SCIENTIFIC ABSTRACT FABRICHNYY, B.P. - FABRIKANT, T.L.

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• Sequence Number: 12
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

Or, the Synthosin of the 3-(2~-thionyl) Alanine 62-1-17/29
ASSOCIATIONs InEtitute 6t Organic Chemistry imoni N. D. Zelinskiy
., AS USSR
(Institut urganicheskoy khimii im. N. D. Zelinskogo Akademii
nauk SSSR)
SUB'.=TED: July 12, 1957
AVAILAJLS: Library of Congress
1.16 -(2-T:Lerql) glanine-Synthesis 2. Alanines-Synthesis
Card 2/2
ItTl
i OKI

R I C f4 y 79-1-45/63
AUTHORS z Golldfarb, Ya. L. , Fabrichnyy, B. P. , Shalavina, 1. P
TITLEs The Synthesis of Amino Acids of the Aliphati c Series From
Thiophene Derivatives (Sintez aminokislot alifaticheskojo ry-
ada iz proizvodnykh tiofena) II. The Synthesis of P-Amino
Acids (II. Sintez P-Aminokislot)
PERIODICAL: Zhurnal Obahchey Xhimii, 1958,Vol28, Nr 11, pp.213-222(USSR)
ABSTRACT; In recent years new data were published in periodicals on
the investiE;ation of P-amino acids, as biolo~;ically active
compounds, of vibom earlier little notice had been taken.
Thiophene as initial product (references 4 and 5) beean to
play an important part. The way from thiophene and its ho-
mologues to amino acids is illustrated by the formulae M,
(II) and (III). The second sta-e of this process consists
of the condensation of the aldehyde, which can easily be
produced, with malonic acid and ammonia to P-anino acid ac-
cording to V. It. Rodionov. The final staje is brouGht about
Card 1/3 by the reducing desulphurization with the aid olf" nickel. The

79-1-45/63
The Synthesis of Amino Acids of the Aliphatic Series From 'I'hiophene Dori-
vativea. II. The Synthesis of P-Amino Acids
given synthesis of P-amino acids contains all possibilities
which were characterized by the authors in papers devoted to
the methods of synthesis of amino acids of another type. From
the above-mentioned scheme follows that tile acid of a rami-
fied structure must form when ever the substituent or the al-
dehyde group are in positions 3 and 4, or when the substituent
in position 5 has a ramified structure. Thus the following com
pounds were obtained from the corresponding 2-thiophene-alde-
hydes according to Rodionov's method: P-(2-thienyl)-P-amino-
propionic-, P-(5-methyl-2-thienyl)..P-aminopropionic-, P-(5-
.-ethyl-2-thienyl)-P~-aminopropionic and P-(5-tert-butyl-2-
-thianyl)-p-aminopropionic acid. By the hydro-enolysis of
these amino acids of the thiophene series the authors synthe-
sized V amino-n-heptyl-, F-amino-n-capronic, V amino-n-pelar-
gonic acid. By hydrogenolysis of the acetyl derivatives of
P--(5-athyl-2-thienyl)-F-aminopropionic andy~-(5-tert-butyl-
-2-thienyl)-taminopropionic acid the acot derivatives of
P-amino-n-pe argonic and 4, &-dimethyl-amino-n-pelargonic
,acid respectively are obtained. By saponification of the acc-
Card 2/3 tyl derivative of _11~ , 9--dimethyl-p-aLiinopelar~;onic acid

79-1-45/63
The Synthesis of Amino Acids of the Aliphatic Series From 'Thiophene Deri--
vatives. II. The Synthesis of P-Amino Acids
with hydrochloric acid the hydrochloride of rdimethyl-
-P- aminopropionic acid was obtained; by neutralization free
amino acid was liberated. There are 19 references, 10 of
which are Slavic.
ASSOCIATION: Institute for Organic Chemistry All USSR
(Institut organicheskoy khimii Akademii nauk SSSR)
SUBMITTEDs December 15, 1956
AVAILABLE: Library of Congress
Card 3/3 1. Mwmistry 2. Amino aoide-Synthesia 3. Aliphatio compounds
4. Thiophene

YABRICHNYY, B.P.; SHALAVINA, I.F.; WITARB, Ts.L.
Synthesis of alip-hatic amino acids from thiphene derivatives.
Part 3: Synthesis ofk)-amino acids. Zhur.ob.khim. 28 no.g:
2520,-2530 S 158. (MIRA 11:11)
1. Inatitut organicheskoy khimii AN SSSR.
(Amino acids)

.9 (3)
AUTHORS: Golldfarb, Ya. L., Fabrici '-B V179-29-3-30161
-'Imizz So
Shalavinag I. Fe
TITLE: Synthesis of the Aliphatic Amino Acids From the Thiophene
Derivatives (Sintez alifaticheakikh aminokislot iz pToi---
vodnykh tiofena)- IV- 5-Acyl-(2-thienyl)-alkanic Acids as
Initial Products for the Synthesis of the Aliphatic Amino
Acids (IV. 5-Atsil(2-tiyenil)-alkanovyye kisloty kal- iskh-
adnyye veshchestva dlya polucheniya alifaticheskikh ami-
i,okislot)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 299 Nr 3, PP 891-697
(USSR)
ABSTRACT: There are comparatively little data available on the highest
aliphatic amino acids of the structure 'C'(N'
COOH'
)(C'
)
2
2
n
where R. alkylq although they are interesting as polyeondensa-
tion objects (Ref 1) or as derivatives for physiological
investigations (Ref 2). Their general method of synthesis is
so far unknown; for the synthesis of some of these amino
acids natural products were used; thus, for instance, the
Card 1/3. 10-amino-undecanic acid (Refs 1,2) was obtained from

Synthesis of the Aliphatic Amino Acids From the SOV/79-29-3-30/61
Thiophene Derivatives. IV- 5-Acyl-(2-thienyl)-alkanic Acids as Initial Pro-
ducts for the Synthesis of the Aliphatic Amino Acids
undecylenic acid which is formed on the pyrogenetic cleavage
of castor oil. The method previously suggested by the authors
.which is based on the reductive desulfurization (hydrogeno-
lynis) of the oximino and amino acids of the thiophene
series (Refs 3-8) yields aliphatic amino acids of any kind.
The thiophene-keto acids previously used by the authors permit
only the synthesis of such amino acids in which the carbon
atomg as carrier of the amino group, is combined with an alkyl
which contains not less than 4 carbons. This restriction was
partly removed with the oximes of the aldehyde acids as
initial products (Ref 8). In the present paper the synthesis
of the highest amino acids of the mentioned type fy'om. the
oximea of the keto acid (II) according to the given scheme
is described. In this way the highest aliphatic amino acids
can be synthesized which have the amino group in the required
position to the carboxyl and an alkyl radical at the carbon
atom combined vrith the dmino Group, with the necessary number
of carbon atoms. The experimental part gives details on the
Card 2/3 carrying out of the reaction scheme nentioned. By the

Synthesis of the Aliphatic Amino Acids From the SOV/79-29-3-30/61
Thiophene Derivatives. IV- 5-Acyl-(2-thienyl)-alkanic Acids as Initial Pro-
ducts for the Synthesis of the Aliphatic Amino Acids
hydrogenolysis of the oximes which were obtained from the
thiophene keto acids the following acids were synthesized by
means of the skeleton-nickel catalyst: The 10-amino undecanic,
11-aminolaurict 9-amino undecanic, and 11-amino tridecanic acid.
There are 3 tables and 8 references, 6 of which are Soviet.
ASSOCIATION: Institut organicheskoy kbimii Akadamii nauk SSSR (Institute
of Organic Chemistry of the Academy of Sciences, USSR)
SUBMITTED: January 20, 1958
Card 3/3

