2(5H)-呋喃酮|金属催化|偶联反应|Sonogashira反应|Suzuki反应|Michael加成反应

Chin. J. Org. Chem. ›› 2011, Vol. 31 ›› Issue (9): 1377-1387. Previous Articles Next Articles

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金属催化的2(5H)-呋喃酮反应研究进展

毛超旭，汪朝阳*，谭越河，薛福玲

(华南师范大学化学与环境学院广州 510006)

收稿日期:2010-11-21 修回日期:2011-01-24 发布日期:2011-02-25
通讯作者: 汪朝阳 E-mail:wangwangzhaoyang@tom.com

2(5H)-呋喃酮|金属催化|偶联反应|Sonogashira反应|Suzuki反应|Michael加成反应

MAO Chao-Xu, WANG Chao-Yang, TAN Yue-He, XUE Fu-Ling

(School of Chemistry and Environment, South China Normal University, Guangzhou 510006)

Received:2010-11-21 Revised:2011-01-24 Published:2011-02-25
Contact: Zhaoyang Wang E-mail:wangwangzhaoyang@tom.com

The unique carbon skeleton of 2(5H)-furanone is widely present in a variety of natural products, and many compounds containing 2(5H)-furanone skeleton are important synthetic intermediates. Recently, more and more attentions have been attracted to the organic synthesis based on 2(5H)-furanones, especially via the metal-catalyzed reactions of 2(5H)-furanones. Classified as different types, the recent progress in metal-catalyzed reactions of 2(5H)-furanones, mainly including Sonogashira reaction, Suzuki reaction, Stille reaction, Michael addition, Friedel-Crafts al-kylation, Baylis-Hillman reaction, nucleophilic substitution, and reduction reaction, