SCIENTIFIC ABSTRACT KAZANSKIY, B.A. - KAZANSKIY, D.A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000721320004-2
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 13, 2000
• Sequence Number: 4
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

-.--.--KkMSKIY9 B.A.
Academician I?Lkolai Dmitrevich Zelinskii; on the 100th
anniversary
of his birth. 12v. AR SSM. Otd. khim. nauk no.2:193-196 F 161.
(MIRA 24:2)
(Zelinskiip Niko2al. Daitrevich, 1861-11,153)

5/204/62/002/004/003/019
9071/E433
AUTHORS: -Kazanskjy,-&,A,, Dorogochinskiy, A.Z., Sterligov, O.D.,
Lyuter, A.V., Dmitriyevskiy, M.L., Nazatov, P.S.
TITLE: Dehydrogenation of isopentane into isoamylenes on an
alumochromopotas3ium catalyst
PERIODICAL: Neftekhimiya, v.2, no.4, 1962, 448-456
TEXT: A systematic study of the process of dehydrogenation of
isopentane into isoamylenes under conditlons of a stationary and
moving layer of granulated catalyst K-544 was carried out on
experimental installations of Groz NIX, Tests on the stationary
layer were carried out on a laboratory and.an enlarged
installation. The reactors with a stationary layer of the
catalyst were of the capacity of 40 and.500 cm3 respectively.
Tests in the moving layer were made in a co-current continuous.
pilot plant with a reactor (4 litres) and a regenerator (4-7
litres).
T.he volume of the catalyst - 35 litres, throughput - about
100 litrea/day, the velocity of circulation of the catalyst
up to 16-litres/hour. The analyses of the reaction products were
made by chromatographic and other chemical methods. The influence
of the temperature, volwme velocity and rate of recirculation of
Card 1/2

S/2o4/62/002/004/003/019
Dehydrogenation ofisopentane ... E071/E433
the catalyst on the main parameters of the process as well as the
behaviour of tile catalyst were studied. It was found that the
catalyst had a good and stable activity. During an operating
period of 1100 hours in a stationary layer and 400 hours in a
moving layer its activity remained practically unchanged. Under
the optimum condition of tile process (temperature - 5400C and
volume velocity - 1 hour-1) the yield of isoamylenes amounted to
30 to 31 wt-l" calculated on raw material (98.6% of isopentane)
with a total yield of unsaturated hydrocarbons C5 of 34 to
38 wt.%. The catalyst has a satisfactory strength and good
regeneration characteristics. The velocity of burning out of
coke from the most inaccessible layers of catalyst K-544 amounted
to 20 litrea/litre of catalyst per hour, in comparison with that
for aluminosilicate catalysts of 13 to 16 litres/litre of
catalyst per hour. There are 6 figures and 5 tables.
ASSOCIATION: Inatitut organicheskoy
im. N.D.Zelinskogo (The
Chemistry AS USSR imeni
khimii AN SSSR
Institute of Organic
N.D.Zelinakiy) GrozNII
Card 2/2

LIBMW, A.L.; BRAGIN, O.V.;,. KAZANSKIY, B.A.
Cataiytic dehydrocyclization of diethylamine with the
formation of a
five-membered heterocyclic system. Izv.AN SSSR
Otd.khimarAlsk noe3t
525-527 Mr 161, (MIRA 14:4)
1. Institut orgimicheakoy khimli imeni X.D.Zeliuskogo
AN SSSR.
(Diethylwdne) (Pyrrole) (Butylazine)

Boris Aleksandrovich-laxp-QU J j on the seventieth
anniversary of h,
Izv.AN SSSR Otd-khimomuk no.4:537 AP '61-
(y,azanekii, Boris Aleksandrovich, 1891-)

S/02o/61/136/005/019/032
B103/B208
AUTHORS: Khromov, S. I., Shokova, E. A., Sterin, Kh. Ye.,
and
B. A. Ka?,ax~ekiy_, Academician
TITLE: Contact; conversions of cyoloootane in the presence
of a
nickel catalyst
PERIODICAL: Doklad), Akademii nauk SSSR, v. 136, no- 5,
1961, 1112-1115
TEXT: The authors studied the conversions of oycloootane
on a catalyst
consisting of 50% nickel on kieselguhr, a) at 2500C, and
b) at 2500C in
an intense hydroger stream. In case a) - 61% of
cyclooctane was con-
verted, in case b) - 81%. The composition of the fractions
obtained
by distillation of the final catalyzates was studied by
means of Raman
spectra (methods described previously in Ref. 7). The
authors concluded
from the results that three processes take place at the
rather mild
temperatures applied: 1) hydrogenolysij of the 8-membered
ring giving
n-octane (in analogy to an identical process with
substances with
smaller rings, Refs. 2-5), which was detected for the
first time by the
Card 116

Contact conversions of oyoloootane ...
S/020/61/136/005/019/032
B103/B208
authors; 2 ') a transannular dehydrogenation which yields
cis-pentalane,
and 3) a stepwise isomerization of cyclooctane to
compounds with
7-, 6-, and 5-membered rings. At ?OOOC9 the following
compounds were
formed: n-heptane, cyclohexane, methyl oyclohexane,
cyclopentane, and
cis-1,2-dimethyl cyclopentane. The latter may be formed as
a result of
the afore-mentioned ii3omerization. About 46.5 wt% fall to
the share of
the unreacted cyclooctane. Very small quantities of
cis-bicyclo-(0,3,3)-
octane-(ois-pentalane') were also found. On the basis of
these results
the authors suggested the reaction scheme at 2000C.
Card 2/6

S/020/61/136/005/019/03
Contact conversions of cyclooctane ... B103/B208
W-Citill- if -Citill
C 1. CHS
Cl f
-Clis
-0, 71

SIM161113610051019103
Contact conversions of cyoloootane ... B103/B208
The oatalyzate consisted at 2500C of -., 8 wt% of cis-pentalane,
11% toluene, and , 2% benzene (apart from the unreacted cyclooctane).
Besides, the following compounds were obtained: methy-1 cyclohexane,
cyclohexane, cis-1,2-dimethyl cyclopentane, and gem-dimethyl
cyclohexane.
CH,
HS
CHa XD CH.
C.
-ZOOC
L-Ca 4/6

S/020 61/136/005/019/032
Contact conversions of oycloootane ... B103 208
The reaction temperature was found to play an important
part in the
quantitative interrelation of the afore-mentioned three
processes at
200 and 250OC- Marked hydrogenolysie of oyaloootane occurs
only at
2000C, and practically ends at 2500C. The formation of
pentalane, on the
other hand, is characteristic mainly of 2500C. The ring
isomerization
which is accompanied by hydrocracking takes place both at
200 and 2500C,
but is in addition complicated at 2500C by an aromatization
of hexa-
methylene hydrocarbons. The authors assume that small
quantities of
cis-lp2-dimethyl cyclopentene are formed at 2500C owing to
competitive
processes: from methyl cyolohexanev the latter compound is
formed on
the one hand, benzene and toluene on the other hand, with
the
equilibrium being shifted toward the latter two. No
aromatization
occurs at 2000C. The transannular dehydrogenation of
cyclooctane to
ois-pentalane, and the isomerization of the hydrocarbons
also take place
on platinized carbon, but at a higher temperature (3100C,
Refs. 60).
The experiments of the authors showed that this does not
apply to cyclo-
octane at 200-2500C. There are 4 tables and 8 references: 4
Soviet-bloc
and 2 non-Soviet-bloo.
Card 5/6

