SCIENTIFIC ABSTRACT GUNAR, I.I. - GUNBINA, M.N.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000617330008-3
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 21, 2001
• Sequence Number: 8
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

RATLY, XEtrel [Rataj KELroll; UNNOT, M.P. Etranalatorl; GUNAR, I.I., red.;
rummo, S.Y., tekhn. red.
[Chemical control of weeds in flax] [Translated from the Czech]
Xhimloheskals, bor'ba o sorniakead T pose'vakh l1na. Pod red. I.I.
Gunara. Moskva, Ind-yo inostr. 'Lit 19L122 p. (MIRA 11110)
(Wood cont';'17, (

u J;
IVA I
It
19
ILI 11 .3
9 A 2 q A j
91
I F

YEMEL'YAIIOVA, N.A. [translator]; LISGVSKAYA, O.V. [translator]; GUNAR, I.I.,
red.
[Chemical control of weeds) Khimicheskaia bor'ba B sorniakami. Pod
red. i a predisl. I.I.Gunara. Moskvap Izd-vo inostr. lit-ryj 1959a
226 p. (MIU 14:10)
1. British Weed Control Council,
(Weed control) (Herbicides)

GMIAR, I.I.-, SINYMUN, A.M.
Electrophysiological charactnr is tics of irritability in
plants. Report 1: Principles, history and mathodu of research.
Izv.TSI'hA no.4-7-22 159. (14IRI, 12:11)
(Blactrophysiology of plants)
(Plantq--Irritability and movem3nts)

GUNAR, i.I.;i~liASTII;A,Ye.Ye.;PZTROV-SPIRIDOI[OV, A.Ye.
How the proportion between potassium and calcium in the nutrient
solution and in the plant affects the cold resistance of corn. Izv.
TSKU no.5:19-28 159 (KIR& 13:3)
(Gorn(Maine)) (Plants. Effect of potassium on)
(Plants, Effect of calcium on)

14 0,1.4--w-
GUNAR, I.I.; SINYUKHIII, A.M.
Effect of action current an the circular movement of proto-
plasma in the cells of nitella (Nitella flexilis Ag). Izv.
TSHhA no.3:7-17 160. (MFHA 14:4)
(Nitella) (Protoplasm)

GUIIXR, 1.1,; IM~STIUA, Te.Ye. ; BRYUSEK017-I'l, N.A.; ye.M.
Diurnal periodicity in the synthetic activity of roots. [with
summary in graglishl. Izv. TS&Li. no-5:18-34 160. (HUIA, 13:11)
Poots (Botany))

GUNAR, I.I., prof.; KALINKEVIC119 M.I.0 kand.biolog.nauk
Using chemicals for regulating the flowering and fx-uiting of
apple trees. Izv. TSKU to.1:22-41 161. (MIRA 14:3) ,
(Apple) (Cresol) (Phenols)

GUNAR LT biit'~7T!',~Hii,,'J' AJI. ; L;ulNA , L. Ya . ; TAkEV A, "LI.A,
ft~
Eluctrophy6i(jlogical characteristics of irritability in
plants [with wwamuary in 'Englishj. Izv. 'D~Khfi no.2:7-19
(MIRA 14:8)
(Z'lants--Irritability and movements)
(Plants, Effect of electricity on)

I.I.; BOGACHEVA, I.I.
How the movement of kidney bean chloroplasts within a cycle
of 24 hours is related to photosynthesis [with summary in
English). Izv. TSKILA no.2:215-220 161. (DIIRA 14:8)
(Chlorophyll) (PhotosynOwsis)

GUNARY !.I.; KRASTINA, Ye.Ye.
Effect of light-darkness balance on the rhytbm of movements
in plant leaves. Izv. TSKhA no-5:55-70 161. (MIRA 14:12)
(Plants, Effect of light on)

KRASTINA, Ye.Ye.; GUNAR, 1.I.; KASPSHIK, M.
Role of external and Internal factors in the daily dynamics of
root feeding in tomatoes. Izv. TSKhA no.6:32-42. 161.
(HIM 16:8)
(Tomatoes) (Plants-Nutrition)
(Plants, Effect of light on)

GUNARY I.I. , prof.; I,ETHOV-3l,jjtIDOtl(-jV, 11-Y0.2 Btal-iihiy nauchnyy sotrudnik,
Respiration and transformation of or anic acids in the ontogenes.Ls
of soybeans [with summary in Englishl. Izv. TSKHA no.1:61-73 162.
(MIRA 15:6)
(Plants-Rospiration) (Acidsp Organic)

KWTIWA. YeeYe9j, kandobriolog.nauk; GUNAR, I.I., prof.
Specific characteristics of the photoperiodic reaction of
organisms to short and long days. Izv.TSKU no-053-63 162.
(MIRA 15t12)
(Photoperiodism)

GUNAR, I., prof.
Life revolted against grassland farming. Nauka i zhiznI 29
no.5:2-10 My 162. (MIRA 1511l)
1. Zsveftushchiy kafedroy fiziologii rasteniy Timiryazevskoy
sallskokhoayaystyennoy akademii.
(Agriculture)

GUNAR, I.I.; SINYUKHINq A.M.
The propagating wave of excitation in higher plants. Dokle
AN SSSR 142 no.4:954-956 F 162. (MIRA 15s2Y ....
1. Moakovskaya sel'skokhozyaystvennaya akademiya im.
K.A.Timiryazeva. Predstavleno akademikom A.L.Kuraanovym.
(Electrophysiology of plants)

KWTINA, Ye.Ye.; KOVRIGO, N.M.; GUNAR. "
Connection of the photoperiodical reaction of Perilla and
spring wheat with chronometric characteristics. Izv. TSKHA
no.6:32-48 162. (MIRA 16:6)
(Photoperiodism)

GUNAR, I,I.; SINY110111, A.M.
Functional significance of action currents affectinF ~rc L, . , exchange
of higher plants. Fiziol. rast. 10 no-3:265-274 IV-je 163.
(MIRA 16:6)
1. Kafedra fiziologii rasteniy i laboratoriya iskusstvennogo klimata
Moskovskoy sellskokhozyaystvennoy akademii imeni Timiryazeva.
(glectrophysiology of plants) (Plants-Respiration)

ZH1JRB1TSKIY, Z.1., otv. I-ed.; GJ,'KLL1, J;.A., red,; GUNAII,,,~4,t
red.; POTAPOV, N.G., red.; YjiMILINIKO A-"G"V'." ' d izd-va;
Y . re .
GUSIKOVA, O.M., tekhn. red.
[Physiological basis for the plant nutrition system] Fizio-
logicheskoe ob0snovanie sistemy pitaniia rastenii. Moskva,
Izd-vo "Nauka,n 1964. 339 p. (MIRA 17:3)
1. Akndemiya nauk SSSR. Institut fiziologii rostenly,

ZHURBITSKIY, Z. 1. 9 otv. red.; GETIKEEL P. A.., red. red.;
FOTAFOV, N,G., red.; FOTIEKHINA, N,A.j red,
Nole of mineral elements in the metabolism and productivity
of plants] Roll mineralln-ykh elementov v obmene veshchestv i
produktivnusti rastenil. Moskva, Izd-vo "Naul(a," 1964. 358 P.
(MIRA 17:7)
1. Akademiya nauk SSSR. Institut fiziologii rastenii.

