SCIENTIFIC ABSTRACT BELSKIKH, V.I. - BELSKIY, I. F.
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CIA-RDP86-00513R000204520008-0
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RIF
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S
Document Page Count:
100
Document Creation Date:
November 2, 2016
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8
Case Number:
Publication Date:
December 31, 1967
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SCIENCEAB
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BSLISKIKH V I kandet6khnrAUk
Automatic temperature regulator. Avto prom. 27 noo 5:19-20
My 161o (MIM 14:5)
1. Visesoyuznyy nauchn6-issledovatellskiy institut makhanizataii
sellskd~b khozygLystvao
(Temperature regulators)
BELISKIKH, V.I,j kand.tekhn.nauk-
Efficient cooling system for internal combustion engines.
Avt.prom. 27,no. 6&34-17 je 161. (MMA 14:6)
1. Vsesoyusnyy nauchno-iseledovatellikiy inatitut mekban4sataii.
Bellskogo khozyaystva.
(Motor.vebicles--Engines--Cooling)
S/262/62/000/008/014/M2
IM711207
AUTHOR~ Bel'skikh, V. 1.
TITLE: Suitable cooling system for an internal combustion engine
PERIODICAL: Referativnyy zhurnal, otdernyy vypusk. 42. Silovyyc ustanovki, no. 8, 1962, 56, abstract
42.8.300. Avtomob. prom-st', no. 6,1961, 14-17
TEXT: The author devised and experimentally chocked a water-circulation system ensuring thermo-siphon
cooling of cylinder liners for the case of forced cooling of the combustion chamber. The proper operation of
such a self-adjusting system requires even distribution of water supply to each chamber and uniform hydraulic
head; uniform arrangement of parts linking the block jacket with cylinder-head jacket to ensure even distri-
bution of temperature in the circumference of the cylinder liners; arrangement of the water outlet connection
above the cylinder head thus ensuring convective heat exchange between the water within the block and that
circulating through the cylinder head as well as the absence of steam pockets. There are 4 figures and 4
references.
[Abstracter's note: Complete translation.]
Card 1/1
PASECRNIKOV, N.S., kand. tekhn. naukj__4U_~SK;KH, V.I., kand.
tekhn. nauk; YALOVENKO,, F.I.-p-RA-n-d-.7T-ekhn-.-NMwT--
KASPEROVICH, V.V., inah.; VASIKOVSKIY, S.Ye.p red.;
GRISHIN, L.V., red.
(Technology of the maintenance of the "Belarus'" traktorb)
Tekhnologiia tekhnicheskogo ukhoda za traktorami, "Belaruel,n
Moskva., Biuro tekbno informatsiij, GOSKITI, 1964. 298
(MIRA 18: z
1. Perovo. Gosudarstvennyy vsesoyuznyy nauchno-isoledovatell-
skiy tekbnologichaskiy institut remonta i ekspluatateli
mashinno-traktornogo parka. 2. Goaudarstvannyy vseaoyuznyy
nauchno-isoledovatellskiy tekbnologicheskiy institut remonta,
i ekspluatataii mashinno-traktornogo parka (for PasecbnJkovp
Bellskikhj, Vaslkovskly). 3. Gosudarstvennyy soyuznyy nauchno-
issledovatellskiy traktornyy institat (for Yalovenko).
4. Minskiy traktornyy zavod (for Kasperovich).
BELISKIXHP VoL ka.nd. tekhnonauk; BAGDASAROV,, N.V., Inzh.
Determining the~loading degree of an engine by means of an electrio-
light signaling mechanism. Trakt. i sallkhozmash. no,3:11-13 Mr 165.
(MIRA 1&0
1. Gosudarstvenn*yy vsesoyuznyy nauchno-issiedovatellskiy tekhnologi-
cheskiy institut remonta i ekspluata-tsii mashinno-traktornogc O&pk&4
(for Belittkikh), 20 Vaesoyuznyy nauchnc~-issledovatellskiy institut
mekhanizatsii seltakogo khozyaystva (for Bagdasarov).
MIKHAYLk. M.-, SINUSHAS. A.; HILISKIS, V., mekhanik; BALITRUSHAYTINE, B.,
kontrollny7 master.
Advanced methods used in manufacturing asbestos slate. Stroi.mat,
3 no.11:14-16 N 157. (MIRA 10:12)
l.Daugelyayakiy kombinat stroitellnykh materialov. 2. Glavnyy
inzhener Daugelyayskogo kombinata stroitelInykh materialov (for
Mikhayla). 3.Nachallnik shifernogo tsekha Daugelyayakogo kombinata
stroitelinykh materialov (for (Sinushas).
(Daugeliali--Asbestoe cement)
BELISKIY, A,., kontr-adairal zapaaa
On the batt3- watob. 'roan. 2nan. 38 m.10:4-5 0 162,
(14IR& 15-10)
Russia- (Cmmunist Youth Lea
gue)
p ". II N ~ -IV
,Z:~, IS, ~ , ~y I ~
BILISMY, A., insh.
Slaughterhouse became a meat combine. Rias. ind. SSSR 28 no.6.#34-35
'57. (MIRA 11:1)
1. Glavny7 inzhener Melovskogo mvasokombinata.
(BIblovo-Phoking houses)
BZLI SKIY.. A.,--,-
Maldng foremen responsible for technological control. Mias.
ind.SSSR 30 no.1:22-23 '59. (MIRA 12:4)
1. Belovskly myasokombinat.
(Heat industry-QuAlity control)
.MMISKIT, A., inzh. I
Redesigning tho "MookviCh)m" saw. Hias.ind.SSSR 31 no.1:51
'6o. (MIRA 13--5)
1. Belovskiy mrasokombinat Kamerovskogo movuarkhoza.
(Belov-Packing houses--Zquipment and supplies)
11
IJBLISKIr, A.
Mobile platform for the unloading of cattle from railroad care* Mias,-
ini. SSSR 33 no.3:46 162. (MIRA 15:7)
1. Yeletskiy ptitsemyasokombinat.
(Cattle-Transportatibix)
(Ioading and unloading-Equipment and aupplies)
BZLISKIT, At A*
32677, Zkopertmentallwya provorlm uslovly Ilky1distall vygreboy v royous, stroltellst
novoy lumnalizateli leningrada. 4&klad na konterentmile sozve naveh*-Issled. In-Som
tmumle Ihozyaystva ispolkoma longorsoveta. Kay 1929, 0:7HAterialy pokommunal.
Khoz-yug 19499 SB* 3o me 67-72
801 Letoplel Zhurnallafth Statoy, Vol. 44. Moskva, 1949
T.G.; IMLISKITI, A.A.; SHCHUPANOVSX&TA, R.r.
Characteristics of magnetic fields of drum separators with closed
circuit. Obog. rod. 3 no 03:26-32 '58. (HIR& 12:1)
(Yagnetic separation of ores)
EELISKIY, A.A.
CaleiLlati~g ~hs susceptibility of open magnetic systems in
~.separators. Obog. rud 5 no-3:42-4 160. (KM 14-18)
~ tMagnetic separation of ores)
BEL'SKIY*-..A.A.- . II
Calculation of permanent magnets in magnetic field patterns. Obor
rud 5 no.6:41-44 160. (KIM 14:8i
(Magnets)
EELISKIY., A.A.
