SCIENTIFIC ABSTRACT MINKIN, A. S. - MINKIN, V. I.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001134420011-4
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 14, 2000
• Sequence Number: 11
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

MINKIN. A.S.
...... mummustwAbAwwa
[Repair and servicing of metal-mitting muchine tools] Remont i oboluzhiva-
nie metallorezhushchikh stankov. Leningrad, Goo.naachno-tek:hn.izd-vo xmL-
shinostroit.lit-ry [Leningradakoe otd-nie) 1953. 235 P. (MMA 6:7)
(Machine tools)

KINKIN, A.S., kand. tekhn. nauk (Ioningrad)
---
Reorganiss the eyeten of planned preventive maintenance of
manufacturing equipment. Shysin. prom. no.4:12-14 Jl-Ag 159.
(MIRA 13:2)
(Sewing machines-Naintenance and repair)
(Clothing industrr)

HASLMMXOVA, T.F., kand. takhu. nauk; MNXIN, A.S., kand. tekhn. nauk
Qualifications of young technicians. Shvein. prom. no.4:24-27
JI-Ag 159. MRA 13:2)
l.Leningradskly tekhnikus legkoy promWahlonnosti.
(Technical education) (Glothing industr7)

MINKINg Anato Samailovichp kand. tekhn. nauk; CiLkITERZON, Yevgeniy Ki-
------~roiovich; ANDREM,, X.-I. t red.; FREGER9 D.P., red. izd-va;
GVIRTS9 V.L.v tekbn.'red.
[Repair and operation of certain kinds of machines and electric
equipment at garment factories in Leningrad] ROMOnt i ekpluata-
tAia nekotorykh vid6v tekhnologicheskogo,i elektrotekhnicheskogo
oborudovaniia na i3hveimykh fabrilrakh Leningrada; obzor. Leni adt
1961. 87 P. (MIRA 24:7T
(Leningrad-Clothirg industry)

VMKIN, A.S..,kand.tekhn.nauk; GELIBERG, B.T.
Using resins in repairing. Mashinostroitel' no.11:16-19 N 161.
(KLRA 14:11)
(Epoxy resins)

KINKIN, A.V., inzhener.
Setting brick clay in double lengthwise rows on cars. [Suggested by
A.T.Makin.] Rats.i isobr.predl.v stroi.nol46:16-17 '56. (KLVA 10:2)
(Bricb--king)

T, // i/, rj, i~,-`
i , "-1 1
HnMIN, A.T. Insh.
~---~-I-rcu-,-atlng waste heat in tunnel
v strol. n0.3:74-75 157.
(Bricks-Drying)
Vr
dryers. Rate.
(Waste heat)
Isobr. predl,
(KIM IItI)

AVDUSIN, D.A.; HUMORTSEV, I.D.; BTJDAYEV, D.I.; RTABKOV,
G.T.; IN, A.M., ITANOT, I.P.; XROLIX, D.; N.V.;
VALIZDTA, X.,-red.; 7ZLIPPUKOVA,~K., tekhn.red.
[Smolensk; a gutdebook] Smolensk; spravochntk-putevoditell.
[Smolensk] Smolenskoe kutzhnoe Izd-vo, 1957. 217 P. (KIRA 11: 1)
(Smolensk-Desertption)

SOV/ 137-58- 7- 143 H
Translation from: Referativnyy zhurnal, Metallurgiya, 1958, Nr 7, p 52 (USSR)
AUTHOR- Voznesenskiy, A.A., Minkin, B.M.
TITLE: Effect of Zinc on Blast-furnace Firebrick (Vliyaniye tsinka na
ogneupornuyu kladku domennoy pechi)
PERIODICAL: Tr. Sibirsk. metallurg. in-ta, 1957, Nr 4, pp 3-22
ABSTRACT: The influence of precipitations of zinc in the brickwork of
the lower portion of a blast-furnace shaft upon the condition
thereof is examined. It is noted that the precipitation of Zn and
compounds thereof cause increasing portions of the brickwork
of the upper portion of the shaft to be partially or totally resist-
ant to cooling, and destroy the brickwork in the lower portionof
the shaft, and that the processes by which these phenomena
occur are the following: 1) formation and precipitation of ZnO
in the brickwork in a clearly-defined crystalline form, 2) con-
densation of Zn in the brickwork and oxidation thereof in the
solid and liquid state to ZnO not crystalline in exterior appear-
ance. A listing is given of procedural steps with the purpose of
reducing the harmful effect of Zn on the firebrick and increas-
Card 1/2 ing the life of blast-furnace operation without damage to the

SOV/ 137-58-7-14314
Effect of Zinc on Blast-furnace Firebrick
integrity of the shell of the shaft: Smelting of hot, readily reducible and
low-oxide fluxed sinter of the maximum basicity attainable without damage
to its mechanical strength; diminution in the upper limit of the size of the
Tashtagol ore being smelted to 35-40 mm, an increase in the size of the
sinter, with reduction of the 0-10 mrn fraction to the minimum possible; and
reduction in the intensity of the peripheral gas flow without interference with
the evenness of the process, particularly when furnaces are run at high
pressure.
M.M.
1. Furnaces--Deposits 2. Zinc deposits-.-Thermal effectr, 3. Zinc oxide dpposits--Therma
effects 4. Refractory materials--Performance
Card 2/2

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wepws gloom" owup amomd" awtud ewe salmalm
ftele NOUN"" we MWWIML omwdml~ aL A. a. ftIm OMM), wow.

KIRSANOV., V.Ij MINKIN, E.B.
Features in using synchronous start-stop systems an vire
communication lines, Elektrosviaz' 15 no,8:58-61 Ig 161.
(MMA 24:7)
(Telegraph)

KOROTKOVA, N.U., inzh.; KIRS101OV, V.I.; MINKINr 111I.B.
Electronic regenerative transminsion. Vest. sviazi 21 n0-4:4-5
Ap 16-1. WIRA -14: 6)
I* 14ookovskiy elektrotekhnicheskiy institut svyazi (for Korotkova).
2. TSentrallnyy nauchno-issledovatellskiy institut avyazi (for
Kirsanov,, Minkin). (Telegraph-Automatic systems)

M161tv", G. S., 9vaNufleft of VON* spdr4s. (in Russian), F1
5b. tr. LIM-P.-M -V -ea. rtauch. inzhotelthn. ahva, Yod. uunsp,
an. 2. 60-95. 1955: Ilef. Zh. M*AA. no. 12. 195(,-Rcv. 8681.
Elementary calculadons, ate ustd to deteridne the endumace of
An investigation Is
in ;? statically and an 4;"pt ofkti
am , .1 the relsti*n between th14 (taq-u-enzy-01 ascucst oscillstiort
of the aptings GAil the safety factor for fatigue, and a ftmule Is
oixalatd linking the calculated rpm of the cam shaft of a (ftc-
stfok engine and the safety factot of the valve- spdat.
A. F~ RoAnysmakil
COWICSY R (eW!Wri ibumet, ~ qrlt
rraffslat&~ Courtesy Ministry Sup 7filland
-'01Y.

MINKIN, I.I. (Rostov-na-Donu); SHATILOVp V.V., inzh. (Rostov-na-Donu)
Information and centralized freight delivery. Zhel. dor. transp,
47 no.505-36 Yq 165. (MM 18:6)
1. Nachaltnik Roetovokoy gorodskoy tovarnoy stantaii (for Minkin).
10

MINKINj L~Mo
Distribution and age of Mosaftic intursionB in the Aldan massif.
Mat. po goal. i pol. iskop. lAk. ASSR no. 2: 3-22 1 60,
(Aldan Plateau-Rooko (NM 15:10)
., Igneous) (Geological tibe)

L 4o364-66 M(1) JM
,ACC NR: AP6014249 SOURCE CODE: UR/0109/66/011/00510936/0938
':AUTHOR: Golubentsev, A. F.; Minkin, L. M.
1; ORG: none
TITLE: Minimizing the noise factor of a TW tube with an allowance for the.
;current precipitation at the delay-system entrance
SOURCE: Radiotekhnika i elektronika, v. 11, no. 5, 1966, 936-938
TOPIC TAGS: TW tube, noise factor
ABSTRACT: The slight effect of current precipitation on the minimum noise
'factor of TW tubes has been noted by W. R. Beam (RCA Rev.. 19S5, 16, 551) and
;by B. A. McIntosh (Canadian J. Phys., 37, 285). This finding is criticized
!:because it is based on the affect of the current precipitation only on the
noisiness" of the electron beam. If the current precipitation occurs only in the
:Card 112. UDC: 621.385.632:621.391.822

