Rh(I)-Catalyzed [(3+2)+1] Cycloaddition of 1-Yne/Ene-vinylcyclopropanes and CO: Homologous Pauson-Khand Reaction and Total Synthesis of (±)-α-Agarofuran

被引:109
作者
Jiao, Lei [1 ]
Lin, Mu [1 ]
Zhuo, Lian-Gang [1 ]
Yu, Zhi-Xiang [1 ]
机构
[1] Peking Univ, BNLMS, Coll Chem, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China
关键词
DIELS-ALDER REACTIONS; DONOR-ACCEPTOR CYCLOPROPANES; ALPHA-AGAROFURAN; ENE-VINYLCYCLOPROPANES; BETA-AGAROFURAN; MECHANISM; ALKYNES; SESQUITERPENOIDS; 1,3-DIENES; ALDEHYDES;
D O I
10.1021/ol100625e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
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, a-agarofuran, in which the bicyclic skeleton was constructed by the [(3 + 2) + 1] reaction of 1-yne-VCP and CO.
引用
收藏
页码:2528 / 2531
页数:4
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