Enantioselective Construction of Oxindoles Bearing a Quaternary Carbon via Ni−Al Bimetal‐Catalyzed Formyl C−H Alkylation

Enantioselective transition metal-catalyzed C-H alkylation emerges as one of the most atom- and step-economical routes to chiral quaternary carbons, while big challenges still remain with acyl C-H alkylations. Herein, we use a Ni-Al bimetallic catalyst to facilitate a highly regioselective and highly enantioselective C-H alkylation of formamides with alkenes, constructing various oxindoles bearing a chiral quaternary carbon in up to 94 % yield and up to 95 % ee.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2024-09-26
DOI
https://doi.org/10.1002/anie.202413652
Citations
12
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
3.00
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article

Enantioselective Construction of Oxindoles Bearing a Quaternary Carbon via Ni−Al Bimetal‐Catalyzed Formyl C−H Alkylation

Mengchun Ye, Jiang‐Fei Li, Qi‐Lin Zhou, Haorui Wang et al.
12 citations
Angewandte Chemie International Edition
Catalytic C–H Functionalization Methods
3.00
article

Enantioselective Construction of Oxindoles Bearing a Quaternary Carbon via Ni−Al Bimetal‐Catalyzed Formyl C−H Alkylation

Mengchun Ye, Jiang‐Fei Li, Qi‐Lin Zhou, Haorui Wang, Weiwei Xu, Mengying Xu
article en
12 citations

Abstract

Enantioselective transition metal-catalyzed C-H alkylation emerges as one of the most atom- and step-economical routes to chiral quaternary carbons, while big challenges still remain with acyl C-H alkylations. Herein, we use a Ni-Al bimetallic catalyst to facilitate a highly regioselective and highly enantioselective C-H alkylation of formamides with alkenes, constructing various oxindoles bearing a chiral quaternary carbon in up to 94 % yield and up to 95 % ee.

Angewandte Chemie International EditionVol. 64(2)
Wannan Medical College (CN), Nankai University (CN)
Openalex Percentile: Top 8%
Catalytic C–H Functionalization Methods
3.00
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