L 4o364-66
~ACC NR: AP6014249 0
J.e.lectron gun, the above finding is true. If, however, the current precipitation
Jakes place at the entrance of the delay system, the TW-tube noise factor cannot
i be expressed in terms of electron-beam noisiness. A formula for the minimum
ITW-tube noise factor covering the latter case is developed. Orig. art. has:
i 2 figures and 8 formulas.
:SUB CODE: 09 / SUBM DATE: 23Jul65 / ORIG REF: 000 / OTH REF: 002
I Card 2/2 hs

MINUN, M.
Closer to actuality. Sov. foto 19.no.6:.42-46 Je 159.
(kNA 12:9)
OPhotographs)

SOV/156 -58-3-~Vr'2
AUTITO'~~S: Ardashev, B. I., Yin,',-in, V. T., I'linkin, !-.. B
HTLE: On the Mechanism of' Q!~~ T-an.--.-formation of Lcylated
Arylamines (0 MC-11. *11 Fill. i ZMC- `--rej-,rLIppirovok atsilirovannykh
arilaminov)
P' Z-11 TOD IC AL Nauclinyye dokla(ly sh~-ol,r, Khlmiya i khimichec!kaya
tokhnolo,,;iya, 1958, N~- 3, ... r,,26-52n, (USSR)
ABSTRACT: The mechanism of the tr,~n.,~foruiaf,jon of the acylarylamines
under the action of ~~atE,.Iyots was investigated. This tr--r-"-
formation taken place at higher tem-peratures in "he presence
of acid catalysts. "Nic ri-action of the transformation of
acetanilide with the natalyst Znrl. in an HC1 current was
experimentally carrled out. After Keating to 150-2Ato for
3o minutes NN'-diplienylact-tamidine was formed in good yield.
On a further increase in t-.-mperature this compound converts
to flavaniline. The NN-dirhenylacetamidine crystallyses in
the form of white needles; the yield is 76 ~',. On the addition
of anhydrous ZnCl, and after heisting for several hours
Card 1/2 (5 hours) to 25006 in a vauk HCI current flavaniline is

S, V/156 - 513 - 3 - 31
On the Ilechanism of the Trann"f,,rmatlon of Acylp-ted iryiamines
formed in a yield of about 41 "fl. There are 11I references,
4 of which are I;oviet.
ASSOCIATION: Wedrs ~)ry-.;nk!heskoy i organicheskoy
khimii Novocherl.,.-iaskogo voiit.--',,.hnicheskogo instituta
(Chair of lnorpiiniQ Chemistry at the Novochorkass-r-
Polytechnical I ruAitutp)
SUBMITTED: February 17, 1958
Card '11/2

ACC NR: AP6022213 (N'VA) SOURCE CODE.
AUTHOR: Xinkin, M. B.; Tsyrultnikov, B. N.*
UAG: none
TITLE: Induction magnetometer for weak magnetic fields
SOURCE: Izmeritelinaya tokhni1ca, no- 5, 1966, 90-91
TOPIC TAGS; magnetometer, radio noise
ABSTRACT: Intended for measuring alternating magnotic flolds of 0.008--60 amp/m
intensity and for determining field frequency spectra within 25--500 Cps, the now
instrument consists of a 10000-turn coil ferrite-core sensor, a proamplifier, a
spectrum analyzer, a reference-frequency oscillator, and a power-supply unit. Only-
a few features of each component are given. The total error of the instrument is
13 /7fo :E 0.002 amp/m; it is made up of forrite-permoability frequency error, emf
compensation error, proamp error, and phase-sensitivity element error. Orig. art.
has. 1 figure and I formula.
SUB CODE- 09 / SUBM DATE: none / ORIG REF: 001
Cardli/I UDC: 681.2:538.122

2 i. !. 11.
A
C!
Stortln,7 Car and I-Proctor Dicoel 1948.

KATTEM, A.I., kandidat takhnichookikh nauk, redaktor; CHAKOV, A.M.,
inshenw. redaktor; GOLID, B.T., kandidat tokhnlcbosklkh usuk,
r*tsenssnt; DYBOF. O.T., kandidat teMalcheskikh nank, reteen-
gente. N' X.L., kand1dat takhnicheskikh nauk. reteensent;
.. kandUat tekhnicheskikh nauk, retsensent;
TIOCIM. A.Ts.. takhatcheskly redaktor.
[Studies In construction of automobiles; collection of scientific
research problewis of the Kolotow Automobile Factory and the
Vhdanaw PblytechnIcal Institute at Gorkly] Issledowanils, v oblasti
konstrairawanlia awtomobilla; sbornik nowhno-looledovatellskikh
rabot artosoblllnogo swods, IwnI Molotova, 1 Gorlkawskogo
politekhn1cheskogo Institute, 1menI Zhdanova. Moskva, Go*. nwchno-
takhao 1sd-vo, mash1nostroit. 1 sudostrolt. lit-ry, 1953. 249 p.
[Klcrofils] (KIRA 9:2)
(Automobiles --j)esign and construction)

HINKIH.M ;L., kandidat takhnichaskikh nauk; TRAKTOVYNKO,I.A., kandidat
texhUbheskikh nauk; OSIPTAN,A.V., kandidat takhnicheakikh nauk,
otvetstvennyy redaktor; ZILIMT-MG,Ya.G., inshener, sekretarl
BRILM,N.R., doktor takhaicheskikh nauk, KAWSH,G.G., professor,
doktor tekhnicheskikh nauk; PNVZM,Ya.N.. doktor tekhalcheakikh
nauk; RAMATYA,K.S., doktor tekhnichookikh n--k; KHRUSHCM,N.K.,
professor, doktor tekhnichoskikh asuk; KOZLOVSKIY,I.S., kandidat
tekhnicheskikh neuk; KATVNMA,Ye.N., tekhnicheskiy redaktor.
[An investigation of Soviet automobile radiators] Issledovante
otechostvennykh avtomobilInykh radiatorov. Moskva, Gos. aauchno-
tekhn. izd-vo mashinostroit. lit-ry, 1954. 43 P. (Moscow. Gosudar-
stvennyi nauchno-isoledovatellskii avtomobillnyi i aytomotornyi
institut. [Truftl. no.74) (KLAA 8:9)
(Automobiles--Radiators)

HINKIH,K.L.
~ -- ---Nft
Answer to Y.Y.Anokhln. M.L.Minkin. ATt. trakt. prom. no.6:31
Ja '55. (KLRk 8:9)
1. Nauchno-isaledavatel'skiy avtomotornyy institut
(Gunpowder) (Automobiles--Fuel systems) (Anokhin,V.V.)

IMMN. Icandidat teklirilchcslri~:h rmulr.
vi KWPWSI*
6aving nonferrous rctals in -arnlpcv.i:-in.~ ra~iatorc. trskt.nror.
nn46:4-6 is '57. (.17,-.,--! lo:pjl
l.ilauchnc,-insledc,vatollsici.,- avt~-/)tornyy inotttut.
(Ilorfnrroun metalo)

SOV/113-58-2-11/15
AUTHORSt-,' Minkin, M.L., Candidate of Technical Sciences, Moiseychik;
X.N. - - -'- -
TITLE% Methods of Pre-Start Heating of Liquid-Cooled Engines (0
sponobakh pred uskovogo podogreva dvigateloy a zhidkostnym
okhlazhdoniyem5
PERIODICAL: Aytomobilinaya promyoklennost', 1958, Nr 2, PP 37 - 40
(USSR)
ABSTRACTs Reliable starting of an engine is determined by the resist-
ance to the turning of the engine and by the temperature of
the cylinder and the air in the fuel mixture. The resist-
ance to turning depends on the viscosity of the oil. The
SU-type oil gas a viscositY of 50 centistoke8 at a temper-
ature of +50 C and 29,000 centistokes at -20 C. A.N~ Khvat-
kov of the NIIAvtopr1boj7found that starting an engine is
possible onl up to a viscosity of 2,000 oentistokes. Ac-
~
cording to 2
Ref 17 the viscosity may reach 10,000 centi-
stokes. High viscosity leads to a higher resistance and
makes the heating of rubbing surfaces necessary. The use of
special oils, fuels etc, without heating inoreases wear.
In the experiments described here a Vebasto-80WII liquid
Card 1/2 heater and a Vebasto-65BL3:.air heater were used in a GAZ-51

Methods of Pre-Start ffeating of Liquid-Cooled Engines
SOV/113-58-2-11/15
engine filled with antifreeze. A combined method in which
both heaters were applied showed the best results (see Table),
In the engine 20 thermocouples were installed to measure the
temperature at different places. The liquid heater supplied
5,000 large calories per hour, the air heater 3,000 large
calories per hour. At a temperature of -30 OC a heating of
30 min at this rate proved sufficient. There is 1 graph,
1 table, and 3 references, 2 of which are Soviet and 1
Engliah.
ASSOCIATIONs NAMI
1. Internal combustion engines--Starting 2. Interna! combustilon
engines--Heating 3. Heaters--Performance 4. Temperetwe
--14easurement 5. Lubricants
Card 2/2