..HigUy..ef.ficient.rfiapatic,is-sparators. Obog. rud 6 no.3:41-43
161. (ILTRA 14: 1-1)
(Magnetic separation of ores-Equipment and supplies)
C~11~-z".i~zM-IM-dMI --7 ---r
BELISKIY~L,k.A.LMYSUMOVAP Hope
Ceramic magnets made of baritim ferrite. Obog. rude 8 no-3;
30-32 163. (MIRA 17--l)
U 8 S R
MtAtt-. ~ZA&,L, Tc"; t i;i-
c ' 11 ~.t
1934. 2k (3). 8211-8 R",.' - hj. it 6 onfir w,,l I
&ymft""~s e"me vxtlficat-"~~'. rl!'
Go= thiLt with Ii :Sa %;epirm. However.
Qf high r"twu-a
tho C*--M of reat'la(miall >' It), w r%% tlo syewm w of ao
pma!j"I haportallea: Other experimsiqta witil tho voatApt
arrungod in the crdtr Mmt,-l (2) pyd t~o
fallowkq mtulta; (1) Appr.. of lia, Hg to-Sa to makn lig,"-w
tivcA Mt',tler cmdiwtivity. b'a no 6AEer motiL.-ail3n thail if
is aj,;lled from vapwr.
thermal of tho So.
(3) &UT.C.. at the evilta'at Vcu. (1)1~3* i4 ewIlAxable
in 'mr.*pitntl(i 44,tls th%k it tl4e- &jjlg&- al;u 'ai~ 1u
C
Awl A). 41 frXC41CMtX4# A; IfAA
tillue t , ~s h-A f.uparlm71%,
VIQ WZAL tX'r
'v cl
idTij !y rt kt~'4'td Wy (NI, a
TZPXRMAN, Yefim Yakovleiich; BELISKIY A.M., otv.red.; LIBMWN, S.S.,
- i ='- ~-- ' ~-7 I-
red.isd-va; ANDREYEf, S.P.. tekbiii6d.
(Mine dewatering pump; a manual for schools and training courses
for mine foremen] Rudnichnyi vodootliv; uchabnoe posobia dlia
shkol i kursov masterov. Kharikov, Goo.nauchno-tekhn.izd-vo
lit-ry po chernoi i tavetnoi metallurgii, 1959. 151 p.
(MIRA 13:9)
(mine pumps) (Mine water)
iA.
ectricity - So.iconductors G-3
Abs Jour Ref Zhur - Fizike, No 3, 1957, No 7006
Author -Bel-I skiy, A. S.
Title Froceduro for Moasuring the Electric Conductivity of Di-
electrics and Semiconductors Using Fulses in Strong Electric
Fields.
Orig Pub i,Uch. zap. Tor-skiy gos. pod. in-t,-1955, 14, 535-539
Abstract The author considers a nothod for measuring the electric con-
ductivity of somiconductors with the nid of rectangular pul-
ses of 10-3 -- 10-5 see duretion. The generator is a cethod6-
coupled multivibrator with one steble state. The resultant
pulse wrs.first r-mplified with r single totrodo stage, The
loed was the invostigrted spociron (RO; CO) and P stnnderd
resistence (Rt) connectect in series with it. By verying the
capncitence C in Farrllol with R,t, the condition RstC = R0Co.
In this case the wavefor--: of the output pulse acroes the
lower and of the divider (ecrosE R ) does not become dis-
torted. The voltego in -casured WIth on oscillograph.
Card 1/1
BELISUT, A.Vo, dotaent,
Prevention and surgical treatment of relapses of jaundice after
palliative operations in cancer of the ampullar zone MArurgiia
no.3s8Z-86 163.. imin .1625)
1. Is kafedry obabobey khirurgii (zav,-doteant N.Merasimor)
Saratovskogo meditsinskogo institutas
Moms) (Bra Duas-waa)
POPOWYAN, I.M., prof., otv. redJ'
Oaratov); NAPALKOV, P.N., zasl.
deyatell nauki prof., r4- ZAKHAROV, N.V., prof., red.
(deceased]; BELISK ....-A.v-,#.,dots., red.; KOSHELEV, V.N.,
dots., red.; CIIAKOV3 L.G.; red.1 CIMNYSHEV, N.V., red.;
BLINER, M.S., red.; ANDREYEV, P.P., red.
(Transactions of the Second Congress of Surgenns of the
R.S.F.S.R.j Trudy vtorogo s"ezda khirurgov RSFSR. Saratov,
Vser. naucbn. med. ob-vo khirurgov., 1963. 583 P.
(MIRA .17; 8)
1. Sllyezd khirurgov RSFSR. 2d, Saratov, 1962.
BELISKrY, A.V.
Furcate drain with two or three branches for hepatic ducts,
removable in separate parts. Eksper. khir. i aneste noel
40-43163. (MIRA 16:10
1. Iz kafedry obahchey khirurgii (zav. - dotsent N.V.
Gerasimov) Saratovskogo meditsinskogo institutae
(BILE DUCTS.-SURGERY) (DRAINAGEl SURGICAL)
BMISKIY dotsent (Saratov, Sovetskaya ul., d.31, kv.6)
1---.1 .1.
.I Primary inflamma ory and cioatrioial narrowing of the hepatocyatic
duat. Vest. Kbir. 91 no,1000-34 0 163, (MIR& 17&7)
1, Iz kafedry obahchey khirurgii (sav. kafedroy - dotsent N.V.
Gerasimov) Saratovskogo meditainskogo inatituta (rektor - dotsent
N.R. Ivanov).
BELISEY, A.V., dotsent
WPM
Direct anastommila of two or three hepatio ducts with intestines
having ~,-Icatriaial stru,,turaa, above their Junction. Sbor* nauch.
rab. Sar. Cos-. mod. inst. 44-.246--251 164.
almd-Lce in mali
$ treatment bf pant t=ors of the porta
he -)a tis. lbid.:251-256
OMM, 18; 7)
1. .1-, kafedry obshchey khimrgii (zav. dotsent N.V. GerasiTrov) J-
Saratavskago lnsti,~uta (rektor dotsent lvanov).
BELISKIY A-Ye-- KUYSLEVA, T.A.
.I.avestigati-P4 the movement of mztor vehicles cn mountain --cads
with prolonged upg--Mes. Avi. pron. 31 no.9118--19 S 165.
(MIRA 18:9)
lo Khabarovskiy pclitekhnichenkly Institulto
BELISKIr,, A. Te.
BELISKIYj A. Ye.s "Investigation of the movement of an automobile on the
vertical curves of autombbile highways". Khar1kov, 1955. Min Higher
Education U&M. Khar1kov Automobile and Road Inst. (DiBsertations for
the degree of Candidate of Technical Sciences.)
SOs KnizhLan LetoRis I No, 50 10 December 1955, Moscow.
5 E L2 S t;~ I ~' ~)- 1-1 e
MOGIINTSKIY, Dmitrly Alsksandrovich, dotsentl BABKOV. Valeriy Fedorovich,
prof.. doktor takhn.nauk-, SHMOV. Andrey Sergeyevich, kand.takhn.
nauk; AMAKOV, Leonid Tikhonovich, kand.tekhn.nauk; ZA'YTSEV, Fi-
lipp Takovlevich# kand.tekhn.nauk; ZAMAKEIATHV, Kitrofan Samenovioh.
kand.takhn.nauk; NIKITINO Bergey Kikbaylavich, inxh*,* BIMIA, A.K.,
prof., retsenzent; DUDKIN, P.A., kand.tokhn.nauko reteensent; AVIMUT,
V,N,g retsenzent; KARTASM, V.A.. retsenzent; PALICHEV, A.G., re-
tsenzent; POPOV, A.N'b retsentent; PTITM. I.G.,.reteanxent-, ROKA-
IMO, I.A., prof... retsenzent; BARATS, L.A., prepodavatell, re-
teenzent; BlSMICH,,N9Iw, prepodavatall, retsenzent; BILISKIY, A.Ye.,
prepodavatell, retsefilent; MUZHMIY, Ya.A., prepod"ai;l ~.re~een-
zente, CHYAROV, V.G.,'red.,; HALIKOVA, N.V.., takhn.red.
