Irda-1 0", etbyk*cl MYWAfiew, bm 135.2-4 51
an 3mortmed te in the.14 a f4M, d. 0.8150 1071), ve- a catalyzate conig
~iftllmyl as methytertei; win j, 24
and allyl) sludialify stArtift material, 14 I-etrVI-2-cyclollexene qrAI
"re'llooltop to I-Aftdohexenem whei, are in put trans. HtPh flWA and 4 a ethyleycloheolarle. 1-BfAy1-2-ejK1O-
54A a mbsequent reaction. 1 hexew, In* 131.7-2.0 a 1.4,500, d. 0.8101 (1651), gave a
YI-2-cycloalkents passed over the above catalyst at catalyzate catotg. 25*y starthig material. rA% I-cthylcyclo-
filonterized to I-alkylcycloalkenes, which t;h.aiitil7cethyfc)-clohexitne. AU*
rj*'~ n f.45(g), d. ('11,8135 916411.
'41N* 11001 Stable to the above catalyst at. Atkylcycle. cyclahexame, Not' 1,51.2-1
with other Positions of uttsatn. in the ring under gave a catalyXate con(K. 15 dating ill;
AM conditions undttgo togislightextent,oltmpaormstiou kyr-tobexclic (1071).
r1am, 2T Iwoopy eyclidieltatic, I-
~Wc 1"MYthentmot ana alky1cyclollexatte. Tlm hydro- PrPk iW90, atilt
'catbotio-with lonsatit. side chalso wefe frepti. by pyrolysto of
(~Ifryit 1.4373, if. O'em
If
tm WOM, of the corresponding a Co., obWrml by the AfeMytefteryelapedhime, 1.~sl 7341.'J', pi 1.4342, 41.
(1053), gave catalpovite of poirr I-methy1c)-clopcii-
d rbuto For the followiliff Complis, at given % V7 1
tent, boos 73.2-1.5'. so L-1314, eL 0.771,41 OW"17). I-AfdhYr-
P.Pilly, %lateortykdrbioto), 30, bot- 1.4321% d. 0.7765 (1657),
1.4579, '9:112(acef4fe, 10. N&" 1.4378,0.9574); c~,r'lapentexe No, 74 , .
kft*4fbi4OI, :15, 11111-if P3-9% 1.4650, Mr-85 (4cefale. ixylep-lopenlane, Ijjj or 1.4375, d. o.M4
b's.-to 75--G'. 1,41174), 0.9(05; cyclopentyfelkaod, 40, 1 (1641), pvc a cat.-dymte fit pure 1-cilivIc),cloomillelle. I-
'bj is 74s, 1.4578, O.IP2:jf WpWe, 75, bijs 7S", 1AMS, ElAodyclopaxlem., N. 110", n 1.4414, it. O.W11r, I.,
bli, 99-100". INH9, 0.0190 stoic so"Ited by Immage cover the eamly%l. I.RMYNNYIl-
b' 07-8% JAM. 0.05110). 1-17thyl-2-cyclts-
0 And -fiellesic 'vLm llfqA. ill 50-4% y1cid (too Kt-
or 1.1mitio-2-cyclithex-
1.1 a &VI(wentefte Alld -Itexclit were obtained 'L7 p
M?

Y,, Lc V AR
$I rp a A'A
0- 0: bw oo,74-0.4*. oo 1.4119, d. 0,7833 (1017). cave a
awraft w(tir 0 stafthis mataw "d 40% Idhyt.
t"MA1631 Allykydopeigame, bw 124-4.5*, to
d. 0 2 (104O.-Save a catalytate with 33 un-
fftycltng ovel tk*
W7w"4s-rfg tn;,kr%pmt,,e mW 43% troext.
I*ydo#txkw hm 120.3-Me

r
LEVINA.R.Ya.; NUINSOVA,N.N.; LZBEDIOV.03.
Synthesis of hydrocarbons. Part 49. Spiro-(2,4)-hsptRdiene-1,3 qnd
spiro-(2,4)-haptans. Zhur.ob.khtm.25 no.6:1097-1100 Je'55-
(PlAfi 8:12)
1. Moskovskty qooudaretyennyy univerettet
(Haptndione) (ReptRne) (Spiro compounds)

