SCIENTIFIC ABSTRACT NIFANTYEV, E.Y. - NIFONTOV, B.V.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001136910015-4
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: July 13, 2001
• Sequence Number: 15
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

F7TV1, 7..A.;
Syn t?ie s i s and a I., y i c n
gliIC03e. a~ir. c;L. :~i:n,

yr., t1r. e B F)
kii! m. -3,,, nc.

Pc-h/Pr-4 HYL TRATI
Woo-/9/64/034/011/3850/3850
OMION MR.- Ap5onos
AUTH09:'
f derivatives of phosphorous
TIM: o. Alev YPOS-0 -uitrog~u containi
bih"
-S- 00M. iErita 64 ~-38W
V,
-~T; agen compound:"
orga a
16joua- acid,o kanic aaado
-0.
Abstract.,. -Inv ewof the -low reactivity of amide derivatives of phosphoro
Iscid as intermediatta in the production of augar phosphites, sugar phoaphatest.-
'iand other phosphorus containing eaters of carbohydratea,~ the authdr synthesised
;new types of nucleophilic nitrogen-contataing phosphorous acid derivatives.
..N-methaxyamide of 1,3-butylenephospliorous acid wen synthesized by the reaction
,of 1,3-butylene chlorophosphite (1) with 0-mathy1hydroxylamine; the reaction
of (1) and ITA-dieihy1hydroxylamine produced the 0-ph6sphorylation product
of the latter. The chlorophosphite of (1) readily phosphorylates 3,5-dimethyl-
pyra~ole aud 4-ethyl-5-mthyl-delta2-pyrazoline, producing phosphorylated
heLerooyales. A hydravide was synthesized from (1) and nonsymActrical

F17ROV, K. A.; N I FV.' E. Ye . ; t, I; i -,.I! "-J()l .-: - V, L, .,- .
A. ' . ; . ~ - . . , . ,
Synlnes!s ar.,~ chrand --ul -r-,pe-tilp-q if ~ - ', .c "i pE t f,
carl)ohydra'les. Zhur. cb. khim. 314 r .1 -CK4-409~) " I I,
I - ,:;~; ;-)

ACCESSIGIT NR: A24018072 S/0080/64/037/002/0429/0433
AUTEORS: Petrov, K.A.; Nifant'yev, E.Ye.; Ly*senko, T.N.; Sinogeykina,
L.P.
TITLE: Synthesis of certain derivatives of phenylphosphonic acid
SOnICE: Zhurnal prikladnoy khimil, V. 37, no. 2, 1964, 429-433
TOPIC TAGS: phenylphosphonate, synthesis, phosgenation, phenyl-
phosphonic acid ester
A3STR,LCT: The synthesis of phenylphosphonates by the following
procedure: PC], Sop, ROU
C'11, C,11,PCI, - AICI, ---0. C,[I,POCI, - AIC13
ICI.
- C,11,PO(OR), - AIG13 H.0 C'116PO(OR)SI
and the subsequent phosgenation:
Card 113

LccBssioN NR: A24o18072 0
C'11 //OH
C,ifspo(OR)l
C,11,poci..
were investigated. The dibuty, dihexyl, di-2-ethylhexyl and diphenyl
esters of phenylphosphonlo acid were prepared according to the first
equa~.ion by reacting a mixture of Dhenyldichlorophosphine and AlCl
with SO C12, removing the excess S02C12, and then reacting with tN
appropriate alcohol. The monobutyl, hexyl and octyl esters were
prepared by reacting in absolute ether the dichloranhydrlde of
phenylphoznhonic acid (I) with the appropriate alcohol and pyridine.
T'--e butyl and isoamyl esters of diethylamidophenylphosphonio acid
were prepared by reacting In absolute ether a misture of I, the ap-
prop.-late alcohol and triethylamine, and then diethylamine. Phosgen-
ation of the diethyl aster of phenylphosphonio aoid at 40-50C gives
t-'-.e mon-ochlorar-hydride of the monoeth3rl ester of phanylphosphonic
acid; at 120-130C. I Is formed almost quantitatively. Phoggenation_,
Card 2/3

.LCC-ESSION NR: A24018072
at the lower temperature of
ranhydride of the monohexyl
art. has: 1 table and 3 equations.
ASSOCIATION: None
SU31111-7TTED: 23Jun62
SU3 CODE: CH
the monohexyl ester gives the monochlo-
ester of phenylphosphonio acid. Orig.
DATE AOQ: 1914ar64 ENCL: 00
NR REP SOV: 002 OTHER: 004
Card 3/3

PETROV, K.A.; NIFANTIYEV, E.Ye.; SOPIYOVA, I.I.; LFVITAN, L.F.
Synthesis and 3om- p:-or-;-!.eS of dialky'Lcyclohexyl phosphates.
Zhur.prikl.khim. 37. noI. 5s1132-1135 My 164. (MIRA 17t7)

NIFANTIYEV, MO.;
Synthesis
Vysokom..soed.
BELOVF~TSEV, M.A.; LEVITAN, L.P.
and some properties of cellulose acid phosphites.
7 no.3:513-516 Mr 165. (MIRA 18:7)

PREDVODITELEV, D.h.; N.'FANr'YEV, E.Ye.,- R(Xj')V!11, Z.A.
Spit he s ie of -911-u, )se hypophosphi teq. Vysck 0m. Saed. - rr,. ',- ~ '191-19L
My 165. , _ ik
I . le:~
1. MosKovskly tekstillay-y

FREOV(SITEIEV, D.P. L_EFAlq~IAW
~A,E.Ye ~ ROG(ArIN, Z.A,,
..-!J,
SynthesJ.3 Of CellUlOSe phosphites by the reaction of moncmathyl
phosphite with cellulose and their subsequent transformatlom.
Vysokom. soed. 7 no.6:1005-1009 Je 165. (MIRA 18i9)
1, Mogkcv8kiy tek-gtillnyy institut.

Z
L5167- !L
1-6
504
-J:
--50
V- t. 00.16' -.X0 --,-They.---
-t eoug- Sol do he -Aead - - -mm 5~ o-
- A ir- m0 ar
are.mo era 1 -1 b in dimethyl-forniaqW, and* in chidtofoft, They Are slowly
~,_y:eo u e
hydrolyzPd lif vater with cleavage of the P-N bond. Treatment with carbon tetra-
Chloride results in cross-linking of the linear polymerg, apparently by the Arbuzov
reaction_:
4
P=
PIO
Ccl
4--
4"V'
rA=
71.
4-
-77 77
7

.1 - ~;. ~'T -, -
4 ~ . - a . . . r, ~ '. . " . 1 1.
--., - -- --t -~It- :- - '1-1 ~I - . I
-, r,,,, t~ n : ~-, t, ,~j , :. ~ I ~ . -1 - I . . I
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'1TFAYT7YLl,-lj, J~OX.Ooi ,
I i ~-V.
Alcoholyst-t, ~),, '. fluccrcrithyl phosph'tes and phosphon'Ltos.
Zhur. ob. kk4--,T. -~ ~ r. D. -. C, .88 , 5
- - 1. 0 16, (IMIFLA 'L81:10)