4ocating and designing airfleldej Isyskamlia i proaktirovaule
sarodromov. Pod red. VJF.Babkovs. Koskya, Nauchno-takhn.isd-vo
H-va avtomobillnogo transports i shoseeiuykh dorog R~M, 1959.
566 p. (MMA 13:3)
1. Kharlkovskiv avto'mobillno-doroshnyy Institut (for Romanenko,
Barats, Baskevich, Bellskiy. Kalushaki
- tT
(Airporti-Planni j
BELISKIT, A.Ye.
I
I
Analytic calculation or motor-vehicle speeds taking into consideration
the variable value of the coefficient of rolling resistance,
Avt.orom. 29 no.10slO-13 0 163. (MM 16:10)
1. Frunzens*Kiy politekhnicheskiy institut.
BEL'SKIY, P.B.
421+65. Kul'tura Kok-Bagly" V BSSR. Izvestiya Akad. Nauk. PSSR, No. 4v 1948, S. 71-76
DEWATY B.T3,
BZLISKIY B.B* "The effect of'the koplication of mineral fertilizer on the yeild
of kok-iagyz" Izventiya akad. Nauk DSSa, 1948 no 6, P 83-94 Idbliog: 8 items
SO: U-3261 10 april 53,, (Letopis 'Zhurmal triykh Statey No U 1949)
I I
tT:VS`Yl S.
36325
Kulstura Kok-Sagyza Na Torf)ranykh Fbahvakh V Kolkhozakh Polesskoy Ob.".ftsti Izvestiya
Akad,. Nauk Bssr, 1949, NO. 5, S. 119-28
SO; Letopist Zhutmalinykh Statey, No. /+9, 191+9
!~fj:skz. IsKy. Abod. %".M,:eSyz
No 'rVO-10L.-Lituing tht oil Improves kok-%kl;hyi
1xi;t; in TCSPeCt to the d. of pL-mt growth atid in.
=,Ilk wt. of wet or dry roots. Although the M-
mlitagir of rubber latex Igopb, the yield per unit arm i,
%ignifimlitly inirruzed. lk*t atilt. is oF l1k.
hv,trolvtk- arwitv of the "I. G. It. KO-IIA;~Ufl
BELISKIYj B. B.;
. 6763. Bellskiy, B. B. , Kulakovskaya;.T.N. J Nyastyuk, N. N.
I ~ Primeneniye udobreniy na torfyano-bolotnykh pochvakh nizinnogo tipa.
Peredovoy opy-t. Minsk, Izd-vo Adad. nauk Belorus. SSR, 1954.
86 a. 20 sm. (Akad. nauk belorus. SSR. In-t melioratait', vodnogo i
bolotnogo khozyaystva). 4.000 ekz. 1 r. 25 k. - Bibliogr: s. 84.
-Na Belorus. yaz. - (55-2204) 631.615: 631.8 (47.60) & (016.3) '
SO: Knizhnaya Letopis' No. 6, 1955
9!
BELISKIY, B.B.
475 SKOROPANOV,, S. G., PECHKURO,VA.IIF*i BII~KIY, B. B.
Osusheniye i sellskokhozyaystuannoye osuoyeniye bolot v
Belcrusaiio M. Se3!khozgis. 1954. 133 a. sill. 20sm.
5,.000 ekz. lr. 80k.-Na obl. avt. ne ukazanv.-
L 54-544317 . 631.615(47-60)'
SO: Knizhnaya Letopis, Vol. 1, 1955
% &V i Q11A 4B."kandidat sell skokho2yaystvannykh nauk.- IODNDYMVA, A.1h.,
-- 6W
sotrudnik.
Effect on crops of the type of underground drainage. Tray InBt.
mel., vodA bol.khoz.AN BSSR 7;154-167 '56. (MI2A 10:5)
(Drainage) (Oats) (Rya)
BALISIIIY, Bronislav Bronislavovich
-
[Using fertilizers on bottom peat soils] Ushyvanne uhnsenniau na
tarfiana-bolotnykh hlebakh nizinnaba typu; persdaV7 vooyt. Xinsk.
Alcadleinia navyk Belaruskai SSR 1954. 83 p. WERA 10:9)
(peat soils) ; (rartillsere and manures)
USSR/Soil Science. Mineral Fertilizers. J-3
Abs Jour: Ref Zhur-Biol.j, No 6, 1958, 23742.
B.
Author Bel'skiy) B.; Kulakovskaya) T.
Inst
Title- Mobility of Phosphoric Acid In Peat-Bog Soil.
Orig Pub: Vestsi AN BSSR, ser. biyal. n.) Izv. 0 BSSR) ser.
biol. n.., 1956, No 2, 25-28.
Abstract: Experiments were conducted in the Minsk Marsh
Experimental Station on peat-bog soil in lysi-
meters. Radioactive superphosphate was applied
in the capacity of phosphorus fertilizer. The
highest assimilation of the phosphoric acid by
barley plants occurred with the application of
fertilizers to a depth of 10 cm.
Card 1/1
USSR/Soil Science. Tillage. Land Reclamtion. Erosion. J-5
Abs Jour: Ref Zhur-Dioi., No 6., 1958, 24836.
was identical In distances of 5 and 10 m. between
drains. The yield of oats on the lot with the
clay drainage was hi(Shest at a 10 m. distance between
drains. The lowest effectiveness of phosphorus-po-
tassium fertilizers was registered on fields with clay
drainage. The effective action of the slit drainage
on the yield of agricultural crops is caused by the
best conditions of aeration of soils.
Card P/P
USSR / Cultivated Plants. Grains. M-3
Abs Jour: Ref Zhur-Biol., 1958, No 16, 72920.
Author : LLLqKiy2 B. B.
I b
Inst :Not given.
Title :Fertilization of Corn on Peat-Marsh Soils.
Orig Pub: V.3b.; Kukuruza v BSSR. Minsk, AN BSSR, 1957, 191-
200,
Abstract: Experiments of the Institute of Amelioration were
conducted at the Kossovskaya Experimental Marsh
Station in 1955. The corn harvest, especially of
the ears, and their ripening increase with the in-
crease of P and K doses. With a dose of P30 KlOO
of active substance the harvest of green ri;ass of
the corn was innreased by 10.8 and of ears by 14.2%
in comparison with the control (311.7 centnera/ha.
of green mass and 87 cwt/ha. of ears). increase
Card 1/3
USSR / Cultivated Plants. Grains. M-3
Abs Jour: Ref Zhur-Biol., 1956, No 16, 72920.
Abstract: the seeds 2-4 cm away. Cu, Co and Mo applied in
the soil before planting at 5 c/ha in the form of
pyrite cinders or cobalt wastes increased the har-
vest of green mass and ears. Soaking the corn seeds
in weak solutions of microelementB provided an ad-
ditional harvest of green mass by 20.5-24.7 and of
ears by 15.6-29.5% in comparison with the control.
M, A. Novoderzlikina.
Card 3/3
SKOROPANOV, S.G., glavnyy red.; PECHKUROT, A.F., kand.sellokokhoz.nauk,
red*; KHOTIKO,,A.I., kand.sel'skokhoz.nauk, red.; IVITSKIT,
AvIs, doktor takhn.naukq red.,; MISKITO B.B., k9nd.sel'skokhos.
nauk, red.; MARIKS, L., rad.izd-va; VCLOEI"OVICH. I., takhn.red.