LIVIIA. R.Ta.; K=BNTSOVA. M.N.; TMHCHOTA, Ta.G.
Syathasis of hydrecarboas; oyathasis of hes-dimethylcyclop'sataae
from cyclopentadionfo.Dokl.AN SSSR 104 ao.4:549-551 0 055.
(KLRA 9:2)
I.Hoskevskly gosudaretveapyy univereltet imeni K.T.Lemenosovs.
Predetavleas akmdaalkom A.M.Nesuepmovym.
(cyclopeatame)

/V/M Ole,
-N~ nd N
kh ilk
DiArt Mal j/V~cV d. C.A II
-AYLcyclopeixtants are prep-L by thr ~~n of ell$. CHCH2-
M Br an 1-chloro-l-alky~ topeataues in tbt- presence of
_jjkl2 A~~v,"d of..- F4. 49, 9930.)~ - I-Ethylcyclo..
pentau S. Treated at 0' vrith 8W nit. cnied. -RCI,
the layerl zn~ -chlorr-l~thYkyclopentane (1)
with ~ am the I
washed I dried With ClIC11, and vAcuum distilled,
800 Yk-ld, bit 53', nlt* 1.452a, doc 0.9643. An ether sola.
., 1~
.72 1 WAS slowly addcd to an ellier
9- ti-An. of 0-4 g. Mg,
109 g. UtUr, and 4 g. ligClt, rtfluxed. 10 hts.. the ether
distd., the residue refluxed 8 hrn. with dry toluene at 110*,
d ith 11,0 aj)d IIOAc. tb,- tolume boiled off.
:,nd
d 2 hr3. with Na nictal ind di3tilled y d_
itic 205,: 1.1-diethyleyclopentaiie, bn, 149*. nJO 1.4388,
dn 0,9015, AIRD 41.40 (caled. 41.4%). The 'Ramon spec-
trunt Shows if C3 aE GEM-
(0.8), 60(j(') 769(0.2). S. 001(a),
970(l.5), 00(1.5), 1022(2), 1010(2:55), 1094--3-
(0.8). 1220(0.5). 127,0(3), 1206(2). 1.023(l), 1354(1.5-).
1380(2.5), aud 1410-1,;U2(10) cm,-1 AJ-Di-n-prupyl-
cyctopentanc was prep-acd shitilarly Irmn 146 g. 1-n-
-propylcyclopentuot by way of
pentauc (15.7%, lia 78-80, nV 1.457(y) n.,d jr-l'r.*,jgj, Ir + 3 g.
lfgCl, (it 121% yield, bm uJ2 )A 1~) 0.811-16
AfRj, LO.M (valcil. 30,71,J), F. It. k."(~iluijlill_

/Raman Spectra 0~ SAlauted Art-M r r7rIft bjdr.~
b
F
V
cu
0n%
!~-
I . . I - litsova, and q' y 4: -ld
-
--:Ml Mer! 0, 660-4(IU31J). t)f6-
rements detd. as
AM-tgTi precisu n is clanned for the me.-ts
described by Treshcheva, Vastnik Muskov. Go~ujarst. Univ.
T6g- ri? and RaRv..n.
-
-'
--
--
--
'
-
-
-
4o
d
r
o
ca
ns
r
vmatg.
spectra are Sivert ior the followmg
~y
efive-memberrd ring:
Propylcycla-
e, 1-buty1c/clopentene, mcthylc,-wcy4wwntane, and
clopentane. __Y4,Nf bterr.Irrg
=

TURITW. Tu.X.; MMNTSOVA. N.M.; SADDVATA. N.I.
1. 1
Progress in the chemistry of selenophene. Vast. Vosk.un.Ser.mat.
wkh. astron. f4s. khIm. 12 no.4:201-222 157. (KIRA 11-5)
l.Kafedra orgsnicheakoy khimit Moskovskogo gosudaretvannogo
universitata.
(Selenophene)

