Issue 43, 2022

Iodine promoted cyclization of N,N′-diphenylthiocarbamides with enaminones: a protocol for the synthesis of poly-substituted 2-iminothiazolines

Abstract

An iodine promoted cyclization reaction between N,N′-diphenylthiocarbamides and enaminones was achieved, providing a series of poly-substituted 2-iminothiazolines. This protocol is transition metal free and simple to perform, with a broad functional group tolerance and good to excellent yields under mild reaction conditions, showing potential synthetic value for the preparation of a diversity of biologically and pharmaceutically active compounds.

Graphical abstract: Iodine promoted cyclization of N,N′-diphenylthiocarbamides with enaminones: a protocol for the synthesis of poly-substituted 2-iminothiazolines

Supplementary files

Article information

Article type
Paper
Submitted
15 Aug 2022
Accepted
12 Oct 2022
First published
13 Oct 2022

Org. Biomol. Chem., 2022,20, 8533-8537

Iodine promoted cyclization of N,N′-diphenylthiocarbamides with enaminones: a protocol for the synthesis of poly-substituted 2-iminothiazolines

X. Xu and Z. Dong, Org. Biomol. Chem., 2022, 20, 8533 DOI: 10.1039/D2OB01477G

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