EAchiavements of the science of land reclamation in the White
Russian S.S.R.; works of the institute dedicated to the 40th
anniversary of the White Russian S.S.R.) Dostizhenlia malio-
rativnoi nauki v BSSR; Lastitut k 40-latiiu BSSR. Minsk, Akad.
nauk BSSR, 1958. 193 p. (MIRA 13:6)
1. Minsk, Beraruski naukova-dasledchy instytut meliiaratayl i
vodnoi haspadarki. 2. Chlen-korreapondent AN BSSR (for Skoro-
panov).
(White Hassia-Peat soils)
ZUBETS9 V.M., red.; SECROPANOT, SoG., red.;IBMISKIT, B.B.. red.; LASURY CH,
G.I., red.; KHOTIKO, A.-I., red.; SA OTA, A* o. red.; 13MMMOT,
T*M., tekhred.
(Cultivation practices for groving field crops on peat-bog soils]
Agrotekhaichaskie trebovanlia po, vozdolyvanliu seliskokhosiaistyennykh
kulltur no torfiano-bolotnykh pochvakh. Minsk, Izd-vo Akad.sellklios.
nauk BSSR. 1960. 79 p. (mmA 14:1)
1. Minsk. Havukova-dealledchy inetytut meliarateyi i vodnal haspa-
darki.
(Field crops) (Peat soils)
SKORCFANOV, B.G., glavnyy red.; PECHOROV, A.F., kand.sellskokhoz.nauk,
red.; KHOTIKO, A.I., starshiy nauchnyy sotrudnik; red.; ITITSKIT, A.I.,
doktor takhn.nauk, red.; ~and.sellskokhoz.nauk, red.;
FROKOFXNKO, D.P., tekhn.red.
[Principal results of research carried out by the White Russian
Scientific Research Institute of Land Reclamation and Water
Management in 19571 Oanovnye resul'taty nauchno-issladovatellskoi
raboty institute za 1957 god. Minsk, 1958. 280 p.
(HIRA 14:2)
1. Minsk, Belaruski navukova-dasladchy instytut maliaratayi
vodnai haspadarki. 2. Chlon-korrespondant AN BSSR (for Skoropanov).
(White Russia--Drainage research)
(White Russia--Agricultural research)
BELISKIY, B.B.; KULAKOVSWA, T.N.; ROZINA, M.S.
Determining phosphate availability in peat-bog soils. Pochvovedenie
no.11:93-98 N 161. (MIRA 14;12)
1. Belorusskiy nauchno-isslei*vatellskiy institut melioratsii i
vodnogo khozyaystva.
(Peat soils) (Soild--Phosphorus content)
ZUBETS, V.M., otv. red.; LASIIKEVICH, G.L., red.; PECHKUROV, A.F.,
red.; IVITSKIY, A.I., red.; BELISKI'Y'a' B.B., red.; LUNDIN,
K.P., red.; IAISHANOVA, Ye.A., red.; ThfitHCHUK, R.S.3,
tekhn. red.
[Draining and utilizing peat-bog soils) Osushenie i ispoll-
zovanie torfiano-bolotnykh pochv. Minsk, Gos.izd-vo sell-
khoz.lit-ry BSSR, 1963. 316 p. NLRA 16-.12)
(Peat soils) (Drainage)
BELISMY, Bvonislav Brcnislavcvi,:h;, Ye-~,- I.A.
[P.Ole of chemistry In the efficient utilization of peat-
bog soils] Roll khimii v effektivnom ispoltzovanil tor-
fiano-bolotryykh pochv. Elnsko Izd-vo "Urozhai," 1.9b4.
36 p. WdiL't '117 :"?;,
DEL: stf tY, 13. E- .
I N"i" - SeJL ( L-C_
BRLISKIY, B.I.
Collophane blinds
(FLIMS)
against flies. Gig. i san. 21 no.11:96 N 156.
(WINDOWS) (MMA 10:2)
meow,
Portable trap for synanthropic flies and blood-sucking insects
[with eumwy inIngliable Medeparax. I, paraz.bol, 26 no.2:222-225
.Nr-4P '57. (MLRA 10:7)
1. Iz Rovenskoy oblastuov sanitarno-spidemiologichaskoy stantaii
(glavuyy vrach L.Y.Bulanov)
(PLISS
portable fly trap)
AUTHOR: Rel'skiy, R.T., Candidate of Agricultural ')cience 26-58-6-54/56
TITLE: Mass Transmigration of Caddis Plies (Massoviye perelety
rucheynikov)
PERIODICAL: Priroda, 1958, Nr 6, p 127 (USSR)
ABSTRACT: The author reports two incidents where caddis flies migrated in
large numbers during daytime. The flights were apparently
caused by heavy clouds and strong winds. The swarms varied
between 200-1100 m in length and were rushing along with the
Card 1/1 wind at 10 to ICO m altitude.
ASSOCY-MM Oblastnaya sanitar.Wa epidemloloWichesk7m stantaiyaga Rovno
(Oblwt Sanitari-m Epldw--olloglcal Stet-_!On, c:Lty of Rovno)
1. Fl-ies-'Kigration
SAVVA) David Abramovich; VLASOV) Nikolay DmitriyevichIBELISMY B.R.
spets. red.; SHEMTTO, Ye.P., red.; ZAYTSEVA,-L-.X., ~.-;red,
(Using the production-line method for vatch and clock repdrel
Remont chasov potochno-operatsiowWm metodom. Vloskva, Gas.izd-vo
mestnoi. promyshl. i kbudozh.promyslov, IWSR, 1961. 133 P.
(MIRA W-12)
(Clodke and vatches.-Repairing and adjusting)
(Assembly-line methods)
KOROBOCHKIN, I.V., kand. tekhn. nauk; _B&L'SKIYA B,.&, 14. ; MIKHAYLOV,
Ye.A., inzh.; GUTENMAKHER,. L.I.,, laureat Stalins4 premii
doktor tekhn. nauk, nauchnyy red.; SEVOSTIYANOVA,'M.V., doktor
fiz.-mat. nauk, prof., nsuohnyy red.; RUSEVICH, I.M., lnzh., red.;
OSTROVSKAYA, Ye.G., otv. za vypusk
[Catalog-manual of laboratory'devices and equipment] Katalog-
spravochnik laboratornvkh priborov i oborudovaniia. Moskva,
Masbgiz.,No.21.[Calculating machines and~Aevices] Schatno-
vychislitalinye priboryi apparaty. 1948. 22 p. Wo*27. (Micro-
scopes and lensea] Mikroskopy i lupy. 1950. .87 p. (MIRA -16:4)
1. Moscow. Vseaoyusnava vyatavka otecheBtvennogo priboroatroyeniya,
1948.
(Calculating machines-Catalop)
(Microscopes-Catalog3) (Lenses-Cataloge)
BELISKIY, D.D.
Measurement errors ol dial and lever-type indicators with racks.
Izm.tekh. no.7:60 J3. 162. (MIRA 15:6)
(Recording instruments-Testing)
OMELICHEM, P.; IMLISKIT9 I* -W-4
We are repairing our dredge. lolyms 21 no,2:8 7 159.
(MIRA 12:7)
1 ~Irags No.173 pritska im. Gastello (for Omellchenko). 2*"Draga
i0*174 priisks, N .3.74 (for Bellskir).
