1,3‐Dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to nitrobenzene annelated with azoles

1,3‐Dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to nitrobenzene annelated with azoles Full article

Journal

Journal of Heterocyclic Chemistry
ISSN: 0022-152X , E-ISSN: 1943-5193

Output data

Year: 2011, Volume: 48, Number: 4, Pages: 824-828 Pages count : 5 DOI: 10.1002/jhet.599

Authors

Starosotnikov Alexey M. ¹ , Bastrakov Maxim A. ¹ , Pechenkin Sergey Yu. ¹ , Leontieva Margarita A. ¹ , Kachala Vadim V. ¹ , Shevelev Svyatoslav A. ¹

Affiliations

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

he 1,3-dipolar cycloaddition of unstabilized N-methyl azomethine ylide to mononitro benzazoles was studied. Depending on the nature of substituents and annelated azoles, the reaction affords previously unknown isoindole fused heterocyclic systems. The reactivity of the cycloadducts was examined.

Starosotnikov A.M. , Bastrakov M.A. , Pechenkin S.Y. , Leontieva M.A. , Kachala V.V. , Shevelev S.A.
1,3‐Dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to nitrobenzene annelated with azoles
Journal of Heterocyclic Chemistry. 2011. V.48. N4. P.824-828. DOI: 10.1002/jhet.599 WOS Scopus OpenAlex

Web of science:	WOS:000293745900012
Scopus:	2-s2.0-79953673639
OpenAlex:	W2315795373

DB	Citing
OpenAlex	29
Scopus	29
Web of science	26