环加成
化学
双环分子
催化作用
Pauson–Khand反应
全合成
烯类反应
天然产物
倍半萜
立体化学
药物化学
组合化学
有机化学
作者
Lei Jiao,Mu Lin,Liangang Zhuo,Zhi‐Xiang Yu
出处
期刊:Organic Letters
[American Chemical Society]
日期:2010-05-13
卷期号:12 (11): 2528-2531
被引量:129
摘要
A novel Rh(I)-catalyzed [(3 + 2) + 1] cycloaddition, which can be regarded as a homologous Pauson−Khand reaction, was developed to synthesize bicyclic cyclohexenones and cyclohexanones, enabling a new approach for synthesis of six-membered carbocycles ubiquitously found in natural products and pharmaceutics. The significance of the Rh-catalyzed [(3 + 2) + 1] cycloaddition has been demonstrated by the total synthesis of a furanoid sesquiterpene natural product, α-agarofuran, in which the bicyclic skeleton was constructed by the [(3 + 2) + 1] reaction of 1-yne-VCP and CO.
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