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Developments in the Chemistry of α‐Carbonyl Alkyl Bromides
Author(s) -
Ouyang XuanHui,
Song RenJie,
Li JinHeng
Publication year - 2018
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.201800630
Subject(s) - chemistry , alkyl , intramolecular force , intermolecular force , organic chemistry , ring (chemistry) , molecule
α‐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.

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