Green Synthesis of Stereodefined Tri- and Tetrasubstituted Alkenes <i>via</i> 100% Atomeconomic and Regio-, and Stereoselective Halo-chalcogenation and Sulfonylation of Alkynes

Achieving 100% atom economy in an organic transformation is a challenging task but it is always desirable in the context of green chemistry. Difunctionalization of alkynes using a bifunctional reagent is a useful strategy to achieve 100% atom economy, however, the challenge is to control the regio- and stereoselectivity of the reaction. In this article, we discuss the recent advances in developing 100% atom economic, highly regio- and stereoselective halo-chalcogenation and chlorosulfonylation strategies with alkynes for the green and sustainable synthesis of stereodefined tri- or tetrasubstituted alkenes, and its application in accessing valuable molecules including a marketed drug in a green and sustainable manner. The green chemistry metrics are presented to highlight the greenness of some of these protocols.

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Journal
CHIMIA International Journal for Chemistry
Published
2025-09-10
DOI
https://doi.org/10.2533/chimia.2025.622
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Green Synthesis of Stereodefined Tri- and Tetrasubstituted Alkenes via 100% Atomeconomic and Regio-, and Stereoselective Halo-chalcogenation and Sulfonylation of Alkynes

Appanapalli N. V. Satyanarayana, Tanmay Chatterjee
CHIMIA International Journal for Chemistry
Sulfur-Based Synthesis Techniques
article

Green Synthesis of Stereodefined Tri- and Tetrasubstituted Alkenes via 100% Atomeconomic and Regio-, and Stereoselective Halo-chalcogenation and Sulfonylation of Alkynes

Appanapalli N. V. Satyanarayana, Tanmay Chatterjee
article en

Abstract

Achieving 100% atom economy in an organic transformation is a challenging task but it is always desirable in the context of green chemistry. Difunctionalization of alkynes using a bifunctional reagent is a useful strategy to achieve 100% atom economy, however, the challenge is to control the regio- and stereoselectivity of the reaction. In this article, we discuss the recent advances in developing 100% atom economic, highly regio- and stereoselective halo-chalcogenation and chlorosulfonylation strategies with alkynes for the green and sustainable synthesis of stereodefined tri- or tetrasubstituted alkenes, and its application in accessing valuable molecules including a marketed drug in a green and sustainable manner. The green chemistry metrics are presented to highlight the greenness of some of these protocols.

CHIMIA International Journal for ChemistryVol. 79(9)
Birla Institute of Technology and Science - Hyderabad Campus (IN)
Science and Engineering Research Board
Openalex Percentile: Top 82%
Sulfur-Based Synthesis Techniques
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