(Kedging machinery-Maintenance and repair)
BELISKI7, G.M. (Sweromorsk) I
Darmographism in axudative pleurisy. Klin.medo 38 no.10t41-
420 160. (MnA 13 t3.1)
(DEMOGRAPB3A) .(PLWJSI)
BELISKIY., G#Pq, podpolkovnik
Important condition for the care of material, Veat.protivovoide
obor. no.9-.61-63 S 161. (MM 14:8)
(Commmications, Yd1itary-11hintenance and repair) ,
BELISKIY. G.V.z SHAV10, S.G.
Some regularities in the distribution of metallic elements in
rocks of the central Ralba. Uzb.geol.zhur. no.5:/+3-49 161.
1, Institut, geologli AN Uzbekskoy SSR.
(Kalba Itang&-Metals)
BELISKIY, G.V.
*thods of-sVdyiag the distribution of metal elements in rocks
as revealed by the studies in the Altai. Trudy AltGMII AN
Kazakh.SSR 12:70-75 162. (KMA 15;8)
(Altai, Wuntains-Rocks-Awaysis)
A~kl, 4BUDARIU, P.M., red.ixd-va; TWIN&, Te.L., tekhn.redo
(Stability of compressed steel rods witb flexible fixed ends]
Ustolobivost' ashatykb utallmykh stersbnei a uprugimi sasbehem-
Inniiami kontsov. Moskva, 1959# 144 po (Mmdemila etroltel'stva i
arhitAtury BEBR. lustitut stroltellnykh konstruktaii. Hauchnoe
soobahchenie A0.10) (HIRL 13:3)
(Blaatic rods and vires)
BIMI SXIT G,Te
Gommission on Metal Construction Xlemente of the Ccuuctl of
Coordination. Ixv, ASU no. 3:133 160a (KIRA 13:12)
1. Voheqy sakretarl Koxissit po metallokonstruktsiyan Sovota
po koordinatsit Almdemit atroitellistm t arkhitektury SSSR*
I (Ilectrio lines--Poles)
GEMWRLING, A.V., doktor tekhn.nauk; MIL%LY_ _G.Ye., kand.t.ekhn.nauk
Bearing capacity of frames under elastoplastic conditions.
Trudy TSNIISK no.7:33-62 '61. (NIRA 15:3)
(Structural frames-Testing)
BELISKIY~ Me., kand.tekhn.nauk
TheoretDc'al and experimental investigations of the deformability
and stability of elastically clamped rods. Trudy TSNIISK no.71
125-185 161. (MM 15:3)
(Elastic rods and wires)
IN MW 111 1 1111111
BELISKIY,.G.Ye., kand.tekhn.nauk
Stability of centrally compressed rods and frames under elasto-
plastic conditions. Trudy TSNIISK no.7t239-267 t6l.
(MA 15:3)
(Elastic rods and wires) (Structural frames)
BELISKIY, G. Ye. Cand Tech Sci -- "Strength of rods and frames withib Qoe
ralWe and beyond the now" of elastic deformations*" Mos, 1961 (Min of Railways
USSR. Mos Order of Lenin and Order of Labor Red Banner Inst of Engineers of
Railrond Transport im I. V. Stalin "MIT"). (KL, 4-61, 194)
143-
1 -2w-
%. BELfSKIYJ G.Ye.1 DIGNISIADI, L.K.
Inveatigation of mechanical properties of high-strength steels,
Prom. stroi. 43 no.9t4O-44 165. (MIRA 18t9)
BU SKIY I
The-machines came. Mest.propoi khud. promys. 3 no.1:29 Ja 163.
(HUI 16:2)
1. Direktor Kiyevo-Svyatoahinakogo zavoda khimicheskikh izdqliy.
(Kiev-Chemical industry-Squipment and supplies)
EELISKIY, I.F.; SHUYKIN, N.I.; GRUSHKO, I.Ye.; SHOSTAKOVSKIY, V.M.
Interaction between esters of (3-tetrahydrofurylpropionic acid
andits 0(-alkyl-substituted derivatives and phosphorus tribromide.
Izv. AN SSSR. Ser. khim. no.9;1670-1671 165. (MIRA 18:9)
1. Institut organicheskoy khimii im. N.D. Zelinskogo AN SSSR.
/-?z- Z- , ~ -k,/r / F/7-7-
SHUYKIU,N.I.; TULUPOV,V.A.; BELISKIY,I.Y.
~
On the hydration of the furan ring. Zhur.ob.Wm.25 no.6:1175-
1178 Je'55- (MIRA 8:12)
1. Moskovskiy Gosudarstvennyy universitat -
(Furau) (Hydration)
SHUYKIN, N.I.; IML r -
10-09 1
Disclosure of the tatroliydrofuran cycle vith alumiz= halides.
Tzv.AN SSSR,Otd.khim.x&uk m9.6:747-748 JTe 156. (Km 919)
I.Institut orgamichaskey khimii imexti N.D.Zelinsk*ge AksAamii
itauk SSM.
(Awan) (Alwimum halides)
..~~L ~ I
1=
Category: USSR B-9
Abs Jour: Zh--Kh, No 3, 1 957, 7592
Author : Shiykin, N. I., Grushko, 1. Ye. , and Bel'skiy, 1. F.
Inst : Academy of Sciences USSR
Title : On the Utilization of a Nickel Catalyst in the K zhner Decompo-
sition of Hydrazones.
Orig Pub: Izv. AN SSSR, Section on Chemical Sciences, 1956, No 5, 622-6Z4
Abstract The catalytic decomposition of the hydrazones of cyclohexenyl-
cyclohexanone and o< -acetylfuran in the presence of platinized
alumina (20% Pt), reduced nickel-alumina catalyst (3076M), or
Ni-mud has been investigated. It was found that finely dispersed
Ni-catalysts give product yields which are not lower than those
obtained with platinum catalysts.
Card ill -44-
Ti -J"
IM
S,
50A
K
'C.A 51 0--
j
f,un 2-un,
64- V", - " ,
~j--Ouz, T.NX'. ~
mud SOC~it
sli,-,rwaW
"I
7 vi,
BEL I SKIYZ9 I, F, Cand ChemaSoL, ('diBs) "Cata-lytic: NIFAMSEW93:10
H~dro 13nolysis of tht-iibumt, 2n.�
9 MoS919-571.
10 pp 22 =4 (Academy o~saiences USSIV, Inst of Org=ic Chemistry
im N". D. ZeUnskly), 1130 copies (XL, 25-5719 109))
- lg)-
Catalytic Hydrogenolysia of Furan Compounds 79-2-27/58
reason for that should be sought in the shielding effect of the side
group on the neighboring C-0 and C-C bonds. The by4rogenolysia reaction
of furan homologues is raccamended as a method for the obtaiment of*
certain less accessible alkyl alcohols and ketones.
There am 19 references ofvhich 9 are Slavid
ASSOCIATION: USSR Academy of Sciences, Institute of Organic Chemistr7
PRESENTED BYr
SUMUTTED: March 24j, 1956
AVAILAZZ: Library of Congress
Card 2/2
On the Interaction of Tetrahydrofuran with Silicon
Tetraohlorid.
robutanol as well as sicilic ae id. The correctness of the assu-
med structure is confirmed by the fact that the entire quantity
of tatrahydrofuran and approximately half the quantity of the
silioon-tatr&ohloride enters into the reaotion if it is carried
out by equimolar quantitLes of these substances. Thau 1.4-dich-
lorobutane and Di (0'0'-olorobutoxy)-dichlorosilane develop from
this as the main products. Furthermore, the carrying out of the
reaction is described in detail.
The reaction under consideration can serve as a method for pro-
duoing oxygen-containing silico-organic and clorino-substitutod
aliphatic alcohols.
(With 9 citations from publications).
