Enzyme-Catalyzed Asymmetric Domino Thia-Michael/Aldol Condensation Using Pepsin

The novel catalytic promiscuity of pepsin from porcine gastric mucosa for the asymmetric catalysis of the domino thia-Michael/aldol condensation reaction in MeCN and buffer was discovered for the first time. Broad substrate specificity was tested, and a series of corresponding products were obtained...

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Veröffentlicht in:Journal of organic chemistry 2016-07, Vol.81 (14), p.6042-6048
Hauptverfasser: Xiang, Yang, Song, Jian, Zhang, Yong, Yang, Da-Cheng, Guan, Zhi, He, Yan-Hong
Format: Artikel
Sprache:eng
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Zusammenfassung:The novel catalytic promiscuity of pepsin from porcine gastric mucosa for the asymmetric catalysis of the domino thia-Michael/aldol condensation reaction in MeCN and buffer was discovered for the first time. Broad substrate specificity was tested, and a series of corresponding products were obtained with enantioselectivities of up to 84% ee. This specific catalysis was demonstrated by using recombinant pepsin and control experiments with denatured and inhibited pepsin. The reaction was also shown to occur in the active site by site-directed mutagenesis (the Asp32Ala mutant of pepsin), and a possible mechanism was proposed.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.6b01132