C-H nitrogenation and oxygenation by ruthenium catalysis

被引:356
作者
Thirunavukkarasu, Vedhagiri S. [1 ]
Kozhushkov, Sergei I. [1 ]
Ackermann, Lutz [1 ]
机构
[1] Univ Gottingen, Inst Organ & Biomol Chem, D-37077 Gottingen, Germany
基金
欧洲研究理事会;
关键词
INTRAMOLECULAR PROTON-TRANSFER; CARBON-CARBON BONDS; DIRECT ARYLATIONS; DIRECT AMINATION; ATOM-TRANSFER; MECHANISTIC INSIGHT; CHIRAL RUTHENIUM; TRANSITION; PALLADIUM; AMIDATION;
D O I
10.1039/c3cc47028h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Remarkable recent progress has been accomplished in direct C-H functionalizations for the formation of C-N and C-O bonds through the use of readily accessible ruthenium catalysts. Particularly, ruthenium(II) complexes allowed for challenging direct C(sp(2))-H hydroxylation of arenes. These catalysts set the stage for step-economical C-H functionalization with electron-rich as well as electron-deficient (hetero) arenes and, therefore, provided versatile access to diversely decorated phenols. While a number of synthetically useful protocols for ruthenium-catalyzed C(sp(3))-H bond nitrogenation have been elaborated, the analogous transformations of more stable C(sp(2))-H bonds were very recently achieved.
引用
收藏
页码:29 / 39
页数:11
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