502723,

Ivs Y

-:MH Rgr-.-:
SUB.~Cc SM""VATE
oplia -002f ATD
Pmm

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NIF~.NVYFV, f Yr-.; KUiJKOl, V.11~
Corte In reactl nni -,~ [i ke~?mt, r~!uptp Is .zmur~ crg. fl~lv, i
no.llil9l~5-1959 '0 lb~. . , , ~.J, ~,'
1. Moekovg~rly go5.idar-2~venn:fy tiniva-sitet imeni M,tl, I ,

'~ -, " , '~. ~ -;' ,r . . , , -
.: " .! '- -. ~ -.- , -_,-
d
: '; - ~ .; r" -.. - - .
...--.:, ' -'~ 0 u It,, "
i y - .1 , ,I ~~
I , -a- LIT Ce,'~L!(,Se
. -- - . .
~ I rl -. ~ r,---~ . . .~ - D:' r, n' . - - -- '! . '?.
I~ M, "i , '- F.'. 1 1,

PREDVODITELEV, D.A.; TYUGANOVA, M.A.; NIFANT'YV, E.Ye.; ROGOVIN, Z.A.
Synthesis of phosphorous cellulose esters by reesterification
of dimethyl phosphite and their subsequent transformations.
Zhur.VKHO 10 no.4:459-461 105.
(MIRA 18:21)
1. Moakovmkiy tok.4tilInyy inFtitut.

NIFANTOYEV, Z.Ye.; 3"iCHEGIMEV, A.A.
Synthesis and alkylation of dipropyl oho9phir".es
I ~ 2- 5,6--di cyc.'ohexylidene glucose.
glucose, and 3,4-iso~TolDylidene-pqneth-ylarabi.rcfi,ir~. V~3t. '4r-~JK.
Ser. 2tKhim. 20 no.4:80-82. ii-tg 165.
1. Kafedre khimicheskoy tekhnologit !Iaskovskogc
wdversiteta.

NIFANTIYEV, E.Ye.; '.VANOVA, N.L.
Synthesis ai;d chemica.2 properties of phosphorous biamides.
Vest. Mosk. un. Ser. 2: Mim. 20 no.6:82 N-D 165.
(AURA 19:1)
1. Kafedra khimicheakoy tekhnologil M03kovskogo universiteta.
Submitted S,ipt. 20, 1965.

T 398k--66 RMA.=',r
ACC 111, 'p_~
06016658 SOMCE COOE'- ' UR/0079/65/03-5761-6
A1JTHORt klifantlyev, E. Ye.; Fursenko, I. V.
ORG: none
TITIZ: Alcoholysis of beta-fluoroethyl phosphites and phosphorites
,SOURCE: Zhurnal obshchey khimii, v. 35, no. 10, 1965, 1882
TOPIC TAGS: vacuum distillation, phosphorylation, ester, polyvinyl alcohol, or-anic
phosphorus compound, fluorinated compound, alcohol, fluorohydrin, organic qrrnthetic
process
ABSTRACT: It has been shown for the first time that various
phosphltes and phosphonites can be obtained In high yields by the
alcoholysis of beta-fluoroethyl estern of acids of trivalent
phosphorus at 20-400C. The method opens up new horizons for the
synthesis of labile phoophorus-contaInIng compounds. The beta-
fluoroethyl ester of 1,3-butylenephosphorous acid and an,equimolar
amount of octanol were maintained for 10 hours at 200C. Ethylene
fluorohydrin was then driven off (95%) under vacuum, and the mix-
ture was distilled. Octyl-l,)-butylene phosphite wag obtained
In 80% yield. Dioctylphenyl phosphonite (62% yield) and propylene-
10-bla-10-butylene phosphIte (83% yield) were obtained In siml-
lar fashion. The fluoroethyl esters can be used for the phos-
phorylation of high-molecular compounds, e&g,t P_q~ly~~Lnyl alcohol. L- ;~_371_
SUB CODE- 07 SUM DATE-. 13May(')5
Card 1/1 j_j- UDC: 547J61118

ImtArIvOletit, vImj*Qm-cQnUIGUW organic caqmmm~i
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Y". UW
-1~~r'ocivbc* m~abl-anrcmu"arA:divboti~tati~tieblorldog as well as altromethave VA
to ~Vthe chromistograpby of xmW
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vhciphttei'~ ink.. vh~i~6'tdtes its* the s i ~ leading tollarring of the
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;the,, ciompmads 'et~dled gave.- i6rew'disttnct "chrovat am In-the case.or determi-
'3:1istion 111111imedliteli. after. application W_ tbe. substance to the plate. Certain
Dqv- M6.181.5/+3 5",~:

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ACC. NRv AM28501
i orth6r or -triLvelent.iboorhorm-ecii:ftlulimi powpoundi -such an a
wid
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'Jlcould UWU'~,dbir_seterlzed, although-, tetr's-'e-ith 8 -a gl 16cpim-and
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YCOV
on-Slu'alnum Oldd4i A 4~-finli4--rtilotlotWblp'voa.fatind b
etween the Rf values and
am~_ uAd: atudled: ~Abrl~~ljhom are cha a te x
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-a po. d phitem r c rl
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t
r. f We ,t it! d1a1*1phosjh1
lky1j)bosph1tei'.eih1b1i -evellAosier mAllity. Dbilk,*1&64phlndus~ sold* (dlalkyl.~
a
~A
phodybilie OX1444Yliko~ebaricterized. bUh_ lu4s. h
e ho& OU thin-P spV.
Uyer. 0 hj IA 11ableAd a. gniter. amber of
J C.6 mitations or txllw"
out
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Method of
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56roeWdn 'A i~, 1P
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orgiud h wd~ Oristnic.amide
g Ap, orue.compot
--ABSITRACT-f ~.~HAId.;~~and'oyanddesoxvaugars -beto ed.by the
caii btaln
A.Arbukdv aftiiLotlo-n from: airallible -tdt!i:~4ak,*Idiadidbglyoophosph a
1-bilddipho4phonites o~ A2101- Lod and..'bromides
!Anddialk Ades and
y
-fluo
ef; era a as -ind~mono roacet aoldis are used
t et to
L ' t
n
*3kylaitba, Won s*
'6-lodo
-were
6-desoxy-1 92-3 1 4-~p
ho.folldwin compoun a,
7
_J Spip pylldefiigalaotose (73% yield) -bromo -&-desoxy-l, 2-
3*
L , 6-4-dexosy-l 2-3,,
11donega so ose. eld 6-ohlor
AlLio 56%
11doneg a jg%,~*Iild 6-refludro--&-desox it
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tioils Of for
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kiii:~ i4initle ~,a-A-'Idophqsph*tes anC:aftif hItes,-,!?f,,.oarboIvdrato44
78M -UTZ ~:.,G