5 0) -
AUTHORS: Colldfarb, Ya. L., Polonskaya, M. M., SOV/20-126-1-23/67
Fabrichnyy, B. P., Shalavina, J. F.
TITLE: Reductive Acetylation of Thlophene Series Nitrocompoundo In the
Presence of Skeleton Nickel (Voestanovitellnoye ateetilirovaniya
nitrosoyedineniy ryada tiofena v prisutsvii skeletnego nikelya)
PBRIODICAL: Doklady.Akademii nauk SSSR, 1959, Vol 126, Nr 1, pp 86 - 89
(USSR)
ABSTRACT: The"first and the third author proved earlier (Ref 1) that(f-
-amino-valeric acid is produced with a small yield by the ef-
fect of skeleton nickel (Ni k) on the 5-nitro-2-thiophene-car-
boxylic acid (I). On the strength of reference 2 the authors
tried to increase this yield by the application of acetic acid
anhydride as medium. However, they succeeded only in isolating
the acetyl-amino acid (II) from the reaction mixture. The re-
cognition that this acid produces (III) in the case of the ef-
fect of Ni sk in-the aqueous medium (Ref 3) led to the conclusion
that the acetic acid anhydride deactivates Ni sk' This conclusion
Card 1/3 was confirmed in the case of two other examples. Thus the react-

Reductive Acetylation of Thiophene Series Nitro- SOV120-126-1-23162
compounds in the Presence of Skeleton Nickel
Ion of Ni A with thiophone-nitroderivatives remains under the
mentioned conditions in the production stage of an acetyl-amino
compound. That is to say, the result of the process is a re-
ductive acetylation. Although the effect of the solvent upon
the reducing properties of Ni sk in the case of the hydrogena-
tion of the thiophene derivatives has already been published
(Ref 4) the authors could not find data concorning the capa-
city of the acetic acid of suppressing the desulfurizing func-
tion of Ni A in such cases. The authors found contradictions
in the publications concerning the properties of the 5-acetyl-
amino-2-thiophene-3arboxylic acid (II) (Refs 6-11) when they
identified the latter. Since the melting point 230-232 0 of the
acetyl-amino acid (with a II-structure as is assumed) produced
by the authors did not agree with that of the publications
(2720) they determined the position of the acetyl-amino group
in the nucleus. Thus the structure II was confirmed. On the
Card 2/3 strength of these data the authors doubted whether the experi-

Reductive Acetylation of Thiophene Series Nitro- SOV120-126-1-23162
compounds in the Presence of Skeleton Nickel
mental results of reference 8 were right. The authors then re-
peated the experiment of reference 8 and obtained acid potas-
0
sium tartarate with a melting point 273-274 . The authors as-
sume that Campaigne and Archer (Ref 8) erroneously regarded
this acid salt as the acetyl-amino acid (II). There are is ref-
erences, 3 of which are Soviet.
ASSOCIATION: Institut organicheskoy khimii im. N. D. Zelinskogo Akademii
nauk SSSR (Institute of Organic Chemistry imeni N. D. Zelinskiy
of the Academy of SciencesqUSSR)
PRESENTED: February 25, 1959, by B. A. Kazanskiy, Academician
SUBMITTED; February 16, 1959
Card 3/3

FAMaCMffrjP B. P - . (prof . )
"A Now Principle of Synthesis of Amino Acids.",
report to be submitted for the Symposium on the Chemistry of Watural
Products, Intl. Uhlon of Pure and Applied Chem. (IUPAC), Melbourne, Canberra, and
Sydney, Australia, 15-25 Aug 60
Inst. of Organic Chemistry im N. D. Zelinskly, Moscov

FABRICHNYY, B.P.; SHAIAVINA, I.F.; GOLIDFARB, Ya. L,
Backmwm rearrangemmit of thiophanoMloalkanons oximse.
Zhur. ob. khim. 31 no.4s.1244-1253 Ap 161. (MIRA 2.4:4)
1. Institut organicheakoy khiaii Akademii nauk SSSR in,.eni N. D.
Ze2.inakogo.
(Oximes) (eyolobexanone)(CZclohaptanone)
(Beckma= rearrangmeut)

GOLIDFARB,, Ya.L.; FABRICHNYY B.P.; SHALAVINA, I.F.
Synthesis of aliphatic amino acids from thiophene derivaties.
Part 6: Preparation of e - and,7 -amino acids and C-substituted
lactams. Zhur.ob.khim. 31 no,,6t2O57-2064 Je 161. (MA 14t6)
1. Institut organichaskoy khimil imeni N.D.ZelinBkogo AN SSSR.
(Amino acids) (Lactams)

FABRICHNYY. B.P.1 KRASNYANSKAYAY E.A.; DOLIDFARB, Ya.L.
Preparation of higher aliphaticO(-amino acids from 2-phenj,1-4-
(thenylidene)-5-oxazolines. Dokl. AN SSSR 143 no.6:1370-1373
Ap '62. (MIRA 15%4)
1. Institut organicheskoy kbimli im. N.D.Zelinskogo AN SSSR.
Predstavleno akademikom B.A.Kazanskim.
(Amino acids) (Oxazoline)

S/190/62/004/012/008/015
BIOI/B186
AUTHORS: Volokhina, A. V., Fab -richnyy, B. P., Shalavina, I. F.,
Golldfarb, Ya. L.
TITLE: Polymerization of C-ethyl and C-propyl substituted
enantholactams
PERIODICAL: Vysokomolekulyarnyye soyedineniya, v. 4, no. 12, 1962,
1829-1832
TEXT: The susceptibility of t-ethyl-t-enantholactam and of ~-n-propyl-i-
enantholactam to polymerization was investigated. Synthesis: The lactam
of 6-(3-aminothienyl-2)-valeric acid, or the lactam of 6-(3-amino-5-methyl-
thienyl-2)-valeric acid was obtained from V,V-thiopheno-1,2-cyclo-
heptan-3-one o'xime or from 5'-methyl-21,Al-thiopheno-1,2-cyclohoptan-3-ona
oxime by Beckmann rearrangement in the presence of benzene sulfochloride.
At the same time the sulfur was eliminated with skeleton nickel, and the
double bonds of the thiophene ring were hydrogenated. The polymerization
was carried out at 220-2800C with 2~, H 0 as catalyst in N atmosphere.
1 2 0 2
Solid, glass-like substances with m.p. 170 C were obtained, which can be
Card 112

S/190 62/,~04/012/008/015
Polymerizati6n of C-ethyl and.'.. B1~1/D/ie6
pulled out to filaments at 1750C and from the hot alcoholic solution of
which films can be formed. th6 polymer yield was more than 99;C, the
intrinsic viscosity reached 0.50 for the ethyl derivative, Lind 0.30 for the
propyl derivative. Conclusion: In contrast to the seven-membered
caprolactam ring, the polymerization susceptibilitiyof the eight-membered
enantholactam ring is not affected by substituenta.. There is 1 figure.
The most important English-language reference is: H. K. Hall, J. Amer.
Chem. Soc., 80, 6404, 1958-
ASSOCIATION: Vsesoyuznyy nauchno-issledovateliskiy inctitut iskusstvennogo
volokna (All-Union Scientific Research rnstitute of Synthetic
Fibers); Institut organicheskoy khimii im. N. D. Zelinskogo
AN USSR (In3titute of Organic Chemistry imeni N.D.Zelinskiy
AS USSR)
SUBMITTED: July 7, 1961
Card 2/2

VOLOKHINA, A.V.; FABRICHNYY, B.P.; SHALAVINA, I.F.; GOLIDFARB, Ta.L.
Polymerization involving ethyl- and propyl-substituted
enantholactams. Vysokom. ooed. 4 no.12:1829-1832 D 162.
(YJRA 15:12)
1. Voesoyuznyy nauchno-iBoledovatellskiy institut
iskuostve=ogo volokna i Institut organicheskoy khimii
imeni N.D. Zelinskogo AN SSSR.
(Azicinons) (Polymerisation)

GOLIDFARB, Ya.L.; FABRICHNrY, B.P.; ROGOVIK, V.I.
Syntheses based on aldehydes of the thiophene series. Part 1.
Synthesis of some aliphatic hydroxy amino acids from thiophene
derivatives. Izv. AN SSSR. Ser. khim. no.12:2172-2177 D 163.
(MIRA 17:1)
1. Instit-at organicheskoy khimii im. N.D. Zelinskogo AN SSSR.

