Issue 17, 2022

One-pot two-step dithiocarbamylation of styrenes: metal-free stereoselective synthesis of styrenyl dithiocarbamates

Abstract

Styrenes have been functionalized to produce styrenyl dithiocarbamates by a one-pot two-step procedure without using any metal catalysts. Styrene was transformed into a bromo-derivative, which undergoes a domino nucleophilic substitution followed by elimination in the presence of a dithiocarbamate anion and triethylamine to produce trans-styrenyl dithiocarbamates exclusively. The reaction shows a wide substrate scope and good yields of products.

Graphical abstract: One-pot two-step dithiocarbamylation of styrenes: metal-free stereoselective synthesis of styrenyl dithiocarbamates

Supplementary files

Article information

Article type
Communication
Submitted
15 Feb 2022
Accepted
01 Apr 2022
First published
02 Apr 2022

Org. Biomol. Chem., 2022,20, 3491-3494

One-pot two-step dithiocarbamylation of styrenes: metal-free stereoselective synthesis of styrenyl dithiocarbamates

M. Mondal and A. Saha, Org. Biomol. Chem., 2022, 20, 3491 DOI: 10.1039/D2OB00315E

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