Asymmetric Induction With Chiral Carbon‐Bonding Donors

Carbon bonding has recently been introduced as a new tool in organic synthesis. Yet, it remains unclear whether this unique weak interaction can induce chirality or not. Herein, we report the synthesis of chiral carbon-bonding donors, and present the proof-of-concept study on asymmetric induction using this noncovalent force. Employing the oxa-Pictet-Spengler reaction as a benchmark, the experimental results demonstrate that chiral carbon-bonding donors can exert asymmetric induction over oxocarbenium ion intermediates. While the enantioselectivity in such a very first attempt is modest, it unequivocally validates carbon bonding as a feasible method for asymmetric induction, paving the way for its future development in more efficient asymmetric synthesis.

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Publication Details

Journal
Chemistry - A European Journal
Published
2026-02-23
DOI
https://doi.org/10.1002/chem.70827
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
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article

Asymmetric Induction With Chiral Carbon‐Bonding Donors

Lei Feng, X. Z. Li, Yuanling Pang, Hang Zhou et al.
Chemistry - A European Journal
Axial and Atropisomeric Chirality Synthesis
article

Asymmetric Induction With Chiral Carbon‐Bonding Donors

Lei Feng, X. Z. Li, Yuanling Pang, Hang Zhou, Yao Wang
article en

Abstract

Carbon bonding has recently been introduced as a new tool in organic synthesis. Yet, it remains unclear whether this unique weak interaction can induce chirality or not. Herein, we report the synthesis of chiral carbon-bonding donors, and present the proof-of-concept study on asymmetric induction using this noncovalent force. Employing the oxa-Pictet-Spengler reaction as a benchmark, the experimental results demonstrate that chiral carbon-bonding donors can exert asymmetric induction over oxocarbenium ion intermediates. While the enantioselectivity in such a very first attempt is modest, it unequivocally validates carbon bonding as a feasible method for asymmetric induction, paving the way for its future development in more efficient asymmetric synthesis.

Chemistry - A European Journal
Shandong University (CN)
Openalex Percentile: Top 44%
Axial and Atropisomeric Chirality Synthesis
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