SOV-113-58-10-3/16
AUTHOR: Minkin, M.L., Candidate of Technical Sciences
TITLE; Automatic Fan Control of Cooling Systems (Avtomaticheskoye
upravleniye ventilyatorom sistemy okhlazhdeniya)
PERIODICALi Avtomobil7naya promyshlennost', 1958, Nr 10, p 8 - 12 (U,33R)
ABSTRACT: The author first considers various foreign fan control sy-
stems, designed by, for example, Schwytzer Corporation,
Thompson Products - US, Schwytzer-Kammins, Bendix-Westing-
house, General Motors Corporation, Ford, and others. He
then describes the electromagnetic pulley for the "ZIL-120".
A thermostatically fan control based on the suggestion of
I.G. Shekhell was developed by NAMI. At the Khtaisekiy a-vto-
zavod (Kutaisi Automobile Plant) an experimental series of
thermostatically controlled fans is being manufactured, which
embody the results of preceding experiments in this field.
There are seven diagrams, one graph and one photo.
ASSOCIATION: NAMI
1. Automotive industry---USSR 2. Cooling fans--Control systems
Card 1/1

cc)v/ 11 x-rQ-2-13i'20
AUTHORS: Minkin, M.L., Candidate of Technical S,',_c-ncE:_P, Ki;::el.
FIT~Skly'Tye,
TITLEx Some Experience in the Production of Plate Radiators (1z
opyta proizvodstva plautinchatykh rndiatorov)
PERIODICALg Avtomobil,naya promystilenriosti, 1959, Nr 2. pp 27-28 (USSR)
ABSTRACT: The author describes the tests conducted by NAMI with plate
radiators, used in "Moskvich" automobiles, upor, request from
the Moscow Small-Displacement Car Plant. The tests showed
that the heat emission of the radiators can be increased up
to 1W~fo by using corrugated plates (Fig 2) with ridges and
cavities. Furthermore, the use of copper instead of brass
for their construction would further increase the heat
emission by 16-18c7f . There are I photograph. 2 graphs, and
/0
4 Soviet references.
ASSOCIATlON: IIAMI; Moskovskiy zavod malolitrazhnykh avtomobilley (MOSCOW
Small Car Plant)
Card 1/1

MIEKIN, M,Li, kand.tekhn.nauk; INITSKIT, I.Te.; SHAYEVICH, A.G.; KARAVATET,
-
Now radiators for the ZIL motor vehicles. AT-t.prom. no.9:10-14
S 160, (MIRA 13:9)
1. Gosudaretyennyy soyuznyy ordens, Trudayogo Krasnogo Znameni nauchno-
issledovatel'skiy aytomobilluyy avtomotornyy institnt i Moskovskiy
avtogavod imeni Ukhacheva.
(Motor vehicles--Radiators)

MINKIM. M.L.. kand.tekhn-nauk
Oil coolers of automobile eogines. Awt.pron. no.6:29-32 Je
16o. (MM 13:8)
1. (iosudarstvennyy sayusayy ordena Trudovogo Krasnogo Znameni
nauchno-issledovatellekLy avtosobilinyy i avtomotornyy institut.
(Automobiles-Maginee-Gooling)

)IMIN,-Ma~vey Iazarevichv kand. tekhn. nauk;TRGOROVp L.A.t kand. tekhn.
naUkq reteen"nt; DMANt B-1-1 insh.v red.; SMIRNOVAt G.V.,
tokhn. red,
[Starting devices for motor-vehicle engines] ftskoM ustroi-
stva aytomobillufth dvigatelei. Noskvaq Goo* naueboo-tokhne
isdwyo mashinastroit. 3-tt--ryt 1961. 138 p. (MM 14:6)
(Kotor vehicles-Ignition)

MOMMt-A-149 kan.d.tekhn.naukp- KiWLINITSHY, E.Ye.; BRAYEVICH9 A.G.; KARAVAYEV,
BJ.j PAPINV A.A.
Increasing the effectivness of coolin g systems for autcimobile
engfnes. Avt. prom. no.2.,10-13 F 161. (MIRA 14:3)
1. Gosudarstyepnyy ooyuznyy ordeha Trtidbvogo Krasnogo Us ni4vivokino-
UeleAovatel.4kiy aytomobilln'yy i aytomotomyy instiUt i Moskovskiy
avtozavod iseni Likhachava.
*tomobileo--Engines-Cooling)

MINKIN, M.L., kand.tekhn.nauk
New standard for motor-vehicle radiators. Avt.prom. 27 no.12:
40-41 D '61. (MIRA 15:1)
I
1. Nauchno-issledovatel'skiy avtomobil*nyy i avtomotornyy inatitut.
(Motor vehicles--Radiators--Standards)

LEYBZON, Z.I., kand. tekhn. nauk; MINKIN, M.L., kand. tekhn. nauk;
DERYUGIN, P.Ye.
Influence of air temperature and humidity on the efficiency
Indices of the GAZ 21A engine. Avt. prom. 30 no.12:5-9 D 164.
(MIRA 18:2)
1. TSentrallnyy ordena Trudovogo Krasnogo Znameni nauchno-
issledovatellskiy avtomobillnyy I avtomotornyy institut.

1 -3 3~;65
.11Rt~,4P50CO66
ACOMIM

ACC N 7,&006514 SOURCE CODE: UR/0113/65/000/01-1/0012/001h
AUTHOR: Karnitskiy,.,V. V.; Minkin, M. L. (Candidate of technical sciences)
ORG: NAMI
TIT12: Starting cold engines by using highly flammable liquids
.L
;
SOURCE: Avtomobillnaya promyshlennost', no. 11, 1965, 12-14
'TOPIC TAGS: motor vehicle, engine reliability, engine starter system, engine ignition
!system, diethyl ether C/,r-av
ABSTRACT: T,he authors discuss various liquids and their respectiye injection systems
for introducing them into engines before starting. American, French and English
istarting aids are discussed. A test was set up to determine the effect of diethyl
:ether content in the starting mixture on starting time, using the SMD diesel at -100C.
'.The results show that a diethyl ether content of 40% and less is effective at -20 to
:-250C.
On the basis of these data all other control starting was carried out with a
,~60% diethyl ether content in the otarting mixture. A starting mixture was developed
,at the Central "Order of tne Red Banner of Labor" Scientific Research In3titute of
Automobiles and Automobile Engines for diesels with the following composition: 65%
'diethyl ether, 12% light mineral oil,':120% petroleum ether, 3% aldehydes and 0.2%
~antioxidant. This mixture ensured diesel starting down to -400C with omooth engine
Lq-rd 1/2 uDc: 621.431-73:62-57

- ----- --- ----
ACC NR, Apko6514
operation. The NAMI-5PP-110 and IIA14I-6PP-40 starting attachments were produced as the
result of a series of tests carried out on diesel and carburetor engines. These
~starting attachments can be used both for diesel and carburetor engines up to 40
.liters. They spray the starting mixture into the intake manifold instead of sprayino
lit directly into the cylinder. This is more economical than the latter. A diagram is
;given for one of these starting attachments. It differs from the French "Start-piloi!!
;in that it has many more channels and ensures a uniform distribution of the starting
;emulsion to each individual injector or valve. An empirical formula is presented
which describes the relationship between engine displacement capacity, design charac-
teristics, ambient temperature and the minimum amount of B.tarting-mixture necess
i
;for starting the engine at a given temperature. The starting mixture and attachm=nts
were tested under arctic conditions and proved successful. Orig. art. has: 3 figures,
3 tables, 1 formula.
SUB CODE: 21,131 SUBM DATE: None
j_gard 2/2

.1 ff~ T
~k) SOURCE CODE: UH/0413/66/000 /OOG/0057100--l
P6011222 57
INVENTOR:. Gure
-Kornitskii, V. V.
0R6:'_ none
A. A. ; Sobolev. Ye. -P. ; Shch2goley, N. V. ; Aleksevev. A. I!,
ikin, 1. 1~ - Senichkin, M. A.' L-'%ms~%OS
M
TITLE: Starter fluid for engines with carbur6tors. Class 23, No., 179870
SOURCE: Izobreteniya, promyshlennyye obraztey, tovarnyye znaki, no. 6, 1966. 57
TOPIC TAGS: carburetor engine, starter fluid, engine starter flu id, -antioxidant
additive, antiwear additive -
ABSTRACT: An Author Certificate has been issued describing a starternuid for
engines with carburetors. The fluid has a base of sulfulric etherand a mixture of
low-boiling hydrocarbons with an antioxidant ad4itiveAft is suggested that to improve:
the functioning properties of the fluid, isopropyl nitrate or oxidation products -of* 1.
hydrocarbons plus an antiwear compound be added. (Tra*nslation] INT11,
SUB CODE: 21 / SUBM DATE: - 13Nov64/
1/1 R-f UDC: 661, 17;621, 434. 019-6332