S/020/61/136/005/019/032
Contact conversions of cyclooctane ... B103/B208
ASSOCIATION: Moskov.Dkiy gosudarstvennyy universitet im. M.
V.
Lomono.9ova (Moscow State University imeni M. V. Lomonosov)
SUBMITTED: November 11, 1960
Card 6/6

BUTMiOV, AX',,;KEKULE, A.; KUFER, A.S.; KAITOVEIKOVt V.V.,*
BYKOV, G.V.
[trans ator]; LIBERMAN, A.L.ftranslatorl; RAYTVAM,L.A.[tran
latorl;
red.; GUSEVA. A.P., tekhn. red.; GUSIKOVA, O.F
kAZ
tekhn. red.
(Centennial of -the theory of chemical structurel Stoletie
teerii
khimicheskogo atrooniia; sbornik statei. E~r A.I.I.Butlerov i
dr. No-
skva, Izd-vo Akiid.nauk SSSR, 1961. 146 p. (19RA 14' 12)
(Chemical structure)
P.,

KAZANSKIY9 R-1 akadem:Lk
A life devoted to science and the motherland.
Starsh.-sersh.
no.2:23 F 161. (MIRA 14:7)
(Zelinskii, Nikolal Dmitrievichp 1861-195))
7 7

39439
S/081/62/000/012/023/o63
B166/B101
L"H 0. is Kazanskiy, B. A., Liberman, A. L.
T!TL!;; Catalytic dehydrocyclization of paraffin hydrocarbons
ReferatiVLlyy zhurnal. X'himiya, no. 12, 1962, 212, abstractt
12Zh92 (Sb. Mezhdunar. neft. kongress, v. 3,.1959".
Gostoptekhizdat, 1961, 241-249)
AA. I
`Z~T: In the presence of Pt/C paraffin hydrocarbors having>
carbo-,
"toms in their longest chain are cyclized into cyclopentane
ho:zolo ues.
T'he process is called C dehydrocyclization as distinct from
the reaction
5
o--:' the formation of hexamethylenes from paraffins and their
subsequent,
a-"omatization which proceeds under the sarae conditions (and
which is
called C6 dehydrocyclization). C 5 dehydrocyclization is a
straight
-j--,ocess, which proceeds without preliminary or subsequent
isor-erization
.- t I
lie carbon chain. It is demonstrated by thermo4yna:nic
calculations
o
'low (-Ath increase in temperature) the concentration of cyclic
lVarocarbons increases when they are in equilibrium mixtures
with "he
r'n rd 1 /I
4

S/03 1 /62/000/012/02 31063
Caialjtic dehydrocyclization oX paraffin ... B1606/B101
.dondink; parL,'fins rmixtures of n-pentane (1) and
-cyclopentane (11'~
corres 4
n-hexane (III) and methyl cyclopentane (IV), n-heptane (V)
and
I6,2-dimeth.~l cyclopeitane (VI), (V) and ethylcyclopentane
(VII),
2,2-dimmethyl pentane and 1,1-dimethyl cyclopentane, 3-ethyl
pentane (Vl~-'I)
z:. " d V 1 f~ -Hydrocarbons of normal and iso structur'e
were introduced into
-~)-.,e G- dehydrocyclization reaction (Pt/Ct 3100C, volume
rate
0.2 hours The aromatic and olefinic hydrocarbons which
formed Ln
5:30.1-1 cuantities were saparated by chromatography on
silica eel, %~:hilz;-~
~;.-a :J--raffin-naphthene part was subjected to precise
rectification; the
'-nz-.u!o.---ues of I were identified by their constants and
Raman s-ject::-a.
The -earaffin -hydrocarbon, the product of C 5
dehydrocyclization, the
I
J.
n the yield of arom4tio hydroca,rbons in ~~J -and the yield
of oiefinz; L-,
,,, are given as follows. III, IV, 5 ~- 4, 1.0 - 1.5, 0-5. -
0.9i "', cis an"
ti,ans VI and VII, 10, (a triple pa.%sin- throujh), 4 - 5, 1
- 2-1 n-~)ct-nc,
111rz,.ns-1-methyl-2-ethy1 cyclopent aze (I~) and n-propyl
cyclo-jentane W),
1, 0-5 - 1-5i VIII, VII, 12, 1 - 2, 0.7i
2,2,4-trimet'1111.11 ,entane
;,1,'-tx-imethy1 cycloj)antane (XII), 25 - 30, 5.5,
-e
2 2,3 -im thyl pen ane, 1,1,2-trimethyl cyclo-aGntane (X~
O~%rd 2/4

Sloa 02/000/012/027/00'3
101
r,.Aal,ytiQ dehydrocyclization of paraffin...B166XB,
2,3,3-tr�=et.,,yl pentane, XIII, -. C5 dehydrocyclization of
I too1--
.-AaOe 0'11~~ at 350 OC, th,e yield of 11 was 4-5X. The
C5dehydro-
cycliza-tion reaction is also extended to benzene
homolo&ues: from
n-propyl-, sec-butyl- and isobutyl benzene indan, a- and
P-methyl indan
,.-.,ere,obtained respectivelyi the yield of indan
hydrocarbons 'via's 6,.)'. The
,)ocsibility of the closin,r of the second five-momber ring
under
Qonditions of G5 dehydrocyclization in IX and X with the
formation of
.-entalane is su68ested. It is demonstrated that in the
presence of
1',1/0, i;i/c, ,ii/ia 031 OB/C and Ir/C the C
dehjdrocyclization reaction V
2 5
V
ill not ,o. R and 11 pressure retards C deh
.11 C, 2 2 5 ydrocyclization over
P'i/'C. The XII which is formed from XI under conditio.,s of
C5
dehydrocyclizution is partially isomerized (mainly with the
participation
of the gem-group) into 1,3- and 1,4-dimethyl cyclohexanes
which for:i
m.- and p-xylenes (35 and A' respectively of the aromatic
part of the
XI caialysis product). The C 5 dehydrocyclization reaction
proceeds
Card 3/4

S/081/62/000/012/023/00'3
Catalytic dehydrocyclization of paraffin...B160101
'inG to a null order; the value of the apparent a6tivution enardi
accor,
Of C- dehydrocyclization of 111) VIII and XI io 20 kcal/mole, for
C5
dehydrocyclization of alkyl benzenes it is 27.5 kca-l/,Mole. It. is
sun-grested that the active (for C dehydrocyclization)
conformation for
5
VIII, and particularly XI, is achieved more easily than for normal
paraffin hydrocarbons. It is assumed that the C 5
dehydrocyclization
reaction proceeds according to a molecular mechanirm through a
trans.,tion
state, in addition to which there is a geometric correspondence
between
the latter and the surface of the catalyst. Abstracter's note:
Complete translation.

