Double 1,3‐dipolar cycloaddition of N‐methyl Azomethine ylide to meta‐Dinitrobenzene annelated with nitrogen aromatic heterocycles

Double 1,3‐dipolar cycloaddition of N‐methyl Azomethine ylide to meta‐Dinitrobenzene annelated with nitrogen aromatic heterocycles Full article

Journal

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

Output data

Year: 2010, Volume: 47, Number: 4, Pages: 893-896 Pages count : 4 DOI: 10.1002/jhet.423

Authors

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

Affiliations

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

The 1,3-dipolar cycloaddition of unstabilized azomethine ylide 1 with meta-dinitrobenzene fused with nitrogen heterocycles affords the corresponding decahydropyrrolo[3,4-e]isoindole cycloadducts in good yields. This is a first example of [3+2]-cycloaddition of azomethine ylides to nitroarenes.

Bastrakov M.A. , Starosotnikov A.M. , Pechenkin S.Y. , Kachala V.V. , Glukhov I.V. , Shevelev S.A.
Double 1,3‐dipolar cycloaddition of N‐methyl Azomethine ylide to meta‐Dinitrobenzene annelated with nitrogen aromatic heterocycles
Journal of Heterocyclic Chemistry. 2010. V.47. N4. P.893-896. DOI: 10.1002/jhet.423 WOS Scopus OpenAlex

Web of science:	WOS:000280450700016
Scopus:	2-s2.0-77954589305
OpenAlex:	W2006916282

DB	Citing
OpenAlex	32
Scopus	33
Web of science	30