Dearomative (3+2) cycloaddition of 2-substituted 3,5-dinitropyridines and N-methyl azomethine ylide

Dearomative (3+2) cycloaddition of 2-substituted 3,5-dinitropyridines and N-methyl azomethine ylide Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122

Output data

Year: 2019, Volume: 55, Number: 1, Pages: 72-77 Pages count : 6 DOI: 10.1007/s10593-019-02421-9

Authors

Bastrakov Maxim A. ¹ , Fedorenko Alexey K. ¹ , Starosotnikov Alexey M. ¹ , Kachala Vadim V. ¹ , Shevelev Svyatoslav A. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow 119991, Russia

1,3-Dipolar cycloaddition of various 2-substituted 3,5-dinitropyridines and unstabilized N-methyl azomethine ylide has been studied. It was found that, depending on the nature of the substituent, the reaction results in addition of one or two equivalents of 1,3-dipole to the pyridine ring. Eventually, a convenient method for the synthesis of differently substituted heterocyclic systems containing one or two pyrrolidine fragments fused with a pyridine ring has been demonstrated.

Bastrakov M.A. , Fedorenko A.K. , Starosotnikov A.M. , Kachala V.V. , Shevelev S.A.
Dearomative (3+2) cycloaddition of 2-substituted 3,5-dinitropyridines and N-methyl azomethine ylide
Chemistry of Heterocyclic Compounds. 2019. V.55. N1. P.72-77. DOI: 10.1007/s10593-019-02421-9 WOS Scopus OpenAlex

Web of science:	WOS:000461551800011
Scopus:	2-s2.0-85061828659
OpenAlex:	W2917161487

DB	Citing
OpenAlex	11
Scopus	12
Web of science	12