474
AUTHORS: Yuryev, Yu. K., and Mezenteova, N. N.
TITLE: The Chemistry of Selenophene. Part 5. Selenophene-2-Aldehyde,
Selanophene-2-Carbinol and Solonophene-2-Acrylic Acid (Khimiya
Selenofena. V. Selenofen-2-aldegid, selenofen-2-karbipol i
selenofen-2-akrilovaya kislota)
PERIODICAL: Zhurnal Obshchey Khimii, 1957, Vol. 27, No. 1, pp. 179-182 (U.S.S.R.)
ABSMACT: Using dimethy1formamide as a base, the authors synthesized a
hitherto unknown selenophene-2-aldehyde which is similar in its
properties to aromatic aldehyde. The formylation of selenophene
with dimethylformamide was smooth, giving a 75% aldehyde yield.
Oxidation of selenophene-2-aldehyde with hydrogen peroxide resulted
in the formation of selenophene-2-carboxylic acid; heating of
selenophene-2-oldehyde with acetic anhydride and anhydrous sclum
acetate gAve selenophene-2-acrylic acid. This a,Ad was also
obtained through condensation of selenophene-2-aldehyde with
malonic acid in the presence of pyridine with consequent decar-
boxylizing of the forming alpha-carboiW-beta-(2-selenophens)-
acrylic acid. Selenophene-2-aldehyde (when reduced with
formaldehyde in conditions of the Tishcherko-Cannizzaro reaction)
Card 1/2

474
The Chemistry of Selenophene
gave selenophene-2-carbinol 4iich, throut mercuration, yielded
5-chloromercuryselenophene-2-carbinol.
There are 9 references, of which 4 are Slavic.
ASSOCIA TION: The Moscow State University (Moskovskiy Gosudarstvennyy
Universitet)
PRESENTED BY:
SUSKITTED: February 17, 1956
AVAILABLE:
Card 2/2

-, I I - -'.. - 1. .- I.",
YURI-'ftVt Tu.ir,; KEMTSOVA, U.N.; 14ALENT'YETA. T.A. TRIISHCHOVA, Te.G.
The chemistry of selenophene. Part 7: Synthesis and M~Vlatlon
of 3-arylselenophenos and 2.3-benzoselenophene. Zhur. ob. khlu.
27 no.8:2260-2267 Ag 157. (XLRA 100)
1. Mosicovskiy Cosudarstvennyy universitet.
(Selenophene)

7- A,/ ", j
TURITSV, Tu.K.; MZZINTSOVA. N.N.; BAIASHOVA. T.A.
Chemistr7 of selenophene. Part 8: 5-(selenenal-2) - aEines,
2-phen7l-4-(selenen&l-2)- oxazolons-5. 5-(selenenal-2 - thiazolidone
-4- thion-2 selenenal-2-rodanine) and h7drazothiazolynon selenophene-
2-aldehyde. shur. ob. khim. 27 no.9.-2536-2541 S 057.
(HIRk 11:3)
1,MoskovskI7 goeudaretvannyy universitet.
(Selephone)

F r
AU MORS: Yurlyev, Yu. K., Mezertscva, N. N., 7 9 -1 1 - 56
Vaslkovsk-4y, V. Y4.
TITLE: Chemistry of Selenophene (Khimiya selenofena).
IX. Condensation of Selenophene-2-Aldehyde With Methylketones.
Synthesis and Reactions of '-'-'eti;~,ise',enaphere-'~-Aidehyde
(IX. Kondensatsiya selenofen-2-al'decida s metilketonami.
Sintez i reaktsii 2-metilselenofen-1-allde-eida).
PERIODICAL: Zhurnal Obshchey Khimii, 19517, Vol- 117, Nr 11,
PP. 3155-~')60 (USSR)
ABSTRACT: In tht: preaer;t paper the authors continue the J_nvesti'~ation
of the ruactivity Uf -,ri examples of
its condensation wi-.h methylketones. Its condensations Witli
methylketones proceell smoothly i,nd lead to tLe formation
of unsaturated ketDres wl~ioh possess the selenop~,ene-cycle.
In this marner the fc,',,,~wing compounds were obtainei:
selen-anal-2-acetone, x-(selenenal-2)-acetophenone,
a-(selenenp-1-2) lz-,-me thy iacet ophenone,
solenionyl-2 j.)jntadi(jnFj-1,4-on-3, 1-(furyl-2)-5-
seleni-nyl-2~ -pent adi one-1 , I-on-3 und j,1)-di-(3o1onionj1-2)_
The aminomethylation uf s,31enennl-2-
Card 1/2 acet ~.e according to 14annich (Mannikh) !--ads tc the hydro-

