Iridium-Catalyzed Asymmetric Allylic Substitution with Sequential Boron Incorporation

An iridium-catalyzed asymmetric allylic substitution with sequential boron incorporation is reported. The reaction accommodates a wide range of substrates, affording chiral N,O-bidentate difluoroboron complexes in excellent yields with high enantioselectivities. Furthermore, decigram-scale reaction, synthetic transformations, as well as photophysical property investigations of the N,O-bidentate difluoroboron complexes are explored.

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Publication Details

Journal
Organic Letters
Published
2025-05-09
DOI
https://doi.org/10.1021/acs.orglett.5c01366
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Iridium-Catalyzed Asymmetric Allylic Substitution with Sequential Boron Incorporation

Ying He, Le Wang, Lihong Zhang, Wan-Yi Xu
Organic Letters
Asymmetric Hydrogenation and Catalysis
article

Iridium-Catalyzed Asymmetric Allylic Substitution with Sequential Boron Incorporation

Ying He, Le Wang, Lihong Zhang, Wan-Yi Xu
article en

Abstract

An iridium-catalyzed asymmetric allylic substitution with sequential boron incorporation is reported. The reaction accommodates a wide range of substrates, affording chiral N,O-bidentate difluoroboron complexes in excellent yields with high enantioselectivities. Furthermore, decigram-scale reaction, synthetic transformations, as well as photophysical property investigations of the N,O-bidentate difluoroboron complexes are explored.

Organic LettersVol. 27(20)
Nanjing University of Science and Technology (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangsu Province
Openalex Percentile: Top 92%
Asymmetric Hydrogenation and Catalysis
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