SCIENTIFIC ABSTRACT SHCHUKINA, M.N. - SHCHUKINA, YE.N.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001548920019-2
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 23, 2000
• Sequence Number: 19
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

GALSTUKHOVA, N.B.,..; SHCHUK.U;A, M.N.
SYnthesis of thioreau derivatives. Part 1; A711LIhiocarbamyl-
piperazines. Zhur. ob. khim. 31 no.4:1090-1092 Ap 161.
(MIRA 14:4)
1. Vsesoyuznyy nauchno-issledovatellskiy khimiko-farmatsevticheskiy
institut imeni S. Ordzhonikidze.
(Piperazine)

BANASHEK, A.; SHCHUKINA, M.R.
2-(Iq- and ~ -pyridyl)-,42-thiazolines. part 2: S th is of
2-(O~-alkyl-ypyridyl)-,A2-thiazolines, their 4-car=l acids
and (/.g- and ~-pyridyl)-2-thiazol-jl.-,~~methanes. Zhur.obkbiTn.
31 n4.5:1479-:-1483 My 161. (MIRA 14:5)
1. Vsesoyuznyy nauchno-issledovatel'skiy khimiko-farmatsevticheskiy
institut imeni S.Ordzhonikidze. F
(Thiazoline) (Thiazolinecarbcj:ylic acid)
r

BANASHEX, A.; SHCHUKINA.
2-(/4-and I-pyridyl)-,A2-thiazolines. Part 3: Synthesis of
2-pyridylthiazolidones) their 4-carboxylic acids and their 2-
methyl substituted. Zhur.ob.khim. 31 no.5:1483-1488 YT 161.
(mm 11. - 51
ll-,-"Vsesoyuznyy naucho-issledovatellskiy khim:Lko-farmatsevticheskiy
0
institut imeni S.Ordzhonikidze.
(Thiazolidinone)

BANASHEK. A.; SHCHUKINA., M.N,
2-( ~- and ~-pyridyj)-42-thiazolinest Part 5: Synthesis of
oBters of 2-thiazolyl-,d Z-phenyl- and pyridylacetic acids. Zhur.ob.
khim. 31 no.5:148&-1492 My 161. Omm 14:4)
(Thiazoleacetic acid) (Pyridineacetic acid)

SAIMOLOVOVA, V.G.; GORTINSPLAYA, T.V.; SHCHUKINA, I-LN.
...
phenoxazine series. Part 3: Glycide derivatives of phenoxazine.
Zhur.ob.khim. 31 no.5:1492-1497 my 761. (MIRA 14:/+)
1. Vsesoyuznyy nauchno-issladovateliskiy khimiko-farmatsev-ticheskiy
institut imeni S.Ordzhonikidze.
(Glycidol) (Phenoxazine)

PPEDVODIT--:LFiVA. G.S.; SECH.UKINA, K.,N_
Phenoxazine series. Part /+: Acyl derivatives of phenoxazine and
1-carbethox~-3-quminophenoxazine. Zhur.ob.lchim. 31 no.5:1497-1500
W 161. (MM l/+: 5)
1. Vsesoyuznyy nauchno-issledovatel'skiy khimiko-farmatseyticheskiy
institut imeni S.Ordzhonikidze.
(Pyrazole) (Nitrile) (Sydnone)

VASILIYEVA, V.F.; YASHUNSKIY, V.G.; SHICHUKIMI, PLN,
Formation of substituted pyrazoles in the reaction of sydnones with
0(,I4 -unsaturated nitriles. Zhur.ob.khim. 31 no,5:1501-1501+ IV
161. (KMA 14: 5)
1. Vsesoyuznyy nauchno-isaledovatel7skiy khImi n.- armatsevticheBkiy
inBtitut imeni S.Ordzhonikidze.
(Pyrazole) (Nitrile) (Sydnone)

SAVITSKAYA, N.V.; SHCHUKINA, b4N.
Synthesis of 5-amino-3-~ (aminoethyl)indazole. Zhur.ob.khimo 31
no.6:1924-1926 Je 161. (MML l4a6)
1. Vaesoyuzn7y nauchno-issledovatellskiy khimiko-farmtsevticheski7
institut imeni S.Ordzhonikidzes
(Indazole)

YASHUNSKIY, V.G.; S.;'VOYLOVA, 0.1.; SHCHUKINA, M.N.
Substances with comploi-forming properties. I-art 6: Synthesis
of cyciic analogs of nitrilotriactic and ethylenodiaminotetraacetic
acids. Zhur.obkldm. 31-iao.7:2316-2321 J1 161. (MIRA 14:7)
1. _Vsesoyuznyy r-auchno-issledovatellskiy khimiko-farmatsevti-
chesklLy institut imeni S. Ordzhonikidze.
(Acetic acid) (Ring formation)

SAVITSKAYA, N.V.; TARASEVICH, Ye.S.; SHCHUKINA-, M.N.
Some derivutives of 5-nitro- and 5-amino-3-indazolecarboxjlic
acid. Zhur.ob.khim. 31 no.10:3255-3257 0 161. (MIRA 14:10)
1. Vsesoyuznyy nauchno-issledovateliskiy khimiko-farmatsevticheskiy
institut imeni S.Ordzhonikidze.
(Inda2Olecarboxylic acid)

KTIZ1,1.,TS, Ye,,7.; SI]Ajl!KOV,, V~S.j TEF-VAIUATTYAN, L.S.,; PIIE013l-IZHENSUYA, M~N.;
SUVW(Ovy N,X,; SYGIILVA, T,,P,,; ~',HCIIUKINA, M.N.
Differences in the action of some monoamine oxi"aa inhibitors in
vitro and in v-Avo. DoU AN SSSR 136 no-541231-2234 F 161,
(NURA 140)
.1. Predstavleno akad. A.N.Bakule-um-
(AWNS OXIDASE) (PHARMACOLOGY)

P.:IEDVODITELEVA., G.S.; SIICHUKINA, M.N.
Phenoxazine series. Part 5: 2-Aminophenoxazine and other 2-substituted
derivatives of phenoxazine. Zhur. ob. khim. 32 no.1:113-117 Ja 162.
(MIRA 15:2)
1. Vsesoyuznyy nauchno-issledovatellskiy khimiko-farmatsevtiches',.I'Y
institut imeni S.Ordzhoni'ddze.
(Phenozazine)

YASHUNSKIY, V.G.; VASILIYEVA, V.F.; KHOLODOV, L.Ye.; SHCHUKINA, M.N.
Sydnones and sydnone imines. Part 8: Polymethylene-bis-3-dydnone
imines. Zhur. ob. khim. 32 no.1:192-195 Ja 162. (NIRA 15:2)
1. Vsesoyuznyy nauchno-issledovatel'skiy khimiko-farmatsevticheskiy
institut imeni S.Ordzhonikidze,
(Sydnone imine)

