4-R-7-Nitrobenzofurazans in [3+2] cycloaddition reactions with N-methylazomethine ylide

4-R-7-Nitrobenzofurazans in [3+2] cycloaddition reactions with N-methylazomethine ylide Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2012, Volume: 61, Number: 1, Pages: 74-77 Pages count : 4 DOI: 10.1007/s11172-012-0011-z

Authors

Pechenkin S.Yu. ¹ , Starosotnikov A.M. ¹ , Bastrakov M.A. ¹ , Glukhov I.V. ² , Shevelev S.A. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
2	A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, Russian Federation

A number of new tetrahydroisoindole derivatives fused with the furazan ring were synthesized based on the 1,3-dipolar cycloaddition of N-methylazomethine ylide with substituted 4-nitrobenzofurazans. Substituents in the benzene ring were found to affect the cycloaddition process.

Pechenkin S.Y. , Starosotnikov A.M. , Bastrakov M.A. , Glukhov I.V. , Shevelev S.A.
4-R-7-Nitrobenzofurazans in [3+2] cycloaddition reactions with N-methylazomethine ylide
Russian Chemical Bulletin. 2012. V.61. N1. P.74-77. DOI: 10.1007/s11172-012-0011-z WOS Scopus OpenAlex

Web of science:	WOS:000310470000011
Scopus:	2-s2.0-84868362523
OpenAlex:	W2031371181

DB	Citing
OpenAlex	8
Scopus	9
Web of science	4