L-31268-66 EWT(m)/EWP(J) M4
ACC NR1 AP6022804 SOURCE CODE: UR/0079/66/036/002/0319/032
AUTHOR: Nifantlyev, E. Ye.; Tuseyev, A. P.; Markov S. M.; Didenko, G. F.
ORG: none
TITLE: Synthesis of ethyleneamidothiophosphites,and -phosphonites
SOURCE: Zhurnal obshchey khimii, v. 36, no. 2, 1966, 319-321
,OPIC TAGS: chemical synthesis, organic phosphorus compound, phosphorylation,
mercaptan, organic amide, free radical stabilization
ABSTRACT : It was found that totraethyldiamides of acids of trivalent
phosphorus react with beta-aminoothylmarcaptan to form previously unknown
ethyleneamidothiophosphites and -phosphonites. These conversions were the
first oxar..Plos of phosphor1lation of aliphatic mercaptides with auddophos-
phites and amides of phosphonous acids. The synthesized othyleneamido-
thiophosphites and -phosphonites are of interest as Inhibitors of free.
radical reactions,.particularly. those developing in living organims.
Orig. art. has: 1 table. [JPRSI
SUB CODE: 07 / SUBM DATE: 09Ju164 / ORIG RFY: 003 / OTH REF: 002
Card 1/1 UDC: 547-419.1

- T 31266-456- --W-W/ WP(j) RM
ACC SOURCE CODE: uR/o(y79A6/036/002/0363/0363
AUTHOR: Nifant'Zey, E. Ye.; Gavrilova, A. I.; Bliznyuk, N. K..
ORG: none
TITLE: New method of synthesizing ethyleneimides of phosphoru acids
SOURCE: Zhurnal obshchey khimii, v. 36, no. 2, 1966, 363
TOPIC TAGS: chemical synthesis, imide, organic phosphorus compound, chemical
reaction, esterification, organic imine compound
ABSTRACT: Three now methods were developed for synthesizing phosphoethylonei-
midos. Dialkyl phosphites were found to0react with carbon tetrachloride.
ethyleneimino, and triethylamine at 0-20 to form ethyleneimides of
dialkylphosphorous acids. Both acid phosphonites, tetraalkyldismides of
phosphorous acid, and alkyl hypophosphites take part in the reaction; in
tie latter case diethyleneimides of alkylphosphoric acids are formed.
Bthy!Gnaimide asters of phosphorous acid are produced by alcoholysis of
mixoa othylonalmidodialkylamides when anine hydrochlorides are used as
cata3,ysts. Ethyleneiminos of trivalent phosphorous acids can be produced
by reaction of the corrosponding dimethylamides with ethyleneimine under
considerably milder conditions than under transamination reactions. These
reactions are model syntheses and are now being used to produce otherwise
difficulty accessible ethyleneimides of phosphorus acids. [JPRSJ
SUB CODE: 07 SUBM DATE: 13May65
'/I Q UDC: 547.2

7-~
23327-6-67~ -~,. V
AICC'~'Nlk AOW69 /66/004/002/62b W
sw. 0M ARft90
4A-UTqq*RS
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itute," MoskOvskik,
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01
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mwk'P !I, if. 8p Fy a oni or 't sec.
.013 A630 1166.0116io a by- phosphorylitionvif cellulove.
Y ene glycol at~~ or,4i6;4ihjiGiie gi, i -i haspidtas is
-phospi yco
p
th- timptiar- 8 A a ioli--i,1114 aild to 0
of.-t 4i old as, react
!t, 401 :41~bunt.:, fit Afiof,.phosphorus - isic~iperW ed~-In the product was:InvestIgated
clialt go.' PEMZlevie Pho t th a
ivaris y. Of '-re 8-anit the product rized by
Ago* is obialiwd are xu~
L C M-1/3- --UWs--66-095.26 T

I
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1 -1 - - - - -- ~ " - 7... ; --l"' -v I---..-"..,- - .. I - --.- - . - .. . I - ~ .. -- - . - - - - I

L 06~12=�L EWT(m)/E'dP(j) RM
NR:
SOURCE CdDE. UR/O079/&6/*/OO6/l1:i4/di�1
NIFANTIM, E. Ye., TUSEtEV..A. P., TARABOV, V. V.
"Colamine Glycophosphitee and -Phosphonitea"
Moscow, Zhurnal Obahchey 1(himii, Vol 36, No 6, 1966, pp 1124-i129
Abstract: The phosphorylation of colamine and N-methyleolamine by tetraethyl-
diamides of methyl- and ethylphosEhonous acids as studied. The amido-esters
obtained were used to phosphorylate carbohydraiws: 1,2-3,4-diisopropylidenegalac-
tose, containing a free primary hydroxyl, and 1,2-5,6-diisopropylideneglucose,
containing a free secondary hydroxyl group, thereby synthesizing the correspond-
ing colamine glycophosphonites. Colamine glycophosphites were synthesized from
diamidoglycophosphites, such as the tetraethyldiamidophosphite of 1,2-5,6-dia-
cetoneglucose, and the colamine derivative, forming cyclic glycoethylenemethyl-
amidophosphites, which reacted with various alcohols to form neutral colamine
glycophosphites. The infrared spectra and other properties of the compounds
obtained, including a promising Arbuzov reaction, were studied. Orig. art. has:
2 figures and 3 tables. EJPRS: 37,0231
TOPIC TAGS: phosphorylationg organic phosphorus compound
SUB CODE: 07 / SUBM DATE: 25Feb65 / CRIG REF: 008 / OTH REF: 001
.11
Card 1/1 LC
Ilia
1F_

ACC NR, AP6035684 SOURCE CODE: UR/0413/66/000/019/0031/0031
INVENTOR: Nifant'yev, E. Ye.; Komiev, I. V.
ORG: none
TITLE: Preparation of hydrogen alkyl phosphates and phosphonates.
Class 12, No. 186469 (announced by Moscow State University im. M. V.
iLomonosov (Moskovskiy gosudarstvennyy universitet)l
SOURCE: Izobreteniya, promyahlennyye obraztay, tovarnyye znaki,
f
,no. 19, 1966, 31
TOPIC TAGS: acid alkyl phosphate, acid alkyl phosphonate, ozone,)
J-
ABSTRAC-~'. simplity the process and to increane the yields in the
,preparation of hydrogen alkyl phosphates and alkyl phosphonates by
Itreatment of the latter with oxidizers, ozone is used as the oxidizing
I
jagent. [W.A. 501
SUB CODE: 07/ SUBM DATEt 17Nov64
Cord 111 UDCt 547.26.118.07

ACC NRi AP6033455 SOURCE CODE: UR/0413/66/000/018/0039/0039
INVENTOR: Bliznyuk, N. K.; Kvasha, Z. N.; Nifant'yev, E. Ye.;
Varshavskiy, S. L.
ORG: none
TITLE: Preparation of 0-alkyl esters of dialkylphosphinic acids.
Claos 12, No. 185905 [announced by All-Union Scientific Research
Institute of Phytopathology (Vaesoyuznyy nauchno-isaledovaL21'akiy
institut fitopatologii)]
SOURCE: Izobret prom obraz tov zn, no. 18, 1966, 39
TOPIC TAGS: alkyl dialkylphosphinate, phenylaroanic acid
ABSTRACT: To obtain biologically active compounds, dialkylphoaphinic
acids are treated with alcohols in the presence of phenylarsenic acid
as catalyst. The reaction is carried out with excess alco!,)l and azeo-.
tropic removal of water at 180-220*C. [W.A. 501
SUB CODE: 07/ SUBM DATE: 15Nov65
t Card 1/ 1 UDC: 547.26'118.07

ACC NR: AP 6 0 30 Q 014 SOURCE CODE:-UR/-0080/66/039/008/1881/1884
AUTHOR: Fedorov, S. G.; Nifant'yev, E. Ye.
ORG: ,Moscow State University im. M. V. Lomonosov (Moskovskiy gosudarstvennyy
universitet)
TITLE: Phosphites and phosphonites of novolak resins
SOURCE: Zhurnal prikladnoy khimii, v. 39, no. 8, 1966, 1881-1884
TOPIC TAGS: novolak resin,
/ ~).L 't /I I f /k! OA!cn_-~; 'C
ABSTRACT: Previous studies of this series showed that new novolak resin-based
polymers with desired properties, including thermostable biologically
active polymers, may be prepared by replacing the hydroxyl groups of
the novolak resin (I) with various functional groups. Eight reviously
unreported modified novolak resins were obtained by phosphoryYation
of the resin with esters and amides of phosphonous and phosphinous
acids: methyl methylphosphonite (II), dimethyl phosphite (III),
di(chloroethyl) phosphite (IV), and triphenyl phosphite (V). Phos-
phorylation of I with II, III, IV, and V is carried out in a distil-
lation apparatus by heating the reaction mixture for 2 hr, aL 170%
in the presence of Na in an inert gas. The reaction of I with 11
proceeds as follows:
Card UDC: 541.6+546.18

- __ ____4
ACC NR, AP603090
OH
\-CH,S- + C113-p< OH
OC113
CH
0- PIII>IV>V. Phosphorylation of I
Card 3/5 -

ACC NRi AP603ogo4
with amides of 1,3-butylenephosphosphonous acid (hexamethyl amide
V1, hexaethyl amide VII, and dimethyl amide V111) proceeds under
milder conditions than -with the esters. At 100-130% in an inert
gas with an excess of the amide, the reaction proceeds with complete
phosphorylation of the resin!
+(R,N),P
OH
CH2-
O-CH
ZO-CIIf O-P/ >C112
(CI1')3NP I
zC11, O-C11,
;o\ CH2-
At low amide concentration, cross-linked polymers are formed. All
phosphorylation products are solidified by usual methods, e.g., by
heating with urotropine, to form thermostable plastics. They are
highly reactive and may be used as starting materials in the prepara-
tion of polyphospatee, polyesters, and other products. Physical
Card

ACC NR. Ap6o~oqol,
constants an-d reac-tion conditions undcr 'wideh-Ithe phosiphorilated
novolak resins are formed are given in the table. [WA-50; CBE No. III
Pho6 Re M.P. of Composition P and
P~~w -Vept r~conafflooR, , -VIP-actipu N in
Temy)er-!Ti,, p dutt
zLigei Yound Cq1rtjAtad-- Table 1.
~3 ature 4 1 1
hgat: I (0C) (hrs) Q Phosphorylation of
resin (1) P N P N
novolak resin
3:, 160-170 3 30-50 0.051 ig,5~ - 18.45
18.69
3--1 00-175 2 95-t 10 1 0.083 15. Q - 0.85

170 -175
/2: i 3 13. 32
3.58 - 16.85
abo~.%! 360 1 12.01
1
(I V) 3:1 140-145 4
95-100
0.065
13.22
-
13-33
13.49
(V) 3 . 1 170 8 120-150 0.075 1.0. Z8 - 9.63
9. 16
(VI-) 3:1 100-110 0.75 - 0.032 12, . 7 8 It.60 t3.84
12.83 11.75
j.Vll) 3.1 Q5
1 1.5 - 0.036 11.37 10.211 li,07
11.45 10-51
(Vill) Li:j
135-111
3
100-110
0*021
11,27 1 13.84
0.42
Solutian doncentr9lHon 0.1-g/10 mls solvent
Card5/5
- SUB CODE: 07/
- SUBM DATE: 2CO-id64/
ORIG REF: 010/
12.50 OTH REF: 00'3/
10.00

AC C N R iAP6035631 SOURCE CODE-- UR/0413/66/000/020/0037/0037
INVI34TOR: N.Ifantlyev, E. Ye.; Koroteyev, M. P.
ORG: none
ITITLE: PreDaration of alkylphosphonic vcid dichlor' deEL Class 12, No.
1187018 (announced by Chemistry Department, Mosbow St"ate University ime
M. V. Lomonosov (Khimicheskiy falcul'tet Mookovskogo gosudarstvennogo
un:Lversit~eta) I
~SOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki, nu. 20,
;1966,37
ITOPIC TAGS: alkylphosphinyl dichloride, phosphorus toLchlorlde, sodiurrill.
alkylphosphite , 0-"
~
ABSTRACT: To simplify the method for the preparation of alkylphos-
phonyl dichlorides with the use of PC1 sodium alkyl phos-
31
phites are treated with PC13.
[WA-50; CBE No. 14]
IFS
.SUB CODE: 07/ SUBM DATE: o5Aug65
L-qardl/I UDC-.,547.241-.3;21113.07

2Q692
4 "V 3 00 S/12o/6i/ooo/001/030/062
9, 3 2 7 '~ (W 1rOV E194/E,184
AUTHOR: Nifantlyeva, F.P.
TITLE: An Ultra-High-Frequency Range Ferrite Phase Shifter
PERIODICAL: Pribory i tekhnika eksperimenta,1961, No.1, pp.101-102
TEXT: Ferrite phase shifters are becoming w)dely used for
altering the phase of a signal over a given frequency range.
However, most of the work has been done on the development of
ferrite phase shifters for the super-high.-frequency range. One
work has been published on a ferrite phase shifter for the
decimeter and upper end of the metre range giving a phase displace-
ment from 0 to 360 0 and having low losses, but it is complicated
and phase control is difficult- The present article describes an
ultra-high-frequency phase shifter which can alter the signal
phase in the range 0 to 360 OC by altering a longitudinal magnetic
field applied to the ferrite from 0 to 250 oe. The phase shifter
is of simple construction and comparatively small size; it is
illustrated schematically in Fig.l. This diagram shows the
construction of a phase shifter in which the length of coaxial
line is 60 cm, the internal diameter of the outer conductor is
Card 1/ 3

2o692
S/120/61/000/00.L/030/o62
E194/Ej84
An Ultra-High-Frequency Range Ferrite Phase Shifter
9 cm, the external diameter of the spiral -is 7.5 cm, the number
of turns of the spiral is 5 turns per cm, the centre core is
ferrite and the outer hatched cylinder is a dielectric. The
input and output of the phase shifter are connected to coaxial
lines by a plug and socket arrangement. The transformer must be
designed to match the coaxial line of 75 ohms and the spiral line.
The spiral contains two ferrite rods (ferrite L12OZnOFe2O3
grade,a~-25 (F-25); the electrical characteristics of this
mater have been published elsewhere. The magnetic field is
set up by a coaxial spiral winding on the external cylinder
consisting of a two-layer winding of wire grade -1.25
(PEL-1.25), contained in a water bath. The damping in the line
and the phase displacement were measured at a frequency of
150 b1cls. The line attenuation was determined by measuring the
signal voltage at input and output and it includes both losses in
the ferrite and reflections from the ends of the lines due to
imperfect matching with the coaxial lines. The amount of phase
shift was determined from the interference pattern produced on a
Card 2/ 3

20692
S/12o/61-/000/001/030/062
An Ultra-High-Frequency Range E194/E184
detector. An the magnetic field is increased from 0 up to 250 oe
the phase shift increases from 0 to 3600 and the attenuation drops
from 12 to 3.2 db. Acknowledgement is expressed to V.N. Detinko
for valuable indications.
There are 2 figures and 4 references- Soviet, 1 probably
translated from English)
ASSOCIATION: Sibirskiy fiziko-tekhnicheskiy nauchno-issledovatell-
skiy institut (Siberian Physico-technical Scientific
Research Institute)
SUBMITTED: January 2, 1960
LY
Fig. I
Card 3/3

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j.L
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PU-W _q
.-b~ndlil+.A
re a -cmm,- a
A--- of, filte IM 4ad-ldr,vainactin' lWaviziel for the
Isaw"t ~~Mllldilmt Will Orlabillits"i- siblo fail 6,a
--;'Am

PSHONIK, A.T., prof.; NIFAN-TIY I. EVA, L.D.
Ghanges in the higher nervous activity in circurn cribed aeuro-
dermatitis. Vest. derm. i ven. 38 no.4:3-9 Ap 164.
(~ff RA 18: 4)
1. Kafedra normallnoy fiziolcgli (zav. - prof. A.T.Pshonik)
KraBnoyarskogo meditBinskogo -nBtituta.

5.-76oo
SO*
AUTHORS: KocheLkov, N. K. , Nifant 'ycv, E. Ye. NlrLir.t L. V.
13 -Chlorovit-yl Ketones of t.-ie Hetevo,,-/,-' I-- Se~-'-(2-;
TITLE: I
PERIODICAL: Zhurnal obshchey khimlL, 1~)Uo, Vol '10, N'.
245 (USSR)
ABSTRACT: Synthesis of some /3-chlor-ovlnyl keLones, r;ontaLnIng a
five-membered heterocyclic radical, Iy the of
the correspondinE, acid chlorides with ace WL:,3
Studied. It was found that acid chlor-11'es of
carboxylLc, thiophene-2-carboxyli1c, and seienophene-.--
carboxylic acids easily condense with acetyllene ~,) f'orm
/3-chlorovinyl ketones-
corresponding I
,AC0Cj+Ct,EEC,, Air[.
f1C0C11=C11c1
Card 1/4 0 8 Se'

I - 7 2 ) z
-Chlorovinyl Ketones of the Hete-rocyr-lir-
fejr Le s
TZ reaction takes place at 30-1100. The heter-o(,ycIL(,-
-chlorovInyl ketones, like other vinyl ketones, rear-t
ith alcohol In the Dresence of alkalis to form Keto-
acetals: 13
VIC 1(COCj1=Cj1-N(C,H )3CI-
RCOC11=C11C1
Card 2/4
They also readily condense with p-NO C t~ HIINPNH to
c vespondIng pyvazole derivatives. Th erivIl-(
-chlorovinyl ketone condense. ~ -naph"hol 1~'.
tre presence of ferric chloride and YICI.

-Chlorovinyl Ketones of' the
P
er ies

It

NO, Se
Pre,nat-atior; of the following cumpourid-'Ii ve,,
Furyl-( 1ketone
10,2 - I or- - - ~"l 0
chloride op -1 'u ( 10 mm) .Thler,~r I
Card 1/4 vinyl ketone (65%), bp ir-4-11-A).1,~0 (2' mm). Sele,
(2) - /3-chlorovinyl ketone (4-5%), bp l-z2-lzc-.0 (7
.5,

-7
/9 -Chlorovlnyl Ketones of the Heteroc'/211- -(I-J,
Series
ASSOCIATION:
SUBMITTED:
Dimethyl acetal of
12) 2 -1 mm), G 1 4 J' I I c, D.--~e
acetyl or le
14"o mm) , n J,
D
Selenyl-(2')-I-(p-nltropheny'L)-,,)~-razole
0
100-101 2 - T h I e n y 1 - ( 2n a p t hi , 2 ' lu m
ferrichloride (66%). mp There --..--e Sov ie
references.
Moscow State University (Moskovskly gosudarstvenryy
universitet)
September '10,
, /4
Card 't' .

io
c Q.
Oa,~, c
11u, 01
Civil L(.-!'
of
futi
---'0 Of
ar, ani-I
acid d-4c*,-llor.-L,C-' ~,LUC:--,cd l4t, Wa~; 3i~OWl t-a-. -,-,o
--ocoads unJ quoly; oven at roo-.-,, to;-ap~crat o the corresponding
cac ~izn n. Ur
"Jo co 1.0 L
AW.torocyc L~ mpounds are nried 'or example
0 :1 CN
-P
V
0 0
G c +
2 2 6-4 /*
1', Ws G-e..
u
Card 1/2 UDC: 546-18 -1-547 + 711 543_._~,22

L 10303-67
ACC NR: A117003104
Of the fro.-, "~-10 '~----ta of
--C
azialys-z;, rn,01ce"Ilar a;-'C! 'ark~a a-jCCr':-a.
of ~-`Afrarod spoc'--a' W11.1c!" Cs-'aractol.-'Zo z'no
fo=ation of -Chc cycl-_c su'l-istances and
nes of phosphon-I'c acLds. 1-u rhould be no-od t:ho
process o,f tao reaction the t:-,iocyano group is not lost since thore is a
2 1 60 band :L'1 the infrared spoc trurl.
C. p-th- cyanoax-j1dioxophosphozanes ieit;h 'Uno molecular atrucTuro
Zlx Io
wh"-t follo-ws were characterizedz
o 0
R- P ? -R
---eza CH, and Ar C~~hl -SCN-p, SM-3, Le or 5^ -3.4.
Orig. art. has; 1 table. [J PXS .38,9677
TGA-JI0 'L'~GS: Organic 6YnthOtic process, phoap"o-rj!"cion, 1R SPOCLrUM.
phos-.)*.-.r,r;.c 4cid
SI;3- M-,Z: 07 / SUBM DAVE. 28ju,165 ORIc, RE,,?. 002 OTH RZF: 002
Carc., '-/2

EZINETSCV, A.V.; NIFASHEVA, I.F.; GPM,,'WVA~, L.A.; "LIANII,,XA, 7.Y.
Frontal sections in the Arct-.'c iasin and !heir relationa- I
.. ~ P
with the type5 of synopti(- processes. Trudy JUNII 255:11),'-
1112 163. 'MIRA 17:6)