BAIUSHEK, A.; SHC~UKINA, M.N.
2-()3- and r -pyridyl) -- n z -thiazolines. Part 5: Alkyl-phenyl-
pyridyl-2-thiazolinyl ZI,"--carbinols. Zhur. ob. khim. 32 no.1:205-
208 Ja 162. (MIRA 15:2)
1. Vsesoyuznyy nauchno-issledavatellskiy khimiko-farmatsevticheskiy
institut imeni S.Ordzhonikidzo.
(Thiazoline) (Methanol)

SYCHEVA, T.P.; TRUPP, T.Kh.; _qqqHUK-INA,_~!,,N. __
Compounds kith a potential antitubercular activity. Part 3:
Thio Rmides of 2-substituted 4-oxazolecarboxylic acids. Zhur.-
ob.khim. 32 no.4:1071-1077 Ap 162. (MIRA 15-4)
1. Vsesoy-uznyy nauchno-isoledovatel'skly khimiko-Carmatsevtichoskiy
institut imeni S.Ordzhonikidze.
(Oxazolecarboxylic acid) (Amides)

SAMOLOVOVA, V.G.; GOaTINSKAYA, r.v.;_..qKGHUKINA, M.N.--
Phonoxazone series. Part 0': Synthesis of some 1C-substituted
derivatives of phenoxazine. Zhur.ob.khim. 32 no.4:1085-1088
Ap '62. (MIRA 15:4)
1. Vsesoyuznyy nauchno-issledovatellskiy khimiko-farmatsevticheskiy
institut imeni S.Ordzhonikidze.
(Phenoxazine)

VASILIYEVA, V.F.; YASHUNSKIY, V.G.; SIIGHUKINA, M.N.
Sydnones and sydnone imines. Part 10: Reaction of 3-phenyl-
and 3-phenyl-4-methylsydnones with methyl acrylate. Zhur.0-0.
khim. 32 no-5:1446-1451 MAY 162. (MIRA 15-5)
1. Vsesoy-uznyy nauchno-issledovatellskiy khimiko-farmatsev-ticheskiy
institut imeni, S.Ordzhonikidze.
(Sydnone) (Acrylic acid)

KUZIMIE&, K.K.; OSTROUMOVA, N.G.; MARKOVA, Yu.V.; SHCHUKINA, M.N.
Thiazoline and thiazolidine series. Part 2: Acylation
of 2-aminothiazoline and the reduction of acyl derivatives.
Zhur.ob.khim. 32 no.10:3390-3393 0 '62. (MIRA 15:11)
1. Vsesoyuznyy nauchno-issledovatellskiy khimiko-
farmatsevticheskiy institut imeni S. Ordzhonikidze,,
(Thiazoline) (Acylation)

YERMOIAYEV,i V.G.; SHCHUYUKAI-M.N.
Pyridylthiazolylmthane series. Part 1: Synthesis and properties
of 4-pyridyl-21-thiazolylearbinol. Formation of free redicals.
Zhur.ob.khim. 32 no.8:2664-2670 Ag 162. (MIRA 15-9)
1. Vsesoyuznyy nauchno-issledovatellskiy khimiko-farmatsevticheskiy
institut imeni S. Ordzhonikidze.
(Pyridinemethanol) (Thiazolemethabol) (Radicals (Chemistry))

Cor.pounds with a potential antitubercular activity. Part 4:
I'-substituted thioa-,aides of 4-oxazolecarboxylic acids. Zhur.ob..;
Irlim. 32 no.9:2882-2885 S 162. (1-a-RA 1-:9)
1. Vsesoyazrq~, nauchno-issledocatellskiy khimiko-,armatsevt-ichesk-iY
institut ineni S. Ordzhonikidze.
(0KAZ0L'ECA1U=1C kCID:) (~MMES)*
. (TU=CM41SU)

1L. ~~ I i;_~ ~ ~- K I y 3 V. G. ; Vz'- _5 I L I, V. F. ; S hG H LTKI NA , 1- 1. N.
Reactions of sydnones with unsaturated compounds. Zhur.ob.kjn:m..
32 no.9:3107 S 162. (Illpu
(Sydnone) (Unsaturated compounds)

KUZ IMIRA, K.K.; OSTROUMOVA, N.G.; MARKOVA, Yu.V.; SHCH-UKIU_,MN.
--------
Thiazoline and thiazclitdine series. Part 1: Alkylation
of 2-aminothiazoline. Zhur.ob.khim. 32 no.10:3215-3219
o 62. (MIRA 15:11)
1. Vsesoyuznyy nauchno-issledovateltskiy khimiko-
farmatsevticheskiy institut iraeni S. Ordzhonikidze.
(Thiazoline) (Alkylation)

SYCHINA, T.P.; TRUPP, T.Kh.; SHCHUKINA M-N.
Compounds with potential antitubercular activity.
Part 5: Certain derivatives of 5-phenyl-2-cxasolecartqxy~
acid. Zhur. ob. kUm. 32 no.]-1:3666-3669 I? 16~'. (M]ICA"I'5:11)
lo Vaesoyuznyy nauchno-issledavatel'skiy
khimiko-farmatsev-ticheskiy,.-iaot~l,t.uLt imeni.- S. Ordzhonikidze.
((bmzolec;4*AWJU'q acid)
(Tuberculosis)

SYCILEU, T.P.; TRUPII, T.Kh.; LEMIDEVA, I.V.; SIMIUKINA. -M-.N.
Compounds with potential antitubercular activity. Part 6:
Anidoximes, amidrazones, and S-oxides of thioamides of some
heterocyclic acids. Zhur.ob.khim. 32 no.11-:3669-3674
11 62. (MIRA 15:11)
1. Vsesoyuznrj nauchno-issledovatellskiy khimiko-farmatsevticheskiy
institut imeni S. Ordzhonikidze.
(Heterocyclic compounds)
(Amides) (Tuberculosis)

MURAT YEVA, K.M.; SHCHUKINA, M.N.
Laboratory method of producing 1,2--thanedisulfinic acid.
Med. prom. 17 no.6a4O-41 Jet63 (~= 17 24)
1. VsEsoyumyy nauelmo-Issledo-vatellskiy khimiko-farmatserti--
cheskiy institut imeni S. Ordzonikidze.

PREDVODITELKVAJ- G. S.; 4H9-BlKINAT-X--N-
Synthesis of derivatives of benzomorpholins. Part 1. Zhur. ob.
khim. 33 no.1:145-150 163. (MIM 16:1)
(Bezoxazine)

YERMOLAYEVA, V.G.; MUSATOVA, I.S.; SHCIIUKINA, M.N.
Pyridylthiazolylmethane. Part 2: Synthesis and properties
of 2-pyridyl-2t-thiazolylcarbinols. Zhur.ob.khim. 33
no.3:825-828 Mr 163. (MIRA 16:3)
I- Vsesoyuznyy nauchno-issledovateliskiy khimiko-
farma-esev-ticheskiy institut imeni S. Ordzhonikidze.
(Pyridihei) (Thiazole) (Methanol)

YERM)LAYLVA, V.G.;-SHCHUKINA, M.N.
.Fyridylthiazolylmethane series. Part 3; Synthesis and properties
of 3-pyridlyl-21-thiazolylcarbinols. Zhur. ob. khim. 33 no.8:
2716-2720 Ag '63. (MIRA 16:11:11)
1. Vsesoyuznyy nauchno-issledovatellskiy khimiko-farmatsevticheskiy
institut imeni S. Ordzhonikidze.