FABRICHNYYY B.P.; KRASNYANSKAYA, E.A.; SHALAVINA, I.F.; GOLIDFARB, Ya.L.
Synthesis of aliphatic amino kcids from thiophene derivatives.
Part 7: Preparation of some higher a -amino acids from 2-phenyl--
4-thenyliden-5-oxazolones. Zhur. ob. khim. 33 no.8:2697-2702
Ag 163. (KIRA 16:11)
1. Institut organicheskoy khimii imeni N.D. Zelinskogo AN SSSR.
t

FABRICHNIYS B. P.j OOLODFARB,, Yakov Imarevichl SIRIAVIR, I. F.
"On the uynthesis of the 2j,3,4,5-tetr&dITdrobiotin.0
Report preBented for the 3rd Intle SyWosium on the Chemistry of
Natural Products (rmc)s i~voto, Japan, 12-18 April 1964.

FADRIGHM, B.P.; SHAIMIE'A, I.F.; YFI.J!,
Synthesis of aliphatic mrflno aci(b. from dnrivatives.
Part 8: Influenev of certain factors ar. " e jjm.'.urA yield In the
reduction desulfurl7mtinn stage. Zhw,. ~b. 111him. 34 no.12-.3878-
3887 D 164 (MITIRA 'Lb-.I)
1. Innti,tut orgwilch~r,:Iroy khli,.ii. 'rr.. TI.D. Zt-] A I ~S":F,
11

~`NTW /1Z'PF(c)/E-dP(j)/T Pc-'# / P r-4 FM
A6~;(,SSSION Ni~% 05008374 3/01~0/6 5100 7/003 /Oh 65'/Oh 90
AU'THR)F-Si Sal&natina, 0. B.; Bonetskmal A. K.J Skcvratov, S. M.; Fabrichnyy, B.
F., Shalavitia 1. T*.-,.~,;!'dfarb. Ta, It,
TITLE: Kinetics vnd thermal effect of 13-merizati of some C-alkvl substituted
SWFvr,E-. Vysokonoleku1yarnyye soyedineniya,, T. 7, no. 3, 1965, h85-490
TOPIC TAGS- alkylation, polymrization., kinetics, thermal effect
ABSrP,Ar,T: A study was made of the kinotics of polymerization of 5-CH3-1 7CH 3-P
-enantholactams -in the presan-ce
?k'1-2~;[,-and 7C 3H7 -caprolact~Lms and 8-G2H5- and 8C3H7
alone and with different amounts of phosphoric acid at
was synthesized. The others were obtai-ned fron Vlilli. For
J I
,)a,yuierization in water it was found that the prucess is airvocatalytic for -- a)-iW1
!3ub5titiAnad ard ummbstituted lactams alike, that the substitution in a la--tazz
sharply lowers the reaction rate, that the degree of convere-ion from
rLonomer to polymer at maximum rate also declines markedly for both aiRTlated
caprolactams a-.-.d alkylated amtholactams, and that the t1r-z of reachi-nS aaxiimu-
Card 1/2

L i5634-65
ACC=10114 NR: AP5008374
reactiGn rate for these monomers is increased. When phosphoric acid is present
,;i'h tiie water the maximal reaction rate is markedly increased, the rate increasing
with cGncentration of acid; the degree of conversion at the maximnum- r.:ft-e decreazee
nol. JeFend on the acid concentration; and the time for
re-~
-~trungly reduced. It was found that the r-ax1nal rate depondq or.
, ~'Ie with
, 'L Substituted &Ikyl in the ring., and that tl~drs raL,~ -ecrearsE
a -I Iength of the substituted alkyl. Mfettiyl nubsti tut 1. 0 r. ~'-' --aurolactw~s
'Lcw8rs '-ne thernal effect of poly merizet ion. Ethyl substitution incre-azqes the
effect, and propyl substitution does not change it. Orig. art. has: ---. figures
asid 3 tables.
A33XIATION: Roskovskiy gosudarstvannyy universitet im. H. V. Lomonosova (Vioscow
State University); Institut orgardcheskoy khimli im. Ze2jmkogo, ill SSSR
~inuqtitute --- of- 0-rganic Chemistrys AN SSSR)
'RJBICT-1-M.- 3CX4ay64 INGLt 00 SUBCODE: OG, I-C
W REF SOVs 007
Card

FAERICHNYY, B.P.; SHALAVINA, I.F.; GOLIDFAHB, Ya.l,.
New synthesis of 2,3,4,5-tetrahydroblotin. Dokl. AN SSSH 162 no.l:
120-123 My 165. (MIRA 18:5)
1. Institut organicheskay khimit im. N.D.Zelinskogo AN SSSR.
Submitted November 4, 1964.

GOL' -'.;Fil,.B, Ya.' . ; FABRICHOY, B. I .; RCGCV I'K, V. 1.
Syntheuc.s and some trans f omations oP mthrxymet.hylthiophenes.
Tzv. AN SSSR. Sor. khtt. no.3:51.f-52C) 165. (MIRA 18: 5)
1. InstUtit organicheskoy khimil im. N.D.Winskogo AN SSSR.

SALAMATINA, O.B.; BONETSKAYA, A.K.; SKURATOV, S.M.; !~B~ICHIIYY, B.P.;
SHAIAVINA, I.F.; GOLIDFARD, Ya.L.
Kinetics and the thermal effect of the polymerization of some
C-alIql-substituted lactams. Vysokom. soed. 7 no.3:485-490
Yx 165. (KIRA 18:7)
1. Moskovskiy gosudarstvennyy universitet imeni M.V.Lomonosova
i Institut organicheskoy khimii imeni Zelinskogo All SSSR.

FABRICHNYY, B.P.; SHALAVINA, I.F.; GOLIDFARB, Ya.L.
-, ,
Synthesis of aliphatic amino acids from thiophene derivatives.
Part 9i Preparation of L-4-alkyl-F--caprolactams and c'Z-alkyl-
E -aminocaproic acids. Zhur. org. khim. 1 no.811507-1514
Ag 165. (MIRA 18tll)
1. Institut organicheskoy khimli iment Zelinskogo PJ1 SSSR.

FABRICI Imrioh
A note on F-classeo in comnutative Hausdorff bicompact semigrqups.
Mat fyz cao SAV 11 no-4t282-287 161.
1. Katedra matematiky, Slovenska vysoka okola technicka., BratiLilava,
Kollarovo namesti 2.

0-
FABRICI. Inrich
The totally maximal elements in semigroups. Mat fyz SAV 13
no.W6-19 163.
1. Katedra. matematiky a deakriptivnej geometrie, Elektrote-
chnicka fakulta, Slovenaka vyaoka skola technicka, Bratislava,
Gottwaldovo nameati 2.