-tm-- f
T'
di -21 bb~ od
ru y -V' - pik' W -po- romm- olgos o -ld~ proknom pog y
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-,-dj~ka AtkUld (Colledticn 6f artl6le s on
W. ' -- 0 6
or ~ApqdO. Jpp-~,

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SUB ODE-.-*~
P~m

2~ 2"
D299X1304
AUTHORS: Lemberg, V.K,, Bukhtoyarova, Z.M and Nifatov, di.il.
TITLE: The distribution of plutonium in the liver accor6ing to
the results of histoautoradiography
SOURCE Lebedinskiy, AN and Moskalev, Yu.I., eds. 3ioLolciciics-
koye deystviye radiatsii i voprosy raspredeleniya raclio-
abot., Moscow, Gosatontizdat,
aktivnykh izotopov; sbornik r,
1961, 136-144
TEXT: Due to the absence of suitable published data on the sub-
ject, the authors set out to study the course of the micro-distrib-
ution of plutonium-239 in the liver and bones by the histoautoradio-
graphic method, i.e,, by studying histological slides fixed on a
photographic emulsion The tests were run on white rats, plutonium-
239 being introduced intraabdominally as Pu(1403)4 in a single done
of 7,*c/kg at pH - 2, j~f ter 6 and 12 hours, and 1. 3, 71 lzi. 28,
41, 56, 88 and 225 days the rats were decapitated and slides of the
S/58 61/000/000/015/020
Card 1/3

21,244
S/581/bl/000/000/015/020
The distribution of plutonium., IJ299/1)304
bone and liver tissues prep~tred A detailed analysis of the )hoLos
shoTAng the tracks of plutonium alpha-particies at various stages
after the introduction of plutonium-239 is given and tiie rcsuLts UL
the experiments are compared, wi th various f indings in the s pecial -
ized literature on this subject, 'i'lic histoautocardiograms showed
a definite redistribution of plutonium in the stractural eLements
of the bones and liver., Within 6-12 hours after its intro6uction
diffuse di.stributiori of plutonium in all structural parts of the
liver is noted, jubsequently.. from 1-225 days. the plutonj-um, con-
tent in the hepatic cells decreases and oegins to accumulate in the
Kupffer's cells and the macrophages of tne perivascular connective
tissue, ~~ix to 12 hours after its introduction the bones coittain
only a small amount of diffusely distributed plutonium (bone marrow.
compact substance and diplod) 3y the end of the 3rd day a i.arked
increase was noted in the plutonium content of the bo-ne ,iarrow z,t
subsequent stages the plutonium content in tne .3one marrow,
diminished, out increased in the endosteum. and ,3eriosteum "oMe
plutonium. however was retained in the compacr L)onc ~nrouijiout u;-ke
Card 2/3

~"%00/000/015/020
S/581 61
The distribution of plutonium... D299VD!304
whole period of the investigation. There are 6 figures and 17
references: 6 Soviet-bloc and 11 non-Soviet-bloc. The 4 most recent
references to Lnglish-language publications read as follows: j.6.
-rnold cited by L-P. Lamerton "Proceedings of the Second United
Nations International Conference of the eeaceful Uses of itomic
L:nergy", vol. 22, p. 119. Geneva, 1958; M.i?. Finkel, Proccedings
uf the Society for Experimental Biology and Medicine, 83, 3, 494
(1953); M. Heller, Ch. 5 - "Bones" in the book by `W. Bloom. Histo-
pathology of Irradiation from External and Internal Sources, 70-161.
N.Y. - Tor. - Lnd. , 1948; R.J. Schubert, 1,1. Finkel, I.!. White a.
G. Hirsch, J. Biolog. Chem., 182, 2, 635 (1950).
Card 3/3

AUTHOR: Nifatov, ~.P.
2",245
S/58 61/000/000/0L6/020
1)299Y,)304
TITLE: The course of morphological lesions of the liver in rab-
bits affected by plutonium-239
SOURCE: Lebedinskiy, ~~.V. and Mosicalev, Yu.I., eds. 13iologiches-
koye deystviye radiatsii i voprosy raspredeleniya radio-
aktivnykh izotopov; sbornik rabot. Moscow, Uosatomizdat,
1961, 145-154
TEXT: The author's previous observations showed that dystrophic
and regenerative processes occur in the liver of rats affected by
plutonyl sodiotriacetate. Some rats develop cirrhosis and tumors
of the liver. These studies, however, related mainly to morpliolog-i-
cil lesions at remote dates in animals which had died. The aim of
the present work was to study the course of morphological lesions
of the liver in rabbits affected by plutonium nitrate. "'lie Pluto-
nium nitrate solution was injected intravenously in doses of 21, 14,
Card 1/3

2e, 245
S/58 61/000/0001/016/020
The course of morphological lesions ... D299404
7 and 21Lc/kg. Some rabbits were killed off after 2 weeks, 1, 5,
4, 5, 6, 9 and 12 months. The rest were spared to study their
survival rate and the remote effects of the isotope. A detailed
description of the liver lesions (as viewed under the microscope)
at various stages is given. At remote stages the plutonium iiiduced
marked structural hepatic lesions of the annular cirrhosis type.
The morphological lesions had a definite sequence of developuent
and were directly proportional to the total dose of ionizing radia-
tion. Doses of 21 and 14 pc/kg induced cirrhosis of the liver in
77.5% of the animals wit1iin 3-6 months; a dose of 2)Ac/kg itiduced
cirrhosis in 2376 of the animals by the 9th month. With a -lose of
2JAc/kg most rabbits showed symptoms of restoration by the 9th
month, Some of these animals developed regenerative hepatomata
and adenomata of the common bile duct. There are 4 figures, I table
and 12 references: 10 Soviet-bloc and 2 non-Soviet-bloc. The ref-
erences to the English-language publications read as foLlows: G L.
Prosser and oth. Radiology, 49, 299 (1947); Rhades, (.'h, 11
Card 2/3

2M 245
S/581_/61/000/000/016/020
The course of morphological lesions... D299/U304
"Structures accessory to the Gastrointestinal Tract" in the book
by Bloom. Histopathology of lrra(liation from External ond
Internal Sources, 541-549, N.Y. - 'for. - Lnd., 1948.
Card 3/3

Z 248
S/581_/61/000/000/019/020
12 ZID D299/D304
AUTHOR: Nifatov, A.P.
TITLE: The remote consequences of intraabdominal injection of
plutonium acetate
SOURCE: Lebedinskiy, AN. and Moskalev, Yu.I., eds. Biologiches-
koye deystviye radiatsii i voprosy raspredeleniya radio-
aktivTLykh izotopov; sbornik rabot. Moscow, Gosatomizdat,
1961, 174-181
TEXT: A study was made of the remote consequences of plutonium
acetate injected intraabdominally in white rats in doses of: group
I - 21.5, group II - 11.5, group III - 6.3, group IV - 3.3 and
group V - 1.6 ~Lc/kg. Some rats were killed off after 1 arxi 2 weeks
and i, 3, 6 and 12 months. The pathoanatomical lesions in the or-
gans of these and of 99 rats that died were studied. Data on the
life SDans was processed statistically. The death of most of the
group 1 rats was due to aplasia of the hemopoietic tissue and the
Card 1/3 1