SITIOUKINA, M.1,1'.
yrithelic. rliur,~'Jo 4,p
Moden. s -.7-19 03.
(MIRA 16.--7)
1. kbi-railco-farmatsev-
~iy -Lf.u+ imen~
S. Ordzhoriki.-iz;e.
(Di,-j.re-, --~7 aud

PREDVODITELEVA, G.S.; SliGlIUKINIA, M.N.
Synthesis of derivaLives o--.- benzomorpholine. Part 2: N-subs ti -Iluted
amides and thioamides of 2-benzomorpholinecarboxylic acid. Zhur.
ob.kiii-T.. 33 no.12:3975-3978 D 163. (MIRA 17-3)

YFI~~!;;i~AY:~LV.,, ' '.i
II '. , , i .1 1 .
Free radi,.,als fon-,~ed ai produ.~Itss- in the oxidation of
p3rridyIthiazo1yIc!jrbinI-!,,~ ard some oth~--r secondlai-f carbiriols. Dcki.
All SSSR 158 no.2:-"36-439 S I.S4. (MIRA 17: 10)
1. IJsp-soy-azr,.ry
iristit[IL im. Pred-stavIeno alm3emikom L'.L.!Knuriyantsem.

?rr, t G i,!A: i_,--
Cor Inti. r~ocw Inbi.-;friall Wall-sawr
J

h i a zr) 11 ne a.,-,-. Zt la 7 ~~ I i ie 5 a r; r. f
3-alkyl-2-thiazoiidones, Zhur. ob. khim. nc,
64.
Vocsoyl-miyy
institut imeni S.Ordzhoni'idze.

S-,,rn-L,he_-is of 'r,- lo~irea J~r` vaL-' -:~;s . -art 3: 1:-razinv 7
banilides and arylthiccai-ba:.--I,)4,r,,erazlnes. -hur. ob. kh 3
no. 3:1,--,80-~',92 Mr 164. (mi!-J, 17:6;l
1. Vsesovizmw naichnc)--i-ssledovatells',~i,, khimi-ko-faiTiatsevL4.cliElskiy
:nstituL juieni S.C,.,,dzllonikidze.
I

S H,-, f: i 1 7! o as tz~::iZ
s -a i-::-J ne- ani ~n.
41 R -7 -
no 5-,
v
1. Vre ratichno-L-r- j,,~ -ji k i j k i-)- L ~l rf:i a " s r: p s k

1 ff
Ila ---.A
and propAi7--,-e3
~71' dY-! th a - -71 U fn --A naL- alm. Z-"hul~ ob. kh-ur..
MIRA Y! 8
-=na

i k 11

11Z

S,L40LOVOYA, V.G.; GORTINSKAYA, T.V.; SHCHUKINA, M.N.
Phenoxazine. Part 7z Sme 10-substituted phanoxazines. Zhur.
ob. khim. 34 no.110-3791-3794 N 164 (MIRA 18zl)

L 1862- E*-,'-1A(J)1---WTW 'E;PF(c)/I';'e,"P(j)/EWA'b-);..2/EWA(c) RPL -'RM-
6~
AUCEbbION NK: AP.)022536 UR/0366/65/001/009/1688/1691
547.867.8
AUTHOR: Nyrkova,-V. G.. GortinskMa, T. V.; Shchukina M. N.
-diazaphenoxazole, a new heterocyclic system
TITLE: Synthesis of 3,4
SOURCE: Zhurnal organicheskoy khimii, v. 1, no. 9, 1965, 1688-1691
TOPIC TAGS: heterocyclic1base compound, organic synthetic process
ABSTRACT: The reaction of 4-bromopyridazine-3,6-diol with p~osphoryl chloride
produced 3 '4'6-trichloropxridazine.f I The condensation of 3,4,6-trichloropyridazine
with o-aminophe-no-f-l-ormed 2-chloro..;3,4-diazaphenoxazine (1), the structure of
which is proved by reverse syntheses. The reactions performed and compounds o~-
tained are shown in Fig. 1 of the Enclosure. The synthesized compounds are:
3,4,6-trichloropyridazine; 2-chloro-3,4-diazaphenoxazine (I);.-3,6-dichloro-4-
' hy
(2'methoxyphenylamino)pyridazine (III); 3,5-dichloro-4-(2 droxyphenylamino)
pyridazine (IV); 2-chloro-3,4-diazaphenoxazine (1); 3,6-dichloro-4-(2'r-nitro-
phenoxy)pyridazine (V); 3,6-dichloro-4-(21-aminophenoxy)pyridazine (VI); 3,6-
dichloro-4-(2-acetaminophenoxy)pyridazine (Vla); 3,6-dichloro-4-(21-acetoxy.;
phenylamino)pyridazine (M). Orig. art. has: 1 figure.
Card 1/4

-- L 1869-66 --
ACCESSION NR: AP5022536
ASSOCIATION: None .
SUBMITTED: Mugt4 ,
.NO REF SOV: 002
1 Card 2/4
m~

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MUMMARRom
L
I

PREDVODITELEVA, G.S..,, SHCHUKINA, M.N.
Synt,,esis of bo--nzcm,--rpho!:Lne derivall-,sa. Pa~rt
N-substitu Wd benzomorphollne-2-c&rboxylir acid drl-L'-
vatives. Zhur. org. kbim. I no,7:1328-1330 JI 165.
(~,','RA 18:11)

PREDVODIMME-VA, G.S.; ',I0DZ:)RC:VA, Ye.A.; SlICHIRINA, M.N.
S-Tnt~e-is of berzomorpholi.ne derivatives. Part 4: Nitration of
L-enzomorplioline-'-~-carboy.ylic acid derivatives. Zhur. org. khim.
0
1 no.7:1330-1334 J1 165. (MIRA 18;11)

fLi.v,; K.K~; PERP'SUM, Y'e..M,j S[WHUKINA, M.N.
Thl-azallne and thia2olidine series. :)~,4- 5, C.~
- .1 -, .
2--im'Lno-3-phenacylthiazoli-Jines and the--ir conve:-s:on to ir~dEzo
(2,1--b)thlazol-idlnes, Zhu~. org, kh-ijn, I no.,8:1475-1.179 Ae 11C
- 0.3 ~
(MIRA 18..,1l)
1. VaesoyuznTf nau--hnL,,-~-ssledoval,e*Ll.3kiy -~
clikgski-Y Institut tmeni Ordzhon'-kidze..

NMOVA) V.G.; GORTINSKAYA, T.V.; SHCHIJKINA, M.N.
Synthesis of the new heterocyclic system 3p4-diazaphenoxazole.
Zhur. org. khim. 1 no.9:1688-1691 S 165. (KW 18:12)
1. Submitted August 8,, 1964.

