Journal
ADVANCED SYNTHESIS & CATALYSIS
Volume 362, Issue 5, Pages 1015-1031Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201901178
Keywords
chiral lactones; chiral metal catalysis; chiral organocatalysis; cyclic ketones; enantioselective Baeyer-Villiger oxidation
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Funding
- National Natural Science Foundation of China [21702080]
- Open Project Program of Key Laboratory of Functional Small Organic Molecule, Ministry of Education, Jiangxi Normal University [KLFS-KF-201603]
- Foundation of Jiangxi Educational Committee [170223]
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Baeyer-Villiger oxidations, first reported by Adolf von Baeyer and Victor Villiger 120 years ago, are highly efficient methodologies for the syntheses of esters or lactones from ketones. The asymmetric Baeyer-Villiger oxidations using racemic, prochiral and meso-cyclic ketones allow a rapid access to chiral lactones, which are valuable intermediates for the subsequent synthesis of bioactive compounds and natural products. The current review provides a summary on the advances in chemocatalytic enantioselective B-V oxidations. The latest achievements in this field and their applications are presented.
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