A Directive Effect of Heterofunctions in Cyclocondensation Reactions of Acetylenylquinones with Hydrazine | Sciact - CRIS-system of Boreskov Institute of Catalysis

A Directive Effect of Heterofunctions in Cyclocondensation Reactions of Acetylenylquinones with Hydrazine Full article

Journal

Mendeleev Communications
ISSN: 0959-9436 , E-ISSN: 1364-551X

Output data

Year: 2000, Volume: 10, Number: 5, Pages: 188-189 Pages count : 2 DOI: 10.1070/MC2000v010n05ABEH001353

Tags

HETEROCYCLIC SYNTHESIS; ACETYLENIC-COMPOUNDS; ROUTE

Authors

Barabanov Igor I. ¹ , Ivanchikova Irina D. ¹ , Shvartsberg Mark S. ¹

Affiliations

1	Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

The heterocycle formed in the cyclocondensation reactions of 2-acetylenyl-1-chloro-9,10-anthraquinones or 5-acetylenyl-3-diethyl-amino-1,4-naphthoquinones with NH2NH2 is influenced by the presence of a heterofunction, e.g. a hydroxyl group, in the acetylenic substituent; this directive effect was used for the synthesis of naphtho[2,3-h]cinnoline-4,7,12-trione and 4H-naphtho[1,8-cd]-1,2-diazepin-8-one derivatives.

Barabanov I.I. , Ivanchikova I.D. , Shvartsberg M.S.
A Directive Effect of Heterofunctions in Cyclocondensation Reactions of Acetylenylquinones with Hydrazine
Mendeleev Communications. 2000. V.10. N5. P.188-189. DOI: 10.1070/MC2000v010n05ABEH001353 WOS Scopus РИНЦ ANCAN OpenAlex

Published print:	Jan 1, 2000
Submitted:	Jun 30, 2000
Published online:	Mar 13, 2008

Web of science:	WOS:000089962000013
Scopus:	2-s2.0-0040182779
Elibrary:	13349687
Chemical Abstracts:	2000:745532
Chemical Abstracts (print):	134:147578
OpenAlex:	W1985788320

DB	Citing
Web of science	5
Scopus	7
OpenAlex	3