Regio‐ and Enantioselective Rhodium‐Catalyzed Allylic Arylation of Racemic Allylic Carbonates with Arylboronic Acids

Abstract Rhodium‐catalyzed regio‐ and enantioselective allylic arylation of racemic alkyl‐ and aryl‐ substituted allylic carbonates with arylboronic acids using commercially available BIBOP ligand is reported. This reaction proceeds at room temperature without base or other additive to deliver allylic arylation products in excellent yields, regio‐ and enantioselectivity (up to 95 % yield, >20 : 1 b/l, >99 % ee). Rh/BIBOP is disclosed as an efficient catalytic system for allylic substitution reaction.

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Publication Details

Journal
Angewandte Chemie
Published
2025-01-10
DOI
https://doi.org/10.1002/ange.202421596
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94

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article

Regio‐ and Enantioselective Rhodium‐Catalyzed Allylic Arylation of Racemic Allylic Carbonates with Arylboronic Acids

Wenjie Shen, Hu-Chong Wang, Shu‐Li You
1 citations
Angewandte Chemie
Catalytic C–H Functionalization Methods
0.94
article

Regio‐ and Enantioselective Rhodium‐Catalyzed Allylic Arylation of Racemic Allylic Carbonates with Arylboronic Acids

Wenjie Shen, Hu-Chong Wang, Shu‐Li You
article en
1 citations

Abstract

Abstract Rhodium‐catalyzed regio‐ and enantioselective allylic arylation of racemic alkyl‐ and aryl‐ substituted allylic carbonates with arylboronic acids using commercially available BIBOP ligand is reported. This reaction proceeds at room temperature without base or other additive to deliver allylic arylation products in excellent yields, regio‐ and enantioselectivity (up to 95 % yield, >20 : 1 b/l, >99 % ee). Rh/BIBOP is disclosed as an efficient catalytic system for allylic substitution reaction.

Angewandte ChemieVol. 137(6)
Shanghai Institute of Organic Chemistry (CN), State Key Laboratory of Organometallic Chemistry
National Natural Science Foundation of China
Openalex Percentile: Top 30%
Catalytic C–H Functionalization Methods
0.94
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