Chinese Journal of Organic Chemistry >
Development of the Asymmetric Hydrogenation of Enol Esters
Received date: 2015-12-07
Revised date: 2016-01-06
Online published: 2016-01-15
Supported by
Project supported by the National Natural Science Foundation of China (No. 21572131) and the Science and Technology Commission of Shanghai Municipality (No. 14XD1402300).
Chiral alcohols are an important class of compounds and possess a broad array of applications, thus their asymmetric preparation is an important area of research in the field of organic synthesis. Amongst methodologies for the preparation of such compounds, catalytic asymmetric hydrogenation has gained widespread interest due to its efficiency, environmentally friendliness and economic advantages, and is gradually becoming a technology with great potential for the industrial preparation of chiral alcohols. This review provides the first overview for the catalytic asymmetric hydrogenation of enol esters for the synthesis of chiral alcohols. A comprehensive and up-to-date introduction are given for a number of different substrates. A thorough analysis is provided concerning the advantages and disadvantages of different chiral ligands and their transition-metal complexes. Finally, a brief discussion relating to developments and potential areas of further research concerning new substrates, new ligands and new catalytic metals, is presented.
Key words： enol esters; chiral alcohols; asymmetric hydrogenation; Ru-catalyzed; Rh-catalyzed
Wang Zhihui , Zhang Zhenfeng , Liu Yangang , Zhang Wanbin . Development of the Asymmetric Hydrogenation of Enol Esters[J]. Chinese Journal of Organic Chemistry, 2016 , 36(3) : 447 -459 . DOI: 10.6023/cjoc201512009
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