Transition Metal Catalyzed Alkene and Alkyne Hydroacylation

被引:645
作者
Willis, Michael C. [1 ]
机构
[1] Univ Oxford, Dept Chem, Chem Res Lab, Oxford OX1 3TA, England
基金
英国工程与自然科学研究理事会;
关键词
CHELATION-ASSISTED HYDROACYLATION; C BOND ACTIVATION; DENSITY-FUNCTIONAL COMPUTATIONS; ONE-POT SYNTHESIS; SELECTIVE INTERMOLECULAR HYDROACYLATION; ASYMMETRIC CYCLIZATION REACTIONS; REDUCTIVE ALDOL REACTIONS; ALDEHYDE OXIDATION LEVEL; S-SUBSTITUTED ALDEHYDES; CARBON TRIPLE BOND;
D O I
10.1021/cr900096x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Several researchers conducted studies to demonstrate metal catalyzed alkene and alkyne hydrocylation. A team of researchers developed a method for the synthesis of cyclooctenones using the intramolecular hydrogenation. Eight-membered ring formation was achieved by the incorporation of a cyclopropane ring in the substrate to demonstrate metal catalyzed alkene and alkyne hydrocylation. The key step of the method involved the fragmentation and isomerization of rhodacycle 25 into ring-expanded rhodacycle 26. The researchers investigated the reactions of the two isomers of a deuterium-labeled substrate to explore the mechanism in operation. Another team of researchers prepared a series of medium-ring sulfur heterocycles using intramolecular hydroacylation to demonstrate the investigations.
引用
收藏
页码:725 / 748
页数:24
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