Cycloaddition Reactions of Carbonyl Ylides Derived From Enones

被引：2

作者：

Yu, Yang ^{[1
,2
]}

Cornelissen, Loic ^{[1
,2
,3
]}

Wong, Wing-Tak ^{[1
,2
]}

Chiu, Pauline ^{[1
,2
]}

机构：

[1] Univ Hong Kong, Dept Chem, Hong Kong, Hong Kong, Peoples R China

[2] Univ Hong Kong, State Lab Synthet Chem, Hong Kong, Hong Kong, Peoples R China

[3] Catholic Univ Louvain, Dept Organ & Med Chem, Louvain La Neuve, Belgium

来源：

SYNLETT | 2015年 / 26卷 / 11期

关键词：

carbenoids; ylides; cycloaddition; diazo compounds; domino reaction; BETA-KETO-ESTERS; 1,3-DIPOLAR CYCLOADDITIONS; ACID-A; CYCLIZATION; CASCADE; TANDEM; CARBENOIDS; CYCLOISOMERIZATIONS; KOMAROVIQUINONE; CONSTRUCTION;

D O I：

10.1055/s-0034-1379926

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The formation of unsaturated carbonyl ylides via rhodium-catalyzed carbene cyclization with enones and their subsequent inter- and intramolecular cycloadditions to construct functionalized oxapolycyclic rings have been realized.

引用

页码：1553 / 1556

页数：4

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