Hill
41. 1,11; R T
Tl '111IN

KU8TIVAI Yn.yfj., starohly nauchnyy ticitrudnik, kand. Walog. iiauk;
GUIIARY I.T., prof.
Effect of thermal stimulation on the exudation of sap by sun-
flower roots. Izv. TSKHA no.3:71-81 164.
(14IRA 17: 1.1)
1. Kafedra fiziologii rasteniy Moskovskoy !3ellskokhozyaystvennoy
akademii imeni Timiryazeva.
L: -j!

451~-
ACCESSION NR: AR5003961 S/0299/64/000/023/R036/11036.
,SOURCE: Ref. zh. Biologiyao Sv. t.v Abs6 12R270
AIMIOR., Gunar$ 1. 1.* Sinrx~in;, A. ff.; OzolinI4 A!
TITLE: Role of bivalent cations-in excitation of A sittgle. plant- oell
CITED SOURCE: izv. Timiryazevsko S.-kh., akadp noo' 3P 1964s 62-86
TOPIC TAGS: nitellap plantp call, fon conaontrdt,11,10.np q6x'~,, itat Loh$
protoplasm flow# calcium iong rutgneaiu~m ionp substitultion roactiOn
A
TRAITSLATIOU44 The possibility o P substituting ?4gP4,,' :for; aa2+ il-L :Ei
medium was investigated with aotion currents ~ gat0oted., by single,
nitella calls, Change In I%?-^It* concentration frovi 0 to 0*006 M., 'ha-A
little effoot on the rest otential of the cells4. With tho
substitution of Ca24' by Mj+ the cells were capablo of' generating
action currents Vaich viere expanded in fbM and ot long duratiC1114
The eat-ion substitution affeoted the exoitation V.11vauhtild, mz.2+
-also affoated struotural changes of the protoplasino, ia~. the moiiont
action current passage,, the oircular flow of the pri:Alfoplasm didl
i Card

,I,l fill.!
34555-65
ACCESSION HR. AR5003961
not stop as under normal conditionsp but 6nly-.s1,dv6d dlwji by 5CYJ ae.
proto lAth" a
compared to the movement rate for PIQUM at rea
tenfold reduction of Y& in the medium Mg Z+ aq63antt-atioiis of 0
and 0,0002 n*q tha cireular flow of protoplasm stappadljn e.11 callos.
when action currents were generated# but with a Irs4"' ooncentratlizi
of 0,0006 ne the flow stopped only in some of the eal-14i, With Ixteb
Mg2+ concentrations and a decreased K+ level# no atoppagp oactuired"
L. Tsofina.
SUB COM LS, EENGLO. 00
re
ca
.. ... .....
"-M,

T YC' UO 77~ T,
S7 j3D ~r;

GUNAII, OZOLINA, I.A.
Action potential of flitella flexilis cal-Is fil:r:id -,4-,t.*- arr.-Jficia -"
salt solutions. Dokl. All SSSR 160 no.4:956-959 F ItI5.
18:2)
1. Mfoskovskaya sellskokhozyaystvenraya akademiya im. Timlryazeva.
Submitted March 21, 1964.

7 ;,., r
ir r~,xr, i ed rlqnt collEi. zv.
r a !,-i
ov

GUIM, I.I., prof., FANTALOV, O.S., InWi.
Laboratory of artificial climate of the Tirdriazev Agri-
cultural Academy. Izv. TSKIIA no./,:220-240 165.
(MIJU 16:11)
1. SuInitted April 29, 1965.

'7 ;-, : '. ;T
J I . 1. , , . , .
!, i . - ~ on C, ~ lan,~s furt:,,er uI,L C-1, ~_:- -, -~ I --- - .,- -.11 t , . . ~-,)
of L., , -4 . -
. c Z L- - G- I - . - Y-
i Bile i I -. -: " ~
F:'I,-,-OD.k k-,i-~erdi-a 11,-n,..~:ite) Sofiya '1`01 -3 '*o I J,:u: / I -!, .-, -~
l')f-11
S(): E,-Ist Eui-opo-m Acc~s7fton3 List Vol 2 i,'o "(' "IC I-) ~

T
GUIIAR, V. I.
USSR/Chemistry - Growth Stimulants
"Synthesis of Some Chlorophenoxy Derivatives, "V. P. Rama~iev, N. 11. Suvorov, and V. I.
Gunar, Moscow Chem-Tech Inst im D. I. Rendeleyev
2hur guthch Xhim, Vol 9-3, No 7, pp 1206..1209 -IlD
Synthesized the following: A,-(~-chlorophanoxy)-pheny-lacetic acid, A-(2,4-dichlorophenoxy)
pheaylacetic acid, A-(2,5-dielilorophonoxy)-pheiVIticetic acid, V-(14-chloropheno3W)-
crotonic acid, V-(2,4-dichloropheno)W)-crotonic acid, V-~2,5-dich:lorophenoxy)croto.,iie
acid, aud 2,4--1ichlorophanoxyace-tone.
272T19

and amtuouJn In pea L, A- A,
Butidel,nnd V. 1. (kalar i A ;~,M, in
pu f,witi, v.;
Z"'j
W'd tiprmtk from 'J.101 llj~ illj~
s1ritkS licit to rAlize. mlif G'kull (C.A.
and the cozvma~p was pq)(J. imin bak,ni'
scribed earlier (Biec~rvx. tilv; ih
purity confirmed spectT of) hotmifati leall v. 4". 1 itt; v I 01, 6 1
was detd. chrnmatozr~ijillicallv by the jjr,--~~Ame of
vich ard Bundc] (C.A. -1-1. 16i(Xln)~ M-Alullil., %0-1 iq
formcd in the gtowing plant ;1~ a rclult of th~ enzyndo
of acid by . 'I tic
addn. o! ccnzymase and ol plixose inter-sif- eiv reavtiri ;t:r
whi:h pH 7.7 -um3 tub! tile uptilnum. E~Vfnwtioll.ll
with (N1-L)2SO4 from reagircvt exts. Wa.3 iscl.-Acd an e-irvil-ii,
prcpu. which ~tnlyzed the -kafoghjwric acid malinizil"i'm
VOU13 by NILOH. 11- S.
INglity"
I is it t; I L,;!! 1 J~ i
lom~.'Jfl , M1.1 I
OR
ME
In

GUNPdl, V.I.; ZAVIYALOV, 6.1.
liew Y.-iethod of synthesizing quinolizidine derivatives. Dokl. AR SWSSR
139 no.2:367-368 Jl 161. MIRA 14:7)
1. Institut organichaskoy khimii im. H.D. Zelinakogo AV SSSR.
0
Fredstavleno akademikom B.A. Kazanskim.
(Norlupinane)

~~OV, I.N.; GTOSEV, B.P.; GUNAR, V.I.
Complete synthoBia of isopropenoid alcohols. Izv. All SSSR Otd.
khim. nauk no.10:1267-1270 0 157. (MIRA 11:3)
l.Institut organicheakoy khimii im. N.D. Zelinakogo AN SSSR.
(Alcohols)