L 1C296 '7
ACC NRZ, ;jNZ03088 SOURCE CODE: UR/0292/66/000/010/OWI/000L~
j'%UT',-:OR: Belentkiy, Yu. M. (Engineer); Gertsov.. S. M. (Engineer); 4L~senko, V. Ye.
nkin, M M.I(Engineer); (Candidate of technical scie-
0.rigineer); aMi nces)
OIRG: none
TITIL: Serial pr.o.du9tion of step electric motors
SOURCE: Elektrotokhnika, no. loo 1966p 1-4 10
TOPT TAGS: electric motor, electric industry
IC
As a resILLt Of exm~
ABSTRACT: lensive theoretical and experimental work it was
most reliable step motors are of the split-phase magnitoelectric
and four-ohase inductor type.
li-x USSR Jndustry a~ present manufactures 14 models oftsplit-phase mag-
n-L
Itoelectric step motors,~which designated by letters ShDA:'~ All these motors
I
..ave 3-6 steps :Ei~ each complete revolution and operate on a voltage of 14 or
28 volts; they weigh from 110 to 1,500 grams.
Mle A'Our-phase inductor type step motors are manufactured in 15 models
!and are desianated by letters ShDR. These motors have 24, 40, 56 or 120
~stc-,)3 for each complete revolution; they all operate on a voltage of 10
volts; their weivht ranges from 100 to 700 grams. Orig. art. has: 4 figures and
2 t abI e s -[JPRST*
SUB CODZ: 09, 05- / SUBM DATE: none / ORIG W-: 004.
V 21-313 -13=133.-
cced -_,3..-001.3.Z --N 21-;~i-- I

L o899o-6?
ACC Na: AP6012113 IV) SOURCE COLE; UR/0413/66/000/rJO7/0027/0027
AUTIHOMI: Ivobotonko, B. A.; Gortsov, S. M.; Lovonotakiy, Yu. H.; Lutuanko, V.
Yo.; 11-linkin, M. M.
ORG: none
TITLE: A multiphano stop electric motor. Clans 21, No. 180239
SOURCE: izobrotoniyap pronWshlennyye obraztsy, tovarnyye znakit no. 7, 1966, 27
TOPIC TAGS:, electric motor, torque
A3STRACT: This Author Certificate presents a multiphase stop electric motor of i
;,-,he induction type with control windings and with permanent excitation magnets
located in the stator. The electric motor has a toothed rotor without a winding
(see Fig. 1). The design increases the torque in Given size motors and simplifies:
their Droduction. The stator is made with an internal permanent magnet in the
form o.L
two synmotrical halvo3 magnetized with opposite polarity. The permanent
magnat is enclosed between the halves of the stator.
!Card 1/2 --..UM: .. 621.313.13.025.4-133.3

L o8ggo-67
ACC NR: AP6012113
Fia. 1. 1 - control w-Indings; 2 permanent'
magnet; 3 i3tator; 4 - rotor
Orie. art., has. 1 figure.
SUB COM: 09/ SUBM DATE: 2lJan65
(n.,,: 2 not

ACC NRz
AP7002978 SOURCE CODE: UR/0413/66/000/024/0077/0077
INVENTOR: Veksler, B. Ye; Katkov, G. F.; Malinskiy, S. A.; Minkin, M. M.;
-Remennikov, V. S.-,~Rybakov, L. A.; Sokolinskiy, Ye. A.; Fe(16F&f;-V_.7if_.;' 'Shmulovich,
I
I. Sh.; Gertsov, S. M.; Pishchulin, V. V.
.,ORG: None
iTITLE: A seismic prospecting station. Class 42, No. 189598
iSOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki, no. 24, 1966, 77
!TOPIC TAGS: seismic prospecting, frequency divider, quartz crystal, seismologic
jstation
!ABSTRACT: This Author's Certificate introduces a seismic prospecting station contain-;
ling an amplification-conversion channel, registration unit and power supply. The
,unit is designed for improved reliability and operational convenience. A quartz os-
Icillator with a frequency divider system is used as a precision-frequency power supplyt!
land synchronizing unit. The oscillator is connected through amplifiers to the actua-
iting units of the station.
::SUB CODE: 08 SUBM DATE: 04Jun65
I
1/1
UDC;
550.340.19-Ji,

MNXINOI-N.,-gvardli kapitan
Reading Lenin with one's heart. Kmm- Vooruzh. Sil 4
no.105-57 Ja 164. (MIRA 17,-9)"

Cfi;',H),3JAKC,V, A., prcX.; fl.;
Fj',udies u- the of -1--:nary Jpfectic.,~q
early and Uits surgei-y. ?,f.'-r-jrgJ!a 17
417-418 1 il,
1. -institut %a sr~-ts~alizatsil% i j:;-u.-urshern.~, .-3 na
lekarite, 3ofila, Fated-ra r-,, --irologila
katedratas prof. A. Cherverakcv).

MIIRKIII, II.I.
Unit for loading shor lumber. Mekh.i avtom.proizv. 14 no.2:
34 7 160. (MIRA 13:5)
1. Glavnyy inzhener Dubovitskogo lasopromkhoza.
(Conveying machinery)

MIMIN, R.B.
Peculiarities of the pro-icteric phase of Botkin's dUease in
Leninabad. Zdmv. T-adzh- 3 no.2:39-41 Mr-Ap '56. (NIM 12:7)
1. Is Ieninabadskoy Gorodakoy bollnitsy No.1 (glavvrach A.A.
Abdullayev).
(IRTIMUD--BMTITIS. INY=IOUS)

MINKIN. R.B.
Clinical evaluation of the normal phonocwNdiogram. Trudy ISGNI
48057-380 159. IHFART--SOUMS) (MIPA 14:2)

ARRIGONI,
,B.j- RASPUTIN, A.M.; SOLOV'YEVA, Ye.A.;
TARrAKOVSKIY, M.B.
Now method for a clinical evaluation of the electrocardiogram
(frequency analysis of waves of the ventricular complex).
Trudy LSGNI 0408-433 '59. (KIBA 14:2)
(ELECTRMRDIOGRA,PHY)

I
. ARRIGONIt J.Mqj_,#LkKjgt_Atp.LRASPUTIN, A.M.; SOLOVIYEV4 Xe.A.;
TARTAKOVSKZ4 M.B.
.j.
'dWical significance of the frequency analysis of the ventricular
complex of the electrocardiogram. Trudy ISGNI IS:L4L-"6 159.
~MIRA 14:2)
(ELECTROCARDIOGRAPHY)

MKIN9 R.B.; TARTAKOVSKIY9 M.B.
Significance of the auricular component in the f6rmation of the
first heart sound. Trudy ISGNI 4,8007-511 159. (YJRA 14:2)
(HUn-JOUNDS)

MINKINY R. B.
Impn-tuee of esophagocardiography in evaluating hemodynamic changes
in heart defects. Terap. arkh. no.7:28-34 161. (MIRA 15:2)
1. Is kliniki vnutrannikh bolesney (zav. - Prof. A. A. Kedrov)
laningradskogo sanitarno-gigiyenichookogo meditainskogo inatituta.
(HMT-DISZASES) (CADIOGRAM)
(ESOPHAGUS-EXELORATION)

So MINKIN. R. B.
Frequency and localization of heart ma-mur heard during the
phonocardiographic examination of healthy persons. Kardio-
Iog:U& . 3 no. 3. M-81 My-.Te 163. (MIRA 16:9)
ls Iz kafedry vnittrennikh bolezney (sav. - prof. A.A.Kadrov.)
Leningradskogo sanitarno-gigiyenicheakogo meditainskogo in-
Stituta,
(HEART-SOLTIEG)

MINKIN, R.B. (Leningrad, D-88, ul. Plekhanova, d.12, kv.64)
Results of the evaluation of the effectiveness of a mitral comir-
surotoqr with the aid of asophAgocardiographyo Grud. kh1r. 6
no.4134-37 JI-Ag 164. (MIRA 1g-./,)
1. Klinika vnutrennikh bolezney No.1 (zave - prof. A.A.Kedrov)
Leningradskogo sanitarno-gigiyenicheekogo meditsinskogo instituta.