ASSOCIATION Institute for Organic Chemistry "N.D.Zolinsky" of the Academy
PRESENTED BY
SUBMITTED 27-10-1956
AVAILABLE Library of Congress
Card 2/2
20-2-37/67
AUTHOR SHUYKINJ N.I. Corresponding Member of the Academy
I
and
JEL
SKIY I
TITLE -
The ~a ~aiyl~icHjydrcgenolysis of Sylvan on varied
Catalysts.
(Katalitiohoskiy gidrogenoliz silivana na, razlichn7kh
katalizatorakh.- Russian)
PERIODICAL Doklady 1kademii Nauk SSSR 1957v Vol 1159 Ir 29
pp 330-332 (U.S.S.R.)
LBSTRACT The hydrogenolysin reaction of furan homologs depends
on.-three factors, namely an the operating conditions,
,the nature of the catalyst and on temperature. In the
sylvan hydration in the liquid phase An copper chromite
the furan cycle is split to almost the same extent on
the ether'bondx 1 - 2 and 1 - 5. As a result develop
pentanol-I and -2, In oontzasit to that the sylvan hydro-
genolysis in the liquid phase on the Adams platinum
catalyst occur& only in the direction of a splitting
of the C-4 bond 1-5. The same in true for the hydrogi-
nolysis in the gas phase on nickel and copper catalysts,
however there dOT010PS no alcohol but a ketone
(pentanone-2). In earlier work* t4authors studied
the same reaction of furan homol~es In the gas phase
CARD 1/4
2M~-37/6T
The Cata4tic Aydroffenolysis of Sylvan on Varied
catalysts.
on a skeleton niokol-aluzibAum catalyst and proved that
thereupon takes place a hydrogenolyBis not only of the
other-, but also of the carbon-carbon bonds in the
f-mran cycle. Ill furan homologs with an alkyl- or alkenyl
substituent in an a-position are subject to hydrogenoly-
sis in three directions. k eohema for this Is given.
At I75*C and below the furan oyale undergoes a hydra-
genolys'is only in directions I and II (of the scheme),
above 23500 also in direction III. The present paper
,gives test results of the sylvan hydrogenclysis in the
fa;%5hase in thelvesenae of various oatalysta: platinum
I an,1 palladium (10~) on charcoal, Adkins copper
chromitep nickel (30 ~0 on alumijaiumoxide an& skeleton
nickel-aluxinium catalyst. The re3ults of this study
lead to the conclusion that the direction and depth
of the hydrogenolysis of the furan cycle esjqenfikly
depends on the nature of the catalyst. Platinum on-
charcoal possesses the seleotive ability to cgrry out
the hydrogenclyals of the cycle in sylvan only on the
other bond I - 5. The presence In the remotion products
only of pentanone-2 and unchanged sylvan shows that, at
2T50C the hydrogenolysis reaction on the platinum
CARD 2/4 catalyst occurs iscomparably faster than the hydrogens-
20-2-37/67
The Catalytic Xydrogenolysis of Sylvan on Varied
Catalysts.
tion of the double bonds in the cycle. Pentanone-2
practically forms with a quantitative yield In rela-
tion to the sylvan that entered the reaction,. In
contrast to that the palladium catalyst proves much
more effective in the hydration of double bonds of
the cycle and shows only insignificant activity in
the hydrogenolysis of the ether bond. Just as on pla-
tinum, the furan cycle in the presence of a palladium
catalyst is subject to hydrogenolycis only on the
C--O bond 1--51 whereby pentanonc-2 deyelope. Copper-
chromium catalyst shows a rather weSk activity in the
hydration and hydrogenolysis at 275 C. In contrast to
the bydrogenolysis on copperchromite in the liquid
phase which leads to the formation of two alcoholop
the reaction here in the gas phase takes place dtly
in the direction of a splitting of the other bond
which does,not border the side group. The mentioned
skeleton catalyst and nickel on aluminumoxyde differ
CARD 3/4 widely with regard to their ability to carry out the
20-2-37/67
GARD 4/4 The Catalytic Hydrogenolysis of Sylvan on Varied
catalysts.
hydrogenolysis of the furan oycle. On the latter about
15 % ketones form at 275001 85 % of the ostalyeate
consist of unchanged sylvan, n-pentane and high-boiling
compounds. This indicates that the prooeases of faxrasrXw,
ing decomposition of the furan ring and the formation
of molecules of complex composition is favored by tbis
catalyst. On the skeleton nickel aluminium catalyst
the hydrogenolysis takes place in three directions.
These results are in agreement with those obtained
earlier. Thus only the skeleton catalyst is able to
carry out the reaction as well in the direction of
splitting the other bond 1-5, as of a conjugate aplit-
ting.of the linkages 1-5 and 4-59 and of 1-5 and 3-4-
This permits to obtain aliphatic ketones of various
structure from alkyl furans.
(3 Slavic-references)
ASSOCIATION: Institute for organic chemistryim.N.D.Ze1in9ki* of the
Academy of Scienoesof the USSR.
(Institut organiaheskoy khimii in. N.D. Zelinskogo,
Akademii nauk SSSR)
PRESENTED BY:
SUBMITTED: 27-3-57
IVAILABLE: Library of Congress.
F
AUTHORSt Shuykin 9 N. I Correspooling Member of the 2o-4-26/~i
AN SSSR and
-'ITLE: The Hydrogenolysis of Furane Homologues on a Platinum Catalyst
(Gidrogenoliz gomologov furans, na platinovom katalizatore)
PERIODICAL: Doklady AN SSSR, 1957t Vol- 116, Nr 4, pp. 621-624 (USSR)
ABSTRACT: After an exhaustive review of references the authors make the
comprising statement that the hydrogenolysis of the furane cycle
in a general case depends on the nature of the catalyser, further-
more on the character of the lateral substituent, on the tem-
perature and on thetphase (Liquid and vaporous) in which the re7
action takes place. The auV-.ors investigated the reaction of the
a-substituted furane homologues in the vapour phase on 15%
platinum, deposited on activated Virch coal. The length of the
lateral chain of the furane homologues was chosen from C1 up to
C5 in orderto be able to evaluate the influence of the chain
length ofthe alkyl lateral group on the character of the hydro-
genolysis. It was found that the furane cycle under these condi-
tions at 2750, independently of the chain length, splitted at
the C-LO-binding 1-5 which is not adjacent to the lateral group..
Here aliphatic ketones are formed with yields of 9o-95,P"' of the
theoretically possible.yield. At this temperature (2750) no al-
kyl tetrahydro-furanes were found. However, at 2300 from the hy-
Card 1/2 drated a-n-propyl furane beside heptanon -4 also a-npropyl-tetra-
The Hydrogenolysis of Furane Homologues on a Platinam Catalyst. 2o-4--26/51
hydro-furane was obtained in a quantity of 16,,;.' of the catalyst
weight. Thus the lower temperature favors the re4ction of the
hydrogenization of the double bindings in the furane cycle,
whereas an increased temperature is favorable for the hydro-
genolysis of the other binding 1-5. In the experimental part the
usual data are given. Final oonolusions: It was found that in
the case of hydration of the a-alkyl furanes in the vapor phase
on platinized coal a elective hydrogenolysis of the furane cycle
on the C-0-binding 1-5 taken plaoc, a fact by which aliphatic
ketones with high yields are formed.
There are 2 tables, and 8 references, 1 of which is Slavic.
