Asymmetric hydrogenation of alkyl(vinyl)thioethers: a promising approach to α-chiral thioethers
摘要:
This paper describes the enantio selective hydrogenation of vinylthioethers. We show that thioether derivatives of maleic esters can be hydrogenated with full conversion and up to 60% ee, and that alpha-thioether cinnamic acids can be hydrogenated in 51% ee with modest conversion. (c) 2007 Elsevier Ltd. All rights reserved.
Asymmetric hydrogenation of alkyl(vinyl)thioethers: a promising approach to α-chiral thioethers
摘要:
This paper describes the enantio selective hydrogenation of vinylthioethers. We show that thioether derivatives of maleic esters can be hydrogenated with full conversion and up to 60% ee, and that alpha-thioether cinnamic acids can be hydrogenated in 51% ee with modest conversion. (c) 2007 Elsevier Ltd. All rights reserved.
Asymmetric hydrogenation of alkyl(vinyl)thioethers: a promising approach to α-chiral thioethers
作者:Alex F. Meindertsma、Michael M. Pollard、Ben L. Feringa、Johannes G. de Vries、Adriaan J. Minnaard
DOI:10.1016/j.tetasy.2007.11.020
日期:2007.12
This paper describes the enantio selective hydrogenation of vinylthioethers. We show that thioether derivatives of maleic esters can be hydrogenated with full conversion and up to 60% ee, and that alpha-thioether cinnamic acids can be hydrogenated in 51% ee with modest conversion. (c) 2007 Elsevier Ltd. All rights reserved.