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7
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A near sy~thaali of N-laorm D, Beke,
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'7'krrvs, ZcAr-uM-W'02:'4M7--4 RIMA cf. CA. 43, 41M.-
Amod
Qryit. Smalacol (112 91 Md 83.7 9. thIc"I hydfiste j'F (Witimt further putification) trittimtLd with W2 cc.
d
1) ri) 430% tb* U-1111. AIT" (tflnp, bt!d At "') an aAle. IICI, and the product dried at no, yielcIrA a&2
...-Aynt Qvml. frops 10 g. CuCO, And 15 C. Naj 1110 $411, Wilich, r M-Md. froin 2Y) cc, 11,0 rave 0"1.5
M
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tio
tic,
pn~dmt (a red mom) (1a) washed by rrpmtcd trituru it e4c-M (IV),'dc 2W, &'frC+vv'1 c-m-0--j-
MUk 110, d1swived in 0 1. bolting ILO with anithatC. and kutly voith 4 g. (Tx',M1Zj14'7o 'P-I) In 2ZO "- RION'ot
~qln. cooted. gave WA 04%) pdre I - 0 - MdhD.tY - 4- toom temp. and atm. pres~urc, the cataiy;t filtet(j, F.'!
(2-welbox7-4-hydroxy: filtrate mpd. to dryness gave an oir, let stind I e, v,
~e WhIte cf Itals, in. I I A roftned a 5t. ProdtMI, which, bom
Aud sd.." C'T 1?. 3171). Sind?u n-sults %rete ut'O. y1elifu 2"M x. (80 /-(1
obtained wing 12C. K4Pq and 3 g. NAtM or 4 g. (NI(4)r 2-itaM
6.Wd V), in. V~V' B(Ol..1 s7
'CO3'%nd8j.K$POJ"cata1ytft; Sulatitatlaz6quidguntaw stirred with 40 cc. Coned. ILCI, tile mixt.
for cryxt. gualacol gave 54-58% lb. lb (04.3 C.) and 2.5 1. At 1401 In a bouib tube, the crude crya, product EiAcrvil
140 rtflux'~d 12 bro.' the $01M. decoloritied with anfinki C, washed with a little k*-Lold concd. lICl gave 5.43 g. ~J :L
trea" with 20.5 it. Na.CO. (added In small anits.) to y odatt (demethylation was complete if the produ--
neutralize the film-Ated IICL them with 0-5 S. X11M., =Yed readily In 0 parts 11$0- undissoInq materW P-i
Itt stand 24 bra., the crystab filtered, witshed with xna-anredeted M, which, dimolved In water. the iniAt. decolur.
anit-i. of IGO, dried At room temp, gAvit 69 v. (087c) Y-fted, filtered. the filtrate treated with 2 parts eonvt. JIC!
melhary-44 YPkdMW&1)VX4[1 P6.(1111191" UINVU addm. gave 4.8 J144i
was so pit-pd. (without isolAtion of 1b) V,
255-72*[(Corrimr.1 -1. 43.
Us 1`0110-~S: Is detom by Wijng 12 hrs. with 7 1. H.O. !j;UU), relxwted VI M. 239-4
deco
zhe inixt. treated %-Itv.12-22 g. powd. KIISOv. let stand 24 fit a rnall anit. IIjiO, and the solit. treated jv1tjj*conc,!,
hr;. " '. n 07 ""' whild Vooling fmvt
Kif e"" M~y ardoP&eva", in. W, ydlow needles, seasitive te) light.
,wsp-z 0 1. d. with If (bth t- Catalytic reduction of VI In sq. medium with Pd-C
by
45*). 30 gi lao 'NIfs method of Carrigan, d al, (IM. cit.), yitldf.41 76%
nad NO
Utol . the ralt. -*A&PW
h- dro7pnvo. thr. ratal"St Altered off, tile filtiateirvaittl with
!~;* s. H3COi. kept 1i his. ~i the rtfilgerator, the pvtd.
ptodurt fiftered 61T. idded And r4wilered ravii XowAtivy-0-

110AC to
~A lu ~'C) -
ILU4- With 'j-"" kt-CAU-
Fu'
Pttr

ftuntry : Hungary
Cz-tOi.,r-)r'jr=:Organio Chovdatry,
G-2
Synthotio Org&nla Chemistry.
19502
A"Ibu, Joi;r. : Ref. Zhur,-KhWya No, 6, 1959
i'Llt'- Or Toldy, L.; Fabricius I
'Ins"
tit,dt. Hungarian
Titlc New Syntheses of Chlorpromazine.
Orig. Pub. Acta chim. Acad. scient. hung.9 1958, 11+1
No 1-2, 203-209
Abstract See RZhE2iiw, 1957, 77140; 1958, 64517.
Card: 1/1

FADRIX 14.
USSR/Hadio Phonographs Apr 51
"Radio-Phonograph With Push-Button Tuning," Yu.
Figurovskiy, M. Fabrik
"Radio" No 4, pp 22-25
Model 1 has long- and medium-wave bands and 4-station
'push-button tuning. Also has one button for phono-
graph operation. Special feature is use of cathode
detector, which increases selectivity as compared
with grid detector w~th-some sacrifice in gain.
Parameters of radio-phonograph are: Output paver, 10
.v) harmonic factor, 8%; frequency response, 50-6,000
cps; power drawn from line, 70 W; sensitivity, 100 mv;
seloctivity for 25 ke detuning, 30 db.
1AiqLoA

USW Eloctronica -.Tape recordoro
Card 1/1 Pub. 89 - 22/26
Authors i Kozyrov.., A.) and Fabrikp He
N.-
Title t Triple-mot or tape-roller mechanism
Periodical I Radio 12, 46-50., Dec 1954
Abstract I A simple-type triple-motor maepetie t--pe roller mechanism is described. The
cassetes hold a 700 Llf-ter tape that can be used for 30 rainutes soundscribing
at a speed of 385 M-Vse'c, or 15 minutes at a speed of 770 r=/sec. The
mechanism can be fed from a 110, 127 or 220 volt line. A selsyn gene rutor
syster., desiLmed for a 50-cycle neti-jork, can also be used as a driving
.mcchanism instead of the irotor. Electric brakes are provided instead of the
Conventional tape brakes. A general liyout of the mechanism, the arrange-
ment of jr~rts and detailed shop dra-wings are presented. The principles of
adjw;Unj,: the riechwiisi--ii, revcrsini, its notion, braking and inotantaneous
stopping, by nccms of salectinL the ol-)tjjwm voltaLes are discussed, Diagrams;
drvirinp; circuit di;-.Lr,-ja.
Institution
Submitted

KOMAY, Anatolii Vladimirovie.h-, FABRIK0 Mark: Abramovich; KANIVSXATA,H.D.,
redaktory; TROITSKIT, L.V., redaktor; AIUMORGY, B.I., tekhnichs-
ekiy redaktor
[Design of amateur magnetic recorders] Konstrulrovanis liubitell-
skikh magnitofonov. Moskva, lzd-vo DOSAAF. 1956. 175 p. (MIRA 9:9)
(Kagnetlc recorders and recording)

F A G
MIM/Electronics.7 Sound,reeording
Card 1/1 Pub. 89 17/33
Authors Koz'yrev, A., and Fabrik..M.
Title Magnetic tape recorder Ath amplifier operating on transistors
FsriOdiOal I radio 2x 37-39p Feb 56,
Abstraot I A technical description is given for a magnetic tape recorder of small
dimensions, fed from a battery with its ribbon mechanism driven by a -
spring motor, and intended for taking dictation when traveling. For such
an instrument it is found feasible to use junction transistors in the
amplifier instead of electron tubes. The technical details of this anpli-
fier including a statement-of the parts involved and its construction are
given along with directions for its adjustment. Illustration; block
diagram.
Institution t
Submitted

t
Subject USSR/Radio AID P - 4395
Card 1/1 Pub. 89 - 4/11
Authors Kozyrev, A. and M. Fabrik
Title Magnetophone with triode-transistor amplifier
Periodical Radio, 3. 30-39, Mr 1956
Abstract The operation of the tape, its mounting and design
details are described. Nine diagrams present a very
detailed picture of the entire operation.
Institution None
Submitted No date

AID P - 4929
Subject USSR/Electronics
Card 1/1 Pub. 89 - 13/17
Authors Kozyrev, A., and M. Fabrik
Title Amateur 'magnetic recorder
Periodical Radio, 7, 45-48, Jl 1956
Abstract The authors describe the procedure in producing a magnetic
recorder by the means available to an average radio
amateur. The type described corresponds to the "Dnepr-3"
and "Dnepr-5" types. It permits recording a band of
frequencies from 100 to 7000 cycles with a recording speed
of 381 mm/sec. This speed, may be reduced at will, to
190.5 mm/sec. The first part of the article gives a
detailed description of the driving mechanism. Six detailed
drawings.
Institution : None
Submitted : No date

AID P - 4943
Subject USSR/Electronics
Card 1/1 Pub. 89 - lo/18
Authors : Kozyrev, A. and M. Fabrik
Title : Amateur magnetic recorder
Periodical : Radio, 8, 34-36, Ag 1956
Abstract This is the second and final part of an article by the
same authors (this Journal, #7, 1956). It deals with
the electrical parts of the magnetic recorder, which are
aslo presented in a detailed connection diagram. Two
tables of specifications, I drawing of the assembled
recorder.
Institution : None
Submitted : No date

AID P - 5022
Subject USSR/Electronics
Card 1/1 Pub. 89 - 7/14
Authors : Fabrik, M. and Yu. Osipenkov
Title : Automobile radio receiver
Periodical Radio, #9, 34-38., S 1956
Abstract The authors describe in detail an experimental model
of an automobile radio receiver. It is equipped with
only one vacuum tube and with nine triode transistors
of the PIZH and P3A types. The detector is equipped
with a diode transistor of the DG-Ts8 type. One
connection diagram, 2 drawings of assembled details.
Institution None
Submitted No date

