SCIENTIFIC ABSTRACT DANILOVA, A. K. - DANILOVA, A. V.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001109630003-8
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• Document Page Count: 52
• Document Creation Date: January 3, 2017
• Document Release Date: June 21, 2000
• Sequence Number: 3
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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DA,"ILO'-"A. A.
-CIJ A. L~. anc
'Funda.-ne als of Feeding
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DKNIWVA, A.K.,prof.
Some problems of avian witrItion at the llth International
Congress on Pon1try Brooding. Ptitaevodstvo 9 no.1:31-35
Ja 159. (KIU 12: 1)
(Poultry-Feeding and feeding stuffs) (Pomltry research)

VANNOVA, A.K., prof., doktor sallskokhos7a7stvann7kh nauk.
Significance of the chick-pea in rations for chicks.
rtitsevodetvo 9 no.2:35 Y '59. kKIRA 12:3)
Ohick-pes,) (Poultry--feeding and feeding stuffs)

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KOZHINA, I.S.; DANILOVA, A.S.
Preparation of' trans-isolimonene. Zhur. ob. khim. 31 no. 110781-
3788 N 16.1. (MIRA 14:11)
1. Botanicheakiy institut Akademii nauk SSSR i Laningradskiy
gosudarstvennyy universitet.
(14enthadiene)

DANILOVA, A.S.
Structure of the thermal isomerIzation of ascuridole.
Part 1: Reaction of the thermal isonerizatIon prod,,:r-. of ascaridole
with hydrogen halides. Zhur.org.khim. I no.3:522-525 Mr 165.
(N',:.P,A 18:4)
1. Leningradskiy gosudarstvennyy urdversi; *.-q' .

DANILOVA, A.S.; PIGULFVSKIY, G.V-
Structure of the product of ascaridole thermal isome-ization.
Zhur.ob.khim. 33 nc.6:2076-2077 Je 163. (MIRA 16:7)
1. Leningradskiy gosud&rstvennyy wniversitet.
(Ascqridcle) (Isomerization)

DANILOVA, A S.i BA."ABANOVA, L.P.i RYABININ, A.A.
E-hinocy9t.1c acid in thm root,-; (:,J' -,-,~j-r.(,pO,JtjjM qrl.helininlicum L. Zhur.
ob.khim. 34 ncl.2V706 F 164. rMIRA 17:3)
1, Lanin~,-rqlskiy 94,et-
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dMia. sW 35 CC. lah won tIMCA dowly
th 33.3g. A106 mW at two temp. 24 lan.. then a
fast. ats 4o.-61; latter adals. of HCI the mom waas estd. with
IftlO. from w" then vam obtsiaell awd CQMpL%_.
on of which Rualywd for (diamos"hilh-
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treat dasawas that the lot two arem indivithsal cdmpds.. White
the 3rd wit a mixt. of Uwm. &uaaw caualectiltdow (a CSt
=to . Was. of the above tubstamm. The odoct
by A*.. Con, RtOH am 4.=: oi!
8 -sisthaw ##Oak
(flow litoll"p. .0
(1). an. 1W70, (El eltdr. M.
taw star t).awpAtheo M. m. 191-2" (Et stur.
an. 304)" (Ireals twou)). The I an tant wpd.
by RION crysto. of tbek St cdcM I form an exinw. M.
10-we ((No Ccla); maw of H an. It", (decompas..
from C611.0j; Cleumemaeli re4scUm of I g*vv the car-
r"PalsAwd &M ' acid. us. WIOO* (from RION) (ES
.taw. bb 190-17which. can beadull with PA In Phue.
laidej Map C., 48c
MV a, 4,
0 0 0 0 0 0 0 0 0 a
0 a Ole ~%, A 0 0 Wo 0 0 0 0 0 0 oj"
FS ^eta
gave
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reduced with amatkamisted Zo in Ila-PbMe to 1jj.4.-
an 04.
(from MOM. Clemmmeeta mducsion at U cave the co-
"Spowdeval bwyrk "ad, M. 109~10* (from pear ether),
which. on cyrfizattion with PA In budift PbMe. Fave an
uoww of the k4*p4rawuLArvvw dirrit.. a. 133-4 (from
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dunring that I vad u wit :ds=
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(3-4 Ian.) adda. of water, the Wit. t Weed 2 lam.
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ducd with the MA he dk. Bob. aacidifed ar"
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ud. 11
the mint. tru eztd. B KtoO. the hatter *aid. with 2%
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and trtatted with an cumu of Sa (Off). foGoared by COt
trealitums of the heated win.; the diustat wass lacizad
with 3DCT H&S04 and ead. with EtoO to *0 the Asclovor
acid. m. 6"' (from EtOll). M.
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USM/hoolstry - MaUldm, Sawalo Jun 48
Chw8try - Retramoine, Prm senecio
BM4111180418
*StU4196 Of Ssm*io OUse Alkaloids,* R. Kmovalovs,
A. Dantio", kjkglojd&l S"I AU_Unjov 80,_Res Chem_
Phar In8t 1mml S. Ordzhonlkldzop Noscow, 5 pp
0zhur Oboftch Rhin" Vol XMI (r=), No 6
Studles struotwe of somomilln. Concludee that
It IN IL GY0110 OthW of retronecine vith a moleoulg
of d1basic senicifillic acid.
4=b gAg?28

CZEChOSLOVAKIA
V. - TOMASEK, V. ; MIKE3, 0. ; DANILOVA, A.3.; 301LM, F.
Institute of OrgFinic Chemistry nnd Biochemistry, Czechoslovak
Academy of Sciences, Prague - (for all).
Prague, Collection of Czecho3loyril-, Chemical Co=iiinicationg,
No 11, November 1965, PP 593 - 9
"On proteins* Part 98, Tho disulfide bonds of bovine dip-
trypsin."

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, flak. an 1b. to ,I,- I'v
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lia" are ammuclatly tt"I
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fs~ lq~llt-j I,v et(hel 4 the 1- .... j_, If,(
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A

la ch. A
%o 11di V. 1)311110VQ and R
"on 'Td on kidze ATWnVo-ft-tfi-enCzPha -
V-4f ft,,. fTO rmG
!~Ijs!., Sjoscgw). Zhtir. Ubs, thri hisim. Z2, 2.N17-V(l952)--
(C[IIUI)7 ext. of 14 kg. -,f the maccratcd plaut previd. in
Pric-qence of 10% N114011, votkLd tip %it t.te Lonveittiouml
0 t miumer. yielded a ruixturc -1 products, which, let stand in
HtO solu., deposited 1.22 ) . new substance, named pInn-
log"ine. CqH,,0,N, m. 21 ~ -20*, 1.1 o 30.9*; It CI jalt, de-
170111p. VS-30*; Itratc, fit 159-60* (from 11,0)-. Chfora.
aurntt, ni. 151-2 t; nirlboxi-Ve, 5ulid which is dillicult to
purify. The liquid rrsidue 1 itified by steam di%tn. and the
distillate treated iCith picric & cid gave a picrale ro. 140-50'
And n pirrate tit. 1*-',1-7* (fro it litOll, then 'rout RtOAc). -
The Ist piernte, in. 151- 3 on f irtlicr purification, YiCldvd an
alkaloid, Cjs[1,10N, uainvd in-licaine; the hiftc, picrnte(m.
127-9* after purification), g;t,c an alkaloid named indic-
amint. C,4[f?,ON, which is au unsaid. substance. Both
lattvr alkaloid% are liquidi C.. M. KosolapofT

DANILOVAt
&,~'niigv; w
AT.
.48.691a. H. Lal.~
C,jedcal Abst
Vol. 48 Not 9
u-., -in 10ri. 1% 1.

USSR/Chemistry - Alkaloids Aug 53
"Investigation of Alkaloids of Senecio Species. Vill.
Alkaloids from Groundsel (Senecio sarracenius)
A. DanilovEi,- R. Konovalova r P. Massagetov, and
~M. Garina, All-Union Sci-Res Chemicopharm Inst im.
S. Ordzhonik!.dze
Zhur Obshcn Khim, Vcl 23, No 8, pp 1417-1421
Isolated two new alkaloids, sarracine Cl&H27 0 5N and
sarracine N-oxide C,5k7 06N, from a groundsel
(Senecio sarracenius). Sarracine picrate and bitar-
trate were obtained as well az the picrate and
chloroaurate of sarracine If-oxide.
270r32

117'
USSR/Chemistry - Alkaloids Sep 53
"Investigation of Alkaloids of the Senecio Species.
IX. Structure of Alkaloids from Senecia sarrace-
nius," A. Danilova and'A. Kuzovkov-j All-Union Scl-
ReBearch Chemo-Pharmaceutical Inst im S. Ordzhoni-
kidze, Moscow
Zhur Obshch Xhim, Vol 23, No 9, pp 1597-1600
It was established that the new alkaloids sar-
racine and N-oxide of sarracine, isolated from
Senecio 6arracenius, are diesters of the amino-
glycol platinecine with cis- Q* -dimethylacrylic
26BT35
(angelic) acid and an unsaturated acid with the
composition C H80 , designated sarrac1nic acid.
The latter aced ;L the carbon frame of methyl-
etbyl-acetic acid, differing from it by the pres-
ence of a hydroxy-group and a double bond.
268T35

DANILOVA, A. V.

froall Seved. SarTacenius

T7,

Chemical Abstracts 1
N -Y 2 5, 1954
O
l
Ch
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ry ......

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Rv. Ill, t I'm if t h I it It 7 , lhi,t ield ~ - rrucine This AkA.

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,7~~ 1Y 1.4 6) V4, h, /
pERSHIN, G.N.; FAIST-sKATA, Te.N.; DANILOVA, A.V.: MIWVANOVA. S.N.
Chemotherapeutic effect of deachlorobiomarcln. Farm. i toks. 17
no.5:3-0 IS4. (KLRA 7:11)
1. Vseaoyuznyy nauchno-iseledovatellakly khtmiko-farmataevticheakiy
institut imeni S.Ordshonikidae.
(ANTIBIOTICSO
deschlorobiomycin HC1. phamacol.)

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I
AUTHORS: Koretskaya, N. T-; Dpnilova, 1. V.;-Vtkin, L. M. 19-2-58/~8
TITIEi Svnthesis of Harmine Derivrtives, Part 1. (Sintez nroizvodnyk~ germina.
I.)
PERIODICAL: Zhurnal Obshchey Khimii, 191;7, vol 2, No 2, pp. ~42-545 (U.S.S.R.)
ABSTRACT: This report describes the s-nthesis of certain harmine derivatives for
pharmacological investigation. The new harmine derivatives were identi-
fied as rnd-N-(beta-diethylamino)-et~ylhprmine, dichlorohydrate; P~-R-
chlor-(beta-diethylamino)-hamine ethylate, hydrochloride; Ind-N-benzyl-
harmins; Py-N-iodomethylate Ind-N-b4-nzylharmine: Py-N-chloramethNIRte of
Ind-N-benzy1harmine, et~,yl ether cf norharmine carboxylic acid. The
authors obtained new derivatives of tetrahydroharmins, namely, Py-N-(beta-
diethyl~Rmino)-ethyltatra~,ydrohamine; tetrahydronorharmine cbrboxylic acid.
Card 1/2 T1,ere are 5 references, none of which are Slavic.
V

Synthesis or Harm'.ne Derivativos. Part 1. 79-2-58/58
ASSOCIATION All-Union Scient1fic Research Chemical Fharmaceutical Institute imeni
S. Orrlzhonikidze
PRESENM BY:
SUBMITTED: March 18, 1956
AVAILABLE: Library of Con&-,ess
Card 2/2

