One‐Pot Synthesis of <i>Ortho</i>‐Halogen‐Substituted Aryl(Alkynyl)Phosphinates Via Aryne‐Phosphite‐Haloalkyne Coupling

Abstract The one‐pot formation of two C−P bonds and one C−halogen bond was achieved through a mild three‐component coupling reaction utilizing arynes, phosphites, and haloalkynes. In this reaction, the aryl anion, generated from the nucleophilic addition of phosphite to aryne, directly attacked the halogen of the haloalkyne. The reaction proceeded smoothly with a wide substrate scope and good functional group tolerance. This operationally simple method enables direct access to ortho ‐halogen‐substituted aryl(alkynyl)phosphinates. The synthetic utility of ortho ‐halogen‐substituted aryl(alkynyl)phosphinates with prospective applications in natural product synthesis, medicinal chemistry, and materials chemistry has also been demonstrated.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2024-09-26
DOI
https://doi.org/10.1002/adsc.202400954
Citations
2
Primary Topic
Cyclization and Aryne Chemistry
Type
article
Field-Weighted Citation Impact
0.50

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article

One‐Pot Synthesis of Ortho‐Halogen‐Substituted Aryl(Alkynyl)Phosphinates Via Aryne‐Phosphite‐Haloalkyne Coupling

Eun Gyeong Choi, Seo‐Jung Han, Duck‐Hyung Lee, Suhyun Ji
2 citations
Advanced Synthesis & Catalysis
Cyclization and Aryne Chemistry
0.50
article

One‐Pot Synthesis of Ortho‐Halogen‐Substituted Aryl(Alkynyl)Phosphinates Via Aryne‐Phosphite‐Haloalkyne Coupling

Eun Gyeong Choi, Seo‐Jung Han, Duck‐Hyung Lee, Suhyun Ji
article en
2 citations

Abstract

Abstract The one‐pot formation of two C−P bonds and one C−halogen bond was achieved through a mild three‐component coupling reaction utilizing arynes, phosphites, and haloalkynes. In this reaction, the aryl anion, generated from the nucleophilic addition of phosphite to aryne, directly attacked the halogen of the haloalkyne. The reaction proceeded smoothly with a wide substrate scope and good functional group tolerance. This operationally simple method enables direct access to ortho ‐halogen‐substituted aryl(alkynyl)phosphinates. The synthetic utility of ortho ‐halogen‐substituted aryl(alkynyl)phosphinates with prospective applications in natural product synthesis, medicinal chemistry, and materials chemistry has also been demonstrated.

Advanced Synthesis & CatalysisVol. 367(1)
Sogang University (KR), Korea Institute of Science and Technology (KR), Korea University of Science and Technology (KR)
Ministry of Science and ICT, South Korea
Openalex Percentile: Top 39%
Cyclization and Aryne Chemistry
0.50
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