SCIENTIFIC ABSTRACT PERVAKOV, V.A. - PERVEYEV, F.YA.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001240130004-6
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 15, 2000
• Sequence Number: 4
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

S/126/50/010/001/025/027/XX
i8 0100 1 otj,~ /j., E 03 2/E 111
AUTHORS: Khotkevich, V.1. and
shepelev, A.G.
TITLE: Latent Heat of Plastic Deformation of Silver at
-196 and +20 0C
PERIODICAL: Fizika metallov i mctallovedeniye, 196o, vol. lo,
No. 1, pp. 117 - 121
TEXT: The present authors have measured the latent heat of
deformation Q, on the degree of deformation -'~~d/d and the
vrork A done in comgressing silver specimens at temperatures
between -196 and 20 C. The pulso method described by the
second of the present authors et al in Ref. I was employed.
99.995c pure silver wires, having it diameter of 0.1 mm and
length of 6o nun were used. The d-!formation was produced by
compression between polished steel plates. Fig. I shows the
dependende of Q (cal/g) on ""'d/d at -196 0C (Curve 1)
and +20 0C (Curve 2). Fig. 2 shovs th.e latent heat Q as
a function of A (cal/g) at the same temperatures as in
Fig. I. Fig. 3 shows Q/A as it Curiction of A and Fig. 4
Card 1/4

872-1 d,
S/120/1:)0/010/001/025/027/XX
P032/'E*;i4
Latent Heat of Plastic Deformation of Silver at -196 and 42L,
shows the latent heat Q as a function of the relative change
in the resistance of the specimens,
Acknowledgments are expressed to N,L. Zheldakov for assistance
in building the apparatus and in the measurements.
,rhere are 4 figures and 7 referenco!s: 5 Soviet and
:2 non-Soviet.
-iz.l Fig.2
17
Card 2/4

s/i2c/60/010/001/025/027/XX
EO~'/r3llf
Latent Heat of Plastic Deformation of Silver at -196 and -2G
F ig2 Fig. 4
Q0
-
T 0
0
C,
Q0
30
?0
0
/0
?
II -
0
05
0,2 0 t=.10.
2
0 f-~196
Card 3/4

A-,, ~71 ~,
S/126/60/010/001/025/027/XX
E032,/L314
L,atent Heat of Plastic Deformation of Silver at -196 and +2'(`
ASSOCIATIONS: Fiziko-tekhnichcEkiy institut AN UkrSSR
(Physicotechnical Institute of the AS
Ukrainian SSR)
Kharlkovskiy gosudarstvennyy universitet
imeni A.M. Gor1kogo (Kharlkov State
University imeni A.M. Gor'kiy)
SUBMITTED: February 15, 1960
Card 4/4

PXRVAKOV, V.A.; KHOT M ICH, V.I.
Colorimetric determination of thei energy of formation of vaca,~cies
in gold. Dokl. AN SSSR 134 no.6:1328-1330 0 160. (MIRA 13:10)
1. Fiziko-tekhnicheskiy institut Akademil nauk USSR i Kharikovskiy
gosurlaretvannyy universitet im. A.N.Gorlkogo. Fredstavleno akademikom
A.F.Ioffo-
(Gold)

-PERVAKOV,-I.A. [Pervakov, V-0); KHOTYEVIC], V.I. [Yhotke7yeb, V.H.l
Thermal capticity of plaeticlly deformed copper. Txr. fiz.
zhur. 6 rio.P:240-2" 14r-Ap 161. (MIRA 1j,: 6)
1. Fiziko-tekhnicheBkiy institut jUl USSR i Kharlkovskiy gosudar-
stvennyy wniversitet im. A.M. Gorlkogo.
I (Copper-Thermal properties)
(Deformations (Mechanics))

- FT:HVAKOV I V.A. [Pervakov, V.0.1; monEvicii, vi. (Khotkevych, V.H.]
Applica"',ion of the pulse calorimetric method for dot-er-izing
the solva-~ion energy of oxygen in Ejilver. Ukr. fiz. zhur.
6 no.3,408-411 My-Je 161. WIRA 14:8)
1. Fiziko--tekhnicheskiy institut 0 USSR, g. Kharlkov,
Khartkovskiy gosudarstvannyy unJ.vf:rsitet im. Gorlkcgo.
(Solvation)
(oxygen)
(Silver)

KHOTKEVICH, V.I.; PERVAKOV, V,A.; GENKIN, Ya.Ye.
Low-temperature press, Prib.1 teai.ek.Bp. 6 no.5:20-202 ~-O
161. (MIRA 14.10)
1. Fiziko,.tekhnicheskiy institut, All USSR i Khartkovskiy
goeudarstvow*,y universitet.
(Low-temperature resear(h---Equipment and supplies)

PERVAEOV, V.A.; MERISOV, B.A.; HOTKEVICT.', V.I.
r- -
Effect of the characteristics of crystal lattice distortions on
the temperature dependencp of the electric resistance of silver and
gold. Fiz. met. i metalloved. 12 no.1:38-41 Jl '61. (MIRA 14:8)
1. Khar'kovskiy gosudarstvenRyy universitet inani A.M.Gor'kogo
fiziko-tekbnicheskiy institut A9 USSR.
(Precious metals-Metallography)
(Metals, Effect of temperature on)

S/126/61/012/003/020/021
E073/E335
AUTHORS: Perva-kov, V.A., Petrenko, N.S. and Khotkevich, V.I.
TITLE: Influence of the plastic deformation on eliminating
excess vacancies in quenched gold
PERIODICAL: Fiziha metallov i metal.'Lovedeniye, v. 12,
no* 3, ig6i, 46o - 461
TEXT: According to M.A. Bol'shanina (Ref. I - Ivz. AN SSSR,
ser, fiz., 1.9509 14, 223) plastic deformation of metal does not
only cause formation of crystal-lattice distortions but also leads
to their elimination. According to published work a sufficiently
high deformation at room temperature in Al and Au leads to a
decrease in the concentration of the excess vacancies. Data are
given in this paper on the influence of deformation,at the rate
of 1.00,c/min and 1.05%./min (impact) at. 20 and -196 oC,on the
increase in the resistance caused by preliminary quenching. The
investigations were made on 60 mm long, 0.05 mm dial wire, made
of pure gold (99.99%), which was determined by compressing the
wire with two polished steel plates. The quenching waB by raj)id
submersion of the specimens in water. Fig. I shows the dependence
Card lk!~'

s/ 1:!6/6 i/ol 2/oc-dc.,Wozi
Influence of' tho . . . . E07 / 83 "15
process itself, it can be anticipated t'iat for annealed Au
speciziens which are slowly deformed at room teuperature the
contribution of tLie vacancies to tlie increase in the electric
rosistallco at low dogroes of deformation will be greater than
at hif-h degrees of defomiation. Spocimeno deformod tit lour
tez:iperaturesor specimens deformed by impact at room tem-)0rature
should contain t-,iore vacancies than specimens deformed at a low
rate at room tem,~,crature. These conclusions on t,ie vacancies
are also applicable to other point defects whict-i have a lover
temperature stability than vacancies.
There are 3 figures and 5 references: 2 Soviot-bloc and
3 non-Sovi et -bloc:. The three Englisli-lanZ;uage references
mentioned are: Ref. 2 - M. Wintenbej-~Ter, Symposium by the
1957, Lon(lon, 1952, 201;
Institute of Metals, Dec.,
Ref. 5 - M. Wint anbarger - Acta met - , 1959, 7, 549 and
Ref- 5 - R. MaddLn, A. Cottrell - Pliil. I-lag., 1955, 46, 735.
ASSOCIATION: 11,,~iarlizovs'ziy gosuniversitet im. A.M. Gorlhogo
(KharlIzov State University im. A.M. Gor'l-,iy)
SUDMITTED: April 27, 1961
Card 3/x~

L 11~118~46 EWT(M)/EWp(.w)/T/EWP(t)/EWP(k)/VdF(z)/EWP(b)/EWA(h) 1JP(c) JD/HW/JG
ACC NR: APS028563 ("/V) SOURCT CODEs UR/0126/65/020/005~(0733/0740;>:'I
AU7WDR: Guterman, M. B., Mirkin. 1. L.; F~qvl
yigc, A. A.; Pervakov, V. A.; Petrenko-,
N. S.; Kho~ikevich, V. T.
ORG: TsNII of Technol2a and Machine BuildinK, Moscow (TsNII tekhnologii i mashino-
stroyeii-yaT; Kt~L*~ov osuniversitet im. A. -M. Glor1kiy Kharlkovskiy gosuniversitet)
TITLE: Certain featwes connected with the K-state in Ni-Cr, Ni-Cr-Mo and Fe-Ni-
-Cr-Mo alloys
SOURCE: Fizika metallov i metallovedeniye, v. 20, no. 5, 1965, 733-740
ysics, ordered alloy, friechanical property, resistivity, non-
TOPIC TAGS: metal ph-
ferrous metal alloy, ferr us alloy, metal heal: ,treatment It heat resistant alloy,
high temperature strength, metal hardening
ABSTRACT: Changes in electrical resistivity b-1 Ni + 5% Cr, Ni + 15% Cr + 18% Ho
(VAand F, '+ 25% N1 + ~61' Cr + K M; alloys were ~s~uidlied s i_T~Vlction of low tempera
ture .2formation , m +200 to -1960C) and _ani,iealing14ate (from 2 to 106 deg/min)
Decilosition of're K-state in the alloys -Za-s- obse ved. The effect of the K-state
an high temperature citrength was also noted. The K-state causes microscopic inho-
UDC: 539.4.015
Card 1/2

