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A practical synthesis of 2,3-dihydro-1,5-benzothiazepines

Academic Article
Publication Date:
2017
Citation:
A practical synthesis of 2,3-dihydro-1,5-benzothiazepines / D.C.M. Albanese, N. Gaggero, M. Fei. - In: GREEN CHEMISTRY. - ISSN 1463-9262. - 19:23(2017 Nov 28), pp. 5703-5707. [10.1039/c7gc02097j]
abstract:
2,3-Dihydro-1,5-benzothiazepines have been obtained through a domino process involving a Michael addition of 2-aminothiophenols to chalcones, followed by in situ cyclization. Up to 98% chemical yields have been obtained at room temperature under essentially neutral conditions by using hexafluoro-2-propanol as an efficient medium.
IRIS type:
01 - Articolo su periodico
Keywords:
Condensation-reactions; efficient synthesis; Michael addition; highly efficient; 1,5-benzothiazepines; catalyst; disulfides; 1,5-benzodiazepines; limitations; oxidation
List of contributors:
D.C.M. Albanese, N. Gaggero, M. Fei
Authors of the University:
ALBANESE DOMENICO CARLO MARIA ( author )
Link to information sheet:
https://air.unimi.it/handle/2434/528618
Full Text:
https://air.unimi.it/retrieve/handle/2434/528618/1116875/postprint.pdf
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Settore CHIM/04 - Chimica Industriale

Settore CHIM/06 - Chimica Organica
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