Group 6 Dihapto-Coordinate Dearomatization Agents for Organic Synthesis

被引:139
作者
Liebov, Benjamin K. [1 ]
Harman, W. Dean [1 ]
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
基金
美国国家科学基金会;
关键词
ELECTROPHILIC ADDITION-REACTIONS; DIELS-ALDER REACTIONS; ETA(2)-COORDINATED FURAN COMPLEXES; TANDEM 1,4-ADDITION REACTIONS; HYDROGEN-BOND ACTIVATION; C-H BONDS; TRANSITION-METAL; CYCLOADDITION REACTIONS; CRYSTAL-STRUCTURE; ETA(2)-THIOPHENE COMPLEXES;
D O I
10.1021/acs.chemrev.7b00480
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This review covers publications ranging from 2005 to 2017 concerning the organic reactions of aromatic ligands eta(2)-coordinated to tungsten or molybdenum and the use of these reactions in the synthesis of novel organic substances. An emphasis is placed on C-C bond-forming reactions using conventional building blocks of organic synthesis such as acetals, enolates, Michael acceptors, acylating reagents, and activated aromatics. Substrates activated by the metal include arenes, pyridines, pyrroles, pyrimidines, furans, and thiophenes. General reactivity patterns are elucidated, as well as stereochemical preferences. These trends are compared to those of osmium and rhenium forebears as well as to the reactivity patterns of other methods of stoichiometric transition-metal-based dearomatization (i.e., eta(6)-arene complexes).
引用
收藏
页码:13721 / 13755
页数:35
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