SHOKOVA, E.A.; MO,43V, S.I.; STERIN, Kh.Ye.; KA~KIY, B.A.
Contact conversions of cycloBetane in the presence of an
alumina-
chromium oxide catalyst. Neftekhimiia 1 no.l-.28-32 Ja-F '61.
4MIU 15:2)
1. Moskovskly gosudarstvennyy universitet,, kafedra khistia
nefti
i komissiya po spektroskopii AN SSSR.
(CycloUctane) (Catalysts)
N~,F,

SHOKOVA, R.A.1 XHROMCM, S.I.; WANSKIrs B.As
Catalytic mathod for pl*par-ing cis-bicyclo-(O, 3p
3)--octane.
Neftekhimiaoi 1 n0-3:353-355 My-,To 161. (MM 16:11)
Is MookoveNly gosudarotverwy univeraitet imeni
Lmonosova,,
kafedra kh1mU nefti,
4`
Ri

UM-SKIY, B.AO DDROGOCHINSKIY, A.Z.; ROZENGART, M,L, LYUTER,
A.V.;
NOVP M.G.
Effect,of the feed rate on the process of aromatization of xane
over a aluminum-chromium eatal t. Kin. i kat. 2 no,2:251=
1 ~10!
V, ye
Mr-AP (MIRA 14:6)
1. Insti ut organicheskoy khjmij AN SSSR imeni N. D. Zelinskogo
i Gorzne skiy neft~oy nauchno-iseledovatellskiy itstitut.
Orixane)
(Arnmatimation)

KHROMOVI S.I.; SHOKOVA, E.A.1 STERA., Kh.le.;
KAZANSKIY, B.A.v akademik
Contact tranal,ormations of cyclo6otane in the presence
of a nickel
catalynt. DoILLAN SSSR 136 no.5zl.112-11-15 F 161.
.(MRA 14:5)
1. Moskovskiy gos.universitet im. M.V.Lomonosova.
(CycloBotane)

XOZINAP M.F.j I.MKINA., M.Tu.; ZUBAPIVA., N.D.; SAFONOVA,
I.L.1 SKURATOV, S.M.;
KAZANSKIY B.I. akademik
Heat of combustion of some phenyloyclopropanea, Dokl*AN SSSR
138
no*4:843-045 Je 161~ (MIRA 14:5)
1. Mookovskiy gosudarstvenWy universitet imeni
M.V.Lomonooova i
Institut orgaideheakoy khipii imerd N,D.Zelinskogo AN SSSR,
(Benzene) (Heat of cokbustion)

LUKINA, M.Yu.; ZOTOVAY S.V.,- MARKOV, M.A.; OVODOVA, V.A.;
_~LZANLIIY II.Al
akademik
Transformations of iso~ropenylcyolopropanwin the presence of
kieaelguhr. Dokl. AN SSSR 139 no.2:381-384 Jl 161.
(MnU.14:7)
1. Institut organicheskoy khimii im. N.D. Zelinskogo AN
SSSR.'
(Propene) (Kioselguhr)

ALEKSANYAN, V.T.; SUERIN, Kh.re.; UKHOLIN, S.A.;
BRAGIR, O*V.;
LIMHWI A.L.; HIMMUS -fe,A.1 SM3MOVAl E-N-1 TYUNIKINA,
N.I.
KA=KIY, B.A.
Ra- spectra of certain hydrocarbons of the benzene
series
havong one o-r two side chains. Izv. AN SSSR.
Otd.khim.nauk
no.8:1437-14,0 Ag 161. (MM 14:8)
1. Komissiym po spektroskopii AN SSSR i institut
organicheskoy
kb'Tn" im. N.D. Ze3inskogo AN SSSR.
(Hydrocarlions-Spectra)

STIMM, Kh.Ye.,- AUMIANIAN, Y.T.1 UKHOLIN, S.A.;
BMIR) O.V.:
ZAVRIIDVA., A.Ire.; ZOTOVA, S.V.; LIHEMM, A.L.1
MIKHAYLOVA, Ye.A.
SMIRNOVA, E.N,.- STERLIGOV, O.D.;__r.= A.
Raman epe~tra of isome tri.. and tetraalkylbonmnes
and condensed
aromatic hydrocarbons. lzv'. AN SSSR. Otd.k-him.nauk
no.8:1444-
1450 Ag 161,. (MMA 14-.8)
1. Yxmisiiya po spektrookopii AN SSSR i Inetlitut
organiaheakoy
khixdi im. N.D. Zelinskogo AIR SSSR.
(Benzene--Spectra)
(Hydrocarbone-Spectra)

rjkLZA)KISKI , B.A., DOMaOCHINSKII, A.Z., ALIM,
V.S., KASIMOVA, A.P.
Catalytic dehydrogenation of IV-drocarbons,
Report presented at the 12th Gonfenace on high
molecular weight
compounds, devoted to monomers, Baku, 3-7 April 62
r ~y

GAYUI, Rem 2grust [Ha
S12 Rene-Just]; SIIAFRANOVSKIY2 I.I., prof.;
ZABOTKINA.. 0.. translator); STRATANOVSKIY,
G.A.[transiatorl;
SHUBVIKOV., A.V., akademik,, red.; BOM , G.B., redo;
PETROVSKIY, I.G., akademikp red.; ANDREYEV, W.N.y
akademiks red.;
KAZAVSKIY$ B.A., akademik, red.; YUDIN, P.P.,
akademik-, red.;
DELOTE, B.N., red.; SAYJLRIV, A.M., red.; ZUBOV,
V.P.)-prof.,red;
LEBEDEV~ D.M., prof., red.; FIGUROVSKIY, N.A., prof...
red.;
KUZNETSOVy I.V., kand. filos. nauk, red.;
02110BISHIII, D.V.,kand.
istor. nauk, red.; SUSHKOVA, T.I.j red. izd-va;
WIRNOVA, A.V.,
tekhri. red.
(Structure of crystals; selected works) Struktura
kristallov;
izbrann.ve trudy. Sogtavlenie, stattia i primechaniia
I.I.
Shafranovskogo. Redaktsiia A.V.Shubnikova i
G.B.Bokiia. Mo-
skva, Izd-vo Akad. nauk SSSR, 1962. 175 p. Translated
frox,the
French. (MIRK 15:3)
1. Chlen-korrespondent Akademii nauk SSSR (for Bokiy,
Delone)
Samarin).
(CrystallograplW)

KAZANSKIY,-B,A,_,_akademik; REUTOV, O.A.1 BYXOVt G.V.,
kand.khimicheskikh
nauk
One hundred years of the theory of the structure of
organic c=
pounds. Zhur. VKHO 7 no.3:242-249 162. OURA, 15:6)
1. Akademiya nauk SSSR (for Reutov).
(Chemical structure)

NAIJIAPETYAN, L.A.; SAFONOVAs I.A.; KAZANSUY, B.A.
Reaction of Isoprene witb methy-ne iodide and a
zinc-copper couple.
Izv. AN SSSR, Otd,khim,nauk no,5:902-905 M~r 162. (MIRA
15:6)
1. Institut organicheskoy IdUmii im. N.D.Zelinskogo AN
SSSR.
(Isoprone) (1-lethane)

KAZAMKIYp-a*A,; DOROGOCH114SKIY A.Z.; ROZEILARZ, M.I.;
TYUNIKIM, N.I.;
'~-- - -----KUZNETS OVA) I.Me; iiFITA, A.V.;
KETROFANCIV, M.T.
Aromatization of mixtures of n. hexane with
2-methylpentane.,
with 3-methylpentane or methyloyclopentane. Izv.Ali
SSSR.Dtd.
khim.nauk no.7:1308-1309 Jl 162. (IMA 15:7)
1. In~titut or anicheskoy khimii im. N.D.Zelinskogo AN
SSSR.
~Aromatization) (Paraffim )

BUZLOV., G.A.; KAZAXSXII', B.A.
Results of work on prospecting by the use of radio
waves in
Karamazar complex ore mines. Uch. zap. SAIGIMa no.8:
167-175 162a (MIRA 17-1)
1. Sredneaziatakiy nauchno-isaledovatellskiy institut
geologii. i
minerallnogo sy-r1ya, Tashkent, i Severo-Tadzhikaknya
geofizicheskaya
ekspeditsiya.