-AP603
H2 /Ni
R-CObC,tf, -0
n-CALI ~,.-i C//
N
[]:XN Li
I - \R
I C"3
CH3 III R-CSH4N-4
1 cl13 It X1 R-;c6HS
"2/N1 N NOH H2
~NCHOH Z"/NH40H
N R
cl-13R CH3
V R-CsH.N-4
IV R-CsH,N-4- XII R-CGHI
C.rd 2/4

i'-ACC-NRt AP60333o6--
The molting poirrts of the compounds ware (in 00: (M) - 134.5-135; (IV) - 156-159;
(V) - 252.5-253 (doo.); (VI) 102-5-103-5; (IrrI) - 236-238; (IX) - 171.5; (XI) - 70-
1 71; (X11) - 248-248-5; (MI) 113.5-144; (XIV) - 185-186; (XVI) - 183.5-184.5;
(VIII) - 204.5-206; (X) - 215.5-216; (XV) - 130-5-i31; (XVTI) - 03-135, Qrig. art.
hast 2 tables.
SUB COD-61 07/ SUBM DATES 08FGb65/ ORIG REFS 003/ OTH REFS 004 -
C
Card

1,V~; 6YCHE'.Ap T.P.; SHCHUKINA, N.Y.
%I
Compounds with a potenUal antituberculotic activity. lart 2;
lj-:~ubstituted th-;*.o amides of thiazolecarboxy-lic acids. Zh-ur.
c'b.-':him. 31 no.8:2618-2623 Ag 161.
(Tiliaxolecarboxyli,2 acid)

SIDDROV, I.N., kand. tekhn. nauk; SUNGUROVA, Z.N.; SHCHUKINA, N.A.
Study of gases in Ural coal deposits and amount of methane emanation
in mines. Trudy Gor.-geol. inst. UFAN SSSR no-31:59-82 '58.
(MIRA 12:9)
(Ural Mountain region--Mine pases)

1-1, A.
crmvqrgef)~-e of directions ot' joints and structural valleys jr
thf-. VIIIIIJ Basin. Uch.zap. SGU 7 1, 119 7, - 2,,'0 '60. (HIRA 1-5:7)
(vilylly villoy-JOInta (rv!oloa))

SHCHUKINA, N.A., jnzhener-kbimik
~Jethod of determining the degree of oxidation and the likelihood of
spontaneous combustion of coals from the Korkino open-pit mine.
Sbor. rab. po silik. no-3:87-90 1�1. (MIRA 15:10)
1. Gorno-geologicheskiy institut Ural'skogo filiala AN SSSR.
(Chelyabinsk Basin-Coal-Analysia)

I
SHCHUKINA, N.F.; KUVALDIHA, Ye.D.
Synoptic conditions for invasions from the north Into the south-
eastern regions of Kazakhstan. Trudy Kaz. NIGMI no.6.-83-101 '56.
(K-azakhstan--Meteorology) (MIBA 10:9)

SHCRUKINA, N. G.
"The Effect Of Magnesium Sulfate and Glucose on Chromium-Yegetable-Tanntid Leather Dur-
ing lulling." Cand Tech Sci, Moscow Technological Inst of Light Industry imeni L. M.
Kaganorich, 28 Doe 54. (Vm, 17 Dec 54)
Survey of Scientific and Technical Dissertations Defended at USSR Higher Educational
Institutions (12)
SO- SUN No. 556, 24 Jun 55

ISPMAN, G.P., knnfl teLnauk, dotsent; SHCLUIKTNA,_4.q,,, kjqnfi-,takha.naUk
Calculation method for setting work norms in the manufacture of
leather. Izv.vys.ucheb.zav*; tekholegoprom, no,3:3-13 t61.
(MIU 14:7)
1. Kiyevskiy tekhnologicheskiy institut legkoy promyshlennosti,
Rekomendovana kafedroy ekonomiki ploaYshlennosti, i arganizatsii
proizvodstva.
(Leather :Ladustry~-Production standards)

1SPIRYA'D`2 G.P- kand.teldm-naWk, dotsent; SHCHUMM, N.G._, kandAekhn.nauk
Stability coefficient of time series. Izv,vjs.ucheb.zav.;tekh.
leg.prom. no.2:)9-,,)-,' 162. OLTILI 15:5)
1. Kiyevskiy tekhnologicheskiy institut legkoy promy--hlennosti.
Rtirkomendovana Icatedroy okonomiki promysIOLennosti i organ.-lizatsii
proizvD.3st-,ra.
(Tire study) (Leather industry)

ISPIRUN, G.P., kand.tekbn.nauk., dotserit; SHCHUKINA, N.G., kand.tekhn.nauk
Number of measurements for the time study in leather manufacture.
Izv.vys.ucheb.zav.; tekh.leg-prom. 3:21-27 162. (MIRA 15:6)
1. Kiyevslciy tekhnologicheskiy institut legkoy promyshlennosti.
Rekomendovana kafedroy ekonomiki promyshlonnosti i organizatsii
proizvodstva.
(Leather industry)
(Time study)

S~_qHUKINAI, N.G.. kand.tekhn.nauk; SHESTAKOVA, I.S., doktor tekhnicheskikh
na~lt,-- prof .
Leather filling with a mixture of glucose and magnesium sulfate.
Nauch.trudy MTILP no.23:29-34 161. (MIRA 15:9)
1. Kafedra tekhnologii kozhi i mekha Moskovskogo tekhnologicheskogo
instituta legkoy promyshlennosti.
(Leather)

SHCHUKINA, N.M.
Contribution
Asia (during
260-273 '54.
(Asia,
of Russian geographers to the cartography of Central
the second half of the 19th century). Vop.geog. no.35:
(MLRA 7:12)
Central--Discovery and exploration)

SHGHUXINA, Nina Mikhaylovna; PERVAKOV, I.L., redaktor-. SRCHUKINA, V.V.,
redakf6r; tekhnicheskly redaktor;
EHow the map of Central Asia was made; works of Russian explorers
in the 19th and beginning of the 20th century] Xak sozdavalas' karta
TSentrallnoi Azii; raboty rusakik-h iseledovatelei XIZ i nachala. 11
v. Moskva Goa. izd-vo geograficheskoi lit., 1955. 237 P. (KIRA 8:10)
(Central Asia-Discovery and exploration)

S/ 1062/601/OCO/OC J'/C 1210
B004/'BO64
AUTHOR: Minachev, Kh, M., Kondratlyev,_D A_ and
Shchuk ina 777TC
TITLE: nV. 7st-1611-11 o_n_0T_M_ePoi son i ng of the PlIatinum
Catalyst by Tiophene Under the Conditions of Reforming.
Communication 3 The Influence of Temperature and
Hydrogen Pressure
PERIODICAL: Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh
nauk, !960, No, 7; Pp, -~263 - 1.266
TEXT: In continuation of their investigations (Refs 1.2) of the
poisoning of 1~-_ and 5% plat--num-al-,;minum oxide catalysts. the authors
studied a) the influence of temperature (425 - 5000C) at constant
hydrogen pressure (20 atm) and b) the influerce of H 2 pressure
"between ';0 and 40 atm) upon the dehydrogenation of cyclohexane
containing 2 65% tiophene at 4250 and 4750C A 1% platinum-aluminum
oxide catalyst was used The yield of dehydrogenation stabilized
Card '//2

