Published March 2020
| Accepted Version
Journal Article
Open
Transition-Metal-Catalyzed 1,2-Carboboration of Alkenes: Strategies, Mechanisms, and Stereocontrol
- Creators
- Liu, Zhen
- Gao, Yang
- Zeng, Tian
- Engle, Keary M.
Abstract
During the past decade, many research groups have described catalytic methods for 1,2‐carboboration, allowing access to structurally complex organoboronates from alkenes. Various transition metals, especially copper, palladium, and nickel, have been widely used in these reactions. This review summarizes advances in this field, with a special focus on the catalytic cycles involved in different metal‐catalyzed carboboration reactions, as well as the regio‐ and stereochemical consequences of the underlying mechanisms. 1,2‐Carboboration of other unsaturated systems, such as alkynes and allenes, is outside of the scope of this review.
Additional Information
© 2019 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim. Issue Online: 29 April 2020; Version of Record online: 10 September 2019; Manuscript revised: 20 August 2019; Manuscript received: 09 July 2019. Dedicated to 2019 Wolf Prize Awardees Professor Stephen L. Buchwald and Professor John F. Hartwig. We gratefully acknowledge financial support from the National Institutes of Health (5R35 GM125052‐02). We further thank Bristol‐Myers Squibb (Graduate Fellowship to Z.L.; Unrestricted Grant to K.M.E.) and the Alfred P. Sloan Foundation (Fellowship to K.M.E.). We thank Joseph Derosa and Lucas J. Oxtoby for proofreading the manuscript.Attached Files
Accepted Version - nihms-1603229.pdf
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nihms-1603229.pdf
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Additional details
- PMCID
- PMC8006804
- Eprint ID
- 98554
- Resolver ID
- CaltechAUTHORS:20190910-130904956
- NIH
- 5R35 GM125052-02
- Bristol-Myers Squibb
- Alfred P. Sloan Foundation
- Created
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2019-09-10Created from EPrint's datestamp field
- Updated
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2021-04-19Created from EPrint's last_modified field