21248
S/58 61/000/000/019/020
The remote consequences ... U299X304
appearance of inflammatory lesions in the lungs and gastrointestin-
al tract. Only one tumor was found in this group. Aplasia and
inflammatory lesions were noted in the other 4 groups, but to a
lesser extent. Groups II-V most often developed tumors of the
bone and hemopoietic tissues, gastrointestinal tract, liver and
mammary glands. Group V contained most animals with multiple
tumors. The rate of carcinogenesis increased with a decrease in
the plutonium dose. Yhis conformed with the findings of Z.H. Bukh-
toyarova and V.K. Lemberg (Ref. 3: Vopr, onkologii, 5, 8, 140 (1L)59))
who noted the greatest number of rats with tumors (54 and 40'1-a) after
the injection of plutonium acetate in doses of 1.89 and 4.0,uc/kg,
The most common tumor with plutonium acetate is ostoosarcoma. Us-
teosarcomata were primarily localized in the lon(,.,, tubular bones and
more rarely in the skull, vertebrae avd ribs. The largest percen-
tage of osteosarcomata was noted at a dose of 3.3)j..c/kg. Some rats
killed off after 6 and 12 months showed pathological osteogenesis
in the metaphysics and diaphysis of the long tubular bones, .)imi-
Card 2/~

28248
S/58 61/000/000/019/020
The remote consequences ... D299X304
lar lesions have been ooserved by other authors and from the action
of plutonium nitrate. A combination of dystrophic lesions and symp-
toms of atypical regeneration was noted relatively frequently in
the liver of the test animals: discomplexation of the hepatic oeams,
the appearance of hepatic cells of various size and shape with two
and three nuclei, a large number of mitotically and anitotically
dividing cells. Comparison showed that the number of carcinogenic
i)rocesses in the hemopoietic tissue is greater from plutonium ace-
tate than from olutonium nitrate. The optimum blastomogenic doses
of plutonium acetate are 1.6 and 3.3 yc/kg. There are 4 tables and
18 references: 13 Soviet-bloc and 5 non-Soviet-bloc. The refer-
ences to the English-language publications read as follows. I.I.P.
Finkel, Proc. Soc. Experim. Biol. and Med., 83, 3, 494 (1953); J.1.
Hamilton, Radiology, 49, 3, 325 (1947); L.F. Lamerton, Proceedings
of the c;econd United Oations International Conference of the 1eace-
fuL Uses of atomic Energy, vol, 22, p~ 119, 1958, Geneva; h. Lisco,
P.M. Finkel, A.M. Brues, Radiology, 49, 3, 361 k1947)~
Card 3/3

44062
8/742162/000/000/004/021
101511215
AVIMORS: Lemberg, V-K., Nifatov,-A-P-I-
TITLE: The microdiotribution of plutonium in the liver of
rabbits and rats
URCE so Plutoniy-239; rauprudoleniyet.biolo-L,,icheokoye
deystviye, uakoreniya vyvedeniya. Ed. by A.V.
LebedinE;kiy and Tuale Hookalev. Moscow, Medgiz,
1962, 23-31
TE;(T: The detailed wicrodistribution of this element in the
liver has not yet been clarified* Bxperimento were carried out on
48 rabbits and 44 albino rats. The former received a single dose of
.7X4/kg b.w. of plutonium nitrate (pH a 2.0) intravenously and the
letter were given the same dose iope In additiont a single dose of
J Oard 1/3

S/742/62/000/000/004/021
1015/1215
The microdistribution of plutonium...
3r(ulkg b.w. of sodium plutonyl-triacetate (pH = 6-5) was injected
i.p. to 12 albino rats. The rabbits were ,acrificed by air embolism
1,3,7,14,30,90,135' and 180 days after the injection. Nine rabbits
died during that period of time. The rats were decapit&ted 6 and 12
hours, and 1,3,7,14,30,45,60,90 and 210 days after the Injection. The
rats which received the-complex salt of plutonium were sacrificed 14, V~
30, 90 and 365 days &fter the injection. The liver was fixed in 10'%
formaain solirbion, enbedded in celloidin-paraffin and cut into sec-
tions 5 %1 thick. ~atorndiographa werc. prepared accorelinG to the
method- of Ye.V. Brleksova and EvdLns. ",.cposure time: 4-8 weeks in a
refrigerator. Stain:big with We*Gert's haniatoxylin. It was found that
-Pu was accumulated mainly in t,c.- r,.;ticulo-cndothclial systom eloments
of the liver. The complex ac-dt of plutonitua wao o1istributed relative-
Ay evenly in all the liver tissue clonients and was preacnt in lescer
Card 2/3

S/742/62/000/000/004/021
1015/1215
o" ~lutoiii= ...
azi o u n t s th t'-.
if, th~-
tiic: rate-, -.nd th.~
hours after t1ri~
Kupfer cells and
appearod in hiZh
dy 1 day after the
1" 1 4A t un d s .Thure was a
of Li-,- ~.Iicrodiotri',--,tion of pluton~un nitrat,-, between
rat;Ibits: it wri3 (-diffusely dii~.tributed lur-':~.6 6-12
irij,-cti,,n in th~-,- rats anL~ subsequuntly acc,,imul-.ted in
(1-210 days),wherLas in the rabbits it
co:xentration in the US elements of the liver n.1rea-
iiijection. Tlher,: arc 9 fibures.
Card 3/3

44076
0/742/62/000/000/018/021]
1015/1215
AUTHOR:' Nifatov, A.P.
. .........
TITIZ: Morphologic changes in the liver..of rabbits and rats
following the administration of pluton'A.UM-239
SOURCE: Plutoniy-239; raspredeleniye, biologicheEkoye
deystviye, uskoreniye vyvedeiiiya. Rd. by A.V.
Lebedinskiy and Yu.I. Moskalev. Moscow, Medgiz,
1962, 129-141
TEXT: There ve relativcly only a few aata in the medical lit-
erature about the morpholoGic changes in the liver in cases of Pu
injuries. Experiment3 were carried out on rabbits and rate. The
rabbit's received a single dose of 21,14,7 and 2,m(alkg b.w. of Pu
nitrate (pH = 2.0) i.v. The rats received a single dose of 7,g(a/kg
b.w. of Pu nitrate J.p. The complex sodium plutonyltr4aetate (pH
card 1/3