ACC NRs AT7000712 SOURCE CODE: UR/0006/ ~i60010001001'510050
':AUTHOR: Kozhevnikov, S. N. (Corresponding member AN UkrSSR); Prazdnikov, A. V.
hnical sciences);
(Candidate of technical sciences); Ioffe, A. M. (Candidate of tec
Fabrika, L. P. (Engine4er)
1ORG: None
TITLE: Use of electronic simulation for studying the hydropneumatic system of the
feed mechanism on a pilger mill
SOURCE: Ukraine. Ministerstvo vysshego i srednego spetsiallnogo obrazovaniya.
~
Gidroprivod i gidropnevmoavtomatika (Hydraulic drive and hydropneumatic automation),
no. 2. Kiev, Izd-vo Tekhnika, 1966, 45-50
i I
ITOPIC TAGS: rolling mill, pneumatic servomechanism, hydraulic device, computer ap-
'plication, analog computer
!ABSTRACT: Electric simulation is used for studying the operation of the feed mecha-
-inism on a pilger mill. This method consists of using an analog computer for solving
the equation of motion of the moving masses in the mechanism. Shown in the figure
is a feed mechanism for production of seamless tubes 219-325 mm in diameter. The
unit contains a hydraulic brake consisting of housing 4 with diaphragm 6. Inside th
housing is tapered plunger 9 with a rod rigidly, connected to plunger 3. The entire
.104 N/ra2.
braking system is filled with water which is fed in at a pressure of 58.9
Card 1/3

ACC NRt AT7000712
Rolls I move sleeve with
mandrel 2 as well as
plungers 9 and 3 from the
extreme left-hand position
l
toward the right. During
this process, water from
the main line flows through
check valve 5 into cavities
A and B. After completion
of rolling, the moving
masses are braked by com-
pressed air in chamber C and begin to move toward the left. On the return path,
water from cavity B flows freely through valve 7 into the waste line until the end of
the tapered plunger covers the diaphragm. At this point, the fluid pressure in
!chamber A rises and valve 7 cuts off the waste line. This begins braking of the
.moving masses. The fluid in chamber A is forced through the annulus between the
-tapered plunger and the diaphragm into chamber B and through pressure valve 14 into
~ the waste line. Valve 14 is used for regulating braking conditions. The length of
'the braking path is adjusted by using screw 10 fo,~ setting piston 12 in measuring
i.unit 11. When plunger 9 enters diaphragm 6, piston 12 is moved by fluid pressure to
~the extreme right-hand position. This action delivers a fixed quantity of fluid to
i

ACC NR, AT7000712
)the cylinder of measuring unit 11 without resistance, so that there is no braki 9
!force on a given section of the braking path. When piston 12 stops in the extreme
right-hand position, braking force develops in the hydraulic braking system. After
completion of braking at the beginning of the rolling process, spring 13 returns
piston 12 to the original position while spring 8 returns slide valve 7 to the ncutral~,
position. Electronic simulation was used for studying motion of the masses in this
mechanism as a function of their magnitude, the working capacity of the feed mechanismi
,was determined and operation of the hydraulic brake was checked with variations in
parameters. The program included simulation of both the acceleration and braking of
;the moving masses. The resultant data show that an increase in air pressure consid-
~erably reduces the operating cycle of the mechanism accompanied by a sharp increase in
!deceleration of the moving masses past the permissible value. An increase in the gap
:between the tapered plunger and the diaphra,&n to more than 0.4 mm results in an
texcessive final velocity of the moving masses during braking. Repair measures are
called for when the clearance reaches this limiting value. The given data agree with
,those of dynamic computation. Orig. art. has: 5 figures.
SUB CODE: 13/ SUBM DATE: 29Jun66
~..;P~0_3.

Bulgaria/Organic Chemistry Synthetic Organic Chemistry, E-2
Abst Journal: Referat Zhur Xhimiya, No 19) 19561 61532
Abstract: 8-5 g NaRCO3 and hydrolysis of the formed N-2-6-bram)-furfuryl-
N-acetylsulfonylemidej, yield 65%, MP 135-1360 (from alcohol), with
14% solution NaCH. Attempts to prepare homosulfanilamides from
N-acetylhmosulfanil-chloride and furfurylamine or I. were un-
successful. On interaction ofer-brocomethyl-furan with acetyl
derivative of homosulfanilamide (III) a substance was obtained
which does not melt at 2500 and having the composition correspond-
ing to difurfurylated derivative of III.
Card 2/2

t64 dirfradim.'", n. WO-w-, -W,
Lad homoalftniluddes. t. Comm
ad. . Wleare. scif. It.
Iff LOS g. 5-altrof I bromide with 0.903
'K phthallmide In 30 ml. xylene xt~130-401 12 hrs. giv
~Ppt-. "td. with RtOff to give 0.99 g. N- -aitrofurl
0
plithalimide (1). m. 212-14*, 1 (2.72 g.) heated 12
-50* with a slight excess of concd. HCI, filtered, and
at 140
A". j
mother liquomevapd. gives 1.58g. &ultrofurfurylm1ne-
HCI(11). Treatment ot 1.79S.11 with &q, NaOH and Et%Co
extu. gives 0.64 g. &nitxWud Lae, b" 129*. Meatinj
1.79 %. U with 214 g.. acetyl=suauHyI chloride mA 3,34 g,
Nall Ot 2-3 bts. in MetCO gives 2.48 g. An-(5-nitro-
2-furfuryl)-N4-aceiyUuUanilmide(M m.164-5* (EtOlf).
M Is sapond. with 20% IICI to 07% MI-(6-nitro-2-furfuryl)-,
sulfanilarnitle, in.- 178-80* (1120). N'-(&-N1tro-2-furlury1)-
'N4-acitylbomw1fanitamide and N45-nitro-2-fuffuryl)-
U1
:.5

mide are similarly preod. 0. H. Wbt:eWr-
11

DULGARIA/Organic Chemistry. Synthetic Organic Chemistry. G
Abs Jour: Ref Zhur-Xhim., No 2, 1959, 4685.
Author Fabrikant. A.
Inst
Title Nitrofuran Derivatives. 5-nitrofurfuryl Ethers.
Crig Pub: Xhiniya i Industriya (Dulgaria), LO, No 2, W-42
(1953) (in Bulgarian).
Abstract: 5-nitrofurfuryl alcohol (I), bp 160 /9 rxi, has
been prepared by the acid hydrolysis of 5-nitro-
furfuryl acetate; I is converted in ether solution
by treatment with FbJRj (30 rdn, 260) to 5-nitro-
furAiryl bromide, yield 65c,-, rap 46-47" (from pe-
troleum ether). The latter product is converted
to ethers of various types by treatment with the
Na alcoholates of the corresponding alcohols in
Card V2

PARITKANT, A.
"News in the field of flotation reagents; review of the publications during the last
eleven yearso' 1946-1957 inclusive"
Khimiia i industriia. Sofiiaj Bulgaria. Vol. 30, no. 3, 1958
Monthly list of East European Accessions (EEAI), LC, Vol. 8, No. 6, Jun 59, Unclas

BULGARIA / Chemical Technology. Chemical Products and H
Their Application. Fats and Oils. Waxes.
Soapsand Detergents. Flotation Agents.
Abs Jour: Ref Zhur-Khimiya, No 12, 1959, 43858.
Author : Fabricant A.
Inst : -1Wt--g1v-eE-,
Title : News in Photoreag6nts (Rtview of Literature for
the 1946-1957 Pdriod)i
Orig Pub: Khimiya i Industriya (Bulg.), 1958, 30, No 4, 112-
116.
Abstract: Bibliography of 53 titles. No abstract.
Card 1/1

1?ABRIXLNT, A.
---------
A, source for effective flotation reagents. p. 173.
GODISHNIK. Minno-geolozhki inatitut. Sofiiaj Bulgaria. V01. 5, No. 1, 1957/58
(published 1959)A'
Monthly List of East European Accessions (EUI) LC, Vol. 9, No. 2, Feb. 1960#
UNGL

FABRIKANT, A.
Flotation properties of same thionaphtols. p. 179.
GODISHNIK. Minno-geolozhki institut. Sofiia, Bulgaria. Vol. 5, No. 1, 1957/58
(published 1959).
Monthly List of East European Accessions (EEAI) LC, Vol. 9, No.2, Feb. 196o
UNOL

S/081/62/000/0210/044/120
B1663101
AUTIIDIISz Fabrikant, A., Khadzhiyov, P.
TITLEs Intensification of thickening processes in ore dressin6 worka
made possAble by the use of flocculants
PERIODICALt Referativnyy zhurnal. Khimiya, no. 23, 1962, 387, abstract
23170 (Minno delo i metalurgiya, v. 17, no. 4, 1962t 25-27
[Bulg.; summaries in Russ. and Ger.1)
TEM The results of laboratory and pilot-plant tests on thickening
processes are given. AMp (AMF) flocculants are recommended for use in
Bulgarian ore dressing works. LAbstracter's note*i Complete translation.]
Card 1/1

FALIRJ,~~!N'T) A.; FAXIENO',.') Il.
Preraration of flotation reagents by vc.,2,--anlzed
caoutchouc waste. Pt. 1. D.Im 1 induatriia 36 no.4:136-138
164.