5 (3)
&UTHORS: Danilovag_4~. V., Utkin,
ko.zyreva, G. V. , Syrneva, Yu. I.
TITLE. A New Alkaloid Which Is an Isomer of
alkaloid, izonernyy platifillin~z)
PERIOEICI,L: Zhurnal obohchey kh-imii, '959, Vol "., 7z, ?,'1`-'436 ('J'--l
ADSTRACT; ?latyphyllin bitartrate is irep~.Y~!d fr,)j,,l '.I:e lrov!le,ived .-,enecio
platyphyllus. As to it3 chemical structure the is i~
diester of platyriecin and the ~;e:.eciiic ici~ ('-.of In the
procesoirio of the industrially manufactured -ilcoholic .:.other
liquids a new base which ha~ been call:~,*. neoplat.y:k-11in was
obtained on separation :ind recrystalli-ation of pl-,typhyllin
bitartrate. As to composition :nd functional c~roups, this new
brize is identical with i
,~latyphyliin. P;ieir busicit- and infrared
absorption spectra (Fi , sh;~w little differ-2nce, 'out as far as
the physical properties are concerned, the ceo7-latyphyllln and
its salts differ from platyphyllin ind ito salts. The bitzxtr---te
of neoplatyphyllin shows well pronounced -,ho1iiolyt1c and
spaomolytic properties. As to uctivity ...:~do if ictill it is
closely related with platy-~*llin, but it is ~WiCL :13 toxic.
Card 1/3 Alkaline and acid hydrolysis of both co;-.-,-)u..~-" yicl-i V-t- !"L.e

A New Alkaloid which Is an Isomer of Platyphyll'in, ~)7/79- 7) -7-7 2/87
products. The authors assume t~-~t the t:iffere..c2 ~,et-veen both
bases is due to thu steric co.~,Ii,-ar.jti -~ !)', ,)-e acil cemiponeat
of their molecules because, s in '-.nown, 1.1!e ":-,ecinic- acids ~-:ith
double bonds show in addition to the OT~tiC-! i30MaCJ-SM also the
geometrical one (Ref 2). The structure of the -ez:ecinic acid
corresponds with the formula (1) (`Ief 3). lzi ,.--.er to investigate
further the properti6s of both compoundc t,.e -!!.-uloids were
reduced vith LiA111,. The result--Lrt trivale.-.*. --c-ohols had to
possess structure II), accordiLIg to the stra~.:'-ire of the
senecinic acid. The chemical and 3pectroocopic re-ults obtained
confirm the asnumption of the authors that t,e different spatial
configuration of the esterifying acids ic the cause of the
difference between neoplatypl-.yllin and clut.",%hyllin. The formation
of a trivalent alcohol from the senecinic aci-.1, by treating it
vrith alkali liquor, which is q 'uaiit-tivel~i -'ifferent from the
alcohols obtained by di,-ect reduction if the -lkaloids, confirms
the observation th t the "necinic" acids so -ir -ted bl- alkaline
h,-drolyvis of the alkaloids of the speci-~~f- -enecio - osoess a
configuration which differc frr,,:: that in enter into
Card 2/3 the composition of the aikal-,id :~,.oleculeF:. ':`here -re I figure

I A Now Alkaloid Which is an Isomer of Flatyphyllin
and 3 references, 2 of which are Soviet.
ASSOCIATION: Vsesoyuznyy nauchno-is.,ledovatellskiy ',Lhi,:,.ik;D-far,.aatsevtiihesk.y
institut imeni S. Ordzhonikidze (All-1,Tni-)n --'oientific
Chemico,pharmaceutical Research Institute imeni :~. Ordzhonikidze)
SUBMITTED: Llay 25, 1958
Card 3/3

A J 1, 11 J 1). L V X
PITLE A 1,,.,i I M.,
Afl.'J"MV-r Th-
I I I c f.- N
1- M

Alkai- !.A M-L
H :H7
A cm, C'j C(CHII co
Placrunecine 41 nakro:Ic-t~;yit) (:LL;
z I t an I --utl " ! i, ,-. I " -
by hydruly,~:1~3 -v, I w t.
wil~-,h `iavo
v t
wt,ve