3/742/62/000/000/018/021
1015/1215
Morphologic chani:es in the liver ...
6.5) was also injected to r~iA3 i.p. in a single dose of 6-3m~41kG
b.w. The rabbits iere s,-.crificed 1,3,7,14 days and 1,3,41,~,9 and
12 months after the infection. 2he rats were sacrificed 6 e-nd 12
hours 1,30,14 days and 1,1",2,3 and 7 months after the injection.
The livers of t'nc sacrificed well as of those w."Ach died
were fixed in 10% fori:.alii', t_-nd Zenker's formol solutions arid embedded
in colloidin-par-f fin. 2.'Ic Lit-.ctions were stained with hemato,~ylin-
eosin, with azan for corinective tissue, by Pearl's method for the
detection of iron and with Sudan-3 (frozen sections) for lipids. The
morphologic chanees in the liver of the affected aninials followed a
certain pattern which depended upon the physico-chemical state of th6
isotope, the dose and the species of the animals. In the rabbits li-
ver cirrhosis developed within 3-6 months after doses of 21, 14 and
7r("/kg of Pu nitrate and within 9 months after a dose of 2!4&4,'kg. In
,-Card 2/3

5/742/62/000/000/018/021
1015/1215
Morphologic chanGo8 in the liver...
--the latter hepatonas and bile duct adenomas were present on the 9th
month. In rats, on the other handp a dose of 7,aCa/kg of Pu nitrate
produced len warkud changes redUtin& in only alight rearrangment
in the liver morphology. The 7complex saZt of Pu caused still less
changes in rats th;ui Pu nitrate. There are 4 figures and 5 tables.
.-Card 3/3

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podshiphi.krvyay zavod). v s~: 'pyt novatorov mashin st-,---;er-iya kuytyshei, 11-LE,
S. UL-25
SO: Letopis' ZhurnalInykh State,, Vol. V, 104b
3

1. NIFONTIOV, A. V.
2. USSR (600)
4. Bearings (Machinery) - Testing
7, Certain forms od deposits of magnetic po%der on bearing rings. Podshipn:Lk no. 9, 1952
9. Monthly List of Russian Accessions, Library of Congress, jenktW7 .1953. Unclassified.

lo NIFONTOV, A. V., Ena .
2, USSR (600)
4. Steel-Heat Treatment
7. Dependence of the qualities of EI 161 steel on the heat treatment method.
Podshipnik Mo. 11, 1952
9. Monthly Lists of Russian Accessions,. Library of Congress, March 1953, Unclaseified.

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X, / /,~, 0 /,~-/ )r6) v? /!-, /-,
NIYOMTOV. B.F. (HO13kva)
1 -1 1 * -
Pathogenesis and clinical aspects of traumatic shock. Felld. i
akush. 23 no.2:8-13 -Y 158. (KLRA 11:3)
(SHOCK)

UM/Winee
Mining Methocle
Bauxite
"Agpicl Cutting of Dritte at the North Ural
lauxlte Mines,* B. I. Nifontov, N. P. Kostin,
&i. A. Alekseyevskiy, Engineers, 5 pp
wCIGr Zhur" No T
Peters to success in decreasing time required
for,rapid cutting of drifts. Rapid autting of
39 drifts vas carried out in 1943-1947 at subJect
location. Describes cutting at various times,,
dlwlosing technical operations, speed, etc.
V80/0200 MOW
Gives three tables vith data on cutting operations.

NIFONTQLj W,~Xop KULIKOVY A.V.
Uranium mining metbods in France. Gor.zhur.,no.2:29-32 F 161.
(MIRA 14:4)
(France-Uranium mines and mining)

V IFQn _,-BoXia -va; ILIINSKAYA,
QV _jyq4i_y;LCh; YEROKHIV, G.M., red. izd
G.M., tekhn. red.; SHKLYAR, S.Ya., tekbn. red.
[Rapid drifting]Skorostnoe pravedenie gorizontallnykh vyrabotok.
Moskva, Gosgortekhizdat, 1962. 282 p. (MIRA 15:12)
(Flining engineering)

ITIFONTOV B.I., doktor tekhn.nauk; ROMADIN, N.M., gornyy inzh.;
On.Lanun"O.- L.Yu., gornyy inzh.
Study of the relation between the net drilling rate and the
depth of boreholes. Gor. zhur. no. 12:52-53 D 161.
(KM 15:2)
(Boring)

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NIFONTQV--B-I.; PROTOPOPOV, D.D.; SITFIKOV, I.Ye.; KULIKOV, A.V.;
'~.TVNIK-(A'A, A.I., red.
(underground nuclear explosions; problems affecting in-
dustrial nuclear explosions] Podzemnye iadernye vzryvy;
problemy promyshlennykh iadernykh vzryvr)-,f. Moskva, Atom-
izdat, 1965. 159 P. (MA 18:6)

ACC NR: UR/
AM6035814 (A) Monograph
WQntp .B vich; Kireyev, Vasily Vasillyevich'Kisilevich, Yevgeniy
Mefodiyevich;,Vollftrub, Iosif Arturovich; Sadkovich), Yan Fedorovich;
I Golomolzin; Arkadiy Ivanovich; Petrenko, Andrey Afans'yevich
Construction of ~ndergrouud structures (Stroitellstvo podzemnykh aooruzheniy
Moscow. Izd-,io "Nedra", 1966. 293 P. ilius., biblio. 2450 copies printed.
0 jj-.jA',oyk mining engineering
TOPIC TAGS:
FURPOSE AND COVERAGE: This book is intended for engineering and technical workers
of construction, scientific-research and design organizations studying the
problems of building underground ineiallations; it can also be used by workers
of mine-constriiction organizations. In the book are discussed the basic prob-
lems of conduAing mining 'operations during the construction of underground in-
stallations. There are 97 references, 72 of which are Soviet.
TABLE OF CONTEUrg [abridged)
Ch. I. Basic methods of conducting mining operations during construction of under-
ground chambers -- 9
Ch. II. Foreign experience in conducting mining operations during construction
of underground chambers -- 22
Ch. III. Drilliz* boreholes and blast holes -- 55
Card 1/2 uDc; 623.191.2+622 268.8

ACC_NR._AM60358l4__
Ch. IV. Blasti::ioperations -- 83
Ch. V. Mechani ion of underground loading and transportation operations -- 118
Ch. VI. Progressive methods of reinforcing mining excavations -- 145
Ch. VII. Methods of excavating underground chambers in hard rocks -- 175
I*Ch. VIII. Excavation methods providing for chamber-wall reinforcement during
the excavation~of a massif -- 178
Ch. IX. Excavation methods by which chamber walls remain open during
excavation -- 224
Ch. X. Examples of calculations relative to work organization and the selection
of equipment -- 233
Ch. XI. Ventilation and dust suppression during the excavation of underground
chambers -- 249
Ch. XII. Several problems of underground installation stability -- 280
SUB CODE: 08, 13/ SUB4 D=: May66/ ORIG MF: 076/ OM REF: 029/
Card

ACC NRi AT7004465
SWM3 COM UR/2834/66/051/001/0078/0084
AUTHORS; Borisov, A. A.; Nifquovl B, I*; Homadin, No Ke
ORG: none
TITLE: Computing the stresses in pillars between rooms in mines
SOURCE: Leningrad. Gornyy inatitut. Zapiaki, v. 51, no. 1, 1966, 78434
TOPIC TAGS: mining engineering, otress diatribution, underground facility
AB.rLRACT: Present methods of computing characteristics and requirements of pillars
between rooms in mines and other underground workings involve two-