Synthesis of fused isoindoles via 1,3-dipolar cycloaddition of 1,3-oxazolium-5-olates (münchnones) with nitro benzazoles

Synthesis of fused isoindoles via 1,3-dipolar cycloaddition of 1,3-oxazolium-5-olates (münchnones) with nitro benzazoles Full article

Journal

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

Output data

Year: 2012, Volume: 22, Number: 1, Pages: 35-36 Pages count : 2 DOI: 10.1016/j.mencom.2012.01.013

Authors

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

Affiliations

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

1,3-Dipolar cycloaddition of 1,3-oxazolium-5-olates at benzazoles nitrated at the benzene ring affords the corresponding azoloisoindole derivatives.

Pechenkin S.Y. , Starosotnikov A.M. , Bastrakov M.A. , Kachala V.V. , Shevelev S.A.
Synthesis of fused isoindoles via 1,3-dipolar cycloaddition of 1,3-oxazolium-5-olates (münchnones) with nitro benzazoles
Mendeleev Communications. 2012. V.22. N1. P.35-36. DOI: 10.1016/j.mencom.2012.01.013 WOS Scopus OpenAlex

Web of science:	WOS:000301020400013
Scopus:	2-s2.0-84856515330
OpenAlex:	W2034849509

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Web of science	6