IQ- ~ I - z 1
Chemistry of Selenophene. IX. Ccndensation of Selenophene-2- /56
Aldehyde With Methylketones. Synthesis and Reactions of
2-Methjlse1enophene-5-kldehjde
chloride of 5-dimethylamino-l-(selenienyl-2)-pentene-
1-ons-3. The reduction of selenophene-2-Lldehyde and
2-iLethylselenophene-5-aldehyde according to Kizhner leads
to 2-methylselenophene and correspondinely to 2,11-dimethyl-
selenophene. The condensation of 2-methylsolenophene-5-
aldehyde -aith hippuric ucid, rhodanine and malonic acid
correspondin,ly yields 2-phenyl-4-(2-methyl3elenerial-'))-
oxazolone-5,5-(2-methylselenenal-5)-thiazolidone-4-thion-2
and P-(2-methylselenophene-5)-acrylic acid. The condensation
of thiosemicarbazone of 2-methylaelenophene-5-aldehyde with
chloroacetic acid leads to the hydrazothiazolinc-ne of
2-methylselenop~iene-5-aldehyde.
There are 4 r,--ferences, 911 DI* which are Slavic.
ASS,CIATION: Ijat3caw BUte Univeraity , - 3'
-oy3kiy i-osudarstverinyy universitet).
1. Selenophene-~'-;-I!(-hytie-C,-,tvlen.,-ition re~,ctiors 2. Met,~Wl-ketones-
Condensation reactions 3. 2-~lc~'~kWlselenophene-5-aldghyde-
Synthouls 2-M,A1,,~I-iol iiiopl:pno-5-aldehydo-Coridensation
Card 212 reactions

AUTHORS: Yurlyev, Yu. K., 14(2:!entsovL~,
TITLE: Cliem-irtry of Selenoprene (11,himiya selenofena) XIV.
Reactions of Seienophere-2-Alde.-Yde I'XIV. se-
lenofen-2-alldejida)
PERIODTCAL; Zhurnal obs..,.~',ioy khimii , 1)-18, Vol 2,11 , 1,11~ I
pp 3o4l - 3(-)45 (U32R)
ABSTRACT; Continuing earlier pa,ers (Re's 1-3) t'.-.e
furtner investi,~ Aed t',.~ reactio:.r of
a1de'hyde which are ch~.r ct(-.ric3tl;c of :,r~-
They introduced this aldehyde into th,e
(Ganch) reaction and in a condensation acet.('
ester %rid o'," ".ed t,-.e diet;. e:-,ter t~.e
2 6-di,- t
dicarboxyli, Sc~.e e I T-.p co.--.de.-. s.it ior. of
selrnophene-2-aldehydeo with 'Larbituric acid, na!:,r,.c,
acid and malononitrile yielded the selenenal-2-barbi-
turic, selenenal-2-malonic acids, and se!ene:-,a:-2-
malononitrile (Scheme 2j. Ir. t-c. cioav%,~e of t'-J~
CF,rd 1/2 5-(selenenal-2'~thi,,.zolidone-4-thiorif-,-2 jl~,f 211 viitl,