Ale-al-id
(a colorle8L; liqiAd, a
D
(mP (,mp
mucrophyllii,t, pl,:i,at-
r,ip -c-) j2 - 2 ~4 (-) ) .Tht,-v-
I Clerman, 1 U.K., I U.:'. Dit'- a-A U.K. ref-.-ence~3
ave: Adams, Hamlin, J . Am. S -15 7
(P)42 C,-~Iveri,).,, L. W. Smlt:., A4.;tral. J. lil~lm.
ic), U4 (ic-7).
ASSOCIATIONt S. OrdmorilkidZe Al L-Unlort S.~It-i,tll',--Research ~: i j~- rn I ca
Pharmace.itleal Iri~~l It-ite (vJ "y y nau c h n
Issledovatel Iskly
In,stitut linerii S.
S U BM iTT ED: D--,~ember ~~j,
C,ird 3/3

DARILOVA,._A.T.; KOIWSKATA. N.1.; SHVICTS, Z.I., UTKTN. L.M.
Few method for obtaining platyphylline from Senecic platyphyllus.
Had.prom. 14 no.4:2&30 Ap 060. (NM 13:6)
1. Teesoynan" nauchno-iseledovatel'skiy khimiko-farmtsayti-
cheskiy institut Imeni S. Ordzhonikidze.
(PLATTPHMIXI)

DANILOVA, A.V.; KORETSKAYA, N.I.; UTKIN, L.M.
Structure of "renardin" alkaloid (from Senecio renardi). '?art 2.
Zhur. ob. khim. 31 no. 1-1:3815-3818 N 161. 6-M~A 1-4: 1-1)
1. Vsesoyuznyy nauchno-isaledovatellskiy khi-miko-farmatsevticheakiy
institut imeni S. Ordzhonikidze.
(Alkaloids)

EC) 3 Z/ E3 14
AUTHO-US Garik"yanov, N.S., Danilova, A.V. and
Sha-idullin, R.R.
TITLE: Electron paramaZnetic resonance ancl a.)sorption
spectra in the visible reZion of alcohol In(, .1ycerin
solutions of Ti*++
PE:',I3DICAL: Optilm i spektros"'Zopiya' V. ~' 11c).
212 - 215
TZXT: A study-is reported of CFR Lines of rlie ~;recn and
violet modificatioiLs of TiCl H 0 solutions. ~-Ivcerj.n ai.d
a'Psolute alcohols ~methyl, eLYT" and isoprop)-l)-wore kiFed as
t1le solvents, The lipecimens were rapidly in thin Z;Iass
capillaries since alcohol solutioiis of Ti salts were fouiicl
t'o be unstable and oxidized to Ti"~~. -Ieasure:-.:e:its were c~%ri'ie~!
out at 9320 'MC/s using tae standard raclios )ectrometer
77 0
-1301 (RE-1301) at 400, 295 and K. T'-, eline widta
doter-mined as ti-ie distance between the maxim-,Li Xn,! minim"I~m of the
fir3t ~,Qrivative of the absorption curve. T*,ie results of line-
.;idt:-i measurements and the spectroscopic splittin~r factor at
Card 1/5

5/0~1/62/01~-) / 0 02/0071VC14
Electron paramacLnetic .... E032/E-114
T = 205 OK are -iven in Table 1. T:,,e in-eisitv )f *,,,,a EP-Z lines
~r. liquid violet glycerin and alcohol solutions, is vorv low
Co.m:-,ared with t:ie intensity due to _-reen ~;lyceriu solutions. It
is therefore considered that the EPR I.Lnes of \riolet
solutions are e.-cclusively due to a sniail amiowit of ~;recn
asymmetric complexes of the form:
7+.
Ti(CH 011) C1 Ti(C,11 o1'.) Cl,
3 4 2-~ , -LT'C:2'l~-'0'1)4C12-". '; 1~ 74
and Ti_C H (OH)-! cl')~
1 3 5 -)- lk
In supercooled alcohol and glycerin violet soluti,,ns of' Ti t. e c e
~Qs
is a large low-symmetry f i e.Lci co;-,i,)c)n eiit clue ~ o ),11-t c
,:ie s econd coordination sphere ( the ciot ion is f rozei) a r, -C i.-3
reason, in t.he super-cooled state each parana3netic Ti i on
in violet molutions contributes to the intonsity of tj-,e EPR jj;-jps.
At room temperature, on the other hand, owing to the lonL~ apin
lattice relaxation time, Ti+~ , does not --;-;~Lnificantly
to t'ie intensity of the EPR lines. As t:ie roj:-.i toz.,,:)c-~-ature ;.6
Card 2/5

