Lipase-catalyzed regioselective domino reaction for the synthesis of chromenone derivatives

被引：7

作者：

Yang, Qi ^{[1
]}

Zhou, Long-Hua ^{[1
]}

Wu, Wan-Xia ^{[1
]}

Zhang, Wei ^{[1
]}

Wang, Na ^{[1
]}

Yu, Xiao-Qi ^{[1
]}

机构：

[1] Sichuan Univ, Key Lab Green Chem & Technol, Minist Educ, Coll Chem, Chengdu 610064, Peoples R China

来源：

RSC ADVANCES | 2015年 / 5卷 / 96期

基金：

中国国家自然科学基金;

关键词：

BIOCATALYTIC PROMISCUITY; ALDOL REACTION; ALDEHYDES;

D O I：

10.1039/c5ra13267c

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

An efficient synthesis of 2H-chromenones and 2-hydroxyl-2H-chromenones derivatives has been developed from 1,3-dicarbonyls and alpha,beta-unsaturated aldehydes by a controllable regioselective domino cyclization reaction under catalysis of different lipases. 2H-Chromenones derivatives were synthesized by bovine pancreatic lipase (BPL) in acetonitrile, while lipase from Pseudomonas fluorescens (PFL) can catalyze the synthesis of the 2-hydroxyl-2H-chromenones derivatives in dichloromethane with moderate to high yields.

引用

页码：78927 / 78932

页数：6

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