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An Unusual Heterocyclization of 2,3-Diacetylenyl-1,4-Naphthoquinones Full article

Journal Tetrahedron Letters
ISSN: 0040-4039
Output data Year: 2000, Volume: 41, Number: 30, Pages: 5757-5760 Pages count : 4 DOI: 10.1016/S0040-4039(00)00898-4
Tags 1,3-disubstituted 2H-2-aminobenzo[f]isoindole-4,9-diones, 2,3-diacetylenyl-1,4-naphthoquinones, Hydrazine, Reductive cyclocondensation
Authors Shvartsberg Mark S. 1 , Ivanchikova Irena D. 1 , Lebedeva Nadezhda I. 1
Affiliations
1 Institute of Chemical Kinetics and Combustion, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090, Russian Federation

Abstract: Cyclocondensation of 2,3-diacetylenyl-l,4-naphthoquinones with NH2NH2 affords 1,3-disubstituted 2H-N-aminobenzo[f]isoindole-4,9-diones.
Cite: Shvartsberg M.S. , Ivanchikova I.D. , Lebedeva N.I.
An Unusual Heterocyclization of 2,3-Diacetylenyl-1,4-Naphthoquinones
Tetrahedron Letters. 2000. V.41. N30. P.5757-5760. DOI: 10.1016/S0040-4039(00)00898-4 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Oct 26, 1999
Accepted: Jun 2, 2000
Published online: Jul 17, 2000
Published print: Jul 22, 2000
Identifiers:
Web of science: WOS:000088346600032
Scopus: 2-s2.0-0034702525
Elibrary: 13342525
Chemical Abstracts: 2000:498612
Chemical Abstracts (print): 133:266688
OpenAlex: W2090382111
Citing:
DB Citing
Web of science 14
Scopus 14
OpenAlex 9
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