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NKMI
RAYTS, M.M.; FABRIKANT, G.L.; LIBERMAN, I.
Penicillin in the treatment of syphilis in children. Pediatrita,
Moskva No-1:35-40 Jan-Feb 51- (CIML 20:6)
1. Prof.M.M.PAyte; Candidates Medical Sciences G.L.Vabrikant and
I.S.Liberman, 2. Of the Syphilological Clinic of the Institute of
Pediatrics of the Academy of Medical Sciences USSR (Heacl of Clinic-
Prof.M.N.Rayte; Director of Institute--Honored Worker in Science'
Prof.G.N.Speranskiy, Active Member of the Academy of Medical Sci-
ences USSR.

FABRTKAgT, G,_Lt
US,IR. "Physiology" Anatomical and Physiological pecularities of
the child., I. M. OSTROVSKAYA. Reviewed by G. L. FABRIKANT.,
MED. sestra., U, 1951
Monthly List of Russian Accessions, Library of Congress, March 1952,
Uncl.

FA 43 OQ I KA A-fr, q, k -
FABRIKANT, G.L., kandidat moditsinsidy nauk; RIIZXKOVA, L.S., kandidat
2 FifWnskikh nauk
Dynamics of titer changes in the Wassermann reaction in various
methods of syphilis therapy in children. Vast* van. i dorm. noel:
30-34 ja-F 155. (MM 8:4)
1. Is sifilidologichookoy kliniki (zav.-prof. M.K.Rtayts) Institute.
pediatrii AMN (dir,-deystv. chleno AMN, saslusheraW7 deyatell nauki
prof. G.N.Speranakiy) i earologichookoy laboratorii (zav.-prof.
N.H.Ovehimikov)-2Sentrallnogo kozno-venerologichookogo inst. (dir.-
kand. mad. nauk U.M.Turanov)
(SYPHILIS, in infant and child
there, titer of Wassermann reaction, changes in various
there methods)
(WASSIRMA" MACTION
titer changes iniarious methods of syphilis ther. in
children)

FABRIUNT, G.L., kaudidat meditsiuskikh nauk (Koskva)
0 W-Wiffm --
Physiological peculiarities of adolescents. Yelld. i akush. 21
no.4:8-15 Ap 156. (MLU 9:8)
(ADOISSOUCS)

FABRIXANT, G.L., kandidat meditsinskikh nauk
Present-day methods of treating syphilis In children. Felld. I
akush. 21 no.12:12-18 D 156. (MLRA 10:1)
(SYPHILIS, COMMUITAL. RE ITART AND INUNTILS)

FABRIURT, G*Le, kand,medsuauk (Moskva)
v- ~,
,Pneumouia in Infants. Yelld. i akush 22 no.9:28-36 157 (MIRA 11110)
(FmKU ONIA)

FABRIKANTe-GA., kand.med.nauk (Moskva)
Prdvention and treatment of purulent skin d1seAsee in children. Had.
sestrA 17 no.3:13-19 Mr 158. (miRA 11:4)
(SKIN--DISEASES) (CHILDRIW--CARE AND HYGIM)

FABRIKANT, G.L., kand.med.nouk (Moscow)
Inoculations for children* Felld I akush, 23 no,5;21-30
w 158 (MIRA n:6)
VACCINATION)
IIMWN-DISKASM)
M

FABRIKANTO -
C-, I
Influenza in children. Felld. i skash. 23 no.12:15-22 D'58
( DWWMA) (MIRA 11:32)

FABRIUM, G.L., Icand.med.nauk (Hookya)
I Felld. J (Akush. 24 no.6:21-28
Colientoritto in children.
Jo 159. (MIRA 12:8)
(MICSTINNS-DISHASSS)

YABRIKM, G~L., kand.med,nauk (Moskva)
Urticaria in children. Felld. I almh. 25 n0-3:10-15 Mr 160.
(KnU 13:6)
(URTIURIA)

PAWUKANT,,.G.L.y kand.med.nauk (Moskva)
I---- --
Rheumatic fever in children. Fel Id. i akush. 25 no.4:35-39 Ap '60.
04IRA 14-- 5)
(ROU14ATIC FEUR)

YEREMOV, V.A.., kand.med.nauk (Lugansk); CHERVOIRMi, O.D., prepodavatel,
infektsioanykh bolezney; FABRIKA11T, G.L... kand.med.nauk, prepodavatell
kursa detskikh bolezney --
Instruction on children's infectious diseases in medical schools.
Felld. i akunh. 26 no.501-58 MY 161. (MIRA 34:5)
1. Meditsinskoye uchilishche, Magnitogorsk (for Chervonnvy).
2. Meditsinskoye uchilishche No.21 Moskva (for Fabrikant).
(PEDIATRICS-STUDY AND TEACHING)

JABRIURT, G.L. (Moskva)
"Z---
Treatment and prevention of rheumatic favor in children. 7elld.
I akush. 25 00,5110-17 yV 160, (HIU 1317)
(MMM&TIC 32m)

I---FABRIKkR,v G.L., kand.med.nauk (Mook7a)
Pylorio stenoois and pyloric spasm in children. Feltd. I akush.
26 no-4:16-19 AP 161. (MIRA 14:3)
(PYLORIC SPASM) (PYLORIG STENOSIS)

FABRIKAIJT G L , kand.med.nauk (Moskva)
ti -0-mvp
"The healthy Ng sick child" by A.I. Dobrokhotova and I.M.
Ostrovskaia. Reviewed by G.L. Fatrikant. Felld. i ak-ush.
27 no-4s60-64 Ap 162 jCIIIIDREN-DISEASES) (MIRA 15:6)
(DOBROKHOTOVA- A.I.) (OSTROVSUIA, I.Mo)
p

I
FABRIKANTP G. L., kand. mad. nauk (Moskva)
F~mwia in children. reltd. i akuah. 27 no.6:23-27 je 162.
(MBA 15:7)
(URIn-ANALYSIS AND PATHOLOGY)

SHEYNURI S.; FABgIKANT, L,
W4Iat construoUwo *f the 'U1 Iyanovsk Cement Plant teaches. Na strole
goo. 3 no.2t4-6 F 163. (MIM 16 -.2)
1. Zamotitellnaohallnika otdola stroitellukh materialov.-i abornogo
shelesobetone Gooetroys. RSFSR (for Sheynker). 2. Upravlyvuhchiy
tresta Memotroy Ullyanovokogo soveta, narodnogo khozyVetva Cror
Fabr.ikant).
(Ullyanovok-Cemnt plants)

K -
ZOTINA, R.S.; KIFEMA, A.Ta.; PAR KANT, L.D.; STAVSKIY, A.T., red.,
KAPRALOVA,,4.A., tekhn. red. - e 1. ,
[Collection of problem in mathematical statistics and
probability theory]Sbornik zadach po matmatichookoi statistike
i teorli ver-oiatnostei. Moskva, Gosstatizdat, 1962. 183 P.
(MIRA 16:2)
(Mathematical statistics) (Probabilities)

ULLNuVICH, A.S.; FAEIUKANT, M.A.
New binding material from pyrol7tic resins. Ayt.dor. 26 no.9s
18-19 S 163. (MIRA 16slO)