ASSOCIATION; Institute for Organic Chemistry imeni N. D. Zelinskiy AN USSR
(Institut organicheskoy khimii im. N. D. Zelinskogo Akademii Nauk
SSSR)
SUBMITTED: July 10, 1957
AVAILABLE. Library of Congress
Card 2/2
20-5-24/48
'AUTHORS t Shuykin, N. I., Corresponding Member AN USSR, Bellskiy, I. F. and
Tyant Sin-Khua
TITLEt Hydrogenolysis of o6 :.Methyl-d_'-Ethylfuran on Platinized
C~_farcoal (Gidrogenoliz 0~ etil-061-etilfurana na platinirovannom
ugle)
PERIODICALs Doklady AN SSSRj 1957, Vol. 116, Nr 5, PP- 608 - 810 (USSR)
ABSTRACTs For the purpose of comparison the authors investigated the hydro-
genolysis of silvan at various catalysts. The furan ring in silvan
can be splitted at a platinum-, pa;ladium~v and copper-chroaium
catalyst in the vapor phase at 275 at an ether binding not ad-
joining to a lateral group. This leads to the formation of me thyl-
propylketone. Only the platinum catalyst shows the power of split-
ting the furan ring selectively at the C--O- binding without any
secondary processes. In contrast to all these catalysts the skele-
ton-Ni-Al-catalyst has specific powers to carry out the hydrogeno-
lysis of the furan ring in the direction of cracking of the ether
binding 1 - 5 as well as I - 5 and 3 - 4- In the last case ketones
are produced which contain in the molecule 1 or 2 carbon atoms
less than the initial alkylfuran had. This is to be called the
Card 1/3 "conjugated" hydrogenolysis. In all cases the influence of the la-
20-5-24/48
Hydrogenolysis of o(--JUethyl-ot'-Ethy1furan on Platinized Charcoa ,1
teral-alkyl-8ubstituent effects an almost complete incapability of
the C-0-binding I - 2 of hydrogenolysis. Therefore it was inter-
eating to investigate the comparing capability of the C-0-binding
of the hydrogenolysis which are influenced by 2 alkyl groups with
different lengths of the cai:bm chain. If the reaction at the ether
bindings I - 2 or I - 5 mentioned ir4the title is carried out, hep-
tanon-3 and heptanon-2 are bound to be 8roduced correspondingly.
The first substance was obtained at 235 in the vapor phase with a
yield of 54 %, the latter with 36 ~S. N-heptan (ev7lo) was present
in a con3iderabld smaller quantity. Its fornation is effected by a
simultaneous hydro-enolysis of the furan ring at the C-0-bindings
1 - 2 and 1 - 5. The relative content of the two first ketones in
the products of the hydro.-anolysis leads to the conclusion that
the ethyl group exercises a much more stabilizing influence on the
adjoining C-formation than the methyl group. Theexperimental part
with the usual data follows. There are 3 references, 2 of which
are Slavic.
Card 2/3
Y."
AUTHORS: Shuykin, ff. I., Corresponding Member of the 20-1-25/42
AN USSR and Bel'skiy, I. F.
TITLE: Note on the Selective Reduction of Alkyl-Furyl-Carbinoles
to Alkylfuranes on a Palladium Catalyser (Selektivnoye
vosstanovleniye alkilfurilkarbinolov v alkilfurany na
palladiyevom katalizatore).
PERIODICAL: Doklady AN SSSR,'1957, Vol. 117, Nr 1$ PP- 95-97 (USSR)
ABSTRACT: The hydration reaction of compounds of the type
CH-R f where R may denote a hydrogen atom,
UO I
OH
a alkyl or an aryl radical, has been throughly investigated
with respect to the multiplicity of compounds as well as to
the number of the catalysers employed. According to the
nature of the last and according to the structure of the
compounds the hydration may take three directions:
Card 1/4 1) The double compounds of the furane cycle are the only
Note on the Selective Reduction of Alkyl-Furyl-Carbinoles 20-1-25/42
to Alkylfuranes on a Palladium Catalyser
ones that'are hydratedo in such a way as to produce
alcohols of the tetrahydrofurance series. 2) The hydrolysis
of the cycle takes place at one or at both C-0 bindings,
wherefrom "alkandioles" and alkanoles are produced.
3) The lateral group may be reduced entirely, the hydroxyl
being replaced by a hydrogen atom. Pinally, all or some of
the abovementioned reactions can take place at the same time
under certain conditions. A comparison is Given between the
nickel- platinum- and copper catalysers employed for these
purpooes. As it Is well known, palladium represents an
excellent catalyser of the double bindings of the furane
cycle in the 'liquid as well as in the vapour phase. The
attempt of the authors to hydrate the furane ring of the
compounds mentioned in the title at palladisated coal lead
to surprising results: Instead of a hydration of the double
bindings in the furane cycle a hydrolysis of the C - OH
bindinre and the replacement of the hydroxyl group by a
hydrogen atom took place. This lead to a conversion of the
Card 2/4 ethyl- and methyl-furyl carbinole3 to the coxmsponding
Note on the Selective Reduction of klkyl-Paryl-Carbinoles 20-1-25/42
to ilkylfuranes on a Palladium Catalyser
a-propyl and a-ethyl furanes, yielding 70-80 % of the
theoretically possible production. This ability to split
forms a specific property of this type of compounds. It
does not occur in pentanole 2 at much higher temperatures.
It is a remarkable fact, that the hydroxyl group of the
alkyl tetrahydrofurylcarbinoles is not even capable of
reduction. Therefore the C - 0 binding is weakened only
in. alkylfurylearbinoles to such an extent, that it in easily
broken up by hydrogen on palla disated coal. The reason for
this may be sought in the fact, that the 0 - 0 binding
in the lateral chain is conjugated with the double binding
of the furane cycle, Methods of production for the initial
substances are given. The reaction of the reducing des-
hydroxylisation of the alkylfurylcarbinoles into alkylfurane
constitutes a very interesting instance of the selective
effect of the palladium catalyser. kpart from its theoretical
interest it may be of great importance in a preparative
respect, for it provides for an avoidance of the stage of
the dehydration of the alkylfurylcarbinoles in the synthesis
of the alkylfuranes, which, in general, does not roceed
Card 3/4 smoothly.There are 8 references, 2 of vihich are Ofavic.
Note on the Selective Reduction of Alkyl-Furyl-Carbinolea 20-1-25/42
to Alky1furanes on a Palladium Catalyser
ASSOCIATION: Institute for Organic Chemistry imeni N. D. Zelinakiy
AN USSR (Institut organicheskoy khimii im. N. D. Zelinskogo
Akademii nauk SSSR)
SUBMITTED: July 10, 1957
AVAILABLE: Library of Congress
Card 4/4
F
AUTHORS: Shuykin, N. I., Bel'skiy, I. F.V 62-2-21/28
TITLE: The Catalytic Reduction of Alkylfurylcarbinols to Alkylfuranes.
(Kataliticheskoye vosstanovleniye alkilfurilkarbinolov v al-
kilfurany)
PERIODICAL: Izvestiya AN SSSR OtdelerJye Khimicheskikh Nauk, 1958, Nr 2,
pp. 240-240 (USSR)
ABSTRACT: During the investigation of the hydrogenation of ethyl- and
ethylfuryl-carbinols the authors discovered the interesting
fact of the selective reduction of the above-mentioned com-
pounds to a-ethyl- and a-propyl-furnaces. It was further found
that the capability of the hydroxyl-group, to substitute in hy-
drogen under the catalytic influence of palladium coal depends
on the presence of the alkylfurylcarbinol cycle. In the reduc-
tion of isopropyl- and butylfurylearbinols a-isobutyl- and a-
-imylfuranes with a yield up to 7o~b' are produced. The experi-
ment was performed in the vapor phase at 250-26o0. There are
2 Slavic references.
Card 1/2
The Catalytic Reduction of Alkylfurylearbinole to Alkylfuranes 62-2-21/28
ASSOCIATION: Institute for Organic Chemistry imeni N.D. Zelinskiy AN SSSR
(Institut organicheakoy khimii im. N.D. Zelinskogo Akademii
nauk SSSR)
SUBMITTEDs September 27, 1957
AVAILABLE: Library of Congress
1, A11qlfurylcarbinalB to allqlfuranes-Catalysis 2. Alkylfur7l-
carbinals-Reduction 3. Allqlfuranes-Production
4. Palladium coal catalyst-Applications
Card 2/2
62-58-3-9130
AUTHORSi Shuyking N. I. Bel'skiy, I. F.
