Issue 10, 2024

Synthesis of unsymmetric phosphorotrithioates by sequential coupling of 1,1-dichloro-N,N-diethylphosphanamine with thiols and sulfenyl chloride

Abstract

Herein, we present the first, one-step, direct synthesis of unsymmetric phosphorotrithioates through a process involving sequential coupling of 1,1-dichloro-N,N-diethylphosphanamine with thiols and sulfenyl chloride. This method showcases excellent functional group tolerance, substrate compatibility, and mild reaction conditions, offering a streamlined approach for the challenging phosphorotrithioate synthesis. Additionally, the applicability of this method can be extended to the synthesis of mixed phosphoroselenodithioates.

Graphical abstract: Synthesis of unsymmetric phosphorotrithioates by sequential coupling of 1,1-dichloro-N,N-diethylphosphanamine with thiols and sulfenyl chloride

Supplementary files

Article information

Article type
Communication
Submitted
01 Jan 2024
Accepted
11 Feb 2024
First published
12 Feb 2024

Org. Biomol. Chem., 2024,22, 2007-2011

Synthesis of unsymmetric phosphorotrithioates by sequential coupling of 1,1-dichloro-N,N-diethylphosphanamine with thiols and sulfenyl chloride

F. Hussain, S. Mahajan, S. Ahmed and Q. N. Ahmed, Org. Biomol. Chem., 2024, 22, 2007 DOI: 10.1039/D4OB00002A

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