L 14998-66
ACC NR: APS028563
mogeneities Which retarl the motion of dislocations. In this work, the influence
.of the decomposition of the K-state was studied in terms of high temperature
strength. The temperature dependence of electri.cal resistivity waa obtained as a
function of temperature and heating rate. For nach alloy, the resistivity in-
creased initially and at 50OPC reached a peak, iAiereupon it dropped to a minimum
(about 7000 to 9000C depending on the alloy) and rose again. The drop in resisti-
vity was associated with the decomposition of the K-state. Deformation by compres-
sion (60 to 70%) in the temperature interval fn:in -196 to +20012 showed that the de-
couposition of the K-state was practically independent of deformation temperature.
At higher temperatures (between 5000 and 100000 and at high rates of heating the
decomposition of the K-state was studied by increasing the heating rate to 101
deg/min. The Interval for the maximum decomposition was displaced to higher tem-
peratures (300 to 4500 higher), depending an the type nf alloy. In the K-state re-
gion a significant str*ngthening was also noted when the speed of deformation was
increased from 0.03%/min to 0.3%/min, while in the region of K-state decomposition
no effect on strength was apparent. For fast beating rates, the rise in strength
was mair~tained at higher temperatures than for slow heating rates. In particular,
for Ni-Cr this region itas expanded to 7000C, while for the other alloys to 900 or
IODOOC. Where the K-state was decomposed at rccn temperature, no additional streng-
thening occurmd upon pulse heating. Orig. art. has: 4 figures.
SEIB ODDE: IV SUBM DATE: 06Au&64/ OFXG REr: oil/ OTH REF: 003
card 2/2

A5
-9
TON
D I 72~
ii~ p"f.concen
age,
md1s'6
in

PAVLYUK, A.A. (Pavliuk, A.0 )- FERVAK011, V.A. (Pervakuy, V.().); KHOTKE:VIr,.H,
V.I. [Khotkevych, V.A.T
Effect of an oxygen admixture on the heat capacity of silver. Ar.
fiz. zhur. 10 no.2-.237-238 F 165. (MIRA 18W
1. Kharlkovskiy gosudarstvenny~ universitet.

POPOVA. N.M.. kund-tsikhn.nauk; PERVAKOVA, T.P., gidrobiolog
Improving sanitary conditions of the Mool-va River. Gor.khoz.Mnak. -0
no.2:?9-12 F 159. (MIRA 12:3)
Oloacow-Sewage) (Moskva River-water-Pollution)

15-57-12-16786
Translation from: Referatimy zhu-mal, Geologiya, 1957, Nr 12,
p 12 (USSR
AUTHOR: Pervakova, V. I.
TITLE: The Stratigraphy and Lithology of the Jurassic Rocks
of the Llvov Vpadina (Basin) (K stratigrafii i
litologii yurskikh otlozheniy Llvovskoy vpadiny)
PERIODICAL: Nauchn. zap. L'vovsk. politekhn. in-ta, 1956, Nr 46,
pp 72-81
ABSTRACT: Within the Llvov-Volynia coal basseyn (basin), Jurassic
deposits rest unconformably on rocks of the Carbon-
iferous and the Devonian. At the base of these
Jurassic sediments occur variegated rocks with a
thickness up to 137 m; red, brown, green siltstones,
mudstones, sandstones; and layers of conglomerates and
boulders. The variegated unit is a lagoonal-conti-
Card 1/2 nental deposit and is Middle Jurassic in age. Above

15-57-12-16786
The Stratigraphy and Lithology of the Jurassic Rocks (Cont.)
it occur lithographic and dolomitized
lenses of gypsum'and anhydrite and
limestones of the Upper Jurassic.
and molluscs may be found in these
ranges from 60 m to 300 m.
Card 2/2
limestones and dolomites with
with oolitic and pseudo-oolitic
Rarely, ostracods, foraminifers,
calcareous rocks. The thickness
V. A. Krasheninnikov

PARVAWV, IV.G.
Flotation method for separating imste water from oil and oil
products. TrWy MI no.16:172-l!)4 '58. (MIRA 11:12)
(Sev&8*--PtWificAt1Dn) (Y'Letation)

ROZIN, B.B., inzh.; PUCHKOV, L.M., inzh.; FERVAKOV, V.P., insh.1
Using methois of linear prograumung in planning the charging of steel
smelting furnaces. Stall 23 no.9t845-847 S 163. (KRA 16:10)
1. Zlatoustovskiy metallurgicheskiy zavod.

JEVTIC, Zivojin, doe., dr.; TRNINIC, Borivoje, dr.; BESAROVIC, Kiso, Mr.ph.;
PERVAN, Vatroslav, dr.
%r experience with the treatment of hypertension with ismelin.
Med. glasn. 14 no.12:566-568 D 160~
1. Dijagnosticki centar u Sarajevu (Upravnik: dr M. Gajic-Jankovic).
(AMIDINES ther) A-NTIHYPERTF24SIVE AGENTS ther)

pEp,Vk,-TJ E, F.
chmiciaAbst. A rapid and -..$,-A Me determina-
tion of 1~ W me a
_Um~ ~e i C mmium. titanium
~e'n r 0 0 n-
Vol. 48 No. 3 i~n jk2p, r-11F. -7-0
n . ".
Feb. 10a 1954 _M!=.__The sam JeWi4i'lo'y with HSSO" is
reduced witbpo-A-FM. V-'lsreduccdtoV1'4nmJCr4*
AnalAtcal Chemistxy toct"'. The.1 KMu% is added lit slitht excess until the soln.
retaim a sl4ibt pink coloration. After I tuht. enough
0-02N Fe.A Is added to just destroy the pink color. DI.
phenylamine ioln. (1-3 drops) is added as Indicalor, and the
soln. Is t1trated with 0.02N ferrosullate until the Indicator
color changes from vlolet, to green. The juethod is fairly

ACC NRi AP6035884 SOURCE CODE: UR/0413/66/000/020/0124/0124
INVENTOR: Badayeva, A. A.; Pervaya, A. S.; Tutov, 1. Ye.; Katsnel'son, V. Yu.;
Kuzmintsev,' V. N. ; Koloskov_,__M_7ff._, T-ul-f-n1ch, V. P.
ORG: none
,TITLE: High speed steel. Class 40, No. 187314 [announced by the Central
!Scientific Research Institute of Technology and Machine Building (Tsentral'nyy
'nauchno-iasledovatel'skiy institut tekhnologii i mashinostroyeniya);
'All-Union Scientific Research Tool Institute (Vsesoyuznyy nauchno-isaledovatel'skiy
instumental!nyy institut))
SOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki, no. 20, 1966, 124
TOPIC TAGS: high speed steel, chromium tungsten molybdenum steel, vanadium containing
,steel, titanium containing steel, DOC-Mr-l-rcl , 77.00G,14iU65-3
ABSTRACT: This Author Certificate introduces a high-speed steel containing silicon,
panganese. chromium, tungsten, molybdenum, vanacium and titanium. To improve the
strength, ductility, notch toughness, and oxidation and heat resistance and to
reduce carbide heterogeneity, the steel composition is set as follows: 0.75-0.85%
'carbon, 0.17-0.35% silicon, 0.20-0.40% manganese, 3.5-4.5% chromium, 2.5-3.0%
tungsten, 2.5-3.0% molybdenum, 1.9-2.2% vanadium, 0.03-0.08% titanium.
SUB CODE: 1l/ SUBM DATE: 05Jun65/
J Card - 1/1 UDC; 669.14.018-252.3

L 2886-66 FSS-2 WAS(VL-ACC
,~EWA(dy ~(hL IGSIG~t
AT5023607 UR/ODDO/65/000/ODD/0381/03871
IACCESSION NR:
AUTHOR: Vernov, S. N.; Mtl~nlkov, V. V.; Saveqlko 1. A.; Sayin. B. I a
T. 1.
TITLE: Recording of charged particles of energies of 0.1-10 kev with a spherics
electros tatic analyzer
SOURCE: Vsesoyuznpya konf erenqiya pioL f izike kt)amicheakog!~__plo~~"!!stva..- Hoscow,
-1965. Issledovaniya kosmicheskogo prostranstva (Space research); trudy konferentaij.
J~
SEW, Izd-vo Nauka, 1965, 381-387
TOPIC TAGS: satellite, satellite data storage, particle counter, electron density,
ion'density/Elektron 2 satellite
ABSTRACT: Identical s herical electrostatic analyzer 'ew/ere used to record positive
and neantive varticles mos-151nd
Mth nergies of up to I kev on Cosmos-12 and Cos
UP to 10 kev on Elektron-2~ Each analyzer was comprised of a spherical capacitor
some 60 M in diiiaiiii-,--iil-th input apertures leading to plates spaced 12 mm apart,
on which a periodic high voltage was progimmed so as to allow passage through the
annular Sap.of only.partleles of a desired energy range. A Faraday cylinder at-thel.,
L;TLIJ3

L 2886-66
ACCESSION NR: AT5023607
gap output served as the collector. The input apertures and the faraday cylinder
were furnished with biased grids to eliminate thermal particles and secondary emis-i
sion, respectively. A diagram of the two analyzers used 'on Elektron-2 is shown in
Fig.-1 of the Enclosure; accumulated charge was converted to binary code. The Cos_j
nos data generally showed that electron flux at the 1-kev level did not exceed
107./CIZ2/sec/kev at night and was only slightly higher by day. A maximum was noted
during the vouthernmost portions of orbit, in a region south of New Zealand, attaining
up to 12 x 108/cm2/see/kev. Electron fluxes recorded on Elektron-2 showed strong
variations at sunrise and sunset (referred to the satellite'); these variations
!reached values on the order of 109/CM2/sec/kev. Irregular v"arlationd in flux readin a
9
correlated with known geomagnetic .'e~rents obsez-~ed during the- flight.; Data show that
the satellite was at all times within ihe magnetosphere. !Positive ion flux regis-
tered by Elektron-2 in the 0.1-10-kev range did tiot exceed,, 5X.107/cm2/sec'. Orig
art. has: 5 figure'
br~and I tabl6. ISH
ASSOCIATION: none
SUB CO
ISUBMITTEW 02Sep65: NO
ENCL:. 03. DE! ESt
NO REF SOV: 008 OTHER: OD3 ATD PRE S S
Card
j
_1 M -0-6.

