Geminal acylnitrostyrenes in the reaction with ortho-aminothiophenol View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-06

AUTHORS

V. M. Berestovitskaya, R. I. Baichurin, N. I. Aboskalova, K. A. Lysenko, I. V. Anan’ev

ABSTRACT

The synthesis of previously unknown 2,3- and 2,5-dihydro-1,5-benzothiazepines sontaining nitro group was performed by the easy sondensation of geminal acylnitrostyrenes with the o-aminothiophenol. The structure of the obtained sompounds was studied by physicochemical methods. By X-ray diffraction analysis the geometry and structural parameters of 4-methyl-3-nitro-2-phenyl-2,3-dihydro-1,5-benzothiazepine were determined.

PAGES

1163-1170

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363211060156

DOI

http://dx.doi.org/10.1134/s1070363211060156

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1035279642


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