MMZAXEVA, A.K.; MAGINA, N.V.; STERIN., Kh.Ye.;
KAZLNSKIY,, B.A.
Catalytic conversions of apiro (4,5)deoam on a platimim
catalyst.
Neftekh4mia 2 no.1:31-36 Ja-F 162* (MMA .15:5)
1. MoskovsIdy gosudarstvennyy univereitet, kafedra
khlydi nefti,
i Kominsipt po opektrookopli AN SSSR.
(Spirodecane) (Catalysts, Flatimm)

YELAGINA, N.V.; nIZAYEVA, A.K.; LAVRENOVA, A.S.;
KAZANSKIY, B.A.
Synthesis of spiro[5,5]undecane. Neftekhimiia 2
no.3:265-269
yq-ie 162. (MIRA 15:8)
1. Moskoviskiy gosudarstvennyy universitet imeni
Lomonosova,
kafedra khimii nefti.
(Spiroundecane)

BAIENKOVA,
j Ye.S.; KHROMOV, S.I.; SHOKOVA, E.A.; KUCHERYAVAYA,
N.N.;
ST&RIN., Kb,.Ye.; KAZANSKIY, B.A.
Catalytic conversions of cycloheptane. Neftekhimiia 2
no.3:
275-279 IV-Je 162. (MIRA 15:8)
1. Moskovskiy gosudarstvennyy universitet imeni
Lomonosova i
Komissiya po spektroskopii AN SSSR.
(C.Ycloheptane) (Catalysis)

SHOKOVA, E.A.; KHROMOV, S.I.; BALENKOVA, Ye.S.;
BOBROV, A.V.; STEM,
Kh.Ye.; .~AZANSKIY, B.A.
Catalytic conversions of cyclononane and cyclodecane
in the
presence of nickel catalyst. Neftekhimiia 2
no.3s280-287
My-Je 162. (MIRA 15:8)
1. Mo3kovskiy gosudarstvennyy universitet Imeni
Lomonosova i
Komissiya po spektroskopii AN SSSR.
(Cyc:Lononane) (Cyclodecane) (Nickel catalysts)

AGRIKOLA, Georgiy [tgricolaj Georgl- GALIMINAS,
V.A.[translatorl;
DROBBSKIY, A.I.[translatorl; sELrKHARDIN, S.V., red.;
UY
"L RCJV-SI' , I.G., akadavIkp red.; ADDREYEV, N.N.,
akademikp
red - YJLq1ZK-TY-r4-6A., akadorLik, red.; YUDIN,
P.F., ukademik.,
red:,. -D-
) EUVE, B.11., red.; SAM.0, AJI.p red.; MDR, V.P.9
prof., red.; LEBEDEV, D.M., prof., rcd.;
FIGniOVSKIY, N.A.J.
prof., red,.; KUZITETSOV, I.V., doktor filos. nauk,
red.;
BOHODINA, RX., red. izd-va; YEPIFANUVA, L.V., teklm.
red.;
DOROKHMAI, I.N.,, takhn. red.
[Mining and metallurgy; in twolve booksjO gornom
dole i metal-
lxwgii; v dvenedtsati knigak-h. Red.
S.V.ShukhrArdina, perovod i
primechan-Tia V.A.Gallminasa i A.I.Drobinckogo.
Moskva, Izd-vo
Xkad. naWc SSSH, 1962. 597 p. (MMA 15; 8)
1. Chlen--Irorrespondent Akademii nauk SSSH (for
Dolone, Samarin).
(Mines and mineral resources)
(Metalwork)

KAZANSKIY B Agg DOROGOCHINSKIY, A. Z.; STERLIGOV, 0.
D.; IIYUTER, A. V.1
M. L.; VAZAROV, P. S.
Delqdrogamition of isopentane to inoanrlenes w- in
altmino-
silicate cata3yet. Neftekhimia 2 no.42448-456 JV,4,162,
(MIRA .15910)
1. Institut organicbeeko7 kbimii AN SSSR izeni N. D.
Zelinskogo
i GromensIdy naucbm-iseledovatel'okiy neftyanoy
inatitut.
(Butane) (Butane) (Aluminoailicates)
IJ

GOSTUNSKAYA, I.V.; LEONOVA, A.I.; DOBROSERDOVA,
N.B.;,,.XAZANSKIY, B.A.
Isomerization of hexenso under conditions of
liquid-phage
bydrogenation in the presence of palladium black.
Nefte-
kbirmila 3 no.!+:498-502 n--Ag 163. (MIRA 16::L1)
1. Nbskovskiy gosudarstvennyy universitet imeni
M.V.
Lomonoscva.

KMANSKIYp, ~.A*; DOBROSERDOVA, N.B.-, BAKHKETIYEVA,
G.S.;
GOSTUNSMAYA, I.V.
Isomerization. of hexeneB in the presence of
palladized
acal. Neftekhimiia 3 no.4003-506 Jl-Ag 163. (MIRA
16:11)
1. Hookcrvskiy gosudarstvenny7 universitet imeni
loomonosova,
khimichetskiy fakulltet.

KAZANSKIY, B.A.; GOSTUNSKAYA, I.V.; CHESNOKOVA, S.Ye.;
DOBROSEIMOVA, ,.B.;
A.I.
Stereoisomeric conversions of individual cis- and
trans-3-methyl-
2-pentenes in the presence of aluminum oxide calcium amide.
Nef-
tekhimiia 3 no.61871-875 N-D 163. ONIIRP. 170)
1. Moskovskiy gosudarstvennyy univerai-tat im. Lomonosova,
kafedra
khiinii nef ti.
KAZA14SKIY,--B 14SKIY, A.Z.; ROUNGART, ILI.; GITIS~ K.M.;
A.;: DORUGOCHJ
-IiUTER, A.V.; 14ITROFANOVy M.G.
Effect of the length of an alumina-chr6miap-potassium
catalya".. layer on'the hromatization of n-heptane.
KinA lait. 4 no.2:315-318'th,-Ap 163. (mA 16'75)
1. Institut orgenicheakoy khimii AN SSSR imeni N.D.Zeliw&ogo i
Groznen.skly neftyanoy nauchno-.issledovatellakiy inBtitut.
(IlDptane) (Aromatization) (Catalysts)
L

3
KAZANSKIY B.A.; DOROGOCHIN,',~Y, A.Z.; ROZENGART, M.I.;
KIJZNETSOVA, Z.F.,
-Lyul A.V.; HITROFA OV, lliG.
Changes in alumina-chromia catalyst3 during the
aromatization of
n-hexane. Kin.i kat. 4 no.5t768-772 3-0 t63. (MIRA
16:12)
1. Institut organicheskoy khimii AN SSSR imeni
N.D.Zelinskogo
i Gromenskiy neftyanoy nauchn,,-issledovat-ollskiy
institut.

