Recent advances in the synthesis of azaphenalene alkaloids: first enantioselective approaches

被引：0

作者：

Alujas-Burgos, Silvia ^{[1
]}

Bayon, Pau ^{[1
]}

Figueredo, Marta ^{[1
]}

机构：

[1] Univ Autonoma Barcelona, Dept Quim, Bellaterra 08193, Spain

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2018年 / 16卷 / 37期

关键词：

COCCINELLINE; COLEOPTERA; STRATEGY; BEETLE; 6-PI-AZAELECTROCYCLIZATION; PRECOCCINELLINE; DERIVATIVES; HIPPODAMINE; ARTHROPODS; SKELETON;

D O I：

10.1039/c8ob01443d

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Azaphenalene alkaloids are biosynthesised and segregated by diverse insects of the Coccinellidae family (ladybirds) and are believed to play an important role in the defensive mechanism against their natural predators. The particular unique framework of these alkaloids, along with their potential in the field of biological pest control, has led to several research groups developing synthetic sequences to prepare these compounds. The main purpose of the present review is to provide an update of the more recent synthetic progress towards these alkaloids, including the pioneering enantioselective approaches to chiral congeners.

引用

页码：8218 / 8229

页数：12

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