Investigation of the Poisoning of the S/062/60/000/007/012/01-1/YX
Platinum Catalyst by Tiophene Under B004/BO64
the Conditions of Reforming
C~7,mmuni.cation 3 The Influence of Temperature and Hydrogen Pressure
at 20, 30 and 40 atm and 42c5, 450, 475 and 5000C after 1 - 2 hours
No stabil;.zation cf the yield occurred at 10 atm and 4500 and 4750C;
the a--,.;vity of the catalyst decreased steadily in the course of 20
hours, The stabilized yield increased with rising temperature
(425----2~5000C) and de--reased with rislng pressure (20-440 atm). The
specific surface of the deactivatEd catalyst dc-creases with increasing
temperature, with pressure changes., however it remains almost the same
A complete decomposition of thiophene occurs when both temperature and
pressure rise- There are 2 figures. 2 tabl~--~, and 6 references:
5 Soviet and 1 US,
ASSOCIATION: Institut organicheskoy khimi" im N D Zelinskogo
Akademii nauk SSSR
(Institute of Organic Chemistry imeni N. D- Zelinskiy
of the Academy of Sciences USSR.)
SUBMITTED- January a 1959
Card 212

31746
S/20/61/ool/oo4/003/005
E075/E185
AUTHORS~ Minachev, Kh.M., Markov, M,,A., and Shchukina-, O.K.
TITLE, Dehydrogenation of cyclohexane on the oxides of
rare
z earth eleme-ats
PERIODICAL. Neftekhimiya, v.1, no.4, 1961, 489-493
TEXT~ Eight oxides of rare earth elements and yttrium
oxide were used as ---atalysts for the dehydrogenation of
syclohexane. The catalysts were prepared by dissolving the
~~ommercial oxides in 27% nitric acid) and pre~-�pitating with
129o ammonia solution at 5o.-6o OC. The dried and washed
pre~~ipitates were compressed into 4 x 4 mm cylinders and heated
at 560 OC in dry air for 8 hours. The surface areas of the
oxides so obtained were determined by benzene vapour adsorption.
The dehydrogenations were z~arried out at 515-590 OC under
atmospheric pressure. The catalysts were activated at 56o Oc for
2 hours by passing through them currents of air, hydrogen or
nitrogen. The catalysts with the greatest a:tivity were produced
by the activation with nitrogen, Experimental results show that
all the catalysts dehydrogenate --yclchexane to banz-:,n~,
Card I/

317k6
Dehydrogenation of cyclohexane ... S/20 /61/001/004/003/005
E075/E185
The determination of specific areas of the catalysts permitted the
calculation of the specific activity and specific zoke formation
for the various catalysts, and thus their relative overall
activities could be compared. The results are given in Table 4.
It can be seen that the specific activity and coke formation at
530-560 OC does not differ much inside the yttrium group of the
oxides. The yttrium group oxides exceed the cerium oxide group
in respect of activity. It was shown that there exists linear
dependence between the logarithms of the percentage conversion and
the reciurocal temperature of the reaction. The energies of
a.-,tivation calculated from the slopes of the lines had typical
'ralues for acidic catalysts in the case of neodymium, gadolinium
and bolmium oxides, but exceeded 50 k-al for the remaining oxides.
There are 4 figures, 4 tables and 8 references3 5 Soviet-bloc and
3 nc-n-Soviet-bloc. The English language referenzes readz
Ref.1, R,A Briggs- H.S. Taylor.
J. Amer. Chem, Soc., v,63' 25W 1941z
Re-'A, V,I- Komarevsky, Ind. Eng. Chem.) v.49 2-64, 1957~
Card 2~,A-

MINACHEV, Kh.M.; MMV, M.A.; SHCHUKINA, O.K.
Dehdrocyclization of n-heDtane over rare earth oxides. Neftekbimlia
1 no.5:610-612 S-0 161. (MA 15:2)
1. Institut organicheskoy khimii AN SSSR imeni N.D.Zelinskogo.
(Heptane)(Aromatization)(Rare earth oxides)

s./ 0
AUTHORS: Minachev, Kh. M., Uarkr,-.r. 11,11. A- K
TITLE: Investigation of the ~-~ata;yzi-- -f r~r~ ;earths
PERIODICAL: Akademiya nauk SSSR. 1 z.,., e o ~ -~ -I- aCi - i~- i kh
nauk, no. 8, 1961, ~507-':---
TEXT: The aut1--ors investigated the y d
and a m ixed ca t a lys t f rom 15 er '1 ri r: 'o
i:4: The
ape,-- if ic ourf ace of th,~ ce + -
dynamic method by A. M.
AN SSSR, O'd, khim. n.~ 195h- 9 r r.,I
G a,~d
2
190 m Ig fGr Er 0 /A The proper-t a,.,
2 3 1203
listed in Table 1, The eXDeriment5 wt~i- i,,; a
temperatures from 5450-5906C and qtmoz-~nn~:-.
current. The volume rate of the up~ i
0.25 hr Before each experimen, h
with hydrogen at 5500C. Af t er t h t-- -a :-i'-d -a~
Card 1/6

Investi-ation of the caTalyti ...
',00' --200C wi th air, wh ich was di In t en t
of 5-7 %, During the regenerat-Ion, th~- f
catalyst was determined. The ex~erim-7..'.,
Th~
liquid catalysis products were ana'yLe,~ it. -~i,; C 6:' -a,, n
(Ref. 8: D- A. Kondrat 'yev, M. A Yarkc-
laberatoriya 25, 1301 (19"7;)))- The a D rd i rig
to the method by G. P- Kaufman (Ref. 9: J
zh-*rov, M-L., 10157)1~ A n a d s cr t . r.n r t~ Y;
conductiv--~y de tec tor was used for f ht~ a-'
products. The experiments showed that 2
during the conversion of cyclohex:---ne
at a temperature increase from 5450
gaseous products increases from 14.;
from 0 - 5 % to 1 .2 07,40. During the ccnvk--rD-(--, r Er,O-.
the yield of liquid catalysates amou,-~r! 'c
at
5900C. The yield of gaseous produots % at.
suitable temperatures. The amount c: f L. k ea,- ~i ir,;; a I ~y s tw A-
about equal ir. both cases. During the
Card 2/6

