Special features of 1,3-dipolar cycloaddition of n-methylazomethinylid to nitrobenzazoles

Special features of 1,3-dipolar cycloaddition of n-methylazomethinylid to nitrobenzazoles Full article

Journal

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

Output data

Year: 2011, Volume: 47, Number: 2, Pages: 215-221 Pages count : 7 DOI: 10.1007/s10593-011-0743-y

Authors

Starosotnikov A.M. ¹ , Khakimo D.V. ¹ , Bastrakov M.A. ¹ , Pechenkin S.Yu. ¹ , Shevelev S.A. ¹ , Pivina T.S. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences (RAN), 47 Leninsky prospekt, Moscow, 119991, Russia

Synthetic approaches to 1,3-dipolar cycloaddition of N-methylazomethinylid to mononitrobenzazole are described. The geometric and electronic structures have been studied by quantum chemical methods (HF/STO-3 G and B3LYP/6-31 G*) and the reactivity indexes of compounds have been estimated. It was shown that 1,3-dipolar cycloaddition of N-methylazomethinylid to the dipolarophile has a polar character and proceeds in accordance with the normal (noninversion) electronic distribution.

Starosotnikov A.M. , Khakimo D.V. , Bastrakov M.A. , Pechenkin S.Y. , Shevelev S.A. , Pivina T.S.
Special features of 1,3-dipolar cycloaddition of n-methylazomethinylid to nitrobenzazoles
Chemistry of Heterocyclic Compounds. 2011. V.47. N2. P.215-221. DOI: 10.1007/s10593-011-0743-y WOS Scopus OpenAlex

Web of science:	WOS:000293754200010
Scopus:	2-s2.0-80052605857
OpenAlex:	W2009577734

DB	Citing
OpenAlex	12
Scopus	12
Web of science	12