LIBERMAN, A.L.; BRAGIN, O.V.; GURIYANOVA, G.K.;
KAZANSKIY, B.A.
Sone-problems in the kineticig of hydrogenolysis of
eyelopentane
hydrocar,bons on platimi2ed coal. Report No.li
Hydrogenolysis of
methyl,-,and ethyleyelopentanbe. Izv. AN SSSR
Ser.khin. no.10i
1737-1744 0 163. (MIRL 17:3)
1. Imetitut orgaOnheskoy khimii in. N.D.Zelinokogo AN
SSSR.

BRAGIN, O.V.; GURIYANOTA, G.K.; KAWSKTY B.A.# akademik
Tntea-conversions of cis- and
trans-11,2-dimethyloyolopentanes
in the prevenoe of platinum catalysta. Dokl. M WM149
no.3--
591-!594 Ja 163. (MM 102)
lo Institut organicyeakoy kbimii Ime F.D. ZeliinBkogo
AN SM*
(cyclopentane) (Stwooobeadstry)

BRAGIN, O.V.; LIBFRMANp A.L.; GURIYANOVAp G.K.;
KAZANSKIY, B.A.,p akademik
Hydragenolysis and reciprocal.transitions of cis- and
trans-
1,2-dimethyloyclopentanes in the presende of rhodium,
osmium,
iridium, and palladium catalysts. Dokl. AN SSSR. 152
no.4:
865-868 0 163. (MIRA 16%11)
1. Institut organicheakoy khimii im. N.D. Zelinakogo
AN SSSR.

NESMEYANOU, O.A.; LUKINA, M.Yu.; KAZANSKIY, B.A.,
akademik
Ccuparative reactivity of hydrocarbons of the
cyclopropane
setries. Dokl. AN SSSR 153 no.ltll4-117 N 163#
(MIRA 17:1)
1. Institut organiclieskoy khimii im. N.D.
Zolinskogo AN SSSR.
.4 l'-.

NESMEYANOVA, O.A.; LUKINA, M.Yu.; KAZANSKIY, B.A.,
akademik
Reactivity of cyclopropane hydrocarbons as dependent on
their
structure. Dokl. AN SSSR 153 no.2t35?-359 N 163. (MIRA
16.-12)
k,

GWTUNSKAYA, LV.; MIRONOVA, V.A.; DOBROSEIWOVA, N.B.;
KAZANSKIY,
B..L, akademik
Chemical nonequivalence of active foms of hydrogen
eorbed
by a skeleton nickel catalyst. Dokl. AN SSSR 153
no.5:1071-
1072 D '63. (MIRA 17i1)
1. Moskovskiy gosudarstvennyy universitet im. M.V.
Lomonosova.

N. B. ; Eikll:R~L'l I Y?VA, G..% ; I. G"-",TU I
KA7Ajj11
,;f'ly B.A.
Displacement of double bond3 In hexE;-.cc, In tho
prez~enca
platima a-atrilysts. Noftpl.hlmlla 4
ILIL
khImicbeskiy f!~kulttet.

MAGMA, N.V.; hIRZAY2VA, A.K.: STMIN, Kb.Ye..
B."B'(011, A.V.; KAZZOSKIT,
D. A.
Catalytic conversion of opiro-f.546)-dodecane on a
platinum
catalysts. Neftekhlmlia 4 no.2:4'1"Z:1-245 M--AP,164
(MYL4 1-7:8)
1. Moskovskiy gosudarstvenny.,y urdversitet imeni rom
onosova.

G C, -, 3 F'J* ! %' ~ 1 K A Y A1 V. - CM iFuc Ch
I ir,--'dng ' j-,' E '
) . t j , , -.As
Hydrogenolysie of cyclopentund hyeirocarbnn3 In
the presen,-t
of platinum depogited on alxrainum exiie. i zv.
~liirr. no. 5%832-836 Xq 164. (V-,!?A 1-17r6~
1. 114oskovskiy gosudarstvennyy aritver!3~,Aot
im. M V.~o=nz:~scvr-

BAIZNKOVA, Ye.S.; ALYBINA, A.Yu.; AVDEYEVA, T.I.;
KHROMOV, S.I.;
KAZANSKIY, B.A., akademik
Catalytic conversions of cyclododecane in the
presence of
platinized carbon. Dokl. AN SSSR 155 no.1:118-121 Mr
164.
(MIRA 17:4)
1. Moskovskiy gomidarstvenn~y universitot im.
M.V.Lomonosova.

L I B*,J,MP)4' , ft. 11- 1 hHAG 7 'i ? 0 . li .
;*N")K I Y, , li -A - , a ~-u I ?~
fiydroj,t,n-)Iyaio of cyc,!r-,ht-xalr-t3 with
thl-k formht.t n, rJ -,
at atmosphc-sric provstirA. Dokl . AN S!,SR 156
P,,. r, !'1 114- 1117
I -i a,l Lu k
".) 1(41 .M., A " '
.1. Irtatitut orgunicht-iknj 'k-nlnili ~'-. .~N

- - - . - -, .-?I. i.~V~~- -% 7? -~i -"' ,
-- K4zANSKlyp DJt. . okonomiat
Two suggestions for reducing unfinished construction and
accelerating the commencement of the use of new buildings
and structures. Trudy KTE1 nO-15~454,1+57 161. (IURA 14:12 )
(Cmatraction industry)

GAMIN, I.G.; KAZANSKIY B M naucbmjy red.; WIN.,
V.M..,, red.;
Y=66 A.S., red.; USPENSKIY, V.V.p
red.; LEYKIN, B.P., red.; SaSS, M.Ye., red.;
GIAZUROVA,
Z.M., red. izd-va; BOROVNEV, N.K.,, tekhn. red.
(Problems of rytbm and operation completion in
construction)
Vaprosy ritmichnosti i zadela v stroiteltstve.
ftskvap Gos
stroiizdatp 1962. 168 p. (HIRA .15*9)
(Construction inaustry)

KL=KIY. B.H-, insh.; JKUFFMAZI, Ya.M.,
kand.okon.nauk
Overhead expenses in pipeline construction. Strqi.
truboprov. 7 no.10:26-28 0 162. (MMA 15: 11)
(Pipelines-Cost of construction)'

K.AZA'SKIY, B.A.; DOROGOCHINSKIY, A.Z.; S'MLIGU,
O.D ; LYUTEIR, A.V.;
- - M.L.; NAZAROVA, M.P.; RE 4' IVIAS~iILI, A.N.
Studying the dohydrogenation of isopentane on K-544
and X-5
finely divided catalysts. Trudy GrozNlI no.
15:241-253 163.
(MIRA 17:5)

KAZANSKIY,4 A DOROCOCRINSKIY, A.Z.; ROZENGART,
I.I.I.; LYUTER A.V.;
MITROFANOV-, M.G.1 BRESHCHENKO, Ye.M.; KALITA, L.A.;
OOLIDSHTEYN,
Yu.A.; AFANASIYI;V., A.1.; MAKARIYEV, S.V.; ZAMANCV,
V,V.
Dehydrocyclization of normal hexane. Trudy GrozNII
to. 15:
254-264 16). (MIRA +-5)

HAL~IVIVA, Yu.%; A. Tu.; KI(j,"'Ift" 7" idi" I'!
Ca c~- of cyi-71 at::, It the T' a c f Ei
?if, n ,, T!
t-,-,-3r.ny-;. un

GOSVNSKAYA, I.V.; LEONOVA, A.I.; KAZANSKIY, B.A.
Stereolsomeric converaions of individual cJO- rind
tranti-3-
mathylpentenes-2 under conditiono of catalytic
hydrogenation
in the liquid phase. Neftekhimia 4 no.3:379-381 W-Je
164.
(mIRA 18:2)
1. Moskovskiy gosudarstvennyy universitet im.
M.V.Lomonosova,
KhImicheskiy fakulftet.