L 2886.-66
ACCESSION NR: *T5023607 kki,69 i-Vi
S c
Collve
urre-A Scalerr
witch' 41
owet
Tr 119V auppl
Al uce comma
S. Com
COM- Pwitcb-
mand
unit mand
000'
Lid r
Com-
rc
switc%,
Fig. le Spherical parricte analyzer an EWA 2
Tr High voltage transformurs Cow'-, conmutators;-
Al:-,O.I-l kev range; A2 1-40 keV rang0,1
Cmd 3130,~_

VERNOV, S.N.; SAITNKO, I.A.; 3HAVRIN, P.I.; NESTEROV, V.Ya.;
PISARFNKO, N.F.; TELITSOV, M.V.; FERVAYA, T.I.; YEROFFYEVA, V.N.
Some results of radiometric ob!~ervations at altitudes of
200 to 400 km. during 1960-1963. Kasm. issl. 2 no.lt136~146
Ja-F 164. (MIRA 1'7:4)

PERVPMEY.. A. . p I sa t e 11 . ; HD I VANI, G. . p I sa t a 11 , -, KLEBANOV, S. -.
BLISHTREM. A.; ROSTOTSKIY.S.. rezhisser; SEGAL. Ya., rezhisser;
BYSTRITSKATA,L.. aktrisa-. USHAKOVA, V., aktrisa; PUGOVKIV. Mikh., akter;
TIKHONOV. S.. pktor; ZAKHARCRENKO, V., akter; GINZBURG. V.,
kino-operator; DULITSBV. V., kinc-ciperator; SVFrOZAROV. Ya., direktor
kartin; MARON. V., direlctor kartin.
We ar)eak to you. radio amateurs! FL,dio no. 6:) Je 15B. (MIRA 11:7)
(Radio-Receivers and reception)

PaVFIITSLV, A.
In Iceland; ar, c-x(,-crrt from. , book. -,i-. fron th(: ruoLian. P. I[-.
Vol. 5, no. 7, 1955
mo(aoIIA
So'i
~ )s, i~ulrarizi
6c: Eastern uiro,,ean ticccz~.,,cri vol. I -o. 3. Jan. 1956

P.E;tV-:,~TSEV, Arkadiy
k1ways Ugher an-~ higher. Av.i kDam- 46 no.2:6-9 F 164.
(MIRA 17:3)

FZRVEI;TSIV. ArlmdA7
Reflectio on
M3r '59.
the Soviet officeir. Voen. vest. 39 no.5:15-19
(~VU 12:10)
(Russia-Army-4Tficars)

FIRvmtmv,. Arkad
- - -,
Supung Hydroelectric Pover Station. Smr.mor. 16 no.17:18-19 6 '56.
(Supung Hydroelectric ?over Station) (KM 9:12)

PERVOTSEV. Arkndiy Alekseyevich, MiTYIfOV. Yu.,red.; KOROBOVA, L., teldin. red.
[Put out to sea] VYI--hod v okeali. Nookwal Izd-vo TeX VLESM "FlolodRin
gvnrdlia.' 1958. 131 P (MIRA 11:9)
(Rusgin--NaVY3

PERVENTSEV Vl I
- I -
Mountains call. Sov. voin 43 no.22:3?-39 14 #61. (I'dFCA 15:2)
(Mountaineering)

MMDUNI A.M.; DAMUN, M.G.
-
Ufactive spacing of a bisecting series Of inJeCtion wells uzed
"Monuds, flooding. Azerlb. reft, khose 37 no,3:19-21 Kr 158.
intra . ry (Oil field flooding) (MIRA 11:8)

L 41641-66 EWP_(t)/aI -jjP
ic L---JD
ACC WN, AP6WIU4 SOURCE CODE: RU/0004/65/000/002/0059/OC)68;
AUTHOR: Barosu, Mircea (Graduate chemist; Bucharest); Nastase " Constanta (Engineer;
Head researcher; Eichare8t); Pervescu. Xarlana..(Chemical engineer; Timisoara);
Tatucu, Stela (Chemical engineer; Timisoara); Sudresan, Sever (Chemical engineer;
Timis ra) -5--'
ORG: C?Barosu; Nastasel Laboratory of Electrochemistry, ICE~ (Laboratorul de -11
electrochimie la ICFE); [Pervescu; Tatucu; Sudresan] Electro-Banat Factory, Timisoara
(Fabrica Electro-Banat)
TITLE: Contribution to the establishment of the utilization conditions of some
MnO sub 2 types in manufacturing galvanic batteries
SOURCE: Electrotehnica, no. 2, 1965, 59-68
TOPIC TAGS: battery, depolarization, manganese compound, carbon black
ABSTRACT: The authorjqstudied the effect ot hanging the C/MnO2 ratio as well as
the use of artificiai"*O~ and carbon black 01 the activity of depolarizing agents
and the electrical chir_~acteristlc_s of 3R12 batteries. This led to some suggestions
for improvements in the manufacturing technoloi5r, which have been tested and have
now been introduced in production. The structural analysis of the x-ray was done
at the IFB by Doctor R. Gri&2rovici and R. Manaila. The authors thank them for
attention given the analysis and interpretation of the MnO2 type x-ray structure;
Directors of the Mlectro-Banat" Factory and Tochnicians A. Bol?6, M. Sociu and
W_ of ~_
C. Butum for assistance given in preparing the industrial p aso he solutions.
Orig. art. has: 20 figures and 5 tables. (Baned on authors? Eng. abst.] [JPRSj
SUB CODE: 09 / SUBM DATE: 05Aug64 / ORIG REF: 010 / SOV REP: 003
OTH REF: 009
Card I /I af

B A R 0511 ,Mircea, r-b'mJs' dinlonat (Buc,iresti); NASTA-31-7, Constanta, cfrcetator
nrincipal (Buc,iresti); PE~iI.IE-SCU.- Wiriana, inj~. chimist (Timisonrn);
misoqrq --!~,-,7-ist (Timiscare); SUP7~:FSANI, 39ver, inz.
o n.,3
-)nfributl ons to I.he determ: nati on of' thc u* i 11 zR tion -on~ I
gnlvnni~! batteries.
of' !,.ome MnO~. typos in mnnufficturirV
Llle~-trotRhnlca 13 no.'-:59-68 F 10..
I . ~*, ad o*,' E '.o trochemicql Laborit,orj of the Re search qn(I
PI-innim, In3titul.e (for Ba-rosu). 2. Re3earon
Find i ~hn~ c Planning Ingti tutp, (for HIst-ase) . 3.
Bawi' ' Plart , Timi!-,nqra (for !,erve.?cu, Tqtticu, Sudresan). 1, mi t to-j
Aiigii3, -,, V-4t,4.

PZRV3TINSKIY. L.N.
Use of graphic plotting in computing Leveling nets. Geod.i kart.
no.8:72-75 Ag 157. (MIRA 10;10)
1. Otryad No.23 Sredne-AsiatBkogo AGP.
(Triangulation)

PERVEENTSU,, Arkadiy Alekseyevich
Geography & Geology
Visit to Iceland kloskva, Sovetskii pisatell 1952.
9. Monthly List of Russian Accessions, Library of Congress, August -19W.2 Unclassif ied.

PMENTSEV., Arkadiy
........
Why do we strive for culture? Staroh.-serzh. no.5:29 HI 162.
O-IIRA 15:6)
(Military discipline)

PERM7SEV, Arkadly
Strength of the people is a mighty fCTce. Av.i kosm. 1+5 noa2a
2-5 Ir 063. (KM 16 x2)
(Bissia-Armed forces)

~ I Nh ,
?AACW~iSV. Ark-adLy Alekseyevich, S. . re&'.CtOr~ A . ,
or-
LCreDtive werk of millions] Tvorches--.vo millionov, Mosi-va, Goo.
izd-vo Dc.-lit. lit-ry, 1957. 65 P. UILRA io.1i)
~!Dt-or and laboring CiSE;Bea)

PERV-PNTSEV, V1.
In the boiling of the waves. Starsh.-serzh. no.1,0 Jl 162.
(MIRA 16:6)
(Submarine boats)

