Enantioselective α‑Boryl Carbene Transformations

• Published in: Journal of the American Chemical Society 2024-04, Vol.146 (14), p.9871-9879
• Main Authors: Huang, Ming-Yao, Zhao, Jia-Bao, Zhang, Cheng-Da, Zhou, Yuan-Jun, Lu, Zhan-Sheng, Zhu, Shou-Fei
• Format: Article
• Language: English
• Subjects: carbenes; enantioselectivity; society
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.3c14766

Carbenes, recognized as potent intermediates, enable unique chemical transformations, and organoborons are pivotal in diverse chemical applications. As a hybrid of carbene and the boryl group, α-boryl carbenes are promising intermediates for the construction of organoborons; unfortunately, such carbenes are hard to access and have low structural diversity with their asymmetric transformations largely uncharted. In this research, we utilized boryl cyclopropenes as precursors for the swift synthesis of α-boryl metal carbenes, a powerful category of intermediates for chiral organoboron synthesis. These α-boryl carbenes undergo a series of highly enantioselective transfer reactions, including B–H and Si–H insertion, cyclopropanation, and cyclopropanation/Cope rearrangement, catalyzed by a singular chiral copper complex. This approach opens paths to previously unattainable but easily transformable chiral organoborons, expanding both carbene and organoboron chemistry.