HIMIN, S.L.. prof. (Kharlkov. u1. Artems, d.6, kv.4)
lots observations of amputations for enderteritis obliterans. Ilov.
khir.arkh. no.6:64-65 M-D 157. (WRA 11:3)
1. Wedra obshchey khtrur ii Kharlk vskogo meditainakoro institute.
(AMMATIOll & IMGJ (ARTOOISS-DISSASRS)

HIRKINO S.S. t ekth nik
Machining of botton edges on a boriv4g and turning laths.
KhIm.wLsb. no.1:42 Ja 060. (KML 13:5)
(Chemical enginearing-Rquipment and supplies)

it, - ~ f-i-
ZA. 11 UT .
Unkin, S. Yu. - "Sympathetic decentralization of the upper limb," In symposium:
VIII Sessiya ffeyrokhirurg. soveta i Lenim,-r. iln-ta neyrokhirurgii (Akad. ,,~ed. nauk 3SM),
U
Moscow, 191;31 p. 270-713
SO: U-3600, 10 July 53, (letopis 'Zhurnal Irrfkh Statcy, 48. 6.., 1249.)

Mml S. YU.
Kinkln, S. Tue - *Wthod of operation on the chest section of a borderline nyWathetic
trunk in vegetative disorders of the upper extremities,,w In the syqmims V. N.
Shmovs, Kiev# 19499 pa 29-37
SOt U-4355p 14 August 53v (Letaple 'Zbwml Irykh Statey, Mb* 15, 1949)

-,T~1-1 ~-,. Yu.
11,
Csetinskiy, T. G. and Minkin, S. -lu. - "The effect the removal of the riflit henisphere
of the brain has on the functions of the stor~uch," In t'-e eollection: ',". 'j,. Z-~iaz-.ov,
Kiev, 1949, P. 39-42
SO: U-4355, 14 AuguBt 53, (Letopis lZhurnal Inykh Statey, No. 15, 1949)

1-fiNZIN J,- S. Yu. PA 63A9T62

1, TOITAT07101fj, B. I.-j, KeGARITOVAjGF.j MINKIN S YU. jRUBINj 1. L.
2. USSR (600)
4. Sciatic Nerve
7. Data on the pathogenesis of experimental trophic ulcer of the extremities. Vop.
neirokhir. 16 no. 5. 152.
9. Monthly List of Russian Accessions, Library of Congress, Jawar7 -1953. Unclassified.

1. MINKIN3 -'.i. Yu.: RUDIAN, Z. V.: JVUSLANOVA, R. 11.
2. ~U33R (600)
4. Tissues - Extracts
7. Problem of tissue therapy. Vest. khir. 72 no. 6, 1952.
9. Monthly List of Russian Accesstonsj Library of Congress, March 1953. Unclassified.

PAVLOVSKIY, Ye.N.p otv.red.; VASNETSOV, N.A., prof., red.; VERESHCHAGIN, M.N.,
prof.,-red.; MINKIN,_ .5_,-prof., red.; POPOV, P.I., prof., red.; -
STUDENTSOV, A.P., prof., red.; CHAGIN, V G:, prof... red.;
SABIN, ~A, dotsent, red.;' TANYASHIN, I:F I d6tsent, red.;
BORISOVICH, F.K.; red.i SOKOLOVA, N.N.,,*tekhn.red.; FEVZHER, V.I.,'
tekhn.red.
[The N.9,Bauman State Veterinary Institute in Kazan (1873-1953);
materials on the history of veterinary education in the U.S.S.R.)
Waxanskii gosudaretyerinyi veterinarnyi institut ineni N.E.Bauxans.
(1873-1953); materidly k istorii veterinarnogo obrasovaidia v SSSR.
Moskva, Sellkhosgisi 1956. '182 P. (Kazan,,VeterinALrnyi,institut.
Uchenye sapiski,%vol.63). (MIRA 16:8)
(Kasan-Veterinary colleges)

/7 1,
AUTHOR SHTY.Mff D.A. Deputy Director, Blast-Furnace Plant, PA-3055
Kuznetsk Metallurgical Combinate
SUCHKOV I.A., Supervisor of the Technological Group, Kuznetsk
Metallurgical Combinate
MINKIN V.A., Director, Blast-Furnace Laboratory, Kuznetsk
Metallurgical Combinate
TITLE The Kuznetsk Blast-Furnase Workers. (Xuznetskiye domenshohiki.-
Rusaian)
PZRIODICAL Metallurg 1957, Vol 2, Nr 4, pp 9 - 12 (USSR)
Received: 5/1957 Reviewed: 7/1957
ABSTRACT The first blast-furnace iron was produced about two years after
oonstruation at the*Kuznetsk Combinate had started. Four blast
furnaces were eonstruated, with almost 4,000 m3 work space.
Until 1940, the workers of the combinate solyed different
auestions of working methods. The workers learned to regulate
the working of the furnace from aboye, and, inter alia, sue-
oessful attempts were made to obtain a stability of the blast
and of the heat economics
It was learnt to correct ihe melting 8tock after dust had been
completely eliminated usw. A uniform operation of the furnace
was obtained by careful determination and fixation of the
melting stock at the ore depot, in the ore bunkers, and directly
CARD l/ 4 during the process of charging. During this prooess, the constancy

The Kuznetsk Blast-Furnace Workers.
PA - 3055
of the heat state in the blast furnace was rigidly observed by
changing the ore burden per ton coke. After ten years, the ef-
feetive coefficient of the furnace space rose by 26 % as result
of the elimination of the above shortcomings. The first postwar
Five-Year Plan was fulfilled in 3.5 years. The blast-furnase
iron amount increased by 40 % as result of technological im-
provements. Among these technological improvements were: changed
system of charging the furnace, which regulates the gas ourrenti
the active struggle against freezing of raw naterialsi auto-
matization of the charging of the furnaceal speeding-up of
repairs of furnaces; extension of the metallurgical path. The
following alterations were also introduced: furnase operation
with blast feeding with constant and increased moisture content
and with melting of furnace pig iron of low manganese concentration.
Also the Fifth Five-Year Plan was concluded with high performance
characteristics. The production of pig iron in4reased,by 25 % as
result of further modernization. The Plan.for 1956 was surpassed
by several thousand tons of pig iron, with a saying of 3v8OO,OOO
rubles. For the first time in the entire USSR, the Kuzhetsk
Combinate succeeded in automatizing the weighing scales which
resulted in speeding up the work and making it more accurate.
CARD 2/4 The personnel of the combinate received political and t4ohnologioul

The Kuznetsk Blast-Furnace Workers. PA - 3055
education. Workers from Kuznetsk were frequently sent to other
plants an instructors. Many of then had started in the combinate
as construction and auxiliary workers and then were prozoted
to responsible specialized posts. For 1957, the personnel of
the Combinate plans further measures: further improvement of
the blast-furnace operation in connexion with changed ore
quality, shortening of furnace lay-offs during repair work,
automatic regulation of the gas flow in the furnace by using
a revolving distributor corresponding to the heat feeders of
the throat at several points. Automatization will permit to
change, according to need, the system of charging, the charging
platform, and the amount of the coke charge at a change of the
gas flow in the furnace shaft, It is intended to take into
account the gas drop on different horizons in the furnace, and
to regulate the furnace charge in accordance to the static gas
drop; this regulation is supposed to be automatic. The disad-
vantages must not be forgotten: not all resources have been
used, not all furnaces are being operated uniformly and without
CARD 3/4

The Kuznetsk Blast-Furnace Workers. PA - 3055
interruptions, the discipline of working methods is often
violatedp and not all has been done so far in order decrease
the amount of waste.
(7 reproductions, among them 6 pictures of persons.)
ASSOCIATION: Kuznetsk Metallurgical Combinate, Stalinsk.
PRESENTED BY: -
SUBMITTED: -
AVAILABLE: Library of Congress.
CARD 4/4

01KINt V.I.
YIW,INI V.I. "Some Problems in the Construction of Kolkhoz Ponds."
Min Higher Education USSR. Novocherkas3k Soil'Improvement
Engineering Inst. Novocharkassk, 1956. ( Dissertation for
the Degree of Candidate in Technical Science)
So: Knizhnaya Istopist, No. 18, 1956,

~6 ., g 1),( 1. t,- Jv.)~ Ol r, A"":14ph 1. Added ovil
~ - -I.. ..-I.- I ~- . ~ .... ~~ I.... .. - -.. I Al:~.