ROZENGART, M.I.; GITIS, K.M.; WMZKjX4 B.A.
Developmant of an alumina-chromo-potassium catalyst
for the
dehydrocyclization of paraffin hydrocarbons.
Neftektilmia 4
no-3:406-412 My-Je 1640 (MIRA 18-2)

MIRZAYEVA, A.K.; YELAGINA, N.V.; STERIN, Kh.Ye.1 BOBROV,
A.V.; KAZANSKIY, B.A.
Catalytic convers4 ns of n-a--,ri benzene on a platinum
catalyst.
Neftekhimia 4 no.31417-420 MY-Je 164. (MDU 18-2)
1. Kafedra khimii nefti Moskovskogo gosudarstvennogo
universiteta,
i Komissiya po spektroskopii AN SSSR.

GOSTUNSKAYA., I.V.; GO CHIN-FYN [Kuo Chlin-fgng];
KAZANSKIY, B.A.
Hydrogenolysis of cyclopentane hydrocatbons in the
presence of
platinum deposited on silica gel. Izv. AN SSSR. Ser.
khim. no.6:
l(Y73-1077 Je 164.
Catalytic transformatims of cyclopentane-and its
homolQgs in
the presence of platinum deposited on
aluminosilicate. Ibid.:
1078-1082 (MIRA 17:11)
1. Moskovskiy gosudarstvennyy universitet.

Kinutic-l") of the formation of benzene in the
dehydrocyclization of
n-lif-xitne on an aluminum-chrome-potanaiwa cat,a1yat.
flafteklilvila 4
no.4: 1)0'.1-566 JI-Ag 164. (Mim n: 1o)
1. fru~titk-,A organ 1 clips key khIndi Im. N.D.
Zalinskogo Ali' SSSR.

-NE

ROZENGART, M.I.; MORTIKOIT, Ye.3.; KAZAN.S.KlY,
B.A., akademik
----
DellYdrocyclization of n-heptenes on aA alumina-
chromi a-po tas s i tim
catalyst. Dokl. AN SSSR 158 no.4:911.-914 0 164.
(HIRA 17-11)
1
~. Institut organicheskoy khimii All SSSII.

akademik

ranuforralt~ozl-"

!~ataJyzqLo

Tir-
cf mLtjjy'l~,yvjGnDl,%
AN ssni 158
f
',Ice
0 t(l"

41 3
ruj*

-X~

USPENS!, I Y , Va LA-11Y V 3i -I 'Y6vicll; slUiAYiI,,4LN ,
Ni-'K I ,a I I
KA~l-.!NSKlY, muAn. red.; GIAZ*!:,l':Vt-,
........... .
[E,usjrIo,4j accounting in ck)r,structiunj KliczWoLvermyA
ra:!-
chat v r-troiteltsWo. M-Oskvap Str(AiLdat~ 1%4. 1 ~ 1-1.~ p .
(MILRA lgi---)
-Vq
-Ai
N

I- P

YEKELICHIK, Moisey Solomonovich; M!11ER, Natan
Semenovich),
SOSNGV, Rudollf Llvovich; SIEKHTMJU!, Aron
Yudkovich;
KAZAllSKlY,, nauchn. red.; IZYKINY B.P.J. red.;
MIA~Lljdlll, V.I., red.; USPEENSKIY, V.V., red.;
MIASS,
M.Ye., red.; GERASIMOVA, G.S., red.
(Improving the economic work of contracting
organiza-
tions] Sovershenstvovanie ekonordeheskoi raboty
podriad-
nykh organizatsii. Moskva, Stroiizdat, 1964. 96
p.

ACC NRi AP60211397 SOURCE CODE: UR/0020/66/169/202/0361/0361;
AUTHOR: Yakhontov, L. N.; Pronina, Ye. V.; Rubtsov, M. V.;
Kazanskiy. B. A.
(Academician)
ORG, All-Union Chemical and Pharamceutical Scientific Research
Insti*~ute
(Vsesayuznyy naucbno-iseledovatel'okiy
khimikp-farmatseyticheskiy inot-itut im.
S. Ordzhonikidze)
TITIZ: Anomalous course of the FLocher reaction
dOURCE: AN SSSR. Doklady, v. 169, no. 2, l966, 361-364
a
TOPIC TAGS: benzpyridoastriazone, Fischer reaction., Cqe,41e
iCoMAL7u.010,
CVe'1dH'C4w'V0 'Ve. 6#9MIeA4 leeAle;r-dAl
ABSTRACT:
It was found that in boiling HC1, the reaction of Is with
cyclohexanone,
in addition to the normally formed Ila, also yielded (36.6%,
based on
i.cyclohexanone) thepreviously unreported tricyclic compound
Ills, mp
..77-78*C, i.e., under dertain conditions the Fischer reaction
proceeds
,anomalously. The cyclization proceeds via a partial hydrolysis
of In
Card
ACC NRs AF602097
o-ob.-
R
1A ~oln I
R-H
It. CH,
to form cyclohexanon e. which adds at the C-N double bond of the
'hydrazine Is, with subsequent enolization of the ketone and
elimination
!of H20.- Under the same conditions, Ib reacts with
cyclohexanone to form
!IIIb in 27.6% yield, mp 107-i08%. Orig. art. has; 1 formula-
[W. A 50.,- CBE NO- 101
SUB GoDrs: OT/ SUBM DATE: 1690v65/.ORIG REF. 002/ OTH MF: 008/

KAZAT,ISKIY. B.A.j akademik; SOBOUN, Ye.V.,-
Al,FY6,d,'YM', V.T.:
L.A.; LIKINA, M. Yll.
Certain properties of spiro-[2,4]-hopta-193-di-ene.
Dokj. AN SSSR
159 n0,4&839-842 D '64 (MIRA l81l)
1, Inatitut organiche.9koy khimii Im. N.D. Zellnskogo
i Komissiya
po spektroskopil AN SSSRe

BALFNKOVA, Ye.S.; KHAFIZOVA, N.A.; KHROVICV, S.I.;
KA"I'ANSKY, B~A,
Conversions of mothylcyclooct,ane in the presence of'
pl-atinim,
catalysts. Dokl. AN SSSR 161 no.6:1329-1332 Ap 165.
(14TRA 18, 5)
1. Moskovskiy gosudarstvennyy universitet im.
M.V.Lomoncsova.

