Developments in the Chemistry of α‐Carbonyl Alkyl Bromides

Author:

Ouyang Xuan‐Hui12,Song Ren‐Jie1ORCID,Li Jin‐Heng1ORCID

Affiliation:

1. Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle Nanchang Hangkong University Nanchang 330063 China

2. State Key Laboratory of Chemo/Biosensing and Chemometrics Hunan University Changsha 410082 China

Abstract

Abstractα‐Carbonyl alkyl bromides are powerful reactive species for the formation of carbon–carbon bonds. Strategies relying on intermolecular C−H functionalization and cross‐coupling reactions, also referred to as intramolecular cyclization, have been employed for the construction of alkenes, alkanes, ketones, and other natural‐product‐like ring compounds from simple alkynes, alkenes, and 1,n‐enynes. In view of the importance of these α‐carbonyl alkyl bromides, especially the difluoro carbonyl alkyl bromides, many researchers have focused their efforts to develop facile and mild synthetic methods for compounds with important biological activities. This review aims to briefly discuss the latest developments in the transformation of α‐carbonyl alkyl bromides with emphasis on the related reaction mechanisms.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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