期刊
ASIAN JOURNAL OF ORGANIC CHEMISTRY
卷 8, 期 5, 页码 610-626出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.201900071
关键词
Catalytic asymmetric; aldol-type reaction; alpha-fluorinated enolate precursors; metal catalysis; organocatalysis
资金
- NSFC [21672068]
- National Key Research and Development Program of China [2018YFC1708102]
Optically active alpha-fluoroalkyl substituted alcohols are widely present in drugs and pharmaceutically active compounds. Catalytic enantioselective aldol-type reaction using fluorinated enolates constitutes a powerful method for the synthesis of alpha-fluorinated beta-hydroxy carbonyl compounds, which are versatile building blocks to access alpha-fluorinated alcohols bearing different functionalities through an array of transformations based on carbonyl group. This Focus Review summarizes recent achievements of the catalytic enantioselective aldol reactions using fluorinated enolates derived from five different types of precursors, discusses in detail the limitation of each method, and outlines synthetic opportunities still present.
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