Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1347037 | Tetrahedron: Asymmetry | 2014 | 8 Pages |
Abstract
α-Hydroxy esters are key structural units of valuable synthetic intermediates as well as natural products. In this review, enantioenriched α-hydroxy esters with moderate to excellent yield were prepared via various organocatalytic synthesis reactions.
Graphical abstractIn this review, the synthesis of α-hydroxy esters with moderate to excellent yields and stereoselectivities is discussed through the various synthesis reactions, mainly including heteroatom rearrangements, carbonyl-ene, oxidation of β-keto esters, reduction of α-keto esters, kinetic resolution, and glycolate alkylation (arylation).Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Xin Gu, Lan Wang, Yong-fei Gao, Wei Ma, Ya-ming Li, Pin Gong,