Chemoselectivity and the Curious Reactivity Preferences of Functional Groups

被引:284
作者
Afagh, Nicholas A. [1 ]
Yudin, Andrei K. [1 ]
机构
[1] Univ Toronto, Dept Chem, Davenport Res Labs, Toronto, ON M5S 3H6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
chemical synthesis; chemoselectivity; functional groups; reaction mechanisms; synthesis design; CROSS-COUPLING REACTIONS; ALPHA-AMINO-ACIDS; C-H BONDS; GOLD-CATALYZED CYCLOISOMERIZATION; MANNICH-TYPE REACTIONS; LITHIUM ESTER ENOLATE; IN-SITU GENERATION; HIGHLY ENANTIOSELECTIVE SYNTHESIS; ASYMMETRIC TOTAL-SYNTHESIS; METAL-MEDIATED ZINCATION;
D O I
10.1002/anie.200901317
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Achieving high levels of chemoselectivity has been the Achilles' heel of chemical synthesis. The excitement generated by the successful realization of chemoselective strategies underscores the painstaking efforts to define a set of conditions conducive to selection among the available reaction pathways. We discuss in this Review various aspects of chemoselectivity that have been addressed in a range of synthetic methods over the past decade. We have focused on the proposed mechanistic basis of the reactions under consideration in an attempt to categorize them and highlight the key concepts that have been emerging on the basis of these studies. Our overview of recent advances in chemoselective processes suggests that significant progress has been made, but a lot of challenges lie ahead. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:262 / 310
页数:49
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