Recent Advances in Natural Products Synthesis Using Bifunctional Organocatalysts bearing a Hydrogen-Bonding Donor Moiety

被引：16

作者：

Odagi, Minami ^{[1
]}

Nagasawa, Kazuo ^{[1
]}

机构：

[1] Tokyo Univ Agr & Technol, Dept Biotechnol & Life Sci, 2-24-16 Naka Cho, Koganei, Tokyo 1848588, Japan

来源：

ASIAN JOURNAL OF ORGANIC CHEMISTRY | 2019年 / 8卷 / 10期

基金：

日本学术振兴会;

关键词：

Bifunctionality; Hydrogen-bonding Donor; Organocatalyst; Natural Product Synthesis; CARBON QUATERNARY STEREOCENTERS; ASYMMETRIC TOTAL-SYNTHESIS; ERGOT ALKALOIDS; CASCADE REACTIONS; RISHIRILIDE-B; CHEMISTRY; CONSTRUCTION; NARCICLASINE; DERIVATIVES; HALICLONIN;

D O I：

10.1002/ajoc.201900459

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Organocatalysis is widely used for the asymmetric synthesis of natural products and pharmaceuticals, and bifunctional organocatalysts are particularly effective for controlling stereochemistry. Here, we present an overview of natural products syntheses involving bifunctional catalysts bearing a hydrogen-bonding donor moiety reported during the last five years.

引用

页码：1766 / 1774

页数：9

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