71~11111~stry , Sit
ammietry - 11samerl"Um
'Asmssivb In the Yield of Isamiwic Mmyeralcmi of
Zotmes and Aldehydes of the Aaetilskio Series.
F. Ta. Perveyev, lab Oft Chmip Sol Roi'Ckim Instj,
L=IW&d State Order of Lenin U, 51 PP
wzhw obahch xhim" vol xvin (LM) s No 3
Xotelch's reaction maed to synthesize 1-phoDyl:-3-
m0ftl-h-chlcr-Pentm-l-ol-3 and Its corrospmdftg
wMes,- frcm m~peslum-brcmi=-pbwy3.wAyIvn9 mod
3-abler-butanme-2. IsamerIzation of' oxIdes-by's3m
oblorlae produced I-pbmyl;-3-mothyl-limtm-l-cim-4.
PA 6?11"9
REDIM" Character of laimmis'stl= a l1wift
b6imm-MAID&U. MmItted 10 1* 2#7!Pn
629

rn
UBM/Chemistry - ReatTawgaments Apr 48
Chemistry - Ketones, Acetylenic
"ftudlas in the Field of Isomer ConverBion of Ketonam
and Aldekbydes of the Acetylene Series, II," F. Ya:.
Perrayev, Lab Org Chem, Cbem Inst, Leningrad State
U, 81 PP
"Mur Obahch Rhim" Vol MIJ (I )j, no 4
2p 5-Dimethyl-6-chloro-3-haptyn-5-01 was obtained b7
coadensation of isopropylacetylene with .3-chloro-
2-butanme and converted to the corraepmding oxide
vith povdared potassium brdroxide. The oxide was
zemerIzed. with a 20% oolution of ciftlic eald ~t
1000 to 2, 5-di.-.--.b~,1-3,4-haptadione-6-cr.. Th
UaM/Chamistry - Raarrangemanta (Contd) Apr 48
reWrangemnt of the hydrocarbons of the type RC =
CCR(C~)CCRI is facilitated by tertiary a1)[718 ;nrl
1
to a 1 aser degree, secondary a1kylB as substituente
of the acetylenic hydrogens. Submitted 10 Fab 1947.
4M
8/49Tk3--

USSR/Chealstry - Acetylene Series Jul 49
Isomerism
OR"earch in the Field of the Isomeric Conversion of
.-Utones and Aldehydes of the Acetylene Series, III)"
Ya. Perreyev, Chair of Structure of Org Compounds,
.~Chm Faculty, Leningrad Ord of Lenin State U Imeni,
A. A. zhdanov, 6 pp
athur Obahch Xhim" Vol =, No 7
4-ftthyl-5-chloro-pentyn-2-01-4 was prepared by
ccudensation. of metbylacetylene with chloroacetone- and
.9
Its corresponding oxide formed tiy reacting it with
pmarod c~tlc soda. T1w42-metby1-rMtYZW3-&1 w"
4&rlvod by -acid
on tbis Oxide and debydration'6f the alph&-glycol.
Primary alkyl radicals, Vhen wftUtut*4 for hydro.
gen in acetylene in prototropic system., had
effect of stabilizing enol form. Submitted
26 is= 48.
4M
2/5OT25

USSR/Chemistry - Acetylene Series Jul
Isomerism
"Research in the Field of the Isomeric Conversion
of Ketones and Aldehydes of the Acetylene Series,
IV,," F. Ya. Perveyev, Chair of Structure of Org
Compounds, Chem Faculty, Ieningrad Ord of 14nin
State U imeni A. A. Zhdanov, ~F'~p
"Zhur Obohch "Im" Vol =, No 7
2,5-Dimetb,YI-6-cbloro-hezYn-3-01-5 (1) was pre-.
Wed by condensing Isopropylacetylene with tbi~rv
acetone,, and the corresponding oxide of I pre-"'
pared by reacting It with powdered caustfIc soft.
w" then pmpued by
Ismerization of this oxide Vith a 29% soluticm or
c ac1d. Subadtted-26 Jan 48.
2/50M

FFERVEYEVI F. YA,
Chemistry, CrFanic
Ninetieth nnnlversar-j of Uie theor-
y of cliomicnI qtrnicture of orpanIc compoundi. 7(,, -1 t.
Len. un 6 No. 11, 1951.
Monthl Li3t of Russian Accessions, Library of Congress, 3eptember 195 '71CLASSIFIED.

1. PERVEY114V t F& y&.
2. USSR (600)
,4. Chemistr7, Organic
7. Intramolecular reciprocal action of atoms, 'feat. Len. un., 7, No. 2, 1952.
9. Monthly List of Russian Accessiorls, Library of Congress, February 1953. Unclassified. I

F71T1,177, F. IA.
Perveev, 7. IA., Kuirlashova, '-I. I.- "l-iterac!tIon of -), t'- ''~ v -, -, - ", :! - -, -.- ~ -, r-
sprips with oxyi~en-c:)n'liinin-,7 nni compounls." (r. 15~()
SO: Journn] of 'lenpi-Fil Chemistry, (Zhurnal 01).qhchel Whim-ii), ', o' " -1 '47 '- . ' -,
- - _ --- 12~~_ t

USSR/Chemistry - Acetvlene Nov 52
"The Reaction of their-Oxides of the Vinyl Acety-
lone Series with Oxygen-Containing and Organo-
Magnesium Compounds. II," F. Ya. Perveyev and
N. 1. Kudryashova, Leningrad State U, Chair of
the Structure of Organic Compounds
"Zhur Cbshch Rhim" Vol 22, No 11, pp 1964-1970
During the reaction of 2-methyl-oxido-1, 2-
hexene-5-yne-3 with alcs in the presence of sul-
furic and oxalic acids, tertiary monoethers of
glycol were separated out -- derivs of methyl, propyl,
n.-butyl, isobutyl and hexyl aics. During the re-
action of 3-methyl-oxido-2, 3-heptene-6-yne-4 with
all-co in the P-rc=ce of the
ethers were obtained which were the derivs of methylp
isopropyl, propyl and n.-butyl a1cs. During the
reaction of 2-methyl-oxido-1, 2-hexene-5-yne-3 and
3~-methyl-oxido-2, 3-heptene-6-yne-4 with ales in
the presence of alk catalysts (alcoholates of Na,
II&OH, Ba(CH)2), primary and secondary monoethers
reap were separated out. These were derivs of
mCthyl, propyl and u.-butyl alco. The action of
the Acid catalvats resulted only in the formation
Of tertiary monoethers of glycols. But elk catjL_
lysts produced a primary monoether for 2-methyl-
oxido-1, 2-hexene-5-yne-3 and a secondary one for
3-methyl-oxido-2, 3-heptene-6 yne-4. The rate of
formation of monoethers of glycol in the presence
of alk catalysts decreases in proportion to the
decrease in the acidity of the H in the hydroxyl
group of the reacttng ale; the rate of formation
~H Of the monoether of glycol, in the presence of alk
catalysts, drops in accordance with a decrease in
the 801Y in &lcohO1 of the alk catalyst belog con-
sidered.
23M7

Chemical Abst.
Vol. 48 No. 9 ,'Reaction catylene aties vithV,
of a~gljdll A Awl ~ea
I%Y 10t 1954 beaduS an r.:;
Organic Chemistry pervetv an !11 U.7-3-W
22, 2013-18(1952RBngi. tmnslation).-bee C.A. 41,
10491h.

U3
Reaction of 0 Vlaylatetylene sesin Wilk oxy-
pounds.
-Ceavage of tht oxide ring with RMgX ocr re at the a
atorn. To HtMjDr was added 30 g. C11j: CH0 CFM71
Chemical Abet. CH)-ro.3 (1) in Etoo with cooling, the mixt. let stand over-
Vol. 48 No. 5 night, and treated with 30% AcOH, yielding 54% J-mrAyi-:

Mar. 10, 1954 bjqSl-2', do 0.9215, ditO.M. XV
1

Organic Chemistry 1.49
4 wbkh with cold 3% KMnO4 pve (COoll), and a
110 tc4i, Cill0o, Isolated as the Ca sail. Shnilasly, CIA:-
MCI C&#. (M. and RtM gBr gave 00. 5% 2-mdhyl.
2-dk-d-S4exex4-yn-1-ol, b. 72-3*. d* 0.9041, nV 1.48N,1
whicli with KMnO4 gave a HO acid, CoffiA, isolated as the
,Casch. Passage of 40 g. CHs:CHCiCH into EtMgBr and
'addnof34g.lpvt2Og.Cll,:CHC.CCMeICH(OH)Mol-
'C
034'
b
d
0
7
C
H
(
: Cffs,
.959
i
a 1
" 0.9M. do
, xM 1.5M,
,
which hydrogenated over Raney Ni to the said. analog, blo
107-f;*. do 0.8". dt, 0.9458, n1j 1.4471. Si~~ilarly 4D g.
It ga re 23 g. Cffo: CHO CCAft(MOH) C1 C CH.- CHj, N
109-10'. do 0.1)M~ do 0.0476, ts'al 1.5292. hydrogenated to
;the irid. analog, by 95-8*, do 0 8427 Of I
b
;;~
d
f
l
l
i
h Mji 1
W
t r
ne
t
t
,
ng open
ng w
by the gresterl
~o
p
N
i
n the above oxideal A
pas. charge on the a-C atom of the ring
o
becauK of the Pre3enc-c-of r-!-CJlnk.--G-K-Kml4wA-: Af

7

jrjag7, -aujf-
Va. 1. Kit
Ul.

