Iodine-Driven Three-Component Reaction of Isocyanides, Amines, and TsNXNa (X = Br, Cl): A Facile, Metal-Free Approach towards N-Sulfonyl Guanidines

Abstract This work illustrates an expeditious, highly efficient, metal-, base-, and oxidant-free approach towards synthesizing N-sulfonyl guanidines via a three-component reaction system comprising isocyanides, amines, and TsNXNa (X = Br, Cl). The reaction proceeds via the formation of an isolable carbodiimide intermediate. The synthetic protocol emerges as a promising route for a simple, efficient, and rapid transformation into a diverse range of N-sulfonyl guanidines under mild reaction conditions.

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Publication Details

Journal
Synlett
Published
2025-04-07
DOI
https://doi.org/10.1055/a-2577-0726
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

Iodine-Driven Three-Component Reaction of Isocyanides, Amines, and TsNXNa (X = Br, Cl): A Facile, Metal-Free Approach towards N-Sulfonyl Guanidines

Prodeep Phukan, Sauvik Kashyap
Synlett
Sulfur-Based Synthesis Techniques
article

Iodine-Driven Three-Component Reaction of Isocyanides, Amines, and TsNXNa (X = Br, Cl): A Facile, Metal-Free Approach towards N-Sulfonyl Guanidines

Prodeep Phukan, Sauvik Kashyap
article en

Abstract

Abstract This work illustrates an expeditious, highly efficient, metal-, base-, and oxidant-free approach towards synthesizing N-sulfonyl guanidines via a three-component reaction system comprising isocyanides, amines, and TsNXNa (X = Br, Cl). The reaction proceeds via the formation of an isolable carbodiimide intermediate. The synthetic protocol emerges as a promising route for a simple, efficient, and rapid transformation into a diverse range of N-sulfonyl guanidines under mild reaction conditions.

SynlettVol. 36(15)
Gauhati University (IN)
Openalex Percentile: Top 95%
Sulfur-Based Synthesis Techniques
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