The Baldwin rules: revised and extended

被引:140
作者
Gilmore, Kerry [1 ]
Mohamed, Rana K. [2 ]
Alabugin, Igor V. [2 ]
机构
[1] Max Planck Inst Colloids & Interfaces, Dept Biomol Syst, Potsdam, Germany
[2] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
基金
美国国家科学基金会;
关键词
INTRAMOLECULAR ORGANOMETAL-ACETYLENE; RADICAL TRANSLOCATION REACTIONS; TRANSITION-STATE STABILIZATION; FREE CLICK CHEMISTRY; RING-CLOSURE; 1,3-DIPOLAR CYCLOADDITIONS; BERGMAN CYCLIZATION; COPPER-FREE; AB-INITIO; ELECTROPHILIC CYCLIZATION;
D O I
10.1002/wcms.1261
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Baldwin rules constitute one of the clearest examples of the success which can be obtained through the application of stereoelectronic concepts to reaction design. With thousands of examples, the predictive power of these rules is inarguable. However, time has revealed a number of exceptions and gray areas within these rules, leading to extensions and revisions. In this review, we will present an overview of how subsequent studies of ring closure have clashed with several of Baldwin's predictions, leading to the revision of some classes of ring closure (alkyne cyclizations, electrophilic closures, etc.). We also discuss for which the original rules were vague (epoxides) or absent (promoted cyclizations), and the evidence revealed since Baldwin's work that has allowed for a better understanding of these ambiguities. With the concise summation of these amendments, this review aims to present an overview of the understanding of cyclization reactions to date. (C) 2016 John Wiley & Sons, Ltd
引用
收藏
页码:487 / 514
页数:28
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