H.

i
a

RV-Eysv-
- .:op
7' XeAcfirl~ of VA, Mv- &"!A A. .41b GalibLof the
d ety
an rinyla; &T,
19MORM
ova
tk Zhur. Objrhckel =am. 23, 976-
re of oxides of the CHj and Cffs:-
CHCiCH ii;erim Irith HIS in the presence of Bi(011)i Is a
general tritthod for the prelm. of vinyl- and alkylthlophents.
3%e rftctiork consists prolpiAy of the Initial formation ol
a vicinal th'lul aln., Mydrs%n of this to an unsatd. thlot.
stfid ring claFure by addit. of the SH group across the tr!Ple
bond, 11A pansed into a % 11-alitated'mixt. of 20 1. Ilia-
1(011)~ in 114 ml. 11,0 witfi simultaneous addn. of 30 C.
bis 50-10, do 0.9249. PtV
11.47p, at Slich a rate &a to keep the temp. Wow 50', f61..
'lowed
by pwmire of HIS I hr. longer, acidification ivith
'10, gave 73-5
AcOH .and eibi. with U 0 2-vin 4-Methyl-
bip 67-70% nV 1.5,580, dw M11 10, Mch slowly
ilkilymerlicd in air; It KIVCA A ChArACtefiStIC lodapheninc
reaction with latin and fornis ik ctyst. product with lill-
(OAO~. 113-dr6*ation in V40 over Riney Ni gave a
dih o drpiii., nV I.M. d3a O.W52, wbich
miter MrO, g.-sve 4-trethyl-Z-1hiophencearboxylic acid, tn.
K
_I., -1 compd.
a also obtained on oxidation of the viu)
Similar reaction of Xmahyl-2,3-oxido-6-he fers-I-)7se the
JJ-S streant was:;Wsed lit 8 hirs. at W-7 ') gave .1 g.
4,5~twcthjLWophcr;r, bi 6&-70*, tj'D* 1.5,5-15. d:s
With J1;(0,r(c)3 this yields a solid, decornp. 250%
vrith isatin and HSO, a deep red color is formed. If the
synthesis Is nin at the reaction is complete in 2 hrs.,
with a slightly higher yield, along with tarry by-products.
P
ageof 2()I.,,IeC:Cll intoan LtMgBrsoln. over 12 brs.,
as&
followed by addii. W15 g. R tCOCII%Ct and treatment with
30cf AcOll gave b3 75-7% WLI
1. 4111 1 d-, V,M)", 1. Th k;
-with powd. KOJI in Et2O gave
b, .10-1% 11'ro, 1.4435, d-a OXNW,
ivbkh treated with I ItS as described above at 50-60*,
aed,
.15 K. fro ~~5 K. oxide) tit., 1).
116, d., 0.WJU, 1.5070, giving a violet color ividt
J-14 orld Niminr a rolicl witla lfr(OAc)2; oxida-
iii acid, i;%7ii~-TJ__(Cf.. .8JI(pird.
n
C.A. 26, 4330).' S11111atly the Gripard reagent froin
MeCICH and bleCHCIAc gave 05,~
I,, _,AM5, yielding
4-kexyn-j-ol, bl'66-7.6% WJ 1.4671,
4-hrrypic, bjj 4,
with powd. Koff j-metkyl-2,3-oxida-
d#. 0.8W, n'60 1.4410, which with 1115. a%
1, at 60-001 glive, Itoul .00 g. oxide, sono! 8 it.
Abon
torimet il',Acpie, 1). 162-3*, n'j 1.5)04. tIm 0.9730 for a
t some 10'e. oxide failed to react. At Sfl-
ici
"'Lyth'- " _~- rnpletion In a shorter perirxf.
90 e to Col
3~a? e -4-yrie, bl, 54-'5*, d.-, O.OW5, "'0
3_
G. Al. K0.101alUX

4*

with Loi
--
And Synihe nTWyi,-
Lar af vinyl a
th 0
v an
v an
a,
.1017-:

. Kudfrv
A.
953XEngT, tmnTa.
48-:3219i.
H.L.

q
"R

Y~

f
E, J

J,

48, 8219i.-PIICI CMKBT- (Q.7"
tmted with 80 -4. EtCOCILE
overnight and fretted witkSQ-0/.
CCCOH)m al, c1, b. j4c~l 43

M, d,,j LIDII

IM ral.
HtD~

wt
and extd.-:wlth UtIO yiddi
&yUbioj". bt 1=
,

im
,
,
1, violet rifal(14
4.5=. d3, I M78. gave 5C-51

'Which with Ug iiectate j~klds a saltimi

s-p*exj14,5-diuwA*Uq
gave G2-99L
A
30
t
~

n.
w
W
e
onns with ljjaectxi
7 O=pa isada-1,131104, It gives a c

r!-- yi-
J.
J i
Was
ib 1.7-
yl-
20D H with 2$1 9-
gave.
=UnrAcien Ry ml t" iwf brs
...... coam 9&=n n With BUO, 60M. CAN CHO CCAft_
1.5165, C. oM -bkb.
After
Cff,,VH., b. 91-2'. 22 ;t3;. and-
R,%NI In - McOll: 4!
H and yiddO t t mad., emejer,
, 1 1: L
M-t k up abW 3 IM 0 Mg3 whom 14 jjI,NCO rC%c* i
AM, d!s 0 3,
b, OD 0 mnl,
tim P-ducl, C%'H' with t0) a
KNmj)i6ls bi
.1 CHCJ CCOC(OM, I
MN" dN
to
9 dais P,. 43% df-_' 08
1.6ml, 4!6, b.0771:. CICTIVAt ve 3D%.
97-8
r 9 hrs. whh,
king dg,
'0_75 lc unmOr - W7s. xV 1.4 dis I
Cu.OCI, b. I SO 2
1:1~=
Wafting, witli powd_ y4:)H mder -
-wh ed
IL
bm 13"- oil' 1.4111, d" 0-130 at looo. pve F,
I in sg-&W tube 2" IVS'
-with 38% MWTI ;Tj,,r)C7yj&bj 8" 1. %V 1.4HO* do'
lmywdofBucjfi ILI e UY04 *rif-- MI
wi, 1.;Cijl?N P"
oM Ireacth 0 ter
and an 64- ldn- Of "0 1 . Ets
R~10 1(15 g.) gave io K. CH'.. Ciro CCA(,(OMCffrl
jmm temp. .
hro. at do 0.8915- Itfu 4 days
to 86.0%
7~ fi7
7
Zl!" 7 -
~6
~R, ejt
Al

ozd
C
Per"Yev, F Ya., and Kudryashov.a, N. 1,
Title Reaction of alpha-oxides of thd ao-etylene ~series with hydrogen sulfide.
Part 3,
Zhurb Ob. Kum., 241'~ FAi. 6,,: i019 1025, June 1954
The, reaction of alpha-oxides of Vie acet lene series, with hydrogen sul-
~y
nce of Ba(OH),) led to the.synth,esis of, hydroxvalkyll; hio-'-'
fide, in the prese
117-
phenes: 2-(alphs.~oxyi:sio~ropyl)~4.4wtWthiopbone,, 2-alpha-oiy-secondi
butyl)n-4-methylthiopbene and 2-(aipha,-oxyiso0roPY1)-4) 5-dimethylthioj~h-
ene. Dehydration of hydroxyalkyli~hiophenee with,diluted sulfuric acid,
results in the forration of vinylthiophenes; 2-isopropyl-4-methylthio-
phene, 2-(alpha-mthylpropenyl)-4-~~methyl--thiophene and 2-isopropenyl-j~,
5-dimethylthiophene.. Six references; I G6rman since 1885; 2 USSR sirwe
1914. Tables.
,-Institution State University, Leningrad
Submitted January 15, 1954

llt~=

Name
1A.,-: PubW 22
P, F. Ya. and Kud ashova NI I
__:hue I Reactlow of hydroten sulj1de -with "b;cIdes of the acetylene* la
cetylene' seriell' (synthesi~~-O~ virw,l-;, alkyl",_and phepylthiophene's
Doke All SSSR 98/6p 975-wM' October' 21., 1954
Absuract v.-The ri~aiction between. hydroren - sulfidb . and (nddes of the 3cetylene and
vinylacetylene :i eri e swas investitlatedo It was found that thase wddes,
um ro#
en,reacting idth hydrofen sulf de in the presence of bari hyd de,'
forift all.-yl-J. vinyl-., phenylthiophon(~s and other derivatives depending upon
the structure of the basic acids.. Mher dompounds,.synthesized through
:ddes w:itIvhjrdrof.e4 s,,Llfide, are lis ede Thirteen ref er-
thn iraction,6f m t
ences: 7-USS14' 3-USA: and 5-cerhan .('1899-1952). Tables*,
Fr~-scntcd b,.,r: Acv-demicinr. 1. L.. KnimyantT,, Ikq 20',1' 1954