Chemistry of Selerophene. XIV. ReaAi:)n~: of Selen-,
phpne-2-,,~Idehyde
ASSOCI~il:il.
PUBMITTED:
alkali liquor the 2-thione-3-(oeleni(-,!~yl-2l)-i)ropi,)ric
acid was obtained in __-,or)d yi(,Id, which on thc, -.,~tion
of hydroxylamine 'aas trancl'ormed into t~e 2-oximino-,"-
(sell enienyl-21 )-proi;icnic ac;d 'Sc~,,eme 3,. T,,.e oxi-.,.e
of selenophei~e-2-alde'vle served as b,,--~'c Produrt "-jr
the Belenenyl-2-amine, obtai.,,ed by t-,(,, r~.,J-~ction of
nitrile. The conder.8ation of t:l~;;
aelenophene-2-aldehy(le lead to t.
selenenyl-2-amine, with salicylic a,deh,,,!e to the
-0,- 1ic.,-1-11-(se1enenI-,1-2' ~~-)uld f-rm
Lnd
ow S e
ni vc r:~
September 50, 11):7
Card 21/2

AUTHORS,, Y -r Y--.. K. , We z tj atj c, 1, r. , N. N. 30V/7 ~-28-1 2-22114
r 7 Y,3
TITLEt T*.-~,d Ctem;.utry of S,1einophere 1"Kh)miya splenofena) XV. 2-Vlay~
Se I,- vc phe rie (TI. ~.--Viriiselenofen,
PERICDICALi "'JJU.-ra' CtLfjjL't`tq-/ "9~6 Voi 28, Nr 12, pp 5262-52c)"
CSSR
A.BSTRACT? ~ne:,- pap~41'3 In the field of selenophene
--n9ml9try with r6spe--t to ~.,he selenophene-a -aldehydes (Refs 1-5)
tne aul~Grs qyrt~,ev-zei *re 2--vinyl selenophene; the
oata~ytirt deh~ldrasior, cf methyl-(selanieny)'-2)-carbinol turned
out t., br, a better ~ynthe3is method than the decarboxylation
of 2 ar:i:i, aa it led tc the synthesis
nf 2- 1-. -;,-,nsideratly higher y,ieldal
J t, e
K 9hy I o,~ IOU --eny i-.2 nol, as well as the ethyl- and
phen;(?-- were obtained by the reaction
Card 1/3 of se;en.)phei:,~--2 -~-.ue-~:yds4 vi-Lth alkyl and ary! magnesium halides.

The -r.,-m:dtry Df AV : Vinyl 6elenopri-ne ~CV,, -79-2e-12_22/41
in the investigation ol tne effect of varioLe dehydration
agents on it was found that in
the plesence of a::--d rompounds (of potassium bisulfite, p-
toliaene-su'-fortic acid et- ) as well as in the presence of
,~austj,~ ;C-'tas~. the 2-71nyi se-snopnene formed is almost com-
pletejy polymerized. In the thermal dehydration tnq yield of
their, amounts to 50%, whereae in the dehydration in the vapor
phase with aluminum oxide at 200 0 this figure is 80%. In the
aoove-mentlczed -"ic-irr:..,x,,,iation reaction tne yield amounts
407. zrly, 2 selariophene reacts with diazo methane
and f~~.rm- )-pyrazoline, and with dimet~yl
formamide '" z, prp-gence of phoSDn3rus oxycti cride the
'S_-hame 2). In -he oxidation of
trie iatter witn silver oxiLje tne 9 _kseienleny.-2)-aorylic
a.-id WR9 w;tL nydrotTen peroxi.de. however, selenophene-
2 -~artoxyli, a,-id (5,,Leme 5) There are 1 table and 5 Soviet
refPr(-r. .es,
AS.30CIATIM MOOIK -1K Y g0'3 Aaro " ver: Vy Uri-, ~.'ers ! tL1 t('Njoscow State University)
Card

o o
"TT r
n .ro,:
Tj
to
- ---------------------

mc ::Z-,r".c to ri tick of
ci,.:;(. Acetone
v I Cr -,.I a v: -
0
accor.-'i ii, ;~i I i::. r. u,- 1 c ic
fro--
0- 1~0'~;l co::-(,11.,~:,.~ t C,
;e,. c :-~n,
a.
CO
C u 0 n.,- 1
S.2
se ii na rioy