V, L'
AUTHORSt
TITLEt
20-2-27/60
Nazarov, I. N. , Member of the Academy, Yanovskaya, L. A,
Gusev, B. P. , Yufit, S. S. , Gunar, V. I., Smit, V. A.,
The Synthesis of Methylheptenone and Hetbylheptadienone
(Sintez metilgeptenona i metilgeptadiyenona)
PERIODICAL: Doklady Akademii Nauk SSSR, 1957, Vol. 114, *Nr 2., pp. 331-334
(USSR)
ABSTRACT: The two substances mentioned#n the title of the paper under
review are of importance for the synthB3is of the natural
scenting substances of the isoprenoid type. The authors of
the present paper investigated the production of the former
on basis dimethylvinylcarbinol or isoprene with the aid of
three different methods t(l) by condensation of prenylhalo..
genids by aceto-ethylacetate; (2) by -interaction between di-
methylvinylcarbinol and the same etherl and (3) by pyrolysis
of the same ether of dimethylvinylearbinol. As was shown in
a previously published scientffic paper originatinIq in the
same laboratory, there are produced at influence by hydrogen
Card 1/4 halides on dimethylvinylearbinol corresponding prenylhalides

The Synthesis of Methylheptanone and Methylheptadienone
20 2-27/60
with high yields. They can be easily condensed by sodium-ace-
to-ethylacetate and at a subsequent saponification they yield
methylheptenone. The second ingthod of synthesis takes place
at a temperature of 160 - 170 and yields 60 - 70 5' tlethyl-
heptenone in addition to an almost theoretical amount of
ethanol and CO2. The reaction must be carried out under pres-
sure or by using hiah-boiling Vaseline oil. Tile remainder
after distillation is aceto-ethylacetate of dimethylvinyl-
carbinol. At 160 - 1700 this is subjected -to a pyrolysis,
and here methylheptenone and CO 2 are produced. This supports
the reactions mechanism as illustrated in tile paper under
review. The pyrolysis of pure dimetliylvinylearbinol-aceto-,
acetate was investigated further. It in produced with a yield
of 90 ~6, when diketone affects dimethylvinyloarbinol in pre-
sence of small aRounts of pyridine, best at a temperature bet-
ween 145 and 160 . During this process, m thylheptenone is
produced (65 - 70 ~6). The pyrolysis has also a lateral di-
rection and leads to isoprene, acetone and CO 2' Sometimes
this lateral direction predominates. The authors of the pr'~-
sent paper studied in detail the production methods of methyl-
Card 2/4 heptadienone both by interaction between dimethylethinylcar-

The Synthesis of Methylheptenone and Met~ylheptadienone
20, 2-27/60
binol and aceto-.ethylacetate, and also by pyrolysis of pure
dimethylathinylcarbinol-acetoacetate with a yield of 90
influence of diketone on pure dimok-hylethinyl in presence 0 of
triethylamine. The reaction takes place OnlY at '170 80 -
Below 1600 the initial products are obtained againL. because
no interaction takes place. In the ganeous phase t1l ie reaction
takes place only at 250-300~ There the Y.Iel('] is low (15-20 -j~).
Inert diluting agents, acidf , salts and metallic oxides do
not favor the reaction, but rather frequently lead to a coil.
plete resinification of the substance. Ifere again lateral
procesoes take place, with isopropenylacetylene and acetone
being produced. The experimental p%rt. of the paper under re-
view contains a detailed description of the production meth-,
ods t)gether with constants and yields. There are 5 referen,
ces, I of which is Soviet.
Card 3/4

20 -2-27/Q-)
The Synthesis of Methylheptenone and Illethy1heptadienore
ASSOCIATION: Institut6e oF Organic Chemistry imeni 11. D. '"'elinskiy, AS
USSR
(Institut organicheskoy khimii im. 11. D, Zelinskogo Akader3ii
nauk SSSR)
I
SUBMITTED: January 7, 1957
AVAILABLEt Library of Congress
Card 4/4

'; (3)
AUTHORS: Nazarov, 1. N., Bergellson, L. D., SOV/62-58-11-13/26
Gunar, V. I.
TITLE: kc-eyY-re-n-9--berivatives (Proizvodnyye atsetilena)
Communication 191.Proparatift of Acids From Tertiary
Acetylene Alcohols (Boobahaheniye 191. Polucheniye kislot
iz tretiohnykh atsetilenovykh spirtov)
PERIODICALt Izvestiya Akademii nauk SSSR. Otdeleniye khimicheskikh nauk,
19589 Nr 11, Pp 1354-136o (=R)
ABSTRLCTs Recently it was lamonstratod that cis-dibromo-vinyl carbinols
(1) easily cleave off dehydrates and'hydrogen bromide while
forming unstable 1-bromo-vin acet enee (M). when boiled
1
'
with alkali th
*y produce a4,~
_ or ~ , -unsaturated acids
(Ref 1). In this paper a method of p: rucing unsaturated
acids is described which is based on the mentioned reactions.
To increase the yield in eubstituted dibromo butadienes (II)
dehydration of dibrono-vinyl carbinols (I) were investigated
under the action of heat and various dehydrating agents.
Optimum results were obtained in boiling with dibromo-vinyl
carbinole in petroleum ether with phosphoric anhydride (in
Card 1/3 the case of cis-dibromo-vinyl dimethyl carbinol) or with

icetylene Derivatives. SOV/62-58-11-13/26
Communication 191. preparation, cf Acids From Tertiary
Acetylene Alcohols
p-toluens sulfa said (in the case of cis-dibromo-vinyl
cyclohexanol). If-bromination of acetylene alcohols is
carried out in petroleum other dehydration can take place
without separation of brominated alcohols (I). 3ubstituted
dibrono butadienes (II) and especially vinyl acetylene
bromides (III) are unstable. They partly decompose and
saponify in the course of distillation. For this reason
it in expedient to carry out further processes of
dehydrobromination and of alkali hydrolysis in a single
atags without sapantion of bromine derivatives (II) an&
(III). Under then# conditions the transformation of acetylene
alcohols into unsaturated &aide can be carried out in a great
number of cases in sufficient yield (Table 1). The constants
of all known acids agree wellwithtle data from publications.
There are 1 table and 15 references, 1 of which is Soviet.
Card 2/3

fAcetylene Derivatives. 90V/62-58-11-13/26
Communication 191 . -""PW&t1010 of Acids Yrom Tertiary
Acetylene Alcohols
ASSOCIATIONi Institut organi-7heakoy khimii im. N. D. Zelinskogo Akademii
nauk SSSR (Institute of Organic Chemistry imeni N. D. Zelinskiy
of the Academy of Sciences,USSR)
SUBMITTED: March 27., 1957
Card 3/3

~;(. v ,, 7 9 -2 85/063
AUTHORS: Nazarov, 1. 11. (De,:-~aoqd)~ (loisov, 11.
TITLE: Derivatives o~- Acetjlene (Proizvotinyye atsetilena)
193. A Complete Synthesis of the Isoprenoid Alcohols of
Linalcol, Geraniol, Iferol, Iferolidol, Farnesol, Ceranil-
linalool ', Geranilgeraniol and Phytol (193- Polnyy sintez
izoprenoidnykA spirtov(linaloola, Feraniola, nerola, nero-
lidola farnezola~ geranillinaloolaq geranilgeraniola i
fitola~)
PERIODICAL: Zhurnal obstohey khimii, 1958, Vol- 28, Nr 6, pp. 1444-1458
(USSR)
ABSTRACT: As dimethyl-virylcarbinol has become completely accessible as
technical prodiiet the authors decided to investigate the
complete methods of synthesis of isoprenoid alcohols on its
basis, as well as on that of isoprene; for this purpose
they repeatekl the mentioned reaction cycle several times
(scheme 1). Tb.s way the isoprenoid chain is built in the
way of successive combination zL-4ctions of ethinylation, of
Card 1/3 selective hydrbtion , isomerization ~ad acetony'Lation, the