S/06 2 t' :."3C ~D 'I C ("5/ nlo S/O 1 G
C,
Investigation of the catualytic....
hydrocarbons, the yield of liquid catalyeates on j..ure Er 2G, was mioh
higher than on Er 20 3/A 1203 . However, due to th= 1cwiFr a*ablli~y fAf
n-heptane and ethyl cyclopentane it was riot. 6- I)iq at, foy
A _, e fe-t tha-n Ey-,C IA!
Pure Er 0 thus has a much weaker cracking f The
2 3
analysis of ,aseoiis catalysis products showo,i ~hi-- t' o, ea
c-btained on Er 0 /Al 0 is richer r, hydr, t t
2 3 2 3 1 ~ on
Er 0 During the conlrersion of -tii i i-
2
saturated and unsaturated hydrocarbon i Nt
L
of ethyl cyclopentane, the gas produr,-~ E--.C
lin,iaturated and 10.4 '~' saturated Tre e --114
cat alysJ.sproducts showed that the pr.-~ dic- ~t~
cy-11ohexane consists of unchanged h,,rjr(: 'I L 0; ~t if,
p-~n tane and cyclohexane. The benz~--ne Cr. tre i 4-1 11 t- 1 d o 'n
Rr 0 /A 10 amounted to 4.1 -/, at 515"'~: inj
2 3 2 3
Er 2 0,, the benzene content at 5 4 5:C
Card

Invest!-atic-n of the catalytic ...
,.!,1r)ver.sion of n-heptane. The cont enf-i ;-i ti I'It
in the licit.Ai-I catalysate in 1,ht_- preq,~,, Tile.
yield of liquid catalysa-te, however. vaij mu-_,.Lj 11-~4,~ 11 r,, t i ta rt
"Al 0- More aromatic 77-, -0,
c,n Er2OY
per h.-.rlrocarbcn used thart on Er 0'. Tile rre-~7:- 2,,
2 '1
catalysis products of n-heptane points tow-g-A-, 1 --1 It!-C,_'.nS,;,
When passinC throu--h ethyl cy,-1CF,-3nt1nc. d
Er 0 In the product obtained on Er)C) A C'
2
were found. The iodine numbers of the r -~,l liu
conversion of cyclohexane and n-heutane' on ~;otl --i a inc. t
hiaher than 15, Th e i od in e num b e r c f '.. In ~ -,r c;(, C, tI
hexane on the mixed catalyst at 5900 C, i.e. D,.) r in g
catalyois of ethyl cyclopentane, the iiAln.? rtuw~ ~c, ,-;a t
-were 210 on Er 0and 52 on Er 0_,1A1' C', Th~j-e '1:-
2 2 2
arld 10 references- 6
Sovi e t -bloc -ir. d A r r, r; - 3-
rd

1 .1 S/062/61/000/006/00,3/010.
Investigation of the catalytic... B117/B2o6
references to English-language publications read as follows: R. A. Brigget
H. S. Taylor, J. Amer. Chem. Soc. 63, 2500 (1941); V. 1. Komarevsky,
Industr. and Engng. Chem. A~, 264 71957); g. E. dreen, Nature 180,
N 4580, 295 (1957).
ASSOCIATION- institut organicheskoy khimii im. N. D. Zelinakogo.Akademii
nauk SSSR (Institute of Organid Chemistry imeni
N. D. Zelinskiy, AS USSR)
SUBMITTED: December 13,_ 1960
Card 5/6

IIJQ 22,05, 111H IT 7 5
27493
S/06 61/000/009/008/014
B1 I 7YBI 01
AUTHORS. Minachev, Kh. 111., Markov, M. A., and Shchukina, 0. K.
TITLE; Study of the catalytic properties of rare earth oxides,
2. Transformation of cyclohexene, 1-methyl cyclohexene-1. and
n-heptene-1 on erbium oxide
PERIODICAL: Akadem-1ya nauk SSSR. Izvestiya. Otdeleniye khimicheskikh
nauk, no. 9, 1961 , 1665-1669
TEXT; The present work which continues the studies on the catalytic
properties of rare earth oxides was undertaken with a view to investigating
the behavior of several cycloalkenes on pure erbium oxide and a mixed
catalyst (1% erbium oxide, 65% aluminum oxide) at 5100-5150C. Catalyst
preparation, reaction conditions and method of analyzing the catalfst have
been described previously (Ref. 1: Izv. AN SSSR. Otd. khim. n. 1961, no, 8~
The following hydrocarbons were used: cyclohexenel 1-methyl cyclohexene-1,
n-heptene-"; the yields of liquid catalysis products obtained by passing
the two first-alentioned cy:~loalkenes over Er203 were independent of time
and amourted to 80 7% and 8,1,4%, respectively, They contained no hydr-~-
Card 1/6

27493
S/062/61/000/G09/008/C-,4
St.,jd.y of t~e nata-litic proper-,--'es B-117/3101
carbons of mole~;ular weight higher than that of the initial substance,
Chromatographic analysis showed -.hat the gas formed simultaneously is made
up of 90-96% hydrogen and 4-10% Cl to C4 hydrocarbons. Carbonization on
Er 203-gas insignificant. The product obtained from cyclohexene ove-, Er2o 3
consisted of benzene (20-23%) and cyclohexene. In experiments using
1-methyl syclohexene--i and the same catalyst,, 1-me-.hyl cyclohexene-', a
mil.ture of ~-methyl -y-.lchexe?ie-2 and 1-methyl cy;.-lohexene-3, and toluene
were identified in the zeaction Droduct. The results obtained in the
conversion of 1-methyl .~yslohexene-l) on Er2o 3 are given in Table 2, The
tests wj.+Vh cyclohexene and 1--methyl cyclohexene-1 over Er 203/A1203 showed
that the yield of liquid products increases with time. The gases analyzed
consisted of 85%-93% hydrogen and 7-15% C1 to C 4 hydrocarbons~ As in the
case of Er203V the gas was richer in hydrocarbons towards the beginning ~~f
the experiments. Carborization on Er 20 3/A1203 was higher than on pure
erbium oxide. The composition of the catalyzate obtained from cyclohexene
over Er 20 3Iki2OA ia represented in Table 3. The composition of the
Ca-rd 2/6

27493
S/062/61/000/009/008/OiA
Study of the catalytic properties ... B117/B101
catalyzate obtained from 1-methyl cyclohexene-1 was only partially
clarified,. since the chromatogram was greatly complicated by the formation
of dimeethyl :~yclopentenes- A sample drawn within the first two hours was
found to contain 63~'o toluene. The total yield of catalysis produots in
tests with n-heptene-1 over Er 20 3 was 74.% and over Er 20 3~12'3 68~3~-
The gas formed over Er203/A120 3 contained double the quantity of hydro-
carbons that was obtained over Er 2 03" The liquid catalysis pro~uots
contained 6",0 toluene in the case of Er 20 3 and 8.5% in the case of Er 2YA2~'
The chromatogram of the product obtained over Er203/A120 3 exhibited six
peaks in the C 7 hydrocarbons region, apart from toluene, as compared to
two iDeaks in the ::a.,3e of Er 20 3' Er 203 catalysis yielded products
containing 91.8c/111 unsaturated hydrocarbons and Er 20 3/A120347.0%. In
o2~,n:;lusion, the investigation of these two catalysts yielded the followin
results; They differ inasmuch as the mixed catalysts produced isomeriza-g
tion of the 6 membered ring to a 5-membered ring, whereas this isomeriza-
Card 3/6