ACC NRI AP7013155 SOURCE CODE: UR/0020/66iI71,003/06WO618
AUTHOR: Bragin, 0. V.; Kulllov, 0. F.; Libernan, A, L,; Kazanskly,
B. A.
(Acadenician)
ORG: Institute of Organic Chemistry Im. N. D. Zelinskly, AN SSSR
(Instltut
organicheskoy khimli AN SSSR); Moscow'State University Im. 11.'V.
Lomonosov
(Moskovskiy gosudarstvennyy universitet)
TITLEt Behavior of benzene and some other organic compounds in a
focused
loser bearn
SOURCE: AN SSSR. Doklady, v. 171, no. 3, 1966, 616-618
TOPIC TAGS: laser emission,. laser beam, benzene, acrylonitrile,
hydrocarbon,
chromatography, EPR spectrometryl UV spectroscopy
SUB CODE: 07,20,11
"ABSTRACT: The authors study the effect of laser emission on
comparatively
simple organic molecules which transmit light in the visible region
of the
spectrum. Benzene, n-heptane, cyclohexane, cyclopentane,
cyclopentene,
1,2-dichlorocyclopentane and acrylonitrile were studied by exposure
to
-laser emission at room temperature. The experiments were done in
hydrogen,
'air, and a partial vacuum. Chromatographic, ultraviolet and electron
Card UDC: 547.532
073-3 0966
ACC NR: AP7013155
paramagnetic resonance analysis shoved that elemental dissociation
under
the effect of laser emission is characteristic for.an entire series
of
organic compounds although the process takes place more easily for
some
than for others. The authors thank V. I: SHLYAPOCH14IKOV and A. A.
SLINICIN for taking and idea:~ifving the ultraviolet.and electron
paramag-
zip
netic resonance.apectra jj~i: 40'35

I belle
27675 Osobenno3 Ti funktaiy I gipofiza U r-yb a
portsionqu
Arome taniym, (gistolo ieksperime inaledov
trudy laboritorli c#wv riWvodetu&j Tp 11, 19 9p
s. 64-120 --- Bibliogn 56 nazv.
SO.- Knishnaya Letopis,, Vol. 1,, 1955

KAZANSI,h.- B.N.
27865. VIyunovaya yedinitsa (VE) cUyn ivaerenip gonadotopnoy
aktivnosti
preparatov gipofiza ryb. Trudy Laboratorii osncv rybuvodstwi, t
11, 1949
d. 201z-07. - bibliogr: 9, llIZV.
SO: I.,ctopist 'U'hurn!tllnykh Statey, Vol. 37, 194-9
wa

USSR/Medicine -Fish Apr 49
Medicine - Hormones
"Locating the Antagonist of the
Melanotropic; Hor-
m6ne in Hypopbyeis of Bony FIgh,- B. N..
Kazanakiy,
G. M. Persor, Leningrad State U imeni A.
A.
Manor, 4 pp
"Dok Ak Nauk SSSR" Vol LXV, No 4
For experiments, used icetone-treatecl
bypophysis
of carp, prepared from males and females
in pre-
spawning state (IV stage of gonad
virility). Test
ing of these hypophyses was carried out
on male
and female groundlings in Mar-Amr 118
near the
Im
41/49T60
USSR/Medicine - Fish (Coatd) Apr 49
Lyuban station, Leningrad Rayon. Sixteen
hours
after in~ectlng a sufficient &ose of
hypapbysis
into male and female groundlings,
observed a
marked lightening of the skin, caused b7
contrac-
tion of me1anophores, along the entire
length of
the body. Submitted by Acad L. A. Orbeli,
4 Feb 49.
VW_ 41A9Tr-,7

X&MSKIT, B.N.
Function of ovarian epithelium in sexually mature
sturgeons. Doklady Akad.
nauk SSSR 81 no.4:681-684 1 Doc 51. (CLML 21:5)
1. Presented by Academician To. N. Pavlovskiy 11 September
1951.
2. Biological Institute of Leningrad State University
imeni A.A. Zbdanov.

2. U--)Sii (600)
14. !~rnbrvoloL~v
Kxperijrierital analYsis of b,-Ach-sfawning of roe of fish.
'--70o1, zhur. 31 no. 6. 1952.
9. P.onthl-;- List of .-,usz;iart ccessions, Ldbrar~, of
~;ongrc!;.,, -arch 1953. "Ilnclaroific-d-

1. KAW1SKrYj, B. N.
2. ussR (6oo)
4. Ovulation; Sturgeons
7. Extra-organic completion of ovulation
In sturgeons.
Dokl. AN SSSR 83 no. 6p 1952.
Biologicheskly Institut Leningradskogo
Gosudarstvennogo Universiteta im. A. A.
9. Monthly List of Russian Accessions,
Library Congress,
Congress, September 1952. UNCLASSTFJED.
Zhdanova
rcd 8 Feb. 1952

K A Z 01 a-- I Y, '19. 11.
Sturgeone
R
Maturing and fertilization of the egg of sturgeon. '.)oll.
AN SSF 89, Yo. 4, 1953.
Monthl- List of Russian Accessions, Library of Congrese,
June 1953. UMCLASSIFIT).

1. KAZANSKIY., B. N.
2. USSR (600)
4. Kura River - Sturgeons
7o Spawning and cultivation of the Kura sturgeon during the
autumn season., Dokl,
AN SSSR, 89, no. 5, 1953.
9. Monthl List of Russian Accessions, Library of Congress,
April - 1953, Uncl.

'USSR/Biology - FndocrinoloD-
Card 1/1 : Pub. 22 - 44/,W4.
Authors : Kazanoldy, B. 11.
Title
Nuclear clvanl;cs in the oocytes of s-,bron during c)1wire-ovcr cf
the orc,~~n-
ism into spaiaiinL state after a hypophysin inif.ction
Periodical : Dok. A14 350 98/6, 1045-1048, October 21, 1954
Abstract : Results of ey-toloL-ical investiLL-lions of the nuclear
:In the
ooc,ytcs of saliion (Acip3nror Luldonstvd-Li persient; fro'.1
moiacnt a 1iypor,,h,-,'sU injr-,-ction was
U3SR roftircll,;es (16T'-19513)
Institution : The A. A.
j-, 1. Yi, T. 111,
Presented by: AcaOc,-:-c-,,;-, 'T.
..I. Jpj ill(

PAZANSIM, B. IN.
jazz "Maturation and Fertilization of the Sturgeon Egg."
Trans. Acad. Sci.
U.S.S.R. 61), 757 (1953); "Analysis of the Process of
Egg Cell Maturation,
ovulation and Fertilization in Sturgeons," Confercrence
of Einbryologists,
Leningvad, 25-31 January 1955, PP. 11-13.
USSR-/ General Bi-_,1c)gy. Indi-~idua7 D-3 ve 1 opri-i n
B -!I
Abs Jour: Ref Zhur - Biol., No 6, 1958. 23766
Author Kazanskiy; B. N.
Inst 6-f n
g Ve
Title Analysis of Maturing FrOZe33eS of Ovicells and
Fecundation in Sturgeon.
Orig Pub: V ab.: Frobl. sovrem. embriologii. Leo Un-t~
19569
11-18
Abstract: A cytological Investigation was conducted on
nu-
clear transformations in aocytea of Kura sturgeon,
beginning with stage IV of ovarian maturity up to
the completion of ovulation, as well as the trans-
formations In the egg in fecundation. At stage IV
of maturity nucleoli disappear in the oocyte nucleus
and chromosomes begin to appear. After Injection
of a hypophysis preparation, the volume of Gocyte
Card 112
Wid Iluu.Lear Brrucrures
in Ltnurg-:;on cc_,ytss dilrse.ppear, and '[,-hat after
fecundation a new formation of nucleus occurso