.~! i) V/ 79-28 .6-5/63
Derivatives of Apetylene. 1~*3. A Complete Synthesis of the Isoprenoid LI.-
cohols of Linalool, Geraniol~ Nerol~ Nerolidol, Farnesol, Geranillinalool,
Geranilgeraniol and Phythol
two latter rau-~,tions mostly being carried out in one stage
without separition of the intermediate products. The whole
ccm-3e of this synthesis leading to the isoprenoid alcoholsC.'..~
(of geranilgert. iol and phytol) was investiRated in detail and
represented by the mentioned schemes (see nchemes for the
synthesis of -.!c-.raniol (V), farnesol (IX), fferanilgeraniol
(XIII) and ph;-.-,ol (XXV)). The accessibility of the initial
products, the simplicity of its performance as well as the
good yields al all stages of development of the explicitly
described synthesis make it perfectly suited for the in.-
dustrial production of linalools, geraniol, nerol, nerolidol,
farnesol, geranillinalool, and geranilgeraniol, as these
compounds are of great interest for the perfume industry
and for the synthesis of some important natural compounds
(vitamins, ApE,Kp carotenoids, terpenes, etc.). Thus the
authors for the first time carried out in detail a complete
synthesia of the above mentioned iaoprencid alcohols as
well as of the intermediate products of the synthesis (the
Card 2/3 ketones, and acetylene alcohols) by succes3ivo repeating of
j

jbv/'79-28-6-5/63
Derivatives of Acetylene. 193. A Complete Synthesis of th~ Isoprenoid Al-
cohols of Linalool, Geraniol, Verol, Nerolidol, Farnesol, Geranillinalool,
Geranilgeraniol and Phytol
ASSOCIATION:
SUBMITTED:
the condensations of the ketones with acetylene, the selective
hydration of the acetylene alcohols and of the conversion
of tertiary vinylalcohols to isomeric primary alcohols of
the allyl type as well as to unsaturated ketones of the al-
lylacetone type. There are 24 references, 6 of which are
Soviet.
Institut organicheskoy khimii Akademii nauk SSSR
(Institute of Organic Chemistry )AS USSR)
June 28, 1957
1. Alcohols--Synthesis
Card 3/3

50) soi/62-59-2-31/40
AUTHORS: Gunar, V. I., Zav'yalov, S. I., Krotov, A. I.
----------
TITLE: Synthesis and Anthelmintic Effect of DehydrorC3orcinol Deriva-
tives With Branched Aliphatic Chaina (Sintez i antigellmintnoye
deystviye proizvodnykh digidrorezortaina, soderzhashchikh
razvetvlennyye alifaticheskiye tsepi)
PERIODICAL: Izvestiya Akademii nauk SSSR, Otdeleniye khimicheskikh nauk,
1959, Nr 2, p 358 (USSR)
ABSTRACT: The authors found that dehydroreeorcinol can be alkylated with
branched allyl bromides described in reference 1 in anr- 50%
yield. In this way the following compounds were synthesized:
21
2-(31,71-dimethyl-6 -octenyl)-dehydroreaorcinol, 2-01,71-di-
methyl-A 21'61 -octadienyl)-dehydroresorcinol and 2-01,V,111-
trimethyl-A 21 -dodecylenyl)-dehydroreso.rcinol. On boiling with
acetic anhydride these ketones yielded corresponding enol ace-
tates in large yield. All compounds are anthelmintics. The
21
2-01,7',111-trimethyl-k: -dodecylenyl)-dehidroresoreinol
Card 1/2 proved to be the most active compound. There is 1 Soviet ref-

Synthesis and Anthelmintic Effect of Dehydroresorciriol Derivatives '.Vith
Branched Aliphatic Chains
erence.
ASSOCIATION: Institut organicheskoy khimii im. N. D. Zelinakogo Akademii
nauk SSSR (Institute of Organic Chemistry imeni N. D. Zelinskij
of the Academy of Sciences, USSR) Institut malyarii,
meditsinskoy parazitologii i gellminotologii r4inzdrava
(Institute for Malaria, Medical Parasitology and Helmintholo6y
of the Alinistry of Public Health, USSR)
SUBMITTED: J111Y 10, 1958
Card 2,2
ij~ijjffiffi! Ifl, Iffil P,
Pill ITT'li'll, 171,11: TIM., 111, V Im
UNM

GUNARI V. I. Cand Chem Sci - (aiss) "Synthosis, rearrangement
and biological acLivity of derivatives of aib;ydro-resoreLn
containing isoprene chains," Moscowp 1960, 15 PPf, 180 COP*
(Inat. of Organic Chemistry im N. D. Zelenskiy, AS USSR) (KL., "-60,128)

GURAR, V.I.; 7AV'YAWV, S.I.
Syntheses based on 2-prenyldibydroresoreirol. Izv.A.9 SSSa Otd.khim.
nauk no.5:937 KY '60. (NDU 13:6)
1. Institut organicbeskoy khimii imeni N.D.Zelinskogo Akademii
nauk SSSR,
(Resorcinol)

ZA.V'YAII)V, S. I.; GUNAR,-V.I.; VASILITEV, A.F.
Direct hydroxylation of 2-substituted dihydroreaoreinole. Izv.
AN SSSR Otd.khim.nauk n0-5--938 My 160. (MIRA 13:6)
1. Institut organicheBkoy khimii imeni. N.D. Zelinakogo Alzademii
nauk SSSR.
(Resorcinol) (Erclroxylation)

ZAVIYALOV, S.I.; GUHAR, V.I.-, KUDAMTSEVA, L.F.
Chr,miBtry of dibydr,oresorcinol. RepQrt No. 6: New steps in the
synthesis of phenanthrene derivatives based on dihydroresorcinol.
Izv. AN SSSR.Otd. khim. nauk no.11:20U9-2013 H '60.
(14LU 13:11)
1. Institut orgwdchaskoy khimil im.N.D.Zelinskogo AN SSSR.
(Phenantbrene) (Resorcinol)

GUNAR, V.I.; ZAVIYALOV, $.I.
Chemistry of dibydroresorciaol. Faxt 8: Syntheses based on
2-prenlildihydroresorcinol. Zhur. ob. khim. 30 no.11:
3658-3663 N,6o. (MIRA 13:11)
1. Institut organicheekoy khimii Akademii nauk SSSA.
(P.Psoreinol)

0
AUTHORS:
TITLE:
PERIODICAL:
S/02 60/132/04/26/o64
B011 ~B003
Gunar, V. I., Zav'yalov, S. 1.
A New Synthesis of LbZjol
Doklady Akademii nauk SSSR, 1960, Vol. 132, 110. 4,
pp. 829-831
TEXT: In a previous paper (Ref. 1) the authors showed that the
alkylation of dihydroresorcinol with prenyl bromides (II) leads to a
series of cyclic p-diketones which contain isoprenoid chains. In the
article under review the authors proved that these derivatives of
dihydroresorcinol may be used, inter alia, f-jr the synthesis of phytol
(XIII). In the hydrolytic cleavage of 2-pr6oyl- and 2-geranyldihydro-
resorcinols (III) and (IV) large quantities of corresponding keto
acids (V) and (VI) were formed. The latter reacted smoothly with an
excess of lithium methyl, with the two functional groups participating.
In the dehydration of the keto alcohols (VII) and (VIII) obtained by
means of potassium bisulfate and in the subsequent complete hydrogenation
Card 1/2