O"Rfx"T~ M, 8, (Prof.) Hon 'Aorker of Sci
"Role of Conserved Tijisue in Therapy," Khirurglya, No.10, pp. 18-21s 1947
Translation W-18831, 19 Jul 1951

UMRMedicine - Tissue Therapy mar 50
"Investigations on the Biological Activity of
Dried Tissues," Prof K. B. Fabrikant, Prof N. S.
MNLrchenko, Khar1kov Med Inst' Khar1kov Stomatol
lust, and Khar1kov Republic Jav and Face Hoop
"Sov Med!' Wo 3, pp 20-22
Describes method of preparing dried placenta tis-
sue therapy, implantation technique, and effects
of its use in cases of various diseases in opha-
thal 1, urol, and dermatol practice. 'Also dis-
cusses prepn of dried skin and bone tissue and
effects of its use. Dir, Kha Ikov Med Inst, R. I.
an 176T77
UM/Medicine - Tissue Therapy Mar 50
(Coutd)
Sbarlaya; Dir, Khar1kov Stomatol Inst, Prof
P. V. Vlasenko; Chief, KhA Ikov Republic Jaw
and Face Hosp, N. M. Svet.
-170M

FABRIUINT~ N.JA.
Aerondinanika. Chast'I. Moskva, Gostekhizdat, 1949. 624 p., diagrs.
Title tr.: Aerodynamics. Part I.
QA930-F2
SO: Aeronautical Sciences and Aviation in the Soviet Union, Library of Congress,
1955

1(2)
PHASE I BOOK EXPLOITATION SOV/3265
Moscow. Aviatsionnyy tekhnologicheakiy institut
Nekator7ye voprosy aerodin-1ki i din-1ki samoleta. (Same Problems in
Aerodynamics and Dynamics of Aircraft) Moscow, Oborongiz, 1959- 11 P-
(Its: Tru&y, VYP# 42) 2,,100 copies printed.
Additional~Sponsoring Agency: RSFSR. Ministerstvo vysshego i srednego
spetsiallnogo obrazoymiya.
Ed.: (Title Page).: S.I. Zonshayn, Doctor of Technical Sciences, Professor;
Managing Ed.: A.S. Zaymovskaya, Engineer.; Ed..of Publishing House: S.I.
Vinogradskaya. Tech. Ed.: V.P. Rozhin.-
,PURPOSE: This collection of articles is intended for the engineering and
technical personnel of design offices and scientific-research organizations.
It may also be used by students of aeronautical *uzes, specializing in the
field of aircraft construction.
COVERAGE: This collection of articles contains acme results of scientific re-
search performed by the Aerodynamics and Design of Aircraft Department of KATI
Card 1/6

S.ome Problems in Aerodypazios (Cont.) SOV/3265
(Moscow Aviation Technology Institute) during the period 1955 - 1957. The
collection considers a number of problems in wing theor7 for three-dimen-
Bional flow and in the dynamics of aircraft, and also methods for research conduct-
ed at the initial stages of design and configuration of aircraft. A report by
V.T. Dubasov presents a variational method for approximate determination of the
velocity field for potential unsteady, compressible and incompressible air flow
about bodies. S.I. Zonshhyn considers the methods of research performed to de-
termine rational dimensions of alreAft during the initial design stages. The
problem is solved in a general formulation, but the obtained results are applied
to particular problems, for instance, to the calculation of optimum wing loads*
In a report by N.Ya. Fabrikant, the theorem regarding the lifting force of a wing,
given by N.Ye. Zhukovskiy, is generalized for the case of a rotational three-
dimensional f.Low and a compressible medium. A formula is given for calculating
force arising Prom the mutual interaction of two flows. The results obtained are
used for calculating the effect of the accompanying jet on the lift coefflcien~
of the wing and for calculating the load'distribution along the span in the region
boz*kring on the ving ti-p. A report by S.M. Matveyev deals with one of the im-
portant problems in aircraft dynamics - the loop - first investigated br.-H.Te.*
Zhukovskiy. The problem is solved for the mathematicallysimplest case, amely
a loop with uniform turning bf the flight path. The kinematic and dyijAftie Bmalysis
Card 2/6

Some Problems in Aerodynamics (Cont.) SOV/3265
Translational notion -of a Aircular cylinder 18
Arbitrary motion of in elliptical cylinder 19
Motion of the symetrical9p (Nikolay Yegorovich
Zhukovskiy) profile I
Steady motion of a cylindrical body in a compressible fluid R
7- 2
8. Examples 23
Translational notion of'an ellipse along its
large vxis 23
9. Flow about a circuinference 26
10. Translational notion of a thin," profile 28
Zonshayn, S.I. Data Pertaining to-Investigations of Rational
Dimensions of Aircraft 32
,Eabxik&nt,A.Xa~ Generalizations of Zhukovskiy's Theorem of Lift
Fokces and Some Applications 61
1. Lift force in tw-dimensional rotational flow of an in-
compressible medium 62
2. Lift force in two-dimensional rotational flow of a
compressible medium 63
Card 4/6

Some Problems in Aerodynamics (Cont.) SOV13265
11. Calculation of loop trajectories 96
12. V;rtical velocity component in the loop
13. On the angular velocity of an aircraft in a loop 100
14. Transition from the variablee to the variable t. Barogrm
characteristics of a loop 102
Tupolev,, A.A. Special Features of the Aerodynamic Configuration
of Near-Sonic Airci~ft io4
Conclusions
AVAILABLE: Library of Congress
Card 6/6
105
AC/pp
-4-1-60

NXKRASOV, Borls Borisovich; BWAGO, G.Y., prof., doktor tekhn.nank;
KOSMOV, X.F.. prof.. reteenzent; FABRIMT,. 19 Ta retsenzent;
RUDM, SA. reteenzent; SHILIT , A.M., aid.; SrRKLINIKOVA,
N.A., tekhn.red.
(Hydraulics] Gidravlike.
196o. 26o p.
(Hydraulics)
Moskva, Voen.izd-vo K-va obor.S=,
(KIRA 13:5)

PMLR.'.OV, A.I., kand. tekhn. nauk~~~KANT ~Nja,.,-prof., red.;
PORTIIOVA, Z.S.., red. izd-va; BOROVNEV, N.K.,, tekhn. red.
(Aerodynamic principles of inertia separation] Aerodinamiche-
skie osnovy inertsionnoi separatsil. Pod red. N.IA.Fabrikanta.
Moskva, Gos.izd-vo lit-ry po, stroit.,, arkhit. i stroit. mate-
rialam, 1961. 123 P. (MIRA 15:1)
(Dust-Removal) (Separators (Maohines))

FABRIKANT, Nikolav YakovlevJch; VUBASI,W, V.T..q red.
(Aerodynamics; general coui-.:e] Perodinarrdku; obAchl-I
WIRRA 17.
kurs. Moskva, Nauka$ 1964. E:14 p. .10)

L
ACC NRt AP6011782 SOURCE CODE: UR/0147/66/000/001/0028/0037
AUTHOR: Fabrikant, N. Ya.
ORG: none
TITLE: Velocity distribution in a turbulent flow close to a solid surface
SOURCE: IVUZ. Aviatsionnaya tekhnika, no. 1, 1966, 28-37
TOPIC TAGS: flow velocity, turbulent flow, surf-ace property
ABSTRACT: The author considers the relationship between average velocities and tan-
gential stresses as the basis for calculating a velocity fiVId in a turbulent flow.
Motion transfer theory is utilized as the point of departure for this study. In ac-
cordance with this theory, the averaged tangential stress resulting from turbulent
mixing and involving a case of flow parallel to the x-axis is determined by a standard
equation. The distance of intermixing can be determined both experimentally and theo-I
retically. Experimentally it is determined by measuring the velocities and tangentiall
stresses in turbulent flow. Theoretically, the distance is determined on the basis of'
an accepted turbulent flow model. The study is in agreement with the data in the lit-L
erature on the vortex nature of turbulent mixing. This phenomenon is a direct result
of the rotation of isolated fluid bodies under the effect of a transverse force. The
transverse motion of the fluid bodies and their rotation is retarded by the ambient

