C-H functionalization logic in total synthesis

被引:1135
作者
Gutekunst, Will R. [1 ]
Baran, Phil S. [1 ]
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
关键词
ENANTIOSELECTIVE TOTAL-SYNTHESIS; (+/-)-PENTALENOLACTONE-E METHYL-ESTER; ENANTIOSPECIFIC TOTAL-SYNTHESIS; BOND ACTIVATION; ORGANIC-SYNTHESIS; CELOGENTIN C; INTRAMOLECULAR ALKYLATION; PHOTOCHEMICAL REACTION; NOMINAL DIAZONAMIDES; EUDESMANE TERPENES;
D O I
10.1039/c0cs00182a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this critical review, the strategic and economic benefits of C-H functionalization logic will be analyzed through the critical lens of total synthesis. In order to illustrate the dramatically simplifying effects this type of logic can potentially have on synthetic planning, we take the reader through a series of case studies in which it has already been successfully applied. In the first section, a chronological look at key historical syntheses will be examined, leading into modern day examples. In the second section, our own experience with applying and executing synthesis with a C-H functionalization "mindset'' will be discussed (114 references).
引用
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页码:1976 / 1991
页数:16
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