Name:
Dissertation:
Degree:
Affiliation;
Defense Date, Place:
Certification Datel
Source:
KAZANSKIY, Boris Nikolayevich
Ovogenosia and adaptations connected
with reproduction among fish
Doe Biol Sci
fn-ot indicateI7
25 mar 57, Council of Leningrad Order
of Lenin State U imcni Zhdanov
21 Sep 57
BMVJ 22/~7
KAZANSKIY, B.11.
for irproving the efficiency of sturgeon culture in the Kulla.
ralley based on the analysis of intraspecific biological groups.
Uch.
sap. WU no.228-33-53 157. (MM loril)
(Mm Rive r--St urge on a) (71sh culture)

KAZANSM B.N,
= ~P-~
Experimental analysis of the seasonal reproduction of
sturgeons in
the Volga River in connection with the phenomenon of
intraspecific
biological differentiations Uchozap*IJGU noe311:19-45
162.
(MM 15:8)
(Volga River-Sturgeons) (Reproduction)

KAZANSKIY, B,N*
Experimental and histophyoiological analysis of chnnges in the
nexual
cyoles of fishes under the ipfluence of ecologic factors. Vop.
ekol.
5188-89 162. (MIRA 16;6)
1. Leningradakiy gosudarstvannyy universitet.
(Fishes-Physiolog.v) (Zoology-Eoology) (Reproduction)
UDC:- 62U.173
Card 1/2 629.13.01/06

V__ -1-V VV W 7
ACC NRj AP6033494
cally constructed, grooved coupling which assures the alignment of
the cam for a
certain travel of the spring-loaded plungers.
SUB CODE: Ol/ SUBM DATE! 30Nov64/
Card 2/2

L oe,,~_o6-,-7 E4" tr F L'1.'lT
496g___ M
ACC NR. AP602 1 4 SOURCE CODE: Uil/01,13/66/000/015/0195/0195
INVENTOR: Zhdanov, K. I.; Kazanskly, B. .; I~Aharev, V. 1:,.
39
ORG: none 18
TITLE: Variable-pitch propeller. Class 62, No. 184146
SOURCE: Izobret prom obraz tov zn,'no. 15, 19661 195
TOPIC TAGS:* aircraft propeller, propeller blade, propeller pitch
controls hydraulic
device
ABSTRACT: An Author Certificate has been issued for a
variable-pitch propeller con-
sisting of a hub, blades, a hydraulic mechanism with a piston for
changing the pitch,
and a constant-rpm governor. To prevent the appearance of negative
thrust in flight
in the event of the simultaneous action of several defects in the
power-plant system,
the piston is equipped with a raulic s1 g supportilconsisting of a
spring-
by-d idin I
supported slide valve. The valve has a regulated pressure chamber
connected by a
system of channels with a pressure regulator having power,
altitude, flight-speed,
and ambient-air-temperature transducers. [KT)
SUB CODE:01,, 13/ SUEM DATE: 3ODec64
a S t

Co,d
la

IWOW
KAZANSKIT, B.V.-. LUKIMA. M.Tu.; CHERKASHIRA, L.G.
Isomertratlon of vizTlcyclopropans in the presence of diatoma-
ceous earth. Izv.AN SSSR.Otd.khim.nauk. n0-3:553-554, Mr '59.
(MIRA 12:5)
1. Inatitut arganicheakoy khimit im. N.D. Zelinakogo AN SSSR.
(Cyclopropane) (Isomerization) (Diatomaceaus earth)
41

KAZANSKIY, D.A., kand. md. nauk (Leningrad, D-14, u1. Nekrasova,
d.40, kv.10)
Maiginal resection of the common carotid artery in the excision
of neek
tumors. Vest. khir. no.7-.19-22 JI 164. NIFLA 18:4)
1. 1z otorinolaringologicheakogc- otdelanlya 'zav. prof. N.A.
Karpov)
Instituta onkologii (dir. prof. A.I.S61't'Urov) AMN SSSR.

KAZANSKIY, D.A., kand. ri-ed. nauk
ArtIficla! hypotension during aperationa for the remova! of tumors
from the upper respiratory tracto and Lhe esophagus. i'llur.
u,~Zp. no,9.
1 corl. bol. 23 no.6:18-23 N-D '63. .17:5)
1. Iz o Lori nolaxi ngol ogi che --, k ogo )Ld(.,.!ejjj~jj
prof. N.A. Karpnv) Instiluuta onkolOC,.!;L
dcystvite~ Iny-y ohlen A,QN SSSR 1,,rof. A.] 'Sorf!Iwov)

a
-KAZANSKlY, D.A.
.... . 1, kand. mod. nauk
SYMposium on the claBsification of tumors of the upper respiratoI7
tract. Vop. onk. 10 no.1:134-118 164.
(11,11HA 17: 11)

YAZANSKIY, D.A.
..........
Regional chemotherapy of tumors of the maxilla. the tongue
a.-,d
the pharynx by the carotid perfusion and Infusion method.
Vop.
onk. 11 no.3:42-417 165. (MIRA 18:6)
1. Iz otorinolaringologichaskogo otdeleniyu (zav. - prof.
N.A.
Karpov) Insti-tuta onkologii. AMN SSSR -- kafedry torakallnoy
khirurgii i anesteziologii (zov. - prof. S,A. Gttdzhiyev)
Lenin-
gradskogo gosudarstvennogo instituta d1ya
usoversheristvovaniya
vrachey imeni. Kirova.

KAZANSM, D.A. (Leningrad, D-14, ul. Nakramova, d.40,, kv.10)
Alloplasty of the co=on carotid artery in laryngeal cancer;
a case report. Vop. onk, 10 noogilIO-112 164- (MIRA 1814)
1, Iz otorinolaringologichookogo otdoleniya (zav. - Prof. N.A.
Karpov) Instituta onkologii AMN SSSR (dir. - deystvitel'W
chlen AMN SSSR prof. A.I.Serebrov).
~'F75iP-'~~--'N~*'- V-P
11 A1.1

I:. -i*"i-~'*! T7'
KAZANSKIY, D.A.
Use of intubation anesthesia in stirgery for laryngeal cancer,
Zhur. ush., nos. i gorl. bol. 2-1 no.3:24-29 t~y~e 161. (MIRA
14t6)
1. Iz otolaringologichookogo otdeleniYZL (zav. - prof.
N.A.Karpov)
Inatituta onkologii AMN SWR.
(IAR=--CMGER) (AIUSTFIESIA)

WANSKIY D A
Problem of general anesthesia in oncological
otorhinolaryngology.
Vop. onk.8 no.7:56-63 162. (MIRA 15:7)
1. Iz otorinolaringologicheakogo otdeleniya (zav. - prof. N. A.
Karpov) Instituts. onkologii AMU SSSR (dir. - deyetv. chl. AMN
SSSR, prof. A. I. Serebrov)
(ANESTIIESIA) (ONCOLOff (OTORIIINOLAMGOLOGY)

KAZANSKIY, D.A.
-1
Device for fixing the Intubation tube in anesthesia
carried out
through an opening in the trachea. Zhur.uah., nos.i
gorl.bol. 21
no.6s7O N-D 161. (MIRA 15:11)
1. Iz onkootorinolaringologicheskogo otdeleniya (zav.
- prof.
N.A.Karpov) LeningradskogoAnstituta onkologii ANN
SSSR.
(INTRATRACIM&L ANESTMIA-EQUIPMENT AND SUPPLIES)