Intramolecular donor-acceptor cyclopropane ring-opening cyclizations

被引:639
|
作者
Cavitt, Marchello A. [1 ]
Phun, Lien H. [1 ]
France, Stefan [1 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
基金
美国国家科学基金会;
关键词
HOMO-NAZAROV; ELECTROPHILIC CYCLOPROPANES; SUBSTITUTED CYCLOPROPANES; OLEFIN PARTICIPATION; 3+2 CYCLOADDITION; CARBONYLS; FURAN; CONSTRUCTION; 1,1-DIESTERS; STRAIN;
D O I
10.1039/c3cs60238a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclization reactions of donor-acceptor (D-A) cyclopropanes are recognized as versatile methods for construction of carbocyclic and heterocyclic scaffolds. In the literature, many examples of these polarized cyclopropanes' reactivity with nucleophiles, electrophiles, and radicals are prevalent. Although intermolecular reactivity of donor-acceptor cyclopropanes is widely reported, reviews that center on their intramolecular chemistry are rare. Thereupon, this tutorial review focalizes on new intramolecular transformations of donoracceptor cyclopropanes for cycloisomerizations, formal cycloadditions, umpolung reactions, rearrangements and ring opening lactonizations/lactamizations from 2009 to 2013. Furthermore, the role of D-A acceptor cyclopropanes as reactive subunits in natural product synthesis is underscored.
引用
收藏
页码:804 / 818
页数:15
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