0" SOVI 7~- 1 'A - 1
t
!,)n~ n..- tone an~t I Acetone
T,
.'arci '/5
c o a.,; t,-. n t L ob oo in different system.,; at 2~
C. 1
c ~e!::
Lr
Ct r u4!o.o1(,
5. 4 59to. 009 (.,Y,3 Le~ul IC I
r
5.14510. 010 (SYstem
0 i :Lr 6- 6
of both compounds are independent of
Lhc.ir concert-.-,--tiori in u--t~anic phase (benzene, chlorofo:-m
rc;
t -r- /. o-' tile fact that neither o!* t.- two
compcund~; is in tl.e aqueous nor in zhe oq;anicphase.
-here are fiL-urc-:. 1 c -
and Iij refcr,-~nccs, of' which
are Soviet.
.-ockovskiy gosudar::Ivenny~, universitet im. M. V. Lomonosova
Coscow itate Univc-roi,,y imeni :'. V. ilomonosov)
A-,ril 24, 151-58

50)
ALITHORS Yur 'yev, Yu. K. , blezentoova , N. "I Ka.~; hi t -:.,a ,A
TITLE: Chemistry of Selenophene. XIX. 2-Aceto-selenopncne i:. t,~,e
Synthesis of ct- and 1'~-Keto-aldehydes in the Selenui,%ere
Series
PFRIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr L',
pp 2597 - 26ol (USSR)
A.~ST~LACT In addition to their previous papers (Refs the authors
used, in the present paper, the a-acyl-selencphe.-.es for the
sjnthesis of the (x- and t3 -dicarbonyl compounds in the sele-
nophene series. In this way, they obtained by oxidation of
2-aceto-selenophene with selenium dioxide the selenienyl-2-
glyoxal, a keto-aldehyde, the bright-yellow color of which
is due to a conjugation of the double bonds of two carbonyl
groups and of the selenophene nucleus. The ultra-;iolet ab-
sorption spectrum of the selenienyl-2-glyoxal (iig '' has
two maxima at )~ 275 and 310 mp.,.The compound is easilly cor.-
densed with o-phenylene diamilne, and forms quantitatively
Caru 112 the 2-(selenienyl-2l)-quinoxaline (Scheme 1) By the action

Cne.-istry of Selenophene. XIX. 2-Aceto-selenophene in SGV/79-29-8-3-/8'-
the Synthesis -f a- and P -Keto-aldehydes in the Selenophene Series
of alkali lyes on its monos emica rba zone and monothiosemi-
carbazone, water is split off and, accordingly, the 5-oxy-
and the 2-mercapto-5-(selenienvl-2l)-triazine-1,2,4
(Scheme 2). On condensation of 2-aceto-selencphene wzti; the
ethyl eater of for%Ac acid under the influer.ce of scdia~,
the sodium alcoholate of oxymethylene-(selen4~enyl-2i-ketcre
is obtained which is of dark-violet color in tne tniGpl7iene
series. Its aboorption spectrum is characterized in figire
by curve I, the one of its intramolecular complex coz--_und
with Cu4"+ by curve II. There are 2 figures ana L Soviet re-
ferences.
ASSk2OVIATIM Moskovskiy gosudarstvennyy universitet (Moscow State U n i
versity)
SjB:.:IT-,LL: July 2, 1958
Card 212

B/079/60/030/05/47/074
B005/BO16
AUTHORS: Yurlyev, Yu. K., Itezentsova, N. N.F Vaelkovskiy, V. Ye.
TITLE: Oelenophenelchemi-,s-,t-,r''y."~X,-X"V,I. '2-C'y'yclopropyl Selenophene and
2-Propenyl Selenophene
PERIODICAL: Zhurnal obahchey khimii, 1960, Vol. 30, No. 5, Pp. 1628-1631
TEXT; In the present paper the syntheses of 2-cyclopropyl selenophene M
and 2-prope nyl selenophene (II) are described. The authors synthesized
(1) on the basis of p-(selenienyl-2-)-acroloin (III). Contrary to a
method used previously (Ref. 1), this compound was obtained. by condensa-
tion of selenophone-2-aldehyde with aestaldshyde in the presence of lys.
By treating the unsaturated kecone (III) with hydrazine hydrate,
5-(selenienyl-2l)-pyrazoline (IV) was obtained. This product was not
isolated but decomposed at once according to the well-known method by
N. N. Kishner (with platinized carbon and potassium hydroxide). By this
degradation, compound (1) results with impurities of a selenienyl-2-
alkene. Compound M was also synthesized from the hydrochloride of
2-(P-dimethyl-amino-propio)-selenophene (Ref. 2) by the action of hy4razine
Card 113