Study of' tho properties
27493
s/o62/6! /000/00/cOa/c ',i
B1 17/Bl 01
'_,on does not occur with pure erbium oxide. Both catalysts dehydrogqna-,;e
" I
the tested !y~_-'oalkenes to corresponding aromatic hydrocarbons and cause
shifting of the double bond in the ring. There are 3 figures, 3 tables
and 5 references; 3 Sc-.,-,e-, and 2 non-Soviet. The two referenoes to
English language publications read as follows: F. G. Rossini. K. S.
Pizzer, R. L. Arnett, R. M. Braun, G. C. Pimentd, Selected values of
physical ani Thermodynamic properties of hydrocarbons and related
,-:ompounds, Carnegi Press.. 1053; E. Gil-Avl! J. Herling, J. Shabtai, Chem,
and ~_,hem., Ind. no. 9, 1483 (1957).
ASSOCILTION; Irsi7:ut organicheskoy khimii im. N. D. Zelinskogo Akademi~.
nauk SSSR (Institute of Organic Chemistry .1aeni N. D~
Zeli_nskiy of the Academy of Sciences USSR)
SUBMITTED: December !3. 960
Card 416

DERBENTSEV, Yu.I.; MARKOV, M.A.; ISAGULYANTS, G.V.; MINACHEV, Kh.M.;
BALANDIN, A.A., akademik; Prinlmala uchastiye SHCHUKINA, O.K.
Mechanism of cielohexane dehydrogenation over holmium oxide studied
with the use of radiocarbon C14. Dokl. AN SSSR 155 no.1:128--131
I'tr I /
64. (MIRA 17:4)
1. Institut organicheskoy khimii im. N.D.Zelinskogo AN SSSR.

&BAK, G,A, ; SHChTKELI, Oc Mr
Technical and-e-conomic indices of mire fans of main ventilation
systems used in the U.,S,S.R. Sbor, trad, Inst, gor. dela AN bRSR
no.7t3-9 61, (M-IRA 15:1)
(Pans., Mechanical)

SHGhUKINA' O,m' - - -
Measuring the productivity and zire-z. ure of --n venti-LIation
systems, Sbor, tiq-,d, inst. gor. dela AU MASR nc,7:105-115 161.
0
(MIPJ, 15:1)
(~Iine ventilation)

-Ai"Huylli.A 10--ye,
Methods of geabotanica! research in mountainous countries. Bot.
zhur.42 no.8:1225-1229 Ag 157. (MLRA 10:9)
(PhytogeogrAphy-Reaearch) (Mountain ecology)

SHCHUKIII, Ivrin Somenovich; SLIqMIIIA.. 01'gp_Yevseyevna; DOBRONRAVOVA,
K.O., red.; KONOVALYUK, I.K., m1adshiy red.; G13YKH, D.A.,
tekhn.red.
[Life of mountains; studying of mountainous countries as a
complex of mountain land formal Zhizn' --or; opyt analiza
.-ornykh stran kak kompleksa poiasnyklilandshaftov. Koskva,
Gos.izd-vo geogr.lit-ry, 1959. 285 P. (MIRA 13:1)
(Mountains)

Dd
chttniy.
t r 1y
ncl.
-)r.4rv of C~n~~rt5:s, c'ob-r

HISHIb, V.M.; NAMENOVA, 1,11.Ya.; SHCHUINA, T.B.
-Yearly variation of the frequency of magnetic storms. Geomag.
i aer. 2 no.2:321-325 Mr-Ap 162. (MIRA 15:6)
1. Institut zemnogo magnetimna, ionosfery i rasprostraneni-ya
radiovoln Sibirskogo otdoleniya AN SSSR.
(Magnetic storms)

ACC INR: SOURCE CODE: U!1/020-,/ 66 /006/u"J5 /0-63 6, /l, i'to
J
AUTHOR: Polyakov, V. M.; Shchukina, T. B.
ORG: Institute of Geomagnetism, the Ionosphere, and Radiowave Propagation, SO AN SSSRI
:(Institut zemnogo magnetizma, ionosfery i rasprostraneniya radiovoln, SO AN SSSR)
'TITLE: Kinetics of ionization recombination processes in F2 layer of the ionosphere
'SOURCE: Geomagnetizm i aeronomiya, v. 6, no. 5, 1966, 858-868
ITOPIG TAGS: ionospheric physics, recombination coefficient, ion recombination, linear
:approximation, F layer
!P3SMACT: Kinetics of the ionization-recombination processes summarized by equations:~'
'0+ + 1719 - -'M0+ + M and 1-10+ + e - 'M + 0 (where M and 'M are atoms and miolecules of a
2
:gas), which take place in the F2 layer of ionosphere, is investigated. A new method
:,for dete-r-mination of the parameters of the process by means of analog electronic com-
.puters is evaluated. Values for the effective coefficients for charge exchange and
!dissoc.4ation-recombination reactions in F2 layer are determined. It is suggested that!
:the frequently encountered divergence between the values for recombination parameters
!that are laboratory-derived and theoretically calculated from elementary interactions
ibetween the particles, on one hand, and the values obtained from ionosphere measure-
ments, on the other, is due to the temperature dependence of these parameters rather
!than to the inaccuracy of determination. It was established that the recombination
UDC: 550.388.Z
corri 1/2

ACC INR: AP6-3326S9
coefficient varies witn altitude and time. While in using an altitude function it is
more convenient to employ a linear approximation within the whole inter-Val of the F2
layer altitudes, the time variations cannot be evaluated through the use of linear or.
square functions. Orig. art. has: 19 formulas, 3 tables, and 6 figures.
SUB CODE: 04, 09/ SUB.K DATE: 05Nov65/ ORIG REF: 009/ OTH REF: 010
Card

KOZLOV, K.D.; prinimali uchastiye: ZAGORUYKO, K-Ye; ROZOVAq Z.I.; BtJLATLTS-
KE.A, T.P.; TMSTER, F.Z. ; SRGHIRM_j --Z.MTSEVA, N.Ye.; MID-
p - -Ir , -
VA, L.S.; AMELIYAN, G.Ye.; -t1AYD9VV-.-r, -.--RzZHKOV, A.N., red.; ME-
MESHKINA, L.T., tekhn. red.
[Economy of Sakhalin Province6' statistical collection] Narodnoe kho-
Y
ziaist7o Sakhalinskoi oblasti; statisticheskii sbornik. TUzbno-Sa-
khalinsk, Sakhalinskoe knizhnoe izd-vo, 1960. 103 P. (MIM 14z6)
1. Sakhalin (Province) Statisticheskoye upravleniye. 2. Kollektiv
rabotnikov Statisticheskogo upravleniya Sakbaliziskoy oblasti (for
all except Ryzbkov, Memeshkina). 3. Nachallnik Statisticheskogo
upravleniya Sakhalinskoy oblasti (for Kozlov)
(Sakhalin--S~atistics)

SHCHUKBA, Y.L.
The effect of destroying the integrity of the cortical premotor zone
on collateral circulation of the small intestine. Biul. eksp. biol.
i.med. 41 no.1:68-70 Ja. '56 (14IRA 9:5)
1. Iz kafedry normallnoy anatomil (zav. prof. M.G. Prives) 1-go
Lenin,gradBkogo meditsinskogo instituta Imeni I.P. Pavlova (dir. dots.
A.1. Ivanov) Prodstavlano deyetvitelinym chlenom V21 SSSR V.N.
Chernigov8kim.
(IIMSTINE, small, blood supply
eff. of premotor cortical zone inj., exper.)
(CERORAL CORTEX, wounds and inj.
premotor cortical zone inj., eff. on blood circu. of small
intestine, exper.)
(WOUIMS AIM DIJURIES
premotor cortical zone, eff. on blood circ. of small
intestine, exper.)

