Issue 6, 1991

N-alkenyl acylketene S, N-acetals from 2,3-dihydro-1,3-benzothiazoles and carboxylic anhydrides. X-Ray molecular structure of 2-(butyrylmethylene)N-(cyclohex-1-enyl)-2,3-dihydro-1,3-benzothiazole

Abstract

Depending on the reaction conditions or starting materials used, 2,3-dihydro-1,3-benzothiazoles 1 or their N-acyl derivatives 2 react with carboxylic anhydrides to yield the corresponding enamides 3 and/or N-alkenyl acylketene S,N-acetals 4. The structural assignments of these last compounds are based on spectroscopic data. X-Ray evidence for title compound 4c is also reported. A possible reaction pathway for formation of products 4 is suggested.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 1505-1510

N-alkenyl acylketene S, N-acetals from 2,3-dihydro-1,3-benzothiazoles and carboxylic anhydrides. X-Ray molecular structure of 2-(butyrylmethylene)N-(cyclohex-1-enyl)-2,3-dihydro-1,3-benzothiazole

G. Trapani, A. Latrofa, A. Reho, M. Franco, G. Liso and F. Stasi, J. Chem. Soc., Perkin Trans. 1, 1991, 1505 DOI: 10.1039/P19910001505

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