Selenophene Chemistry. XXVI. 2-Cyclopropyl S/079/60/030/05/47/074
Selenophene and 2-Propenyl Selenophene B005/BO16
hydrate and Kishner degradation of the resultant (9e1enienyl-2)-pyrazc.ir.k'.
This method is simpler and more convenient than the one described above.
The purification of product (I) from the selonienyl-2-alkene impurity was
carried out by treatment with potassium permanganate solution and sub-
sequent working up with 2,4-dinitro-benzene-oulfenyl chloride. Contrary
to the unstable monosubstituted pyrazoline (IV) the disubstituted
pyrazoline derivative 3-mothyl-5-(Belani*DY1-21~-pyrazoline (V) obtained
by condensation of selonal-2-acetone with hydrazine hydrate is a stable
compound which is distillable in vacuo without decomposition. In the same
way, I-phenyl-5-(aelanienyl-2l)-pyrasoline was prepared by condensation
of selenal-2-acetone with phenyl h1drazine This product melts without
decomposition. On degradation of compound iv) according to Kishner,
2-(20-methyl-cyclopropyl)-selenophene (VI) results. This product is con-
taminated by small quantities of selenienyl-2-butene which may be
separated in the above-mentioned way. The ultraviolet absorption spectra
of methanolic solutions of compounds M and (VI) show no differences In
the electron transitions. The spectra were taken on an SP-4 spectro-
photometer. Compound (N) was obtained from ethyl-(selenieayl-2)-carbinol
by dehydration with potassium bisulfate~ The initial product was produced
Card 2/3

Selenophene Chemistry. XXTI. 2-Cyclopropyl S/079J60/030/05/47/074
Selenophene and 2-Propenyl Selenophene B005/BO16
by an organomagnesium synthesis from selenophene-2-aldehyde and ethyl
bromide. In an oxperimental part, all operations performed are described
in detail. For each of the resultant products, yield, boiling (or melting)
point, refractive index, density, molar refractivity, and data of the
ultimate analysis are given. The schemes of the reactions performed are
presented as well. R. T&. Levina and co-workers.(Ref. 5) are mentioned
in this paper. There are 6 Soviet references.
ASSOCIATION: Hoskovskiy gosudarstvennyy universitet,(Moscow State University)
SUBMITTED: June 12, 1959
Card 3/3

YURIYEV, Tu.l.; ME7=TSOVA, U.N.; 14011AEROVA. A.T.
Chemistry of selenaphene. Part 29: 5-*omo- and
nelenophenal. Zhur.ob.khim. 30 no.8%2726-2731
5-ch-loro-2-
Ag 160.
(MIRA 13:8)
1. Moskovskiy gosudaretvenrq3r universitet.
(Selanophene)

YURIIEV, Yu.K,.;_!qMNTSOVA, N.N.
Clhmd try of selenopbene. Part 32: 4-diketones of the solonophons
seiiss. Zhw.ob.khimo 31 no.5-.1449-1452 14Y 161. (MMA 14:5)
1. MoslWakly gosudarstvennyy upiversitat imeni M.V.LOnonoaovap
(selenophans)

YURIYKV, Yu.K.1 MZENTSOVA, N.N.; TRESHCHOVA, Ye.G.
Raman Bpectra of 2-propyl-,, 2-cyclopropyl-, and 2-propenylseleno-
phone. Vest.Hosk. un. Ser.2;khim. 17 no.1:60-62 Ja-F '62.
(MIRA 15:1)
1. Moskovskiy gosiularntvennyy universitet, kafedra organicheakoy
khimii i laboratoriya molekalyarnoy opektraskopii.
(Selonophene--Spectrai

