期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 6, 页码 1814-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja077948e
关键词
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A novel concept of Au-containing all-carbon 1,n-dipoles is advanced. From 1-(1-alkynyl) cyclopropyl ketones, Au-containing all-carbon 1,4-dipoles are presumably generated in situ and can efficiently participate in [4 + 2] annulation with dipolarophiles including indoles, various carbonyl compounds, imines, and silyl enol ethers. Polycyclic, fully substituted furans are readily synthesized under mild reaction conditions.
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