A New Synthesis of Phytol S/020/6o/132/04/26/064
B011/B003
of the unsaturated ketones (IX) and (X) on platinum oxide the following
known ketones were obtained: tetrahydrogeranylacetone (XI) and hexa-
hydrofarnesylacetone (XII) (Ref. 2). In accordance with Refs. 2 and 3
the ketone (XII) can be easily converted into phytol (XIII). Thus, a new
method of synthesizing isoprenoid compounds was elaborated. It permits
extension of the chain of vinyl alcohols (I) by eight atome. Here, large
yields of ketones (XI) and (XII) can be obtained. There are 3 references,
2 of which are Soviet.
ASSOCIATION: Institut organioheskoy khimil im. N. D. Zelinskogo
Akademii nauk SSSR (Institute of Organic Chemista imeni
N. D. Zelinskiy of the Academy of Sciences, USSR)
PRESENTED- February 12, 1960, by B. A. Kazanskiy, Academician
SUBMITTED: January 19, 1960
Card 2/2

GUNAR, V.I.; ZAVIYALOV, S.I.; PERSHINp G.N.; NIIDVANOVA, S.N.;
BLUUI)ANUV , N.S.; MAKEYEVAJ, 0.0.; KROTOV, A.I.
-Dicarbonyl empounds. Part 141. Synthesisp trsnfd"tionsp
and biologgical activity of 2-preftqldihydroremoroinol. Zhur.
ob.khim. 31 no.12:3975-3984 D 161. ( M A 15:2)
1. Insti-tut organicheskoy khimii imeni N.D.Zelinakogo AN
SSSR; Vaeaoyuznyy nauchno-issladovatellskiy khimiko-farma-
tsevticheskiy institut imeni S.Ordzhonikidze i Institut
malyariip meditsinskoy parazitologii i gallmintologii.
(Resorcinol)

GUNAR, V.I.; ZAVIYALOV, S.I.
'. . New possibility of building-up a rinj system of thin CD steroid
.1, molecule. Izv.AN SSSR.Otd.khim.nauk no.3:527-529 Mr 62.
(MIRA 15:3)
1. Institut organicheskoy khimli im. N.D.ZoUnskogo 0 S&-!R.
(Steroids) (Cyclization)

GUM) V.I.; KUDRYAWSEVA) L.Y.; ZAVIMOV, S.I.
1-5-Dicarbonyl. compounds. Report Mo.16: Alkylation of dipotassium
derivatives of cyclic e-dicarbonyl compounds in liquid ammonia.
Izv.AN SSSR.Otd.khim.nauk no.8:1431-]J+35 Ag 162. OURA 15:8)
1. Institut organicheskoy khimii im. N.D.Zelinskogo AN SSSR.
(Carbonyl compounds) (Alkylation)

.LUNAR, V.I. ZAVIYALOV, Scie
Synthesis of trans-anti-trans-l-oxo- A q a) 12- a- -hexadeca-
hydrochrysene. Izv.AN SSSR.Otd.khim.nauk no.2:380-3,82 F 163.
(MMA 16:4)
1. Institut organicheskoy khImii im. N.D.Zelinskogo AN SSSR.
(Chrysene)

GUNAR, V.I.; OVECHKINA, L.F.; ZAVIYALOV, S.I.
Condensation of 1-morpholinecyclohexene with Mannich ketones. Iz-*.
AN SSSR. Otd.khim.nauk no.6:1110-1111 Je 163. (MRA 16:7)
1. Institut organicheskoy khimii imeni Zelinskogo AN SSSR.
(Cyclohexene) (Morpholine) (Ketones)

'096-6_5
.............
nczssicu uR: Ap5w9867 UR./oo62/64/ocx)/olo/18-' 183
2 1.
AUT14OR: Gunar. V. I.: Ovechkina, L. F.; Zavlyalov, S. I.; Nirchin" G. 11 0 "er" aw! a
14.
q
TITIS: 13--ta-dicarbonyl compoundG. Communication 22# Syn e: acti-
thesin anA ftnCiatat.;
vity of,some of the simplcst analogs of the antibiotio Grisifpofulvirt
SOUWE: PJ4 SSSR. Izvestiya. Seriya tdhinicheskayaj no. 10, lf~)64, 115,'~7-3.831
TOPIC 'RAGS: antibiotic, phaxtacolor,-j, eoter, chlorinated orij,anic w-,i p(~ v nd, n1p,
lation, cyclization, organic syntheU(;
-A63'crji~t T A a e-ife- sof enot'eaters of dihydroreso'rainol. 110.tatb St
membered hydroaromatic ring.of Sriseofulvtn,was stUaied i1o an qfl!ort to daketuina t
the sigpiEtcance of vacious atructural elements of the CItibioti.c, Knol eartera
of 2-(31-chlorobutene-21-yl)-, 24p-chlorobentyl)-, and 2-(,p-bremabenzy1)-
dihydroresorcinols were synthesized by alkytatLon of dihTdrorenoreino! with the
corresponding alkyl chlorLdes, followed br treatment of thta 2-subatituted bete-
diketones with diazomethane. Internat enol eaters belonging to the tetrahqdi-o'!~h-
1, romanone sertes were prepared by cyalLeation cE darEvativott of 2-pheny,*1dLhydro.-
i resorcinol in the presence of phosphoric aciA., 5,6,7,8,-T4itrah!pli:ochr-amani)".te-.S
i derivatives were produced by a new method of. synthea is, Wised cm condensati-or, Of
L
C400 V
AF~

L 35096-65
ACCESSION NR: 67
dihydcoresoreinal wEth Hannich ketorted ~.-pn o~
I'selectLve reduct ;he trLkek tit
enolates, followed by cyclization of the 'hydraxyket*oneai~~ Th'e:'gremtemt~
qantifungmt activity was detected in 2-math 1-2~o".6eth'A ent4.!ftqA1 s-A) -5
Y.. " ;,;.,
p
keto-5,6,1,8-tatrehydrachromanone.
Orig. art. haEs:, 20 formulas, I table.
ASSOCIATION. Instiltut organicheakoy Ithimii im. IT., D*_ Zeii6ikop Akademii Wituk 1 A
SSSR (Institute of Organic Chemintryl.kcaidemy of Sc ionceel '4.13SRY*~ 'liamiyu-mir
nauchro-isaledovatel'skiy "imika-farmatsavtlcheakiy insttfat im. S. Ordzbanikidze I
(All-Union Scientific Research Chemi-~opharmaceuLical,Inat~tute,~
SUMMED! -~EX=4i 00 VIB dots, 14, ba
NO R13F SOV t 004 OTRR., i003 JIM$
j
- Ju
Card 2/2
MIN
i V'm, n 1,110"N.1111 H!
MR

ZAV I YPIOV, S. I.; K0NB,--,.AT' Yl-I'll " , G. V. ; GUN A 1', 117. j .
Synthesis of d-ibenzofurar derivatives. Izv. A.' SSSR' Ser. I-him.
no.11:2086-2087 N 161~ 1.8zi)
1. institut organ Icheskoy kh-mli !!.D. iV'. SSSIR.
I

ZAVIYATf)V, S.I.; GIIIIAF., V.I.;
Effect of mere-ory diacetate on the co~irse of the reaction be,.ween
dikeLene and urreas. Izv. AN SSST, khim. no.1:20.1 16r.
(IRIJ'A 18:2)
1. InsLitut organi.cheskoy khimll iin. N.D. Zahn,3kogo AN SSSR.

GUNAR, V.I.; ZAVOYALOV, S.I.
Case of r-py-rone ring formation in the reaction of diketene
with urea derivatives. Izv. AN SSSR, Ser. khim- no.4-047-748
165. (MIRA l815)
1. Instittit organicheskoy khimll im. N,,D.Zelinskogo AN SSSR.