SHLYAMIN, Boris Aleksandrovich; LXBFMVA, N.G., redaktor; SHCOKIK&, V.T.,
khudozbeetvennyy redaktor; KOSBELEVA. S.M., tekhaichi-ii-ty' iedsktdrr,
M&LICIOVSKIY, G.N., redaktor kart.
[The caspian sea] Kaspilskoe more. Moskva, Goa. izd-vo geograficheakoi
lit-ry, 1954. 126 p. (MLR& 7:12)
(Gaspian Sea)

UITAGIN, Georgiy Dmitriyevich; ZIM&N, L.Ya., otvetstvennyy redaktor;
TRUBITSYN, V.I., redaktor; SHCMINA...y Y., khudoshestvennvy redaktor;
- 4 -
.1RIVINA, I.N., tekhnicheakiy iiid~~olr;.G,bLiTSTN, A.Y.,~redaktor kart.
[Geographical study of Italy's inchatries] Geografiia prosWahlennosti
Italft Koskv!!,, Goo. izd-vo geograficheekoi lit-ry, 1954. 363 P.
iltali-industries) (MLU 8: 1)

TIKHO'IIRDV, V.P., radaktor: ROZIN, 4.S., redaktor; SHCHUKINA, Y.T..
redaktor; GI09M, D.A., takhnicheakiy redaktok' *~ '
JIndlap Nepal.Ceylon.] Indila, Nepal. TSsllon. flookya, Gos.1zd-vo
geogr.lit-ry. 1955. 31 P. W.U 8: 10)
(India-Description and travel)
(Nepal-Description and travel)
(Ceylon-Description and travel)

BURKHANOV, Vassiliy Fedotovich; PMVAKGV, I.L., redaktor; SHCHUXINA, V.V.,
redaktor; KOSHKINVA, S.M., redaktor ---A--~-
[Ifew Soviet explorations in the Artie] Novye sovetskie iseledovaniia
v Arktike. Moskva, Gos. izd-vo geogr. lit-r7, 1955. 51 P. (MIaA 8:10)
(Artie regions)

ARSENIYEV, Vladimir Klavdiyovich;KUKKICS, S.N., redaktor; SHCHUKINL
V.V., redaktor; KOSHELAVA, S.M., tekhnichealriy red 0.
[Through the taiga.] Skvoz' Taign. Moskva, Gou.izd-vo geogr.lit-r7
1955. 127 P. (8:10)
(Ussuri region-Description and travel)

DANTSIG, Boris Moisayevich; RETSHER. I.M., doktor 18toricheakikh nauk)
redaktor; KQSTINSXIT, D.H., redaktor; SHCHUKIKA, Y.Y., redsk-cor;
RIVINA, I.N., tekhnicheskiy redaktor.
1
LIraq; a brief sketch of its geography] Irak, kratkii geogra-
ficheskii ocherk. Moskva, Gos.izd-vo geogr.lit-ry, 1955. 134 P.
(Iraq--Description and travel) (24LRA 8:10)

14IL'KOV, Y.N.; KqR4KES, S.N., redaktor; SHCHUKIMA, V.V., redak-tor;
KI)SIDITANA, S.'!., tekhnichefikly r9da7F-o-r-------
[A.N.Krasnov, geographer and traveller] A.H.KraBnOV- geograf
i puteshestvennik. Moskva, Gos.izd-vo geogr.lit-ry, 1955.
173 P. (41AA 8:10)
(Krasnov. iindrei Hikolayerich, 1862-1914)

PETRDV~-'Afkhail Plat&i~ic_b; LATRENTITEVA, Te.J.. redaktor; SHCHUXINk.,
V.V., redaktor; KOSENLEVA, S.M., tekhnicheskiy redaktori-ml ~-- -
W~
sketcbjof..i!~p.physir_a1 geography] Iran; fiziko-
I -
9 geogr.lit-ry, 1955.
183 o. ? (MI~RA 8: 10)
(Iran--Physical geography)

'i AU"~ I M I N, Tullan Gleba7lch; BAROlMlY, N.H., redaktor-, MYACHIN, I.K.,
redal~ftor; SHCfRJKINA, V.V., redaktor; GLEM, D.A., tekbaicheskiy
radak-tor.
i-Moucow; a geographical study] Moskva; geograficheskaia khara:-
I
ktnrlstlka. Moskva. Gos.izd-vo gf-ogr.lit-ry, 1955. 191 P.
(MURA 8:10)
1. ('hInti-korreepondant Akademii nauk SSSR(for Baranakiy)
(Mc scow--J)e scri-Dt Ion)

SHCRUKINA, Nina Mikhaylovna; PERVAKGV, I.L., redaktor; SHCHUKINA, V.V.,
P-'
redaktor; RIVINA, I.N., tekhnicheskiy redaktor;
[How the map of Central Asia was made; works of Russian explorers
in the 19th and beginning of the 20th century] Kak sozdavalas' karta
TSentrallnoi Azii; raboty russkikh issledovatelel XIX i nachala. XX
V. Moskva Gos. izd-vo geograficheskoi lit., 1955. 237 P. (MLRA 8:10)
(Central Asia--Discovery and exploration)

NRS",1WYV,V. Vladimir Klavdiyevich; KUMKBS, I.N., radaktor; SHCHIJKINA,
V.V., rmdalitor; GLEM, D.A., tekhnicheakly rsdAktor.--""'I--
Derau Uzala. Moskva, Gos.izd-vo geogr. lit-ry, 1955. 268 p.
(Ussuri region-- Description (MLRA 8:10)
and travel)

Vladimir Klavdiyevich; XVTES, S.N., reda-ktor; SHCHWINA,
V.11. , rodaktor; RIVIPA, I.N. , tekhnicheskiy redaktor.
Fln the Slkhote-Alin riountains] V gorak-h Sikhote-Alinia. Moskva,
Gos.izd-io geogr.lit-ry, 1955. 324 p. (MLRA 8:10)
(Sikhotlp.-'Llin Range--Discovpry -an," exploration--Des-
cription and travel)

SHIGH"UKRU, V~Ya.
Stratigraphic plan of JjowBr Carboniferous sediments based on
the preliminary studying of the fauna of rugosa corals in
eastern Kirghizia, Mat. po geol. Tian^,-Shania no,3:83-90 162,
(min :L6.-7)
(KirghiziBtan--Tetracoralla)

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