Abstract
A series of optically active β-aryloxy alcohols and β-arylthiol alcohols were synthesized directly by asymmetric transfer hydrogenation of the corresponding β-carbonyl ethers or β-carbonyl sulfides in excellent yields (up to 99%) and excellent enantioselectivity (up to 100% ee) under mild reaction conditions.
Keywords: Asymmetric transfer hydrogenation, β-aryloxy alcohols, β-arylthiol alcohols, β-ketosulfide, β-ketoether, esters, hydrogen, ketones, phenylethanone, sulfides
Letters in Organic Chemistry
Title: Synthesis of Optically Active β-Aryloxy Alcohols and β-Arylthiol Alcohols via Asymmetric Transfer Hydrogenation Reaction
Volume: 8 Issue: 10
Author(s): Zhou Xu, Wei Yin, Nan Wu, Jingjing Shi, Ting Liu, Yu Wan and Hui Wu
Affiliation:
Keywords: Asymmetric transfer hydrogenation, β-aryloxy alcohols, β-arylthiol alcohols, β-ketosulfide, β-ketoether, esters, hydrogen, ketones, phenylethanone, sulfides
Abstract: A series of optically active β-aryloxy alcohols and β-arylthiol alcohols were synthesized directly by asymmetric transfer hydrogenation of the corresponding β-carbonyl ethers or β-carbonyl sulfides in excellent yields (up to 99%) and excellent enantioselectivity (up to 100% ee) under mild reaction conditions.
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Cite this article as:
Xu Zhou, Yin Wei, Wu Nan, Shi Jingjing, Liu Ting, Wan Yu and Wu Hui, Synthesis of Optically Active β-Aryloxy Alcohols and β-Arylthiol Alcohols via Asymmetric Transfer Hydrogenation Reaction, Letters in Organic Chemistry 2011; 8 (10) . https://dx.doi.org/10.2174/157017811799304197
DOI https://dx.doi.org/10.2174/157017811799304197 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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