PEAVEYF-V~
the 0-2 Oxy muntno -is exild
les ol the tYO RCI &M Oj
Va. pcw~vgv. 1 VC-1mix Leftimprad xidt:-i dl
yxe more readily thm
ro -War,, 'em, I Whips. 'lly'lln trbulinfilnud wmkw. Ilia)
LLLLMA~11L
101LA Ing glycols-were prept! widjax IWilli Stirring Lite,
1"A1 41nd vilqlamf~;Vlle - by. I ~! -
... ~,-,ipm "Ad Omcg*'d mcidifint 110,
~-;i. P-)
T 1191itsting the F)Y-
tipc lliO by VAM11111
kejunis, ajcs.~ hulf~: tither by rveryting. 0
Ju e33ew JCjCQOl1)Alr-
kci CNIOX + W-V' (frixii Wis).4 ANO
It If-j)=ft v iteoll), MeMICIcabil).3
f.' riw li. M~-T~ (froui A
,he, Cc
J v4dis (bijo./mm" x9pil - d1st 11f&,i U41rid, AIRP iliv. (OH)
"4 Fftm) 'woe .17 -it. &(On Afe 1Cj ce(OH)WOW11, w,
.4 M.) ;;w I f, ut 1044' PA
1704, j,_C(0jj)k.ejj.0j16~ ns. 49-4)", lb g1-`41'
) C; 1~c(j)jjy 1"Ili. 0
44~79,. 4 (311 65. 105--1(e'1
Alf, 105-6
At /2.1.47
7
W1, ~Cjjs:ClIClCCN1e
~iojj c1 cc J (1)
Asti 4 1 3ommor
Illid, I Cl(,X liMlecili
'hie 11(f.10:0 (11~ (d., C.A. 47.:11lit-thl
i49.61i,18.5.; Th
4
(11111CIICICC X
Inlit, (A
ke f oils
I)_SOj. -woe iLt
Y Lll),,of bi is) awl a 3444 excess of kc
W Ic I
14 Stich tji:%t tlj~ tesup, ilk) not "ceed 400.. The
$jsg~ as~e jgwi AY~ Oij)~jc-CAlli,r j. ji8- ting abow INV.
lAiww,; 0. .11,,( pjl,lewou~tawlitij in air asid expl(sile tm Ima
38-81, W; 1r,itiaLut with Lllkl, 11t504 readily bydffAym thr-no 141
ket6les.11111 klyvolq (lit burr i-MADritiling unsfUr thu re~v-
43-95 43.43 fitif ~ coliditio&is to The foilo.% iug:
VAlf-CHAle-0. 8D- 1.468,'0.9637
xW-Afka culvd.j AIRp lfpnw1,'
Afer
1-4050, OX47
CA _11:
aAj no, Y fire li-,tcd:, C11j: C11Cj C
:41~73, 43. 1)11 C.-CFAfl-ew. 0. J01-2-lim), 3
Fj
111C. vp~'Xifle~ re, CAIN: 2.0, 51 ~'_`/3, (0448,1.4658, 47, 0,. 49.6.1...
AlthOligh' p
act %villi JJ4) Very Slowly Ill the llissrJILL. (if a cawlv~,t, it, the ---- -- ------
4
l!-cF0ftk w3cefif w k;04 the rmct~m I (-;itljlv I ,Ct:%1ll:.Cll3.0.QfrELO.
11, - Weil r",!jOjrk! O1 C. 71-2'/4, f).04 1.46NO,
wilb 13)11,b vvjs)l3jil)jj of brat, lit vdill mw to "Iflitt "Wi.

VC
-r14 0.11378, 1.4
tme,cums.0. .-Vis" 0.11225, 53j,
I ~ W) 1.469
CNCJ
04-
CCA
clis: C11 Cl I -
.47W. 5r..6,: r.7." 1.%*33"
L-I"
Fit
0.9, W, CHO C:CAFe-(V1A1e-O,CMt-
CU)
IV.-!, -L 211
T6 m1hus (Tort 1 W14 U the latter vrere addr#d to.
an'MmktintX. 2-3 droji
r, i HIS(". at. a '~ttc'
"imich tbal'the temp.'did il'ot rme above -Ili% amrtM mht;;
_colorteci.
thm stirztd With: NijOh umb wilift HAW.
issmed,m3thecatalrig, Yor 11 is oddi-A to thf: lwnling st.~
HAO, , With cithvr.03~1:'
qrulc'-f 6t
".8s.-Nao)
ink AW t1be k7121. btaged,jo 6G, W an(I tok-11ted ViLh I I't C~.~
'd
d owe jrmd0j,'tbzrf 11 %i-ilb a6lir orbroir cat. yt;u.
-:9,(cataly-st,
mwDuprtbe: '!,,
ft=M%rjfjtD Wed.. t.A(Rp, '~'rr yiJd)1vqrc prept,
CA1, 76-
Ilz.M.
-:7'14. LOGO, 0.0
3#0, 41).g. 39.8. 1.1"$j; CH$:Cjj,".^-j4
CAMOH)CHAVe, NA *w- NaOH. C~40'tJ. 1.4102,
3, 30.6 11'73, CUs: CHQ CCAfc(OPr)C,11r I
(MOMA, 41, 4 - M, 5D.4. A9.2, 4.2,
k0m, 1TXAOj' 03-5 1.47~ 0.9 58;
U11:471MCC(Oll jC8, Fr. Nik. 01-2*/.0, 1.41pi,
"MCC
(0) Na. W-ODI/B. 1.46M. 0.91,90,
if
53:7. 1.4, 24;--EWo.-CHCiCCM#(CitaCtlMft)(.,!Tr~,
t W., HM4,'PCH */5, 1.4713, 0.9M. 65.2, 63.7. I.6. 14;
~Cti-l-'CIICICCAte-(Or4fl1i)CHSOHP' HIM, IWI"(3,
ifc-
fMi,0.9126, 04.31,029 -14 65- cHs:c1fc'cc
1.4811, O.WW,
45.4,1
44.3,1.1. 6940i,'CU2; CUCI CCXOH)MeC11(OMc)A[c, Pla,
"4~.80/8,1.47rj4,t),9543,45.5.44.3.1.2,3D; c11':c11Qc-i
-13, OSY
CMr(OPr)a1(OH)Me, H.Cj%; 9"*/10, 1.47. t.33,,
M.1 3.t, 4g,
Clill:Ciiciccme(ocillfe-)CII(011)-!
Ale, IVS04 of )TYCA, 72--S'/3. 1.470D, 0.9=,
Z,5.2;. 53A,
C111. CIM CCJ[e(ODti) CH(OW)AIc, I ItSO., K-
lluznonocth~lrs ,
are oArvilm mobilc liq" which on otainding in air in The
h ence of. aWksidunu yellow -and vally - thicivii.)
Vic pute'liquiez distil i absence aAr with little tar
m
f4matips. but the hury products which tam explodcL'on
hi ting Ithove, 140% In all cam the e1hus obtained ~ by
ra

er
*'4 0bus ObtaintJ by; ba4r. cavilysis.- 0 huic it jo
OIL5
4slablW16d tbut ttrthtry tt~us are by QCW cutalli4.
7

rmh bmic tntedysh th-s'lorltolary Ot
I
kcmjal
.
1.01-

t PAiding t~c'eptixidrii to a Wod tue" pf %1% Nit 0.
oy I

l ior aiAut) at room fenip. and atkAut 4 6c miA. unt -111L
Wex-j- di PMT. I'
1~5 'ht fuumilsl (b ./sl
11
N
e
- -
lf". C
I
.
dn. Af D cAfc4.i MRD locind) were meM
acc(OH)MCCHINJI, (III),. 01-T1-1 ~ 1.5165, I.OU78'
.C
- CH
97-8*/7
%6i
4
37
CvC
vjdvHAfe
6
OH)Af
&f
.
.
I:
.
j
;
Q
IZMI O.Wnl. 41.63, 42.47;'Bwc(dH) .
,
AfeClljNll, (IV);
1"1/5, 1,4540, OAM5, 119.47, 30.29; j M.-ClIC.ICC-~
92-W7.1.4762. J)Sg lb, M-99, 57.36-
-1 ponloydrosenatknoat 105utin.and W ~',withj(aucyNi
WMS to I-C.N jNCO dPIV 0
strisirlins Ul tryAlif. - (la'.
-estechmilin t
A 4U%vtw4.hi of ifse. I, r1c. . "( Ow
"'IT
O"Air fitig 4u.1 rcview llllk ~tcj tilt fialmir'i'-
5 01! dut coce.,

PARTRYNT, Y.Ya.; XURSNIGINA, T.N.
Interaction of alcohol oxides of I;he acetylenic series vith
h.vdrogen salfide. Zhur. ob. khim. 25 no.8:1619-1623 Ag '55.
(MI&A 9:2)
1.Leningradskiy gosudarstvenW wiiversitat.
(Alcohols) (Thiophons)

USSR/ Organic Chemistry Theoretical and general questions E-i
on organic chemistry
Abs Jour Referat Zhur - Ehimiya, No 4, 1951, L1590
Author Perveyev F.Ya.
Inst '-Leningrad University
Title Isomerization of Alpha Oxides. III
Orig Pub Vestn_ Leningr un-ta, 1956, No 10, L03-115
Abstract On the basis of literature data and the author s work (Zh. obshch
khimii, 1948, No 18,479, 686; 1949, so ig, 1303; RZhKhim, 1955,
13883) a study was made of the effect of substituents in alpha-
oxides on the nature of rearrangement following opening of the oxi-
de ring. In alkyl substituted alpha-oxides the oxide ring opens
mostly on the side of the least hydrogenated C-atom, and most reac-
tive are the disubstituted oxides having the asymmetric structure
RR'CCH20, which are isomerized exclusively to aldehydes; monosubsti-
tuted oxides RCHCH20 yield predominantly aldehydes; disubstituted
symmetrical oxides RCHCH(R')O and the trisubstituted undergo rearran-
gement to ketones. In oxides with mixed radicals (aliphatic and
Card 1/3

