Biocatalysed olefin reduction of 3-alkylidene oxindoles by baker's yeast

被引:10
|
作者
Rossetti, Arianna [1 ]
Sacchetti, Alessandro [1 ,2 ]
Bonfanti, Marta [1 ]
Roda, Gabriella [3 ]
Rainoldi, Giulia [4 ]
Silvani, Alessandra [4 ]
机构
[1] Politecn Milan, Dipartimento Chim Mat & Ingn Chim C Natta, Pzza Leonardo,Vinci 32, I-20133 Milan, Italy
[2] Local Unit Politecn Milano, Natl Consortium Mat Sci & Technol, INSTM, Piazza Leonardo,Vinci 32, I-20133 Milan, Italy
[3] Univ Milan, Dipartimento Sci Farmaceut, Via Mangiagalli 25, I-20133 Milan, Italy
[4] Univ Milan, Dipartimento Chim, Via C Golgi 19, I-20133 Milan, Italy
关键词
Biocatalysis; Baker's yeast; Oxindole; Reduction; Molecular docking; ENANTIOSELECTIVE REDUCTION; ANTIMICROBIAL ACTIVITY; ALKALOIDS; DERIVATIVES; ISATIN; SPIROOXINDOLES; INHIBITORS; SCAFFOLDS; AGENTS;
D O I
10.1016/j.tet.2017.06.022
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
3-Substituted oxindoles are very interesting molecules both for their potential biological activity and for their role as starting materials toward more complex oxindole-based structures. These molecules can be prepared by the reduction of a 3-ylidene oxindole precursor by classical metal-catalysed chemical reductions of the olefin. In this work we present a biocatalytic approach for the reduction of oxindolebased olefins using baker's yeast. All the substrates were efficiently reduced in high yields. When an alpha,beta-unsaturated ketone was used, the corresponding saturated alcohol was obtained in high yield and ee. To further investigate the enzyme-substrate interactions a molecular docking study was also performed. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4584 / 4590
页数:7
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