Stereoselective transition metal-catalysed higher-order carbocyclisation reactions

被引:259
|
作者
Inglesby, Phillip A. [1 ]
Evans, P. Andrew [1 ]
机构
[1] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
基金
英国工程与自然科学研究理事会;
关键词
INTRAMOLECULAR 2+2+2 CYCLOADDITION; QUATERNARY CARBON STEREOCENTERS; TITANIUM ARYLOXIDE COMPOUNDS; ETHYL CYCLOPROPYLIDENEACETATE; CARBOCYCLIZATION REACTIONS; ENANTIOSELECTIVE CONSTRUCTION; NORBORNADIENE-BUTADIENE; UNSYMMETRICAL ALKYNES; 3+2+2 COCYCLIZATION; 8-MEMBERED RINGS;
D O I
10.1039/b913110h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal-catalysed higher-order carbocyclisation reactions represent an important class of reactions due to their ability to construct complex polycyclic systems in a highly selective and atom-economical fashion. A key and striking feature with these transformations is the dichotomy in reactivity that a substrate displays with different transition metal complexes, which is akin to the manner enzymes direct terpene biosynthesis. This tutorial review details the historical development of higher-order carbocyclisation reactions, specifically the variants of [m + 2 + 2] that involve carbon-based pi-systems, where m = 2, 3 and 4, in the context of critical developments with various transition metal complexes.
引用
收藏
页码:2791 / 2805
页数:15
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