Auxiliary‐Based Stereoconvergent Transition Metal‐Free Cross‐Electrophile Couplings of α‐Iodoboronic Esters

Chiral boronic esters are highly valuable building blocks in organic chemistry and related fields, allowing access to structurally diverse libraries, including those of drug candidates. Herein, stereoselective cross couplings of α ‐iodoboronic esters with various commercial electrophiles are reported. These stereoconvergent coupling reactions proceed via iodine‐metal exchange and subsequent stereoselective capture of the generated α ‐boryl organometallic species without the use of a transition metal catalyst. The presented reactions allow the α ‐silylation, α ‐borylation, and α ‐methylborylation of boronic esters using a common chiral auxiliary.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-09-09
DOI
https://doi.org/10.1002/adsc.70117
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
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article

Auxiliary‐Based Stereoconvergent Transition Metal‐Free Cross‐Electrophile Couplings of α‐Iodoboronic Esters

Max Schwenzer, Armido Studer
Advanced Synthesis & Catalysis
Catalytic Cross-Coupling Reactions
article

Auxiliary‐Based Stereoconvergent Transition Metal‐Free Cross‐Electrophile Couplings of α‐Iodoboronic Esters

Max Schwenzer, Armido Studer
article en

Abstract

Chiral boronic esters are highly valuable building blocks in organic chemistry and related fields, allowing access to structurally diverse libraries, including those of drug candidates. Herein, stereoselective cross couplings of α ‐iodoboronic esters with various commercial electrophiles are reported. These stereoconvergent coupling reactions proceed via iodine‐metal exchange and subsequent stereoselective capture of the generated α ‐boryl organometallic species without the use of a transition metal catalyst. The presented reactions allow the α ‐silylation, α ‐borylation, and α ‐methylborylation of boronic esters using a common chiral auxiliary.

Advanced Synthesis & CatalysisVol. 367(21)
University of Münster (DE)
Openalex Percentile: Top 82%
Catalytic Cross-Coupling Reactions
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