TITLEt The Catalytic Hydrogenolysis of Furan Compounds (Kataliti-
cheskiy gidrogenoliz furanovykh soyedineniy)
PERIODICAM Izvestiya Akademii Nauk BBBROtdeled~e Khimicheskikh flauk,
1958, Nr 39 pp. 309 - 315 (USSR)
ABSTRACTs With the example of the preceding experiments the authors
this time performed the lWdrogenation of the mixtures of
some cA-alkyl- and ol--alkenyl-furans at 2350C. It was assumed
that at this temperature an absolute splitting of the furan
cycle must take place. Then products of the hydrogenolysis
should form. This assumption was confirmed by the experiments.
Moreover a new result of theoretical as well as practical
importance was attainedt It became evident that the C-C-bond
3-4 readilg splits up at 235 0, but that at a lower tempera-
ture (175 G) a hydrogenolysis of this bond does not occur.
In this experiment the hydrogenation of 0the mixture of
oC-n.butyl- and o(,butenyl-furanee (235 C) was performed in
Card 1/2 a flow-system under ordinary pressure. In the presence of the
62-58-3-9/30
The Catalytic Hydrogenolysis of Furan Compounds
skeleton nickel catalysts a complete splitting of the furan-
-cycle in these compounds takes place. It was further found
that the furan-cycle in these compounds is subjected to
hydrogenolysie in the direction of the split of the C-0
bond 1-5) as well as in the direction of the split of the
bond 1-5 and 4-5 as well as 1-5 and 3-470 It was found that
the relative stability of the different bonds in the cycle
of ot-n.butyl- and oe--n.amyl-furans depends on the length
of the side chain. The authors obtained some data according
to which the mechanism of the radicals of the hydragenolysis
reaction of the furan-cycle can be assumed. There are 3 re-
ferences, 3 of which are Soviet.
ASSOCIATIONs Institut organicheskoy khimii im. N. D. Zelinskogo Akademii
nauk SSSR (Institute for Organic Chemistry imeni N. D.
Zelinskiy 7AS USSR)
SUBMITTEDs October 27, 1956
Card 2/2
AUT11011S Shuykin, 21. 1., Bel Iskiy, I. F. 62-58-4-22/32
TITLE: Hydration of Alkyl a-Furylcarbinols on Ni-ZnO-Catalysts
(Gidrirovaniye alkil a-furilkarbinolov na Ni-ZnO-kata-
lizatore)
PERIODICAL: Izvestiya Akade-,aii Nauk SSSROtdeleniyeKhimicheskikh
ITauk, 1958, Nr At, PP. 506-507 (USSR)
ABSTRACT: The hydration of alkylfurylcarbinols can take place in
various directions accordine to the nature of the cata=
lyst and the conditions of reaction. Lately the authors
found (Reference 3) that the primary reaction in the
hydration of alkylfurylcarbinols is not an hydration of
binary bindinGa within the cycle but a reduction of the
hydroxyl (.-group which leads to the formation of u-al=
kylfurans. In +he present paper the authors report on
the investigated hydration of alkylfurylcarbinols in gas
phase on a Ni-ZnO-catalyst. In this they found that this
catalyst (like paladini2ed. charcoal) effects as primary
reaction the reduction of the hydroxjl Group in alkyl=
Card 1/2 furylearbinols without touching the divisible bindings
U 0
Hydration of Alkyl a-Furylearbinols on Ni-Z"JnO- 62-56-4-22132
-Catalysts
in the furan cycle.
There are 1 table and 3 references, I of wlich is Soviet.
ASSOCIATION: Institut organicheskoy khiuii ita. If. D. Zelin3%oCo
Alcaderiii naulc SSSR (Institute for Or-anic Chcmistry
imeni 11. D. ZelinskiyIAS USSR)
SUBMITTED: November 13, 1957
AVAILABLE: Library of Con-ress
w
lo Alky1furylearbinols-41ydration 2. R-UG-Catalysta
-Xppl-teations
Card 2/2
/S7A-
Catalytic deh7dration of tetrahydrofuran homologues. Dokl. AN
Azerb. SSR 14 no-2:115-117 158,, (MIRA 11:4)
l.Institut organichaskoy khimii. AN SSSR.
(Furan) (Dehydration (Chemistry))
I SOV/ 20-12o-3-31/67
AUTHORS: 1~huykin, M. io, Corresponding Member, Academy of Sciences,
USSR, Bellskiy, 1. F.
TITLE: Isomeric Transformation of I-Oxides (Tetrahydrofuranes) of
Aliphatic Carbonyl eompounds (Izomerizatsiya y-okisey (tetra-
gidrofurunov) v alifaticheskiye karbonillnyye coyedineniya)
PERIODMAL: Doklady Akademii nauk SSSR, 1958, Vol- 12o, Nr 3, pp. 548-551
(USSR)
ABSTRACT: Several chemical transformations of alkylene-oxides are under
the action of various agents connee 'ted with an easily Pro-
ceed.ing cleavage of the a-oxide cycle. The reiction mention-
ed in the title i;OaWong those well studied. It proceeds from
a heating to 300- 0 or lower temperatures in the presence
of catalysts. Asymmetdo a-oxides, which possess one or two
alkyl-substituents at one single carbon atom of the cycle,
by a cleavage of the cycle are isomerized preponderatingly
at that binding, which links the oxygen atom to that carry-
ing the substituent. This leads to the formation of aldehydes
(Ref 1). No analogous reaction was knwon to take place with
Card 1/3 the comDounds mentionea in the title. The catalysts, which
SOV/ 2o-12o-3-31/67
Toomeric Transformation of y-Oxides (Tetrahydrofuranes) of Aliphatic Carboni!
Compounds
are most active in the isomerization of a-oxides, with hydro-
furane and its analogs lead to a dehydration reaction. It
yielda diene- and aromatic hydrocarbons, The authors perform-
ed the transformation reantions of tetra~ydufurane and of
Its a-substituents on pla-tinated coal in the vapor phase
0
at from 230-250 . They found that these substances under
these conditions isomerize to aliphatic carbonyl compounds
with a simuitaneous cracking of the cycle at the C-0 links.
Conclusions: 1) The a-oxide ring (tetrah.,-drofurane ring) is
capable of the last mentioned transformations, by which ali-
phatic carbonyl compounds are formed. 2) If an alkyl radical
(CH 3' Y5 t n-C3H 7) is present in arx U-DOSitio'n of the tetra-
hyd.rofurane cycle, the isomerization of the I-oxide primarily
NP to 90-951~f*) takes place with a cracking of the cycle at
the C-0 link. This leads to the formation of corresponding
aliphatic ketones. 3) The aldehydest which are produced in
small amounts in the isomerization of tetrahydrofurane and
of "-alkyltetrahydrofuranes, suffer a cleavage at the C-0
link 112 and are subject to a decarbonylation to the correspond-
.ing paraffin hydrocarbons under the prevailing reaction condi-
Card 2/3 tions.