Enantioselective Vinylogous Addition of Enones to Allenes Enabled by Synergistic Borane/Palladium Catalysis

Herein, we report a method for enantioselective vinylogous addition of enones to alkoxyallenes enabled by synergistic borane/palladium catalysis. The inductive effect provided by borane coordination to the ketone was essential for closing the gap between the conditions needed for the generation of a dienolate and those needed for initiation of the palladium catalytic cycle by protonation of the metal catalyst. Furthermore, we accomplished the first example of stereodivergent synthesis with chiral borane/transition-metal catalysts.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-12-24
DOI
https://doi.org/10.1021/jacs.4c16214
Citations
8
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
2.00

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article

Enantioselective Vinylogous Addition of Enones to Allenes Enabled by Synergistic Borane/Palladium Catalysis

Heng Luo, Zequn Xing, Xiaochen Wang, Ming Zhang
8 citations
Journal of the American Chemical Society
Organoboron and organosilicon chemistry
2.00
article

Enantioselective Vinylogous Addition of Enones to Allenes Enabled by Synergistic Borane/Palladium Catalysis

Heng Luo, Zequn Xing, Xiaochen Wang, Ming Zhang
article en
8 citations

Abstract

Herein, we report a method for enantioselective vinylogous addition of enones to alkoxyallenes enabled by synergistic borane/palladium catalysis. The inductive effect provided by borane coordination to the ketone was essential for closing the gap between the conditions needed for the generation of a dienolate and those needed for initiation of the palladium catalytic cycle by protonation of the metal catalyst. Furthermore, we accomplished the first example of stereodivergent synthesis with chiral borane/transition-metal catalysts.

Journal of the American Chemical SocietyVol. 147(1)
Nankai University (CN), Institute of Organic Chemistry (HU)
National Natural Science Foundation of China, Nankai University, National Key Research and Development Program of China
Openalex Percentile: Top 14%
Organoboron and organosilicon chemistry
2.00
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