GUNARY V.I.; OVECHKINA) L.P.; ZAVIYALM,
Synthesis of 1,3-cxazine derivatives based on diketene. Izv.
AN SSSR. Ser. khim. no.6:1076-1077 165.
(MIRA 18:6)
1. Institut organicheskoy khimil imeni Zelinskogo AN SSSR.

OVECHIKINA, L.7.; ZAVIYALOV, S.1.; PEHSHIN, MILOVANOVA,
11)Acarbonyl compounds. Report No.2a Synthesis and fungistatia
a, vity of some simplest analogs of the antibiotic griseofulvin.
Izv. AN SERSIR. Ser. khIm. no.1031827-1831 0 164.
(MIRA 17:12)
1. In:3t'Atut arganiehaskoy khImii Im. N.D. Zelinskogo AN SSSR i
Veesoyuznyy nauchno -' -Iodovatel'skiy khimiko-tarmatsevtAcheakiy
institut Im. S. OrdAW)Ikidze.

MIKBAYWFULO, I.A.; GUNAR, Y-J.; ZAVIYALOV, S.I.
Selective inethylation of simplest uracils. lz7. AN 3er.
khiui. no.9-1715 165. (MIRA 1819)
1. Institut organicheakoy khjm--Ii ira. N.D. Zelinskogo AN SSSR.

V.I.; L,.F,;
Reactl-cri of d1ketene with ammc,nia and am4df- c'
acids. lzv. AN SSSR.Se.-,.khim. no.10:1885--1-PP6 165.
W.I 18: 10)
1. Institut organicheskoy khir-li im. M.D.Zelir-.,-.k,.)go AN ISSSR.

v 1

..........
lizzuL
L V 12-65 -,1~P(w) /E74'k(,j)/T/:T4,'(t '011P(Q/94P(z)
PSA IJP(c) FUlf/ D/ HU/ JIG
;ACCESSION HR: APS007011 S/0129fG$/000.~1003/0057/000
~%.AUTHOR: Ho hkovich, Ye. 1.
Matkina, B. 1.
7ITLEZ: Study of the properties of M21145T, qteel
MUM-, Metal-lovedeniye 'L tent icheskaya abrOotka me-tallovo n6~ 3,1 Pps, 57-60:
ITOPIC TAGS: phase composition, stenite, trietal ~%I*Vfttetvt
!ABSTRACTi The F)q~j_, 57
Ai_.52Mositia) of ten irAustrial batcheq of vast 1, PIN
/.'Kas studied at mom ztnd blih-i~i-r"peratum%s, and the mechanica). propolvtEei, m-mal
.forg ed from these batches were studied after various heat tN.-eitirentij. Pr')-:-J_Aed
specimens were etched in a reagent made up of 10 g KOH, 10 C =x1d 60 g
H20- It was found that in the cast alloys the amount of the C-_ji~)Onerjt
changed 'I'T"om. 10 to 701" at room temperaturf!, and a defiaite rel.atiarmhip w,_~ oboervad
bet,,.~een the phase composition and the ratic of equivalents of
(see fig. I of the Enclosure). In hardened specim-ens, It-he tensi-e ntreng~h vi%iw-
found to inerease with the austenite content. In order to obl:ain tensi.10 !;trq,-nCtYj I
0b 1 70 no less than 15 to 20% austenite must be preseat in the matal wmo...
-1.9 -rd

L 48-
J19-65
1ACCESSION NR: AP5007011.
~ture. In the hardened state, such a metal has -ara. ivmact strq4ath ol! 20 kgm/crh and
higher. Tempering at SSOOC causes a substantial ch q_ r
ange In the inechunkal'prope~rtids.
ihardening of the matal is associated with a sharp decline in IqDacl: strea h.
9t
Since such changes occur, when the amount of the auatenitic phiwie iiii below 20%, it
is conc1lided that high nr_c~cnica! pmpertios of the steal mquire mi auntenite cv~-
tent of over 20%. The phase composit-lon. of ths rmtal of the ,itilbs vas da"Lem.1-ned
at the central laboratory of the "ZaDorozhstal" under the suria:mrision of N. P.
iCherkashiaa. orig. art. ha---: 4 fi tables.
gums
iASSOCIATIO14: Zavod "Dneprospetas. talt 11 (Dnaoro9i5etsstaV: PIan 1)
!SUBMITTED: 00 EXCL: -al. 5UA WD5. M
'00
RIO REF SOV.# coo
C43rd 2/3

~77 -- -----
-4 9119 S
.
SSION
%

i:

4J

cr/eq Hi
Fig. 1. Pbas6 compositioti of cq- a tWNW steel~ve%%us cheutin,.al edupositLun, t4 th~i
metal

L 18651-63 EWP(q)/EWT(m)/BDB AFFTG/ASD JD1JG
ACCESSION VR: AP3004789 -R/0129/63/000/008/0055/0059
AUTHOR': Boblcovj, T, M.p* Moshkevich, Ye, M, Gunaza, K, P,; Zlatkina, V. 1.
TITLE: Effect of additions of ram earth and their oxides, on properties
of some,2tainleas steels
-
SOURCE; Metallovedeniye i termicheakaya obrabotka metalloy, no. 8, 1963, 55-59
TOPIC TAGS: stainless steel, Khl8NlOr steel, A48I 321 steel, W3N18 steel,
AISI 310 steel, R*7N13M2T steel, AISI 316r steel,misch metal effect, ferro-
cerium effect, lanthanum effect, cerium dioxide effect, lanthanum oxide effect,-
praseodymium oxide effect, steel hot ductility, steel structure., nonmetallic-
inclusion cortentIcast structure, ingot structure
ABSTRACT: Th:! ~Iffect of addition of 0.05-0-35% misbh metal (50% Ce, 25% La,
and 25% varicas rare-earth metals] or 0.05-0.4,4 ferrocerium, lanthan-um,
cerium dioxid-3, lanthanum oxide, and praseodymium oxide on struature,, phate
composition, amount of nonmetallic incluskons, room-temperaturj( mechanical
properties, and hot ductility of-111a9l"AISI 3211, MI293BJVAISI 3101,
JM2~ (AISI 3161 stainless steels has been investigated. None of'
Card 1/2 4

L 18651-63
kCCESSION NE: AP3004789
the additions was found to have a significant effect on the crystal structure
of ingots of any steel tested. The forged metal had a fine-grained structure
vith a law content of oxide and sulfide inclusions. A 0.15-0.2% addition
of misch metal reduced the amount of carbonitride inclusions in all steels
tested. Khl81ql0T steel containing 0.1% misch metal had improved hot ductility,
In the Kh23N18 steel addition of 0.3 and 0.05% misch metal improved the due-
tility.at UOO-1250 and 1000C., respectively. Addition of 0.05-0-15% misch
metal or 0.15-0-30% La improved (juatility. of Khl7Nl3MZr steel at 1000C. k
dition of ferroceriun;,, lanthan=Vfceriumqioxide, lanth== or praseo
o;ddes brought about no improvement in hot ductilit 4r room-temperature me-
chanical properties of Kh17N13M2T steel. Orig. artj has: 4 fiVires and
1 table.
kSSOCIATION: Zayod Dneprospetsetall (Dneprospetestal, P3mt)
SUBHUTED: 00 DATE ACQ: 06sep63 ENCL: 00
SUB CODE: ML NO PJCF SOV: 000 OTMM 000
Card 2/2

MOSHKEVICH, Ye.I.; GUNAZA, K.P~; ZLATKINA, 13.1.
Studying the properties of Kh2lN5T steel. Metalloved. i tem.
obr. met. no.3:57-60 Mr 165. (MIRA 18:10)
1. Zavod "Dneprospetsstall".