A~

,,~ ~4, I..
AUT 110H t Mijl%in, V. 1. 7c)-11-55/56
TITLE: By Way of Discussion(V poryadke diskussii)
boi;iu Remarks Concernill,t; 1,11i. ul' tjl-~ (N,kctoryye
zamechanija k voprouu o
PFdZIODICAL: Zl-.arzrl Obstichey Khimii, 1957, Vol. 27, lir 11, lip. 11173-3175
(LJSSR)
ABSiRACT. In the year 1935 J. Backer arid W. Natan introduced the
conception "hyperconjugation" of short arid simple bi%din.-Is
which was later on given its physical foundation. They
C.1
assumed that a linkage of the simple,- bi,-idi,-i,,,s of the type
0
'Y ~1
H C - C - x
were X only in--nifests itsulf as anion, is The fundam-
Ontal invez;t-*
~,~;atjoris carxernizi,, thoproblcm of the linkage
of siLi,)le (61)-bindinC3 vieru ;erforrik-, by soviet scienLicts
which investi~;ated this effect mrainly in connectic'n with the
organora-etallic coupounds. But the 1i.- ,ka.:e of sim--le 13-*ndizi~,-s may
also sufficiently clearly manifost itself ir', the chemical 1)rocess
of substances without a.,i or,,ano:,iv'Lallic Y-.atur,-, ac it -aa3 3hown
Card 1/2 in soue reactions of alk.y1chlorocarborates. These remar~113 refer

B)W&v of Discussion. Some Remarks Concerning the Problem of the 79-11-55/5~
C a -13.Lnd i nf~, .
to the farther tent to determine the reactivitj of 3o::ie ccrz-
poundB throaf-,,,h the concoption of the Oa-bindin,:.,. The ,lathors lore
especiallj interested in the problem concernir , the difference
in the action of oubstituents such as the Liethyl- and ethyl-
groups upon the chemical bc~iavior of the erters of phenols and
alkylanilines. It was earlier otated thc~ ethyloxy-,froup in aroma-
tic coi,,poundn excrts a stron6,er ortho-para orientating action
than the inetoxyl-Group which vian then by tho authorn brou.-Ilt ill
connection with the --reater capability of polarization -of the
uthyl radical. It seems that the ethirlaiine roup also is more
nucleonhiliz than the methyla...-ine Croup. The above-mentioned fact.,
are proved by exa:.,ple~,. :io strict ar-uni~_-nt Lay, !,owe,,er, be held
on this opinion, a-- there exi_~ts no physical th,~,ory of the linkagi
of simple bizidin(,,s. There are I tab~le, and 21 refer,.-,,-,ces, 7 of
w1iich are ;Slavic.
ASSOCIATION; Rostov State University (Rostovski-y gosudarstvenn~-y unive.-sitct).
3 -j-,, 1'1'T ED O_t, 1. _ " J'=4
1. Metalorga nic compounds-Chemical analysis 2. Metalorganic
compounds-Molecular structure 3. Molecular structure-
Determination 1j. Cyclic compounds-Molecular structure
212

_2
r
q!Ff .0 Mot X
-A
e C26 25 tol
00% IW
f
Wdi
.
,,
n
~
u
-stid 120 V. glycerol at 05-100* vms added graditally (4G-

gh a rcUc mdenser to 27 g. nitruanisrile (1)
00 min.) thm
prebeatedat 1#0', the mi%t.. b. 14&--52', rziluxcd 4.5-6hri.,
-
d
d
:
e
. distd. and dissolved in Et~O (ai
with excess CJIt
filtered
by 2 ponions of 25 and 15 g. ph(halic anhi-dride). yielding
'
6
t
h
. b. 279-84
.
1,647e 6- indine, b. 127-30

SOV/1561-58- 3- ~-; 1
AUTHM': Ardashev, B. I., 1"Inkin, V. T., "inkin, 73.
TITLE: On the 11echaniim or ~i!-, of icylated
Arylamines (0 mc-Vbnni7m-~- -,regrtippirovok Ptsilirovannykh
arilaminov)
PER TO'n IC AL Nauchryye doklad,r T.h--',.niya i khimich,~~-!,aya
tckhnolo,,,?iya, 1956, 1:F. (USISR)
ABSTRACT The mechanism of thp trr-,nr-.forr,.L-.#.ion of the a cylaryln mine P,
under the action of .,attilyats was investigated. This trans-
formation taken place at higher temperatures in the presence
of acid catalyatn. Thc reaction o," the transformation of
acetanilide with the nsitalyst ZnCl in an HC1 current was
0 ,
experimentally carrit-~d out. After Keating to 150-200 or
30 minutes was formed in good yiel(I.
On a further incrQase in tqmperature this comnound converts
to flavaniline. The NN-diphenylacetamidine crystallyses in
the form of white needles; the yield is 76 5% On the addi t4 on
of anhydrous ZnCl, and after heating for several hours
Card 112 (5 hours) to 25006 in a ve;ik HCI current flavaniline is

S OV1156- 59-3- 3
On the I.:echanism of the rip oi~ Acylated :Iry_!.-III.Ine-v
formed in a yield of about i;l There are 18 referencec,
4 of which aro .1"oviet.
AS90CIATION: Wedre -)rp-.-,ni.-:heqkoy i organichesko,v
khimii IIovocII(,]*k:t.'3*CI 'it,
- r. Q ETO r.,o T-:~hnicheskogo instituta
(chair of' -nrt Cir.,-unio Cheiristry at ti-e !Tovoch(-,rkE..s,.!',.
Polytechnical I nctitute)
SUBMITTED: February 17, 1958
Card 2/2

AUTHORS: Ardashev, B. I., Minkin, V. 1. 79-2-59/0'4
TIT12: Investigations in the Field of 'juinoline Derivatives
(Issledovaniya v oblaoti proizvodnykh khinolina).
XV11. Synthecis of Some 6- and 8- Alkoxy quinolines
(XVII. Sintoz nekotorykh 6- i 0- alkoksikhinolinov).
PERIODICAL: Zhurnal Obshchey Khiraii, 1958, Vol. 28, 11r 2, 1)11- 545-540" (USSR)
ABSTRACT., The hitherto applied methods for the synthesis of alkoxy
quinolines according to Skraup (ref. 1), Kon (ref. 4), Dau et
al. (ref. 6) were deficient. With a quiet reaction a good yield
was achieved on the occasion of gradual addition of a mixture
of amino, sulfuric acid, and glycerin to the oxidizing agent
which was heated to a temperature higher than that of the re-
action temperature. This method was suggested by 'Walter (ref,
10) and recommended by Manske (ref. 11). The present method has
some advantages in compari3on to the alkylation of the 8-oxy-
quinoline according to Bedall (ref. 12) or Friinikel (ref. 13)
or to the synthesis with arsenic acid according to KnUppel
(ref. 14, 15). In the present work 6- and 8- methoxy quinoline
as well as 6- and 8-ethoxy quinoline wore synthezized accord-
ing to the above mentioned alterated method. The yields amount-
Card 1/2 ed to 38 - 64;f2, the specific data of the products are Given.

Inve3tieations in the Field of ~jinoline Derivatives. 79-2-59/64
XVII. Synthesis of Some 6- and 8- Alkoxy Quinolines.
There are 17 references, 3 of which are Slavic.
AS60CIATIGII: Rostov State UIIiVOr3ity (Rostovskiy cosudarstvennyy universi-
tet).
SUB"UTTED: January 31, 1951"
AVAILABLE: Library of Congrese
Card 2/2

AUTHORS: Ardashev, B.1, Minkin, Y.,l. SOV/ -t~-26-b-52163
TITLE: Investigations in the Field of quinoline Derivatives
(Issledovaniya v oblasti proizvodnykh khinolina).
XIX. New Method of :3ynthesis of quinoline by Hegrouping
Acylated Arylamines ~XIX, Novyy metod sinteza. khinoiinov
peregruppirovkoy atsilirovannykh arilaminov)
PERIODICAL: Zhurnal obshchey khimii, 1958, Vol. 28, Nr 6, pp. 15'ttJ-
1581 ~UBSR)
ABSTRACT: In the investigation of the lepidine regrouping of the
ethyl acetanilides the auzhors carried out regroupings of
a series of alkyl formalinides which take place on milder
conditions in a nitrobenzene medium. The existing data
permit to make the assumption that the catalytic regroupings
of the alkyl acylanilides make possible the synthesis of
various quinoline derivatives and that it appears as one
of the few quinoline syntheses which have general ch4~racter.
The mechanism of the investigated regrouping differs from
that of the reaction according to Pictet (Ref 12) (Pikte)
and is not connected vith any cleavage of the alkyl radical
Card 1/3 from nitrogenp as theat,o-dimethyl indole to be expected in

SOV/ 79-28-6-32/63
Investigations in the Field of Quinoline Derivatives. XIX. New Method
of Synthesis of Quinoline by Regrouping Acylated Arylamines
this case in the conversion with hydrochloric aniline does
not permit lepidine to be formed. As was found in the first
stage of the reaction N,Nl-diaryl-N-alkyl acylamidine is
formed which is obtained on heating (150-1600) the amine
salts with their acyl derivatives (Refs 16,17). The best
yields of the products were actually obtained in using the
amine salt at equivalent ratios. At higher temperature the
amidines regroup to the anil of the corresponding
o-aminocarbonyl compound which then cyclizes into the
quinoline (see'scheme)., The investigated reaction in
principle appears as a new method of the synthesis of
quinoline. There are I table and 29 references, 13 of
which are Soviet.
ASSOCIATION: Rostovskiy-,na-Donu gosudaratvennyy universitet
(Rostov-na-Donu State University)
SUBMITTED: March 25, 1957
Card 2/3

my 79-28-06-52/63
Investigutions in the Field of Quinoline Derivatives. XIX. New Method
of Synthesis of Quinoline by Regrouping Acylatud Arylamines
1. Quinolines--Synthesis
Card 3/3

