4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide

4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2010, Volume: 20, Number: 6, Pages: 353-354 Pages count : 2 DOI: 10.1016/j.mencom.2010.11.018

Authors

Konstantinova Lidia S. ¹ , Bastrakov Maxim A. ¹ , Starosotnikov Aleksei M. ¹ , Glukhov Ivan V. ² , Lysov Kirill A. ¹ , Rakitin Oleg A. ¹ , Shevelev Svyatoslav A. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation
2	A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991 Moscow, Russian Federation

1,3-Dipolar cycloaddition of 4,6-dinitrobenzo[c]isothiazole to (N-methyl-N-methylideneammonio)methanide (2 equiv.) gives 5,8-dimethyl-3b,6b-dinitrodecahydroisothiazolo[3,4-e]pyrrolo[3,4-g]isoindole, whose structure was confirmed by X-ray diffraction analysis.

Konstantinova L.S. , Bastrakov M.A. , Starosotnikov A.M. , Glukhov I.V. , Lysov K.A. , Rakitin O.A. , Shevelev S.A.
4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide
Mendeleev Communications. 2010. V.20. N6. P.353-354. DOI: 10.1016/j.mencom.2010.11.018 WOS Scopus OpenAlex

Web of science:	WOS:000285910800018
Scopus:	2-s2.0-78649538497
OpenAlex:	W2952199969

DB	Citing
OpenAlex	23
Scopus	28
Web of science	24