GUNAZA, L.
My experience in the maintenance of a jigging machine. Mast.ugl. 3
no.2:16 F '54. (MLRA 7:3)
1. Moyshchik Dobropol'skoy TsOF tresta. Stalinugleobogaohcheniye.
(Coal-handling machinery)
q JfK
V, ji. ppli
F:,9,-;-c 4t

)--------SOURCE -CODE -UR/0114/66/000/008/0008/0011
ACC NR, AP6029618 (N
AUTHOR: Gunbin, B. L. (Candidate of technical sciences)
ORG: none
TIT" : The structure of the relative flow at the exit from a centrifugal compressor
1mpeller
SOURCE: Energomashinostroyeniye, no. 8. 1966, 8-11
TOPIC TAGS: centrifugal compressor, compresso r, compressor impeller, J-woeo
9-40a, -57-,CV07-6,,Ce,
ABSTRACT: The results are presented of an investigation of relative flow parameters
at the exit from the centrifugal compressor impeller. The measurements were made
using a single stage unit with three-channel cylindrical probes, rigidly fixed on the
outer diameter of the impeller. Tested were three impellers with relative thickness
S2/D2 - 0.055 with inlet and exit angles of 0*1 - 32' and 02 - 45% respectively, and
blade numbers Of Z2 -18.24, and 28, at 7800 rpm, which corresponds to a peripheral
speed at the outer diameter of the impeller of 'u140 m/sec. The following conclusions
were reached: a) Flow separation from the trailing surface of the blade was observed
in the exit cross section of the flow passage during low-capacity operation. b) The
discharge component of the relative velocity vector In the peripheral area of the
impeller is transformed in such & way that at rated and low operating regimes, an L
Cctd -333-6-01-001.94
.1/2. 21-515-

ACC NRs AP6029618
increase in the velocity from the training surface of the blade toward the leading
surface is observed. Orig. art. has: 5 figures.

GUNBIN, B.L.
Controlling the operation of centrifugal forcing pumps.
Gaz. prom. 4 no.11:46-48 159. (MM 13:2)
(Gas, Natural-Pipelires)

GUMB IN, B. L.
- -----~
Changes in the effective capacity of gas-turbine units. Gaz.
prom. 5 no-3:46-48 Mr 160. (K1" 13:6)
(Gas turbines)

GUNBIN, B.L., inzh.
-Pressure coefficient of the runners of centrifugal compressors.
Izv. vys. ucheb. zav.; energ. 6 no.6:99-105 Je 163.
(MIRA 16:11)
1. Leningradskiy tekhnologicheskiy institut kliolodillnoy
promyshlennosti. Predstavlena kafedroy glubokogo okhlazhdeniya.

s/115/62/0(;0/004/003/007
L194/L154
AUTHOR: Gunbin, B.L.
TlTLE: All instrument for remote temperature measurernezit5
of a moving medium
I-EAIUDICAL: lzn-..eritcllnaya tekhnika, no.4, 1962, lb-i7
TEXT: in investigations on turbines, heat exchangers and
various aerodynamic equipment it is necessary to measure the
temperature distribution and average temperature in a fluid
medium moving with high speed. This is difficult to do with
ordinary thermometers because their time-constant coefficients
depend on the Reynolds and Nach numbers of the flow. The
present article describes an instrument for making measurements
of this kind with high subsonic flow speeds. The schematic
diagram of the instrument is an unbalanced bridge with a
thermistor in one arm. Any one of four sensing elements may be
connected to the measuring circuit in turn by means of a
selector switch. The temperature range covered is 0 to 100 OC
and besides the full-range scale for coarse measurements there
Card 1/2
; - 71411

An instrument for reinote S/115/62/000/U04/003/007
E19VL154
are five subsidiary ranges covering a spread of 240 each.
Thermistors vary in their properties, and so that a single
calibration curve can be used for all the sensing elements,
resistances are connected in series and parallei with the
thermistors to give them standard characteristics. The error
of measurement dopends mainly on the accuracy of the
galvanometer. Using a inicroammeter type M91 (2q91) with a
full-scale deflection of 10 microamps, the error is 0.2 I)C.
The instrument is easily arranged to take an average of four
readings and if these differ from one another by 2 to 40 the
difference between the instrument reading and the arithnietic
mean temperature is not more than 0.1 OC. The instrument is
powered by dry batteries.
There are 2 figures and 2 tables.
Card 2/2

tj-
ISM., __T
L 19554-65 FxAlaa (1) /tWG M/T-2/ EPA (bb) 'Td,~'F445/1,~i-4 AM , (a)/.8~
T-V ET c (a) izw,
ATDTP Vtoi
ACCESSION NR: AP4048335 S101 14164100a/0 1-0/0043/0044
AITTHOR: Gunbin. B. L. (Engincerl
TITLE* Structure of the relatively -moving flow at, the entrance of a centri.Lujali-
coE~p,E~i~sor impeller
SOURCE: Energoi-nashinostroyeniye, no. 10, 1964, 43-44
TOPIC TAGS: cantrifugal compressor, compressor inlet 914sw
ABSTRACT: Tests on a model of an axial-inlet centrifugal! 6=1 P'Tessor were
performed at 8,733 rpm which corresponded to a peripheral velcicity of 140 irn/sOc,
three impellers, with 18, 24, and Z8 blades, were studied; in.-Ipq1ler outsidq:
diameter, I~ m 305 rm-n; relative width, b,/%, 0.055; D44ID2 ;1: 0.554; i.nl.etand
outlet angles, 32.0 and 450, respectively. It was found tWQ4.:: (1). Zhe angle: of
attack varies differently in diff-erent -sections of the blade and ha.0 a vnaximum
variation at the cover disk; (Z) Under optin-itini-officiencli, 4xinditiona, angl-e~a of
Card 1/2
INN6

L 195.54-65
ACCESSION NR: AP4048335
attack in all blade sections coincide; (3) Aeaction of the 14adlng upon the flow
swirl is p.-actically nil, the swirl being caused only by the impell-er vveb and covq:r
disk. Orig. art. has: 3 figures.
ASSOCIATION: Nevskiy mashinostroitel'ny*y zavad (Ngvaj~;jch~n-~$
-----Plant)
SUBMITTED: 00 ENO!Lt 00
SUB CODE: PR NO REF SOV: 002 OTHZA: 000
Card