E.',~ctron r c, L~ 14
-L*,;zic:i oul t !ic comp,,mjit c) V I ow-s rmiict i-,,, c " oco
4-
7 i ion tends to avera_-e out and e1ectron
-A'o-s3r-3tion is eiitirely daie to Zr(,e., -3
w rJ 0 0.
!).is be(-ji LiscLl to
L:-- :,c It ~X-c
of Lreen coi;iplc,~es in violet soiki~ i, - z,,:i ~1~1 L Ii
U r e - I
t;ic Solveat, all' t:-1(- ;I;Its are ziverl i;L
was t.,.en chec'ezed by carryi.-,~; 0;.~
,,ta3 foLini~ t:iat the abrorption in t:10 V.1 f; i 1) 1
L;.re iii ~,ood . greet~.ient with t:ic al)ov(,, lntei-drotat 1,)!l of L:IL,
EPR s,?ectra. Taere are 2 tables.
S'~B\il'17ED: June 9, 1961
,- ard 3/5

r,-).i par a
....... ....

To 1, it, I

13 %111 T I I AbNI C I J I Ir V

u: 3 Z3 2
(Y. 10TO IW !taCT 111) 11 :1 11
if j1TV

21 10'; 11 It Oll 4.1 11-11VA.1 jl~,CTROl

will." 1; 21
Card 5/5 0.5 12 ~2 i.A-12

DANILOVAY A.Y.; KORETSKAYA, N.I.; UTKIN, L.M.
New alkaloid from Senecio othonnae M.B. Zhur.ob.khIm.
32 no.2:647-648 F 162. (1,111](A 15:2)
1. Vsesoyuznyy nauchno-issledovatellskiy khimiko-farmatsev-
ticheskiy institut imeni S.Ordzhonikidze.
(Alkaloids)

KORETSKAIA, N.I.; DANI-LOVAY A.V.-;-,- UTKIN, L.M.
S',ructure of jaconecic and jacolinecle acids. Zhur.w.khim. 32
no.4:1339-1345 Ap 162. (MIRA 15:4)
1. Vsesoyuznyy nauchno-issladovatel'skii khimiko-farmatsevtickieskiy
irstitut imeni S.Ordzhonikidje.
(Jaconecic acld)

GAFLIFIYANOVO H.S.j DANILOVA, A.V.; sHAGIDULLIN, K.R.
Zlectron paramagnetic resOfmce and absorption spectra in the
visible region in alcoholic wd glycerine solutions of Ti"'.
Opt.i spektr. 13 no.2-.212-215 Ag 162. OUM 15:11)
(Piramagnetic resonance and relaxation) (Titanium,--Spectra)

KCRETSKAYA,, II.I.; DANTILOVA, A.V.; UTKIN, L.M.
Structure and interralation between senecic and
epoxyjaconecic acids. Zhur.ob.khim, 32 no.11:3823-3827
PI 162: ;',141RA 15:11)
1. Vsesoyuznyf nauchno-issledovatellskly kl-,'-Miko-
fw-matse,srtichoskiy iimtit-ut imeni '. Urdshonikidze.
0
(Scnecic acid) (Jaconecic acid)

Of
I PCV,

DANILOVA, A.V.; KOPETSKAYA, N.J.
Structure and propertles of senec~phylllnr-- --'.
35 no.3.584-5R? Mr '65. 18 4"
1. Vaesoyuznyy nmuchnn-"Rsled(-,va~.elli;t:,v "hrmn*
sf;vti~,.heskly Institut imen,' 3.

ge posw ~Jume,,W>ck

15 ~7 D
HL