D16tri:
dio With
W4 80 it., zx= vedg!! "B
aid
Y.
M
Y Md"
7
4, 12"KI956).-MC11) (Rm CM
;,C11 ~x
TUSS fom In CHCII and Aq Bri(OHN undcr Jkn N atin. 2-.
ethY14-jhethYIs--lcuoiAuWe, a2"0'. x1?- 1.5518. dm
.1-3WO, and 2.vhlyt-I keti, 1wiritopbene, be.&- 32*, nj?
1.5". do Lam 0911JUM, -PGIYMCtIC tar$:
if ~;, CV1, I,
form. cwn
1P
reduction.of W-vinyl coo d.- to, The alkyl.
lorru x),a1kVJ-4,ucthyjv r hen
RIW~OH)R - 2-h ydj nap es
Which. can bb - delivdmted to '_I41k-tflYj cmP& Th
mII)p&. girt *pQJounaus, it i-h expostue to the impois 1111jug
injee,
knoph ited I ubztltui~nt, ti.p. min.)
Tf ft, C 0 11
pit, dis Id IM33;
T -3P/2, 1.6T82, RtMeC(OH1. 734*/0.
CHI .C~lv, M
.1.5553,-A-3m, CHOCIII (31-20/0161 1.6 M,A.277401'
Cff2:Cjjw1so, -84/0:5.. j two, I.
77 1847; isf)-41'r$eou,
IX14*10.11. 1.5310, U_1169;-
I-tyrlo nttniYI,,78
IADUY'
Spec ra Averr 0
1U. Infrared t t ained and compared toAhote
are rbarw
of Oie tUVbeun. -The fulU wing.banAs (cm.
W
tedmic., :3075-53, cycEic ~ H; ,. 1578-.57, ~ cyclic duuble
bond; - M-Wi not dm- to ~ ttro atom since it dovt not'
alter In "nj ftom*nkno Iive lo thiophene7 - 760-59i the
baml at M;_ 12 -095.73~25 absent fortht,
Iflophrm,
batitut0i
u4su A thiaphe"t flud" tenDplicne but prewin iii the
2.4-smbstituted cumpds.;~ A vinyl group; 578 and
S
-85., (CH. -his thipawlt for aulp.
D5 thc:.fwcm~" whid
Ing %ba-.8tructurcs asA-alk Ivinyl -con, .'and not its
a I rowe X9"*t--

Ile ve -Air
ABROUQUO i6ewSmfkq_- LX
loft
AU
"Jew
ITAY1401
Airy -AUG:
, W-M, 1=11401
*WS 9, 1
s theds of attwo was de froul'.
unsa . epoxy
i J, the addn, 46 1 APP1*2 td C=P&
Derme -0 side
I oaf eft and bnu of chala Ion a
nop, -the, tIvIty-W-Ho d-
heve lint In
00V,
thalin " thuspjkr*lh
3cen to
ins, -
to, fis Pc Im'-0 only
tow
f
tuisatd. do riva;A 0.6 q
t~ ~O)CIICH'
to I fume JAMSDr. 3 n .1 hr7aad'maddg~
1. CICHIAC,
ve after sm" houre rAjq,- Ilowed by trairagat with_~
t( 16- Lows j and V44
AV 1.4790.* lot the -
g followIng c0
supd1s.). - 61mllarl j'__PrwqOIi1IIIc I CH- gave;
-bi
z
he" A16ri es -wuh pomi'.
You -
11tio r"-P" I'S'7-4rh"#YPI'j4P
-Ant-
I% I.: And
'"Mom-
Pali bw7se i'vo
of' H&-10
"0' 0=.. Ba(OH)t wjLj paj
et w
11nin. Nth: there wax. u4 cd::21W.. 2-mithyw.2.
rXY-vhcxctWI-YAti tht H& - S was cwtinuiDd 16.
W6.0 the truted with A OR and exid. with EtgO
~-Pg.ghtd.;-the Ist fratflontbu tied - being treated with
yl ldh on ~otnblnatl
Irmill-if as . on of the
be 29-
Wil-U18, Me It thbadd t I
A. 1 6 ox do werl
Ifie yldd t* muldemblyj With Ai NiandkIsClith rAvo
the ehlQMMCMU4_i dUIV-, H the above oxide, -
_7Z

146 gm It, At W. lwd if the mixt., It It
ti 4
with lfxS* 4.hrs;i
qd
- M-O flag
mba%, z 2Ad methA;1.2-i
dl
vt 0;1
--s6 mrse
Save 43!&Ml4*b
H :gave 80%
1.1-785, 1 M40.
mtyu-S-ol gave 4M I
hmo, b,4 W-8'. 1.5MI, M84. It ,
=ovyl-laeepay4-11 iin go.
-2-mabyl-4 hydrazycydc
tayt SK J-tyk Wes 1-01
78- j Lom' loul$bj 4-teth)
-Vwilafly-
OMAPAMI bA 03% 1161
to
i With N
rg
i lalvo~
op

X
A l

Ot
*Yd
VIX04-

PXRV , Y.TgL.; VFXMU. U.K.; SMNKOTA, L.N.
W !~In~._7~_..~.-
Interreaction of amonia wA &miaes with Ck -oxidem &ad bydro-
xyoxides of acetylente wA vinylac,etylesic series. Synthesis of
alkyl, -vinyl, -phsay'l yrrolse and prTole-carbisole (with sus-
"5.Vest. Lea. us. 12 no.4:134-144 157.
?mry in Inglish. P.154
M,rrolsa) (Nothazol) (Mlah 10:4)

-if licatt.4
-ink

k

to_
t
i

e pve-
4MS

-,VAth,-- - Z~
4.1
Ktx tJ,!i-!

w1b

Nr

M
gnj~L
sw
~;.Ifa ftht
4l
o
c
li", A
0- 1p 9
tg*. Wit watkg 10
hr~ to I~rve
12 M.
kave
b4-10"
car..
ell
Awil- in,
taw _u'"Law 1414~*Pxyi r,
Ch"
illip
14 Ot I
Wrde. JJwi
th
timll I w 0. -.101L 50 at:
M";- 4311-
N!14 -- t;

~,' R,-- , '.1 . V'~ . ; , .
~ ... . I - . - I . ~ ~ ,
It e ar *1 1 ( y: ( f - G )t ~ d H " , ", 1, r. f, a . m t Y 1 9 1; 1 C 5f! r 1 (- ~, './ ~ 1. ~. 'I I F, . /. y , '. :: . , - ~ , .
. I n~r . o . t '. ~m . -~,. r)( . ! -- 3 1-3-3 1"'? ( ' ( 4 .
,.! 1 1, . 1. .
.. it,?~iv
. y t in I v e r H : t e t .

PERVETMV, F.Ta.; KUZNMSOVA, Te.M.
Interaction of smonis and amirms with oxides Of
vinylacetylene series. Raw synthosim of pyrrole.
28 no.9:2360-2371 S 158.
aceVlOnO ond
Zhur.ob.khim.
(MIRA 11:11)
1. Leningradekly goeudaretvanan, imlversitat.
(Pyrrole)

5(3)
AUTHORS: --XaZyeyev, F. Ya., Statsevic~i, V. Ya. SOV/7~-29-7-6/,-,
TITLEt Investigations in the Field of the Dioxides of the Acetyl,~,~(.-
Series. I (Issledovaniya r oblasti diokisey atsetilcnovL,.,-,-
ryada. 1)
PERIODICAL- Zhurnal obshchey khimii, 1959, Vol 29, Nr 7, pp 2132-21,57
ABSTRACT: The purpose of the present paper was the reaction of
the acetylene series Witt. ILMines, a comparison of the
of di- and monooxides of this seri,;s as vell Fta the so'lliti C
the problem as to how the oxide cycle cpens und,;-,- thi,,
amines, and under which COILditions the forming dian~no
are transformed into the corresponding ~-aminopyrryl ca-r'
Pyirole homologs of this structure have hithe:rt,3 not
scribed in publications. TI.e dioxides of thc a-r-etylene
have equally been little investi.-ated so that thc inv.,~ti
of the openinc, of the oxidc rin- under the n, ti,---. f
in alkaline or acid catalvEis vas of interest. d~~
dimethyl dioxydo-1t2-5,6-~eXYne-3(l) served as
bard 1/3

Iw%estiGations in the Pield of the Dioxilpt3 of 'n 7
the Acetylene Scriec. I
0 0 0
H C/~~ C-C =:O_ - C H
2 __2 -3-'
CH3(1) CH3 CH3
In the reaction of (1) with ammonia, methyl- and et!;yl aminc
it was found that this dioxide has a higher reactivity than tuh,'~
monoxides of the acetylene oeries. Thus, (11) reacts with amine's
x7hen heated in clo3ed ampoules at 1000, in contrast to (1)
reacts explosion-like even Yith methylamine (without coolinG).
By the reaction of methylamine r7ith (1) compound (III) is fornod
which in the case of longer heating passes into compound (IV),.
Thus, N-methyl-2-(I-oxy-2-inethylamino isoPrOPYI)-4-methyl py--rol,-
and 14-ethyl-2-(I-oxy-2-ethyl.-amino isopropyl)-4-methyl pyrrol.?
were synthesized. In the reaction of the dioxide with alcohol
it was found that in the alkt.line catalysis
dimethylhexyne-3-diol-2,5 and in acid catalysis ?,5-dieth-,x-.-
2,5-dimethylhexyne-3-diol-1,6 is formed.
Card 2/3

9')_7-"/,9 3
Investigations in the Field of the Dioxidcs of
the Acetylene Series. I
The spectroscopic inverti~,ntLon confirmed the above
There are 6 references, 3 Of Which are Soviet.
ASSOCIATION: Leningrad3kiy gosudarstvennyy universitet
(Lenincrad State University)
SU13MITTED: July 4, 1958
Card 3/3