ACC NR. AP7002607 SOURCE CODZ: UP/G1,13166/1-,----j/ "/0115/01,16.
INMVTORS: Gunbin, B. L.; Shabashov, S. Z.
ORG: none
-TITLE': An automatic device for disconnecting a dam&,;,-ed bras pipe. Clas:; 47 ANo .
189271
S0TjRC:;1: Tzobreteniya, promyshlennyye obraztsy, tovarnyye znaki, no. 23, !966, 115-116
TOPIC TAGS: Gas engineering, gas conduction, 6-as flow
This Author Certificate presents an automatic device for discor-~ecting a
da.rzged gas pipe. The device includes a distributing assembly (which actlvatas the
drive mechanism of the shut-off organ) and a gauge which controls the chmnol:c or' -,as
flow in a 6-as pipe when the latter is damaged (see Fig. 1). To prevent 'Lh,.; aut0matic
device from being activated by the changing operational conditions and to activate it
when the velocity head exceeds the allowable linLlt, the gauge- (fixed to tlkle auto=atic
device and made in the form of a cylinder) is oriented at right angler, to the
longitudinal axis of the gas stream. The lateral walls of the cylinder contain four
openin,-s. T,.,,o of these are placed centrally in respect to thi! stream duarin,~ its
forwa--d and backward flow. The other two are placed at some to the central
ones. These openings are connected by pipes (located within the casing of the gauge)
to the rigid elements of the distributing assembly which motivates 'the drive mechanismi
Cord 1/2 UDC: 621.640'.83-522 1

j___ eD
ACC NRz ':AP7002607
Fig. 1. 1 gauge; 2 gas Pipe; 3 distributing aosembly;
4 - drive mechanism for tho Bhut-off organ of gas Pipe; 5
rigid elements (a, al, b, bl are the openings in the
cylindrical walls of the gauge)
activating the shut-off organ of the pipe. Orig. art. hant 1 figure.
SUB CODE: 13/ SUBM DATE: 03Aug6i
14 -qj
T'I 1!~ ii, I !t 1
'lip I I I III
tv I IR F 11.1

7!67..
A%oo6523
SOURCE CODE, TJR/037-9/65/000/011/0045/0047
AUTHOR: Gunbin. N. A (Colonel, Candidate of Military Sciences, Hero of the Soviet
Union, Military Navigator lot claco)
ORG: None
TITLE: Maintaining formation with aircraft
- 7-
SOURCE: Morskoy sbornik, no. 11, 1965, 45-47
TOPIC TAGS: navigation aid, navigation oyatem, air force training, air force tact1c
ABSTRACT: Naval aircraft engaged in long overland or offshore flights, and not
equipped with interaircraft-navig~tionlinstruments, use a method to maintain station
in the formation, referred f~_-as the time interval method, but it has inherent diffi-
culties making it inconvenient since it requires giving commands and signals via
radio, a situation which may not be tolerated because of the specific tactical situa-
tion controlling the flight in question. Nor is it accurate enough. Too,, formulas
used to derive information required for station keeping must take into consideration
several human errors such as the error resulting from the impossibility of making a
timely signal of passage through the control point, and the error involved in start-
and stopping the stopwatch. The result is an overall error which can be-exceedingly
large. Thia may have as its end result,the unacceptability of the eyatem for night
I Card

-L JUYUU--07
Adf
I AP6006523
flights or daytime flights in bad weather. The use of linear values, such an kilo-
meters, etc., should be preferred to the use of time values in such system since the
use of the former will permit the crews to graphically represent the position of
own and other aircraft. The use of linear values also lend itself to ready computa-
tion, with resultant values tabulated prior to takeoff and thus are available in
flight. Orig. art. haot 5 formulas, 1 table, and 1 figure.
SUB CODE: 01, 15/SUBM DATE: None
I t

GUNB , Geroy Sovetskogo Soyuza, kand. voyenny/h nauk,
-
polko,mik, voyennyy shturman I-Co klasna
Interaircraft navigation. Mor. sbor. 48 no.2:54-59 F '65.
(MIRA 18:11)

Gel,oy Sovctskogo Soyi-i-,-,,L, kand. voy-.-,,,nilykl,. nail'
CtU?1;31_'!)- N.-A-.1- ~ - I, ..h,
. --., polb-OV1111" ennyy rhLurrun I-fy
voy _,c) klansa
Maintenance of conliat formation by airplaner.
i . - , -
Mor. sbor. 49 no-11:4~1-4? ti 6r,.
(",!L~A 18:12)

d I'll I 1 11 ; 7! : I !r!!!3:..P16,: 13,
1,IAK[),I-,nVTC[l, A,C,., GIRI'liOly N.f,~.y , I 1. 1- . ~'Ii 'i k - ;, ,~ 1 .,-A A. -.
v -- -,-, . *; .. k~. . . ; .. 1l r I L:.. .~, . . I . , . - 7
Irnprav,~ d cX I-,utvlrjrir, 1% *,.'.0
I -t 16~~
rubber plant in 6tp-rIltai7ak. Khim.vr(..r~. J-
OMIRA 18:8)

1. GUIDli-.', N. Ya.; 130CI'ii,~OVSKAYJI, L. Y.: Ri-*;-'G)
2. LSSR (600)
4. Krivoi Rog - 1-1ining Engineering
70 Experience w-ith t.'-..e work of all-arovnd briE;ades Ln tne ::anes of the :srivoL
Rog Basin. Gor. zhur. No. 11., 1952.
9. Monthly List of Russian Accessions, Library of Congress, anuary 1953. Unclassified.

GUNBIN, N.Ya.; GORBATOV, V.S., Forny-y lnzh.; MAKELEV, A.ji.
Industrial test results of multibucket folding scrapers and pros-
pects for using them. Gor. zhur. no.11:48-50 N 61. (MIRA 15:2)
1. Glavnyv inzh. rudnika im. Kirova Krivorozhskogo basseyna (for
Gunbin). 2. Nauchno-issledovatel'skiy gornorudnyy institut (for
Gorbatov). 3. Glavnyy inzh. shakhty im. Ordzhonikidze Krivorozh-
skogo basseyna (for Makeyev).
(scrapers)

GUNBIN, N.Ya., inzh.; VEKSELIMAN, V.M., inzh.
Increasing labor productivity at the Kirov mine. Met. i
gornorud. prom. no.3:43-46 My-Je 62. (NIRA 15:9)
(Krivoy Rog Basin--Iron mines and mining-Labor productivity)
~:,, :. . ..: r
I

GUNBIN, N.YLi,.,,Auzh.; VEKSELOW4, V.14., inzh.; MIKHAYLENKO, F.K.., inzh.
Rapid upraise mining at the-uSevernaia" Mine of the Kirov
Mining Administration. Met.i gornorud.prom. no.5280-82 3-0
162. (KRA 16ol)
(Krivoy Rog Basin-Iron mines and mining)

GUNDINP N.Ya., gornyy inzh.; KOSHELENKO, V.M., gorny Jnzh.
, y
Growth of labor prcductivity etu the Kirov Minti, zhur.
no.5~12-14 My 164. ~MRA 17;6)
1. Rudnik Im. Kirova., Rog.

GUNBIN, Yu*; DFMIDOV, P.; KAZAKOV, M.
Selecting wetting agents. Pozh.delo 8 no.11:16-17 N 162.
(MIRA 15:11)
(Surface-active agents)
(Fire extinction)

Pl, .11DOV kovedlitc! ' p,-cr ekt :t; Kk~:.EOV,
.: j 11.1 BI N, ,"YII.G. 1 .1, 1 , F u U. , vu in " t a
~,.-V_ dlplcmncgo ;,.i,c, I
lj:ie of wetAing agents in fire oxtinction. Po7h. tezop, no.3s
1
'6-87 t64 - (MIRA 1815)

GTRIBINA, M. N.
Ivaluation of functional cardiac state of physical exercise
and athletics; electrocardiographic observations. Klin. med..
Moskva 29 no.7:43-48 July 1951. (CII-IL 21-1)
1. Of the Faculty Therapeutic Clinic, First Leningrad Medical
Institute ineni Academician 1. P. Pavlov and of the Leningrad
Scientific-Research Institute of Physical ciature.

GUNBINA, T. N.
Cartograpby
1962