Optimised Dynamic Kinetic Resolution of benzoin by a chemoenzymatic approach in 2-MeTHF

被引:36
|
作者
Hoyos, Pilar [1 ]
Alberto Quezada, M. [2 ]
Vicente Sinisterra, Jose [1 ,3 ]
Alcantara, Andres R. [1 ]
机构
[1] Univ Complutense Madrid, Biotransformat Grp, Organ & Pharmaceut Chem Dept, Fac Pharm, E-28040 Madrid, Spain
[2] Natl Univ Trujillo Peru, Chem Engn Fac, Biotransformat & Nat Prod Grp, Trujillo, Peru
[3] Sci Pk Madrid Tres Cantos, Ind Biotransformat Unit, Madrid 28760, Spain
关键词
Benzoin; Dynamic Kinetic Resolution; 2-MeTHF; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE REDUCTION; ENZYMATIC RESOLUTION; GREEN CHEMISTRY; LIPASE; KETONES; ACYLATIONS; CATALYSIS; ACYLOINS; ACCESS;
D O I
10.1016/j.molcatb.2011.04.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Different influential parameters in the Dynamic Kinetic Resolution of racemic benzoin via lipase-ruthenium catalyst enantioselective transesterification have been improved in order to develop a more productive process. In this sense, 2-Methyltetrahydrofuran (2-MeTHF) is proposed as an excellent and greener substitute of THF for this biotransformation: on the other hand, by scaling up the reaction, much better results were obtained by using a much simpler one-pot methodology (compared to the previously described three-steps protocol), resulting not only in higher amounts of enantiopure product (85% conversion, >99% ee of the product), but also in an enhanced sustainability of the process, because lower acyl donor concentrations and lower ruthenium catalyst amounts (protected from oxygen deactivation) are required. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:20 / 24
页数:5
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