5(3)
AUTHORS: Perverev, F. Ya., Hartinson, E. SOV/79-29-9-24/76
TITLE: React:,.on of the a-Oxides of the Acetylene Series With
Diamines. A New Method of Synthesizing Dipyrroles.
PERIODICAL: Zhurnal obshchey khinii, 1959, Vol 29, Nr 9, pp 2922-2927
(USSR)
ABSTRACT: Following the papers quoted in reference 1, rhich deal with
the synthesis of pyrroles fr= 1,4-dicarbonyl compounds the
author based their new investi.-ations on the oxides mentioned
in table 1 and studied their reaction with ethylene-, hema-
methylene-, p-phenylene diamine which proceeded according to
the given scheme. Pyrrole derivative (IV), a product of the
reaction of oxide with an amino group of ethylene diamine,
and pyrrole derivative (V), a product of the reaction of
oxide with two NH 2- groups of the diamine resulted from the
reaction of oxide (1) with ethylene diamine. The oxides (11)
and (III) form the conpounds (VI) and (VII) respectively with
ethylene diamine. Oxide (1) together with hexamethylene
diamine yields pyrrole (VIII). Oxides (1) and (II) with
Card 1/2 p-phenylene diamine yield the compounds (IX) and (X). Table 2

Reaction of the a-Oxides of tile Acetylene Series SOV/79-20-9-24/76
With DJamines. A New 1.1ethod of Synthesizing Dipyrroles
shows the constants of the synthesized compounds. The
infrared absorption spectra obtained from six compounds
prove clearly that the synthesized compounds have a pyrrole
structure. Bands from the pyrrole spectrum were found in their
spectra (Ref 2). The intrcduction of a large amount of sub-
stituent8 into the molecule of pyrrole was of course bound
to have an effect upon the oscillations of the molecule. This
makes clear that some of the bands are shifted and that in
several cases double bande occur instead of a single band, or
even several bands which do not occur in pyrrole. Already at
a f:.rst sight a close relationship between the individual
bands and the structure of the molecule can be observed (Table 3).
There are 3 tables ifid 2 references, 1 of which is Soviet.
ASSOCIATION: Leni.ngradskiy gosudarstvennyy universitet (Leningrad State
University)
SUBMITTED: Jul3- 4, 1958
Card 2/2

5 - 3400, 5 - 36 30
SO"
'A
AUTHORSi Per:eye-v, F.. K.
TITLE: Reaction of' Hidro~ren Ph)sphide WI.th Acetylenic a -0.,-,ides
PERIODICALt Zliurnal obshchey khIml.1, 1950, Vol 30, Nr 3, PI) ';-4-
789 (USSR)
ABSTRAM Acetylunile ox'.des (I)-(IV) in reaction with
phosphine gave new acet:rlenlc hydroxyphosphines.
2-methyl-1, 3--ePoXY-3-o.-:tYne (I) stirred for BO hr
with NaPh2gave I-pl)ospiiinyl-2-inc-thyl-2-hydroxy2-3-
0
0
oct.~ne (V, yiEld 73%, bp 64-65
C at 0.5 mm; r1
1.4948,
D
d20 0.9360). Similarly, 2-methyl-1,2-epoxy-3-pentyne
4
(II) ~;ave in 46 hr 1-plic-sphinyl-2-methyl-2-hy
~Bo
-51C) C at 1 mm, 1.506.3,
pen--,y,ie (V!, yield 73% IP 50
11D
20
dij 0.9,980). The ahov~.~ pho,,3phlnes were mobile liquld!3
with the characteristi., phosphine odor; they were

4 readily soluble in metnanol, ethyl acetate, F-chyl ether,
rd 1/ but were insoluble in water.

Reaction of Hydr-o;::F-. Phosphide lviltl~
c
Acetylenic a -oy,,-- 7,
(Ak
-"8
1 25 9
sov//~7
(11) C113
Carcl 2/4

17 J .)
Reaction of Jiydrojre~n
Ac ety I e nic GL-Ox:-d,'3
me'
x -d Y
wi'h NaPHI, the react'Lon product polymerized
cmpletely. ',,-Ilietliyl--I,'~-opoxypeilt(itte (III) 1~,, ---0 1,41,
stIrrIng oilly trace3 of
hydroxy-penty--, photph'-ne. !R sp-~ctra of the nydroxv-
phcsphine5 taken ~.~;ith IKS-11 spectr3graph showed 'lie
characteristic, freq,,~eric,~ of the P-H bond C.1r,
Dehydration of' V arid VI with die thylethylenediam-'n~
gave products with 1bp 1400 C (1 mT,) and -,780 C ( 0 mm.
respectively; the str,--c-.,ire, according to thelr eleme-~,,-al
compcsition, ~~p--~ctral aria ly.-31 -9, a~A
Oc ~,d corr.--9pund to the
Card 3/4

Reaction of HydroFe,-, Pt,c),gplilde 141-1,h
Acetylenic CL -Oxid(--~o
ASSOCIATIONi
SUBIKITTED:
(83259
Tnere are 3 table2; anc r-~ferencess, I ~;.S., '-~.K.,
3 Ger.iian, 4 Soviet. TI e U. S and U.K. referen~:es are:
H. Beachell, B. Katalaf3lly, J. Ch-jTi. Phys, 27 1.82
Ro b er t.,3on, Fox J. Chem. Soc., 120,
(1957); (',)26) .
Leningrad State Uni,,,,ersity (Leningradskiy gos idarst---ennyy
univers'-tet)
JulY 6, 1959
Card 11/4

Ma.; K.G.; N.V.
nt~-ractio:, of QK-oYldes f-,f the a~-etylene 5er't-s j-'t~
pot,aasiain cyatl-,Ae. Part 2. 20, r,0-2"- 1--~--1.49
16%.

RAZUVAYEV, G.A.; STEPOVIK, L.P.; I!WIEM, F. Ya.; DEMIDOVA, V.M.;
ALANIYA, V.P.; SOKOLOV, N.A.; KHAR,HINKO, V.G.; KRUPINA, T.I.;
KLIMBIKO, S.K.; RASSUDOVA, A.A.; GDRELIK, M.V.
Letters to the editors. Zhur. org. khim. 1 no. 12t2244-2246
D 165 (MIRA 19:1)
1. Nauchno-issledovatellskiy institut khimii pri Gorlkovskom
gosudarstvennom universitete (for Razuvayev, Stepovik). 2. Le-
ningradakiy gosudarstvennyy universitet (for Ferveyev, Denidova).
3. Moskovskly institut neftekhimicheekoy i gazovoy promysh-
lennosti imeni Oubkina (for Alaniya, Sokolor). 4. Saratovskiy
politekhnicheskiy institut (for Kharchenko, Krupina, Klimenko,
Rassudova).

PEIMLEV, F.Ya.; VOYTOV, A.P.
Interaction ofcC-oxidea of the acetylenic and vinylacety:enlc
serieB with nucleophilic reuRentD, Part 1. Zhur.org.khim, I
no*2:226-229 F 165, (MIRA 1834)
1. Loningradskly gosudarstvennyy universitet.

~ i .. k . ~ . I ., .
.- - - . ~ - I- . I
- . . I I 'I- C-. - - .
I
n~ : -. ..I I. . . I . I . . . .

PFRVFY7rV, F,Yq,.
Rea 2t r~- S., :~Tqa7~CF 1
primary !inn !!w.*t-,wFiry n I , p .rc- rif*

I., i'. ii'.; V. yfl.
.". i'YEN ) -
Dioxi,,----3 C-f a~C-*.7~t,.%iC SC-r~E:I. L.. ,,ur. ot).
34 no. t *. i'i ~l 1, - 1'/ 3', .'e I ,
. . .3 n ~ !, 'L, -( , v g
,osudarqtvt-rtriyy univ(!r,,iitE,L.

GOLODOVA, K.G.
Oxynitriles and nitriles of the ace-tylenic series. Part 1. Zhur.
ob.khim. 32 m.7:2092.-2095 JIL 162. (MBA 15:7)
1. laningradskiy gosudarstvennyy wAversitet.
(Nitrilen)

MINGEYEV. F.Ya.,i SIATSEVIGH, V..Yu,,
I
Dthyd.roxides of ibp- acetylera., iw-ies. Pa-r-% 3. Zimr,ct,k-hi . -
3-1 662~ (Kru I r ~ -7
1. LeaizX.-,-wl.-Iuy Losudaxet,,eruzyy ia~,Yersltot.
(qplroxy -owjx.-and5) ~ketylene compoiwds)

PERVEYEV, F.Ya.; DEVIDOVA, V.M.
Interaction between OC-oxides of the acetylenic series ~Lnd
alcyl- and dialkylamines., Part 1. Zhur. ob khim. 32 no.l:
1.17-121 Ja 162. (MIRA 15:2)
1. Leningradskiy gosudarstvennyy tniversitet.
(Acetylene compounds) (Amines)

MUM, F.Ya.; DDLEDOVA, V.M.
Interaction between oC--oxides of the acetylenic series and a-Uylamine
and diallylamine. Part 2. Zhur. ob. khim. 32 no.l-.121-126 Ja 162.
(MIRA 15:2)
1. Leningradakiy gosudarstvannyy univeraitet.
(Acetylene compounds) (Amines)

IRMEY, F.Ya.; YMHDVA, V.
~
77
Reactions of hydrazine hydrate and dimet4lbydrazine withinme
oxides of the acetylene series. Zhur. ob. kbim. 30 no.11:
3554-3558 N'60- (MIRA 13:11)
1. Loningradakiy gosudarstven-urr universitet.
(Hydrazine) (Pyrrole) (Acatylene compounds)

PERVIUEV, V.Ya.; STATSEVICH, T.Ya.
Dioxides of the acetylene series. Part 2. Zhur. ob. khir-.
30 no.11:3558,-3561 W160. (JIVU 13: 11)
1. Leningradakiy goeudaretvemly)r universitet.
(Acetylene compoundo)