NIIWKDF, V.I.; ARDASHEY, B. 1.
Now means of.preparing quinaldine bases and N-arylqainaldine
salts by condensation of aryl amines with aldehydes. Part 20.
Zhur.ob.khtm. 28 no.9:2556-2560 3 '56. (KIRA 11:11)
1. Rostovokly-na-Donu gasudaretvennyy universitet.
(QuInaldine compounds) (Condensation products (Chemistry))
I
PS

MMUNP V. I.0 Candidate Chem set (diss) -- "Investigation of the mechanism of
preparation and nev methods of synthesis of certain quinoline derivatives",
Rostov M Dom., 1959. U pp (Rostov State Up Chair of organic Chem)., 150 copies
(KL, No 2k., 1959, 128)

50)
AUTHORSt Ardashev, B. I., Minking V. I., SOV/74-28-2-5/5
(Novocherkaosk)
TITLEj Regroupings and Migrations of Acyls in the Series of
Aromatic Amines (Peregruppirovki i migrataii atsilo7 v ryadu
aromaticheakikh aminov)
PERIODICAL: 'Uapekhi khimii, 1959, Vol 28, Nr 2. pp 218-234 (USSR)
ABSTRACTs In spite of a large number of papers in this field, regroupings
of aoylated aromatic amines described in this paper have not
yet been systematically dealt with in publications. By meana
of regrouping of aoylated arylamines nitrogenous heterocyclic
compounds of the quinoline and aoridine series, difficultly
accessible arylamino ketones and substituted aminoaryl
benzoio acids a. o. can be obtained. The regrouping of
aoetanilide which is accompanied b~ a shift of the aaetyl
grou toward the aromatic nucleus, was detected b, Fischer
and gidolph Ref 2). The regrouping of acylaniliaee in the
presence of acid catalysts is usually-not terminated by the
formation of arylamino ketones. This fact is explained by an
increased reactivity of the substances formed which readily
Card 1/4 enter into condensation and cyclization. During reaction in

Regroupings and Migrations of Acyls in the Series SOV/74-28-2-5/5
of Aromatic Amines
glacial acetic acid by the influence of sirupy phosphoric
acid aromatic amino ketones in the form of acetyl derivatives
can be separated (Ref 13) the latter of which have been
formed by reacylating in acetic acid. Due to the volatility
of o-arylamino ketones with steam the isomers can be easily
divided. 0-arylamino ketones are extremely reactive compounds.
If subjected to strict conditions of regrouping of
aoylanilides they can readily transform into different
nitrogenous heterocyclic compounds. The investigation of the
regrouping mechanism presents great difficulties. Besides,
one and the same regrouping may take place according to various
mechanisms which Is conditioned by the used catalyst. In this
case all regroupings of aoylanilides may be divided into
three kindsi 1) regrouping with AlCl 31 2) regroupings with
phosphoric acidal 3) regroupings with ZnCl 2- Nevqrtheless the
regrouping mechanism is insufficiently investigated and requiroi
further investigations. The regrouping of alkylaoyianilides
taking place in polar solvents and in the presence of ionizing
Card 2/4 catalysts is probably a heterocyclic reaction. Results obtained

Regroupings and Migrations of Acyls in the Series SOV/74-28-2-5/5
of Aromatic Amines
by the regrouping of different alkylacylanilides are given
in Table I . The reaction is bribing in its effeet due to the
accessibility of the initial compounds, however, requires
further investigation. On heating acylated diarylamines or a
mixture of diarylamines and oarboxylie acids, anhydrides or
acid chlorides in the presence of ZnCl 2 at 200-3000 a shift
of the acyl residue from nitrogen into the ortho-position
toward the amino group and a cyclization into corresponding
memosubstituted aoridin*s take place. Acridines can Le
obtained by means of regrouping of the previously synthesized
acyl derivative of the diarylamine. However, the yield remains
unchanged as in the case of the main reaction (Refs 49, 51, 66
Chemical, physiological and oth- nbnracteristics of ao--Idines
are described in detail 1. Albert's monographs (Refs 76, 94).
The problem of the regrouping meananism of diaoylanilides
cannot be considered to be solved. Some investigation results
of this reaction are summarized in Table 2 . A special case
is the regrouping of N-arylphtalimides taking place on its
Card 3/4 heating up to 200-2250 with the alloy NaCl + AlCl 3* The

Regroupings and Migrations of Aoyls in the Series SOV/74-28-2-5/5
of Aromatic Amines
intermolecular nature of this reaction is obvious. In all
cases investigated the reaction took place exclusively in the
ortho-position to the amino group. In conclusion it may be
stated that the regroupings of aoyl radicals are of decisive
importance to the synthesis of aromatic and heterosyclic
amines which are important from a practical point of view.
There are 2 tabl'so and 117 references, 27 of which are Soviet.
Card 4/4
usmm-Da.0842

AUTHORS: Ardashev, B. I., Minkin, V. 1. SOV/79-29-1-43/74
TITLE: Inve3!ifations in the Field of quinoline and Its Derivatives
(Issledovaniya iz oblasti khinolina i yego proizvodnykh).
XXI. Simultaneous Condensation of Aryl Amines 71ith Hydra-
crylic Aldehyde (XXI. Sovmentnaya kondensatsiya arilaminov
a gidrakrilovym alldegiflom)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 1,
pp 200 - 2o2 (USSR)
ABSMCT: In a previous paper (Ref 1) Ardashev showed that hydracrylic
aldehyde (0-oxypropionaldehyde) is capable of reacting in
the Skraup reaction beside acrolein. In this connection it
ras of interest to investigate the reaction of some aromatic
amines with this aldehyde in order to obtain quinolines.
Apart from one patent by Chichibabin ('Ref 5) this reaction
has hitherto remained unknown. It was found that already
under the usual conditions of the Skraup synthesis, i.e. in
the case of addition in drops of aldehyde to the reaction
mixture at 120-1400 quinoline is obtained in a yield of 151'~J.
On using e. lighter oxidizin.- agent, nitrobenzene sulfuric
Card 1/2 acid and by carrying out the reaction in a diluted solution

Investia :1 ationn in the Field of ~uinoline and Its SOV/7"1-29-1-43/74
Derivatives. XXI. Simultaneous Condensation of Aryl Amines TJith Hydracrylic
Aldehyde
ASSOCIATION:
SUBMITTED:
with hydracrylic aldehyde, quinolines are obtained in yields
UP to 501% Thu3q the conclusion can be drawn thut in the
usual Skraup reaction with glycerin (also acrolein if no
glycerin is available) part of the rp-iction in the reaction
with hydracrylic aldehyde formed from glycerin or acrolein.
This reaction was extended to diaryl amines. E.g. n-phenyl
quinoline salt was synthesized from diphenyl amine. Thus,
it was determined that it is also possible to introduce
secondary amines into the modification of the SkraUD synthesis,
with hydracrylic -aldehyde. Among some ways of reaction of
this aldehyde with aryl amines which lead to quinolines the
most probable one is shown in the scheme. There are lo refer-
ences, 7 of which are Soviet.
Novocherkasskiy politekhnicheskiy institut (Novocherkassk~
Polytechnical Tnstitute)
November 21, 1957
Card 212

5(3)
AUTHORSs Min:cin, V. I., Ardashev, B. I, SOV/79-29-4-18/77
TITLE: Investigations in the Field of Quinoline and Its
Derivatives (Iseledovaniya iz oblasti khinolina i yego
proizvodnykh). XXIII. A New Method of Synthesis of
Quinaldine Compounds and N-Aryl Quinaldine Salts
(XXIII..Jovyy sposob polucheniya khinalldinovykh
soyedineniy i N-arilkhinalldiniyevykh 80ley)
PERIODICALs Zhurnal obshchey khimii, 1959, Vol 29, Nr 4, pp 1129-1132
OSSR)
ABSTRACT: The quaternary quinoline salts with an aryl radical on the
nitrogen are important as initial products for the synthesis
of cyanine dyes and photooensitizers (Ref 1). The beat
accessible substances of the quinoline arylates synthesized
according to references 2 - 5 are the N-aryl quinaldine salts
which are obtained according to Skraup (Ref 5). All synthesis
methods known so far have the general disadvantage that they
are little suitable for the introduction of higher fatty
aldehydes into the reaction with diaryl amines. In connection
with the above-said results the authors used the variation
Card 1/3 of quinaldine synthesis earlier devised by them (Ref 7) for

Investigations in the Field of Quinoline and Its SOT/79-29-4-18/77
Derivatives. XXIII. A New Method of Synthesis of
Quinaldine Compounds and N-Aryl Quinaldine Salts
the purpose of synthesizing some hitherto unknown
2,3-dialkyl quinoline arylates from diaryl smines and
higher fatty aldshydes (Ref 7). This synthesis is based on
the separate performance of two steps of developments 1) on
the formation of the dimers of vinyl diphenyl amine, which
possibly exhibit cyclic structure (Ref 8), and 2) on their
dehydrogenation to the quinoline derivatives. The first
step in carried out in neutral, the second in acid medium.
The formation of the N-aryl-2,3-dialkyl-quinoline salts can
be illustrated in connection with the previously suggested
scheme (Refs 7, 9) according to the given scheme. The yield
of the reaction products in the form of their perchlorates
is 20 - 65 %- One molecule of quinoline arylate is formed,
accordingly, from 2 molecules of the initial diaryl amine.
The primary aromatic amines in the form of their acyl
derivatives yield, under equal conditions, also quinaldine
products, probably according to the above scheme. The
reaction described is of general importance. There are 11
Card 2/3 references, 10 of which are Soviet.