MELICHAKOVA, N.V ; MEZENTSOVA, N.N.1 PEN AN [Pl9ng Ang); PESHKOVA. V.M.;
YUR I YF.V:-TT.T.---
Characteristics of some j6-diketones of the pelenophene series.
Vest.Mosk. un. Ser.2tkhiA. i'1 no.1:63-67 Ja-F 162. (MIRA 15:1)
1. Hookovskiy gosudarstvennYy univeraitet, kafedra analiticheskoy
khimii.
(Selanophone)

YUR'YZVP Yu.K4 -MUMSUVA, N-.N.-; SAPOROVSKAYA, M.00
Chemistry of selanophenes Part 37: Synthesis of 5-(21-seleaienyl)
pyrazoles substitutes in the position-3. Zhur.ob.khim. 32 no.5:
14"-1"6 Vq f 62. (MIRA 1535)
1. Moskovskiy gosudarstvannyy universitet.
(Selenium compounds) (Pyrazole)

YMIYEV, Yu.K.; 14EZF21TSOVA, N.N.; KEDA, B.I.
Chemistry of selenophene. Part 38; Synthesis and reactions of
vinylselenophene. Zhur.ob.khim. 32 no.6:1820-1822 Je 162.
(MIRA
1. Moskovekiy g.-.Ahr8tvennyy uriversitet im. M.V.Lomonosova.
(Selenophene)
2-
15:6)

MEZER, Jerzy do, mgr. inz.
"Electronic amplifiers
installations" by Bodo
Pmiary 8 no.7047
for Industrial, regulating, and control
Wagner. Reviewed by Jerzy do Mozer.
J1 162.

I ) I - I , '.L, . r . ., . ,: 'N
i; ' : IT, ' 1. 1 '. , 'I%.- - .11 . 7 1.7 1 .. : . I .- . r . _
'i . It- , , 9 -
- I .

MEZERA, A.
Typology in forestry, future basis for culti,.ation of forests.
p. 249. SBORNIK, RADA LESNICTVI. Praha. Vol. 28, no. 2. Apr. 1955.
SOURCE: East European Accessions List (EEAL) IAbrary of Congress
Vol. 5, No. 7, July 1956.

MEZERA, Alois, prof., inz., dr., ScDr.
Gradual shelterwood cutting as forestry system in high forists.
Los cas 9 no.4/5:279-298 163.
1. Lesnicka fakulta, Vysoka skola zemedelska, Praha.

HOLLAS, Adolf, inz.; LadiSIRV, '.nz.
Let us Improve the -~rganlzat.ijr -.:' pro-iliction. Sklar a 'keramik
14 no. 7gl"43-105 JI '64.
1. Deputy Minister f -'~,nsumrner Goods Industry (or Hellas".
2. Ministry of ',cclal Icir Mpzera).

GOL I I)SHTUM, L. M. ; FROKOF I YEVA)Ye.I.i KEVESEP L.Ye., MERNITSKIT, Ye.p.
h1neiples of roentgenocinematography and the possibility for its
use in the examniation of the esophagus and stomach. Vop onk. 7
no,12.,R-37 161,, ~MIRA 1591)
Iz rentgenologicheskogo otdeletiya (zav. - prof. L.M. Golld-
!
h-te7n) Instituta onkologii AMN SSSR (dir. - deystviteltnyy chlen
AMN W3R prof. A.1. Serebrov).
(SINEBUOROGRAPHY) (STUMACII--RADIOORAPHY)
(ZSOMGUS-RADIOGRAPHY)

WIZES, Lajoa
Pnei=atic device. Vasut 8 no.2:3 of cover 15 Mr 158.
1. Ulitasi eloado.

MWES, Lajoe
Odom --
An outstanding innovator in the Debreceni Vehicle Repair
Shop, Vanut 8 no,3%3 of cover 30 Ap 150.