Acylated benzothiazinesulfoneamides: Synthesis and molecular structure

Tevs O.; Veremeichik Y.; Shurpik D.; Lodochnikova O.; Plemenkov V.

Acylated benzothiazinesulfoneamides: Synthesis and molecular structure

Tevs O., Veremeichik Y., Shurpik D., Lodochnikova O., Plemenkov V.

Дата публикации: 2016

Дата публикации в реестре: 2020-03-01T01:22:08Z

Аннотация:

© 2016, Pleiades Publishing, Ltd.1,2,3,4,4a,10b-Hexahydro-1,4-methano-6H-dibenzo[c,e]-5,6-thiazine-5,5-dioxide has been converted into the corresponding N-acyl derivatives via the reaction with acid chlorides and anhydrides. X-Ray diffraction data have revealed the presence of an intramolecular С–H···O=S hydrogen bond in the molecules of the obtained compounds.

Ключевые слова:
acylation, intramolecular interactions, sulfonamides, X-ray diffraction analysis

Тип: Article

Источник: SCOPUS10703632-2016-86-8-SID84988850933