SCIENTIFIC ABSTRACT DANILOVA, A. K. - DANILOVA, A. V.
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CIA-RDP86-00513R001109630003-8
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December 31, 1967
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SCIENTIFIC ABSTRACT
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DA,"ILO'-"A. A.
-CIJ A. L~. anc
'Funda.-ne als of Feeding
I-TI., published from
(!t. Aca"~
i:ia:--ioe C,.)raz,)vani., v
P7
1. ~A. "';%'I
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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)
Tr, -0
r rar a n
OL f,
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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04111
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COMMON"= d S-8giAMI-I
kow
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Union Chem
J. GM. Cheats
n"Cla. Su.,
.6 Malay
(30 J. I" If.
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-
oweptia1w acid. M. Ids-70'. 0. 191-2% SW Izat; it
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
tu. 101-2* Yfum HIM) (atrawe. m. 147-6* (hum RIOND.
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
HtOlIH01iM- to- lt?J-7t)*)
dunring that I vad u wit :ds=
Zu to III. tkm am 7
1 (3 g.) in 50 cc. 10'1~ XAA~0. was doarty UW Wish 30
x. 30e. Na-I!4 amulcant at room temp. the . I
(3-4 Ian.) adda. of water, the Wit. t Weed 2 lam.
-
estd. with RIO to Mamma: the Tama" ah" W" hatro,
ducd with the MA he dk. Bob. aacidifed ar"
HO (3%) add~31u~"; eteem'. after bolifus to- 13 naba.
ud. 11
the mint. tru eztd. B KtoO. the hatter *aid. with 2%
Nallco.. am The w3khutl Mao voln. was fmj of wall"d
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."
thill"t'Is tst %Oltoclo specto. VII Allial-J. It-.,
wirlo spolat'll % I I . "'.1 14 % K-
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1(6 ~-matphtbcajl Vropixank acift S I "wrtitc-eikara A 'V'
Danduva. ...,art A A I, b,-m-k-, IS All,
'T'nT6n-'('hrt,, hist Xl,~. I A., tif,rikkel
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if AICI, ifh ~tm-ia laid I,- U41 of I I
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.1ji-I A firma "I'l 11,A(mil I hr~ 1. 111, 5' Fre .1tr, Om
'Isual armament "', K "","I an IV-rV, artlers.
fii.im,n .I thi, 1,% r,flumnit 41 he% with *K) nil. VtOll ."d
:111 nil. -mcl I 1'.~ '. .,.,I ~V'ln Inman Floff pve 14.4
(" Af
I"a"'I "11 2 C I-11hilo"W i olv- b;
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mn in C". the v,dd L, much lowet and flit I-CJ1,C0
pre,lonunji" I p.mfml by an IN
unati,riv purifi-1, ,1 1111 5' 1 "-r. an 14&-A' I with
N.ItCl yields ra-1. an~ hwb.
la~ttrcf with Mir "M in. - the : 111) astraloar. an 24#11 1
, flak. an 1b. to ,I,- I'v
Fintl fill If '14 1, - I (-1 411 tr.," Fr, III
k1ernmeraw" "'b" I-. ~ H, I "'-f o" -~' h- c-'-
: , rt, IM 7' 1- aiq
VtOlf, A., I'v : -"j"
4.1 Wit ...... I h, IL 11.4" ~ mA."j t" L,I-.
."I, I I If far L It....
-fuel.., K." 'th'-l 4-1
~ki 4 * Or"m ..I Fl. .11 1 ..... i" 'h' Z %f~
'."Iog gave " mr(ko"I .-d ,, %I I
Wellusing rith" rva -ith A,4)lf.lflfr Cave the .7410 -41,
- I
1.10 t 7 f frmn F, ( -11 , St.. mian 4 ~!lt , ~14-
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ail"t. I st'rall."'ar. 1-- FtI)fI jtO tie,
A
ill lirnwinit and offnecionk acids A~ V
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lJohiidt, AW
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at .1th Ill, sel- I ...... .-I " I-o its, It"Ir"Iyous of
.4 .-Olum m fill,
--1, tm,ma -Sms~ -ft,
pla"o-ak, a-t %III (Ill hcAtil"fla
....d 1111. C.1144.
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14W 11 t.k. up 2 It, YWLI-
do", 1'. sal-'I .11h 1,01,; Itcl all- the
CnIfesillssnilinj sskj"sif I.kj L4'. J,"tW*l 'Jill If* ledt'.
ilit", tw-jucl frm, 111 11, ,, , It ApI.-Ar. I., Ill, a 'I. and 1
a trans tu"tirr 4 cove, ~tmoterr lim"al'Alwo "I III al
CIR-1, go- ill, J, 14, d"', Ift, V. M m*, while
if, an oil 11 A.- fit d.11, . of 11:1 13 lt.'
1.!" 0
tw-llull I
It NO, lisi, ))I. i Nit .4 sj
C./ho.. -.1 . Ilk 1'. of, "'. 1,
in 114 V .[ot, 1,, 2-1.1 kt. A,% I,%, :
"" rhm"t""I " 6 A,
Olklacul I fill
M.- Triblu., lyphal 4 01F CIA.. wnt, 1'.'s
lia" are ammuclatly tt"I
In 'Julask Acid lic-t., fill- -e m'sw
fs~ lq~llt-j I,v et(hel 4 the 1- .... j_, If,(
11,0111, 11 w( ,, V,'
01.011 (pit) (11MOO 1.11, -Its .4 h.h
-f ,( ~Awfvtllm.. '", .111101,11 1-1 1-
-~fthfisll the rmy-t J,q ..... 14
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
i
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e
em
rgan
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ry ......
flu Iilfl~ M
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fillk
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It I I In.) I q. r,f plat , 1,11 , !! Im f tile III, .' rv - I '! it ml
t he 1,1, . ill & It I pi -I im 1".'r i,irit h N I I ( ) II :I I,
J)"'. ibk t. I'\ %It, In :Ilnl,.t ".-InrA
Substanre, 1, N*. fit I Irma Nf(!,Cf )) , ~' I
- "1 6' (p,[, 1" .1 1107 5 .4 .1 1-hl-iiju,41r, Ill I !~f h " ,
Rv. Ill, t I'm if t h I it It 7 , lhi,t ield ~ - rrucine This AkA.
I"id 0111, appi, ,, t.- It, V .,xi,fe of j,j,rj. live. Thi, t, un-
,
firilit of b, if, forrij,ti-i fr,aii -run ill, with 11,0,
Nt
,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.)
mlqjpp~w- 4gaw. t
tic
CIFOMi
k tw Om"ge
Lat. sm- abod 26 gi WIMA 4,
aw 1-14 xi Am-
*"dim, w" a
talmi; am clicksa.- fts** Of w 2.70 X,
t2a had$ WOW
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kh lisma g&"
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sot a" MAWWOOL*w9a. in.
77 G. M.
77
Y
v., m
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