Preparation of peri-annulated indoles from polynitro compounds

Preparation of peri-annulated indoles from polynitro compounds Full article

Journal

Tetrahedron
ISSN: 0040-4020 , E-ISSN: 1464-5416

Output data

Year: 2009, Volume: 65, Number: 34, Pages: 6868-6872 Pages count : 5 DOI: 10.1016/j.tet.2009.06.074

Authors

Samet Alexander V. ¹ , Yamskov Alexei N. ¹ , Strelenko Yuri A. ¹ , Semenov Victor V. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry RAS, Leninsky Pr., 47, Moscow, 119991, Russian Federation

A novel peri-annulated heterocyclic system of 1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole was prepared starting from TNT via 4,6-dinitro-1-tosylindoline as a key intermediate. Base-induced Cdouble bondC bond shift in 1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indoles affords isomeric 2,11-dihydrobenz[6,7]oxepino[4,3,2-cd]indoles.

Samet A.V. , Yamskov A.N. , Strelenko Y.A. , Semenov V.V.
Preparation of peri-annulated indoles from polynitro compounds
Tetrahedron. 2009. V.65. N34. P.6868-6872. DOI: 10.1016/j.tet.2009.06.074 WOS Scopus OpenAlex

Web of science:	WOS:000269282400014
Scopus:	2-s2.0-67650717992
OpenAlex:	W2949692394

DB	Citing
OpenAlex	18
Scopus	14
Web of science	14