L 3818o-66
ACC NR, AP6011782
fluid. It is because of this phenomenon that the distance traveled by these bodies
is limited in a direction perpendicular to the flow. The calculated distance of
intermixing based on this method is determined for the case when vx is independent of
x. The distance of intermixing obtained by the above method is very close to the
experimentally determined distance. This is not true of the distance calculated
according to the standard formulas in the literature. Turbulent flow over an infinite
surface is considered. At a distance from the surface where the effect of viscosity
is imperceptible, the average velocity is assumed to be distributed a=cording to -
parabolic law. This law does not satisfy the boundary conditions at the wall. The
article also deals with an approximate method of computing velocities in the general
case of turbulent flow in the vicinity of a solid surface. Orig. art. has: 6 fig-
ures, 17 formulas.
SUB CODE: 20/ SUBM DATE: 26Jul65/ ORIG REr: 001/ OTH REF: 005
Card 2

1- P, j K A 1VT S,
USSR/General Problems of Pathology - Shock. T-3
Abs Jour : Ref Zhur - Biol., No 1, 1958, 3028
Author : ._Fabrikaat,_ P. B.
Inst
Title On the Significance of Individual Reactivity of the Body
in the Formation of Thermal Shock.
Orig Pub Tr. Kirg. goo. med. in-ta, 1956, 8, 155-163
Abstract A burn of 33-35% of the surface area was caused by a
stream of scalding water. The course of the shock accom-
panying skin involvements of such intensity was characteri-
zed by individual variations in arterial pressure, hemocon-
centration. and survival. Anesthesia (2 ml/kg of a 50% solu-
tion of urethan) shortened the original blood pressure dropo
prevented hemoconcentration and postponed the animals'
death.
Card 1/1

FABRIKAMr, S.I., inzh. (Novopolotsk)
Increasing the operational reliability of an automatic switch.
Energatik 13 no.8;20-22 Ag 165. (MDiA 18:9)

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IXVIB,A.N., doteent. kandidat tekhnichaskikh nauk; FABRIKANT.T.L.,
nsuchnyy sotrudnik
Polymerization rate of vinyl chloride in emulsions., Khim.prom.
no.2:48-50 F'47- (MLRA 8:12)
1. MMM
(Ithylene) (Polymers and polymerization)

FAI321U.''Fr) T. L.
Fabrikant, T. L.
"The development of a process for obtainini- certain copoll ers of
vinyl chloride and acrylonitrie.11 'fin Higher Education "'S.R. "oscow
Inst of Chemical Machine Building. !lo!7cow, 1956. (Dissertation .or
the Derree of Candidate in Technical ."3clences).
Knizhnaya letopist
No. 21, 1956. 'Moscow.

v0 N"Y'. ' -\- I.
KLINOV, I.Ya., prof.; FABRIXANT, T.L., nauchnyy sotrudnik; MTLINIKOY, V.P.,
inzhener.
Use of carbon and graphite materials in the woodpulp and paper
industry. Bum.prom-32 no.8:6-8 Ag '57. (MIRA 10:12)
1. Monkovskiy in8titut khimicheakogo mashinostroyeniva (for
Klinov, Fftbrikant).
(Graphite) (Woodpulp industry) (Carbon)

5(1,3) FWF. I BOOK E)MLOITATION 1900170
,Fabrikant, Tamara Llvovna, and Vollf Leonoviek, Volltman
Asbovinil i yego primeneniye v khimicheskoy prcelyahlennosti (Asbovinyl and Its
Ptilization in the Chemical Industry) Moscow, Goaldhimizdat, 1958-
78 p. Errata slip inserted. (series: Korroziya v khimicheskikh
proizvodstvakh i sposoby zashchity, vjrp. 11) 3,000 copies printed
Ed.: I.Ya. Klinov; Editorial Ccmminsion: N.A. Baklanov, V.Ye. Volodin.,
V..IS. Kiselev (Chair-n)., I.Ya. X:Linov., V.I. Kruchinin (Secretary),
G.V. Sagalayev (Deputy Chairman), and P.G. Udyma.
PURPOSE: This booklet is intended for vorkers speeializing in corrosion prevention
and for design engineers of chemical and related industries
COVERAGE; This booklet desaA with the prevention of corrosion and anticorrosive
materials. It reviews ph7sicochenical and mechanical properties of asbovinyl
which io an anticorrosive mixture, the riasic canponents of which are ethynol
(divinyl acetylene)slacquer and asbestoa. Methods for preparation of the
Card 1/5

Asbovinyl and Its UtIlIzation (cont.) SOV/31TO
asbovinyl mixture and the utilization of thin ml-xture as a protective material
against corrosion are briefly outlined and t--ifotty te,,11niques during pro-
duction are reviewed. Chemical resistance of different types of asbovinyl to
corrosive agents is discussed. The exWri(,rcP of the induRtry in using asbo"l
mixture for the lining of various containers, f liters, gas conduits, pipes, etc.,
is outlined. The procedure for using this mi:rture as a corrosion resistant
material is explained as well as methods of tutoring, transporting, packing, etc.
Studies of A.L. Klenbanskiy, I.M. Dolgopol'skiy and T.P. Shabodalov proved that
asbovinyl mixture can be usel success-fully for protecting equipment of the chem-
ical industry against corrosion. It in now videly used in Soviet industry. There
are 16 references: 14 Soviet and 2 Eng1lsh.
TABLE OF CONTENTS:
From the Editor 3
Foreword 5
I. General Information 7
II. Basic Materials 9
Card 2/5

Asbovinyl and Its Utilization (Cont.) SOV/3170
Ethynol lacqiAer 9
Asbestos 13
III. Production Process for the Preparation of Asbqvinyl Mixture 19
Preparation and dosing of rav material 19
Mixing 19
Packing 20
Storing 20
Production control 20
Consumption of materials used im preparing the initial asbovinyl
mixture 20
Technical specifications for the asbov~nyl ,mixture 21
IVp Properties of Asbovinyl 29
Physical and mechanical properties 22
Chemical resistance 26
V. Use of AsboviMrl as an Anti corroe ion,Materi al 34
Card 3/ 5

Asbovinyl and Its Utilization (Cont.) SOV/3170
Use of asbovinyl as fettling 34
Use of asbovinyl as dyeing lacquer 38
Use of asbov-inyl as a base coating 38
VI. Experience of the Indastry in Using Asbo-Oln.7,y " a Protective
Qoating 42
Lining of bubbling towers used in the prrAu(.,rJ.,,-,. of sulfuric acid 42
Lining of acid tankB 43
Lining of fermentation dr=s 44
Lining of alIcali neutra.Uzers 44
Lining of filters made. of reinforced coner~te 45
Lining of vane vheela of exhoauBt fanfi and smAll tixrbines 46
Lining of gas conduits 47
Lining of pipes 47
Lining of wooden towers and t-heir mptallic bar.6 49
Lining of electrofilters, (selenium precipitation chambers 50
A base coating 51
Asbovinyl cement 54
VII. kebavlnyl Section of the Corro!Aon Pr*-,rentton Department 55
Card 4/5

A8bov.-Inyl and Its Utilization (Cont.) SOV/3170
with
VIII. Safety Techniques During Work/Ethyuol Lac%uer and Asbovinyl
Mixture 61
Appendix 1. Instructions for Using Asbovinyl Mixtures as Fettling 62
Appendix 2. Excerpts From K[KhM Regulations Concerning the
Procedure of Combined Costing of Metal Surface With
Polyisobutylene and Asbovinyl Mixture 67
Appendix 3- Excerpts From VTU MKhr 3109-53 Specifications for the
Asbovinyl Lining Mixture 74
Bibliography 77
AVAIIABLE: Library of Congress
Card 5/5 2-17.6o

KLIKOVp I.YA,; IABRIIANT,--T.L.-,,-
Improving the properties of ambestoo-vinyl blends by modification.
Trudy HIM 22:1,39-158 160. (min 14%1)
(Asbeston) (Vinyl polymers)

KT.-MOV# I*Ta.j KMSEHOKp B.I.; FABRIKUT, T.L.; GnIMANy TS.I.
Chemically stable mastics based on
Plast.massy no.2s44,50 161.
(Plastics) (Protective
a modified asbestos viny2,
(KIRA 34:2)
coatings)