Electrochemical one-pot cascade synthesis of thio(seleno)cyanato-substituted thiazolidine-2-imines without external electrolyte

Abstract

A novel synthetic method has been developed for generating thio(seleno)cyanato-substituted thiazolidine-2-imines via an electrochemical one-pot cascade reaction. This reaction employs isothiocyanates, N-2-en-1-amines, and KSCN (or KSeCN) under mild conditions, obviating the need for metals, chemical oxidants, and external electrolytes. The protocol is effective with unactivated alkenes and facilitates the synthesis of five- and six-membered thio(seleno)cyanato-substituted thiazolidine-2-imines. The versatility is demonstrated by its straightforward operation and scalability to gram-scale production, underscoring its potential for broader application.

Graphical abstract: Electrochemical one-pot cascade synthesis of thio(seleno)cyanato-substituted thiazolidine-2-imines without external electrolyte

Supplementary files

Article information

Article type
Communication
Submitted
08 Oct 2024
Accepted
30 Oct 2024
First published
30 Oct 2024

Org. Biomol. Chem., 2024, Advance Article

Electrochemical one-pot cascade synthesis of thio(seleno)cyanato-substituted thiazolidine-2-imines without external electrolyte

X. Yu, L. Hao, X. Liu, S. Jin, Y. Li, Y. Liu and Y. Ji, Org. Biomol. Chem., 2024, Advance Article , DOI: 10.1039/D4OB01626B

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