Investigations in the Field of Quinoline and Its SOY/79-29-4-18/77
Derivatives. XXIII. A New Method of Synthesis of
Quinaldine Compounds and N-Aryl Quinaldine Salts
ASSOCIATIONt Novocherkaeskiy politekhnicheskiy institut (Novocherkassk
Polytechnic Institute)
SUBMITTEDs January 14, 1958
Card 3/3

. FRA-gy I BOOK MEPEOrTATION SOVA350
Sovishchanly* po khImil, tokhnologil I prLmeneniya proisvod.1fkh
pirldins, 1-khinolina. Riga, 195T
Vx1mlys. takhnologlyn I primenonlye prolzvodnykh pirldina I
khtnolina; materialy moveshchaniya. (Chemlatryt Technology
and Vtillzatlon of Pyrldlne and Quinollne Derivatives;
Materials of the Conference) Riga, Izd-vo JW Littviyukoy
33R. 1960. 2" p. Errata allp Inserted. 1.000 copies
printed.
Sponsoring Agenclems Akademlya naak Latviyakoy 331t. Xnstitut
khImill VaeloyQanoye khledchemkoye obsnehostvo.
Bachanovas Tech. 9d.;* A. X2yaviny&; Llitorial
Sd.
S.
;o
&rd Yu. A. Bankovskly, candidate or Chemistry, R. V.
t
VarAda, Candidate or Chemistry (Resp. 94.), L. P. Zalukayev,
Dcator or ch"lotry. and x. x. Kainyn-.
PMUOSE: This book Is Intended for organic chemists and
ahemd"I engineers.
The 4ollectlon contains 33 articles on methods
of synthesizing or producing Pyridln*, quinollne. and
their derivatives from natural soarces. No PersonLilti,3
are mentioned. Figarea . tables, and references accompany
the articles.
11. SYNTUTIC MW3 OF EPZPARnIC PYRID=3 AND
4 QVL4OL3x-E3
3alykov. A. S.. and 0. 3. Otmahcherko. 13redneazistakly
Lm6nI 7. r7tentna (Central
A&,.& state ur.-.v*r3ity 3-'or-- V. 1. L~n!.%)j . Synthetic. 3tu,11ai
c4r'l 4"'10
v_ B. p. A__X. Kut_
--TY
a
7 a'
-l'od j.'r.-e-4tva
t
("ar's,
'
-
r.,&nt or tr. ximist-1 -~f -,! Cnes~t-`~
Synt!teaez of 2-XetbYl-5-etny!pyrL-1in.
'
I1o&tWn 97
&r.1 and -heir of ApP1
orgiruche3k-ogo minters, Aktdomil mmak

lArviys oy SSE (I-titlate for Oraa:1-1- ST-Ii-,'" is or the
SM
Azide-4 of 3:1entea Latv:yak&7a 53R)I. The Transition
P--= 1,3- Dtdaruijone to Pyridine Derivatives

(Ingtitut vy zn'soyellnonty
M. P. sokoolokulyarny
alar Compoon-la
"&4emu raak 333N (institute for High Malec
USSR)] Synthtsis And POlYwrt-
of the ""By of &tenee
ration of Cnmalura*ed Coa:-unda oe the Pyridine and quina-
119
[Rosto J-, rosadar3tve=n77,QnI ers t

k
Ar's T--j--7 , ;k4ins
;8
I
i&l Synth 31sv f [A
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nlv#rALr
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)
127

44l'skokhGzyLYs.v1n:'yj institut

ifez-a toral nn3tltut~ Atalr.. 3jrntha.113 ~r
it
Q~xinoltn'-! Bases F.,0m Am'-nos Wul A~-tYl-v 131
pr~plrxtton of
State Unlv*rs!t7l
qal..lain.s From 3-3,111wa Atyl JLr-tl*-dld %A Synt.-~,ais .. or
139

qatnai-unq StIta
N-Ary.,

reakt1wc*0 (Al' -Uijn
jnst~,tate for C."W.-.al St'1-17 If the
nthesizing quinolinic N""d 14.s
'
thod or S
lne Me
y
"yjroXyqujno.
T*r"v. 5. A. R~stov State unjv."tty) 3jntn*,im or
-auinjl-n- aml So-d H-ArYlItPldl" Salt-
15L
Kazlov, X. S.. and 0. K. K.2-mii-kh !Pornukty go"Ur-t--yy

C&Wytic 3ynthes.3 or 2-pmnyl- 5,6-bonzoqainoilne Derl-
Vatives 159

r. -st-v State Universitr] Catalytic Cols-
:j
~h
rs f
Ac
tsd Aryl Amino. to Qai~.ilno. 171
...... T - P~ P-d~t& Ar th, P-1-1-lan '2 An'.11no -1

HINK3, V. I.; DORanffAXO, G.N.
C----- -------------
Formylation andarylation of organic coupounds with substituted amides
of carboxylic acids, Ump. khIm. 29 no-11:1301-1335 1 160.
(MIRA 13:11)
I. Jkletovskiy-ma-Donu gosudaretvemW universitet I Laganskly
sell skokhozyayetvewi~yy instifat.
(Formylation) (Acylation) (Amides)

,t- kf
3/079j60/030/05/53/074
B005/B125
AUTHORS: Ninkin, V. I., Ardashev, B. I., Takhadadze, K. A.
TITLEs The Condensation of Diaryl AminesiWith Isovaleraldehydel
PERIODICALt Zhurnal obshchoy khimii, 1960, Vol. 30, go. 5, Pp. 1647-1649
TEXTs -The synthesis of several previously unknown derivatives of N-aryl-
2-isobutyl-3-isopropyl quinolines in described in the present report. The
derivatives named wore isolated in the form of their.perchlorates. The
production was carried out according to the Doobner-Niller reaction by th:e/,"
condensation of secondary aromatic &mines with the aldehyde of the is
valeric acid. The mechanism of this reaction was already investigated
previously (Refs. 1, 2). The authors assume that the ring closure in
asymmetrical diaryl &mines occurs towards the more strongly nucleophilic
aryl group. This assumption is in accord with the data of G. T. Pilyugin
(Ref. 4). The reaction according to Doebner-Niller was also applied to
secondary aliphatic-aromatic &mines. The N-methyl quinaldinium perchlorate
formed in negligible amount in the corresponding reaction of the methyl
aniline. The formation of this product can be explained by the decomposition
Card 1/3

The Condensation of Diaryl Anines With 3/079/60/030/05/53/074
Isovaleraldehyde D005/B125
of the intermediately forming dimer of the vinyl methyl aniline under
the separation of methane (vide also Refs. 8, 9). The schemata of the
formation of the normal reaction product and the by-product mentioned are
given. The reaction worked out by the authors can be carried out on the
one hand with various aromatic and aliphatic-aromatic secondary and
acylated primary amines, and on the other hand with various aliphatic
aldehydes; and it can generally be used for the synthesis of arylates and
alkylates of quinaldine and of 2,3-dialkylquinoline. Nitrobenzene or an-
other polar solvent can be used as a solvent. o-Nitrodiphenylamine,
294-dinitrodiphonylamins, and N-phonylanthranilic acid form no quinolinium.
salts, since these amines are too weakly basic. Also indole forms no
quinolinium salt. All of the syntheses carried out are thoroughly de-
scribed in the experimental section. The yield, melting point, and
chlorine content are given for each synthesized product. The influence of
the solvent on the yield of N-phenylquinaldinium perchlorate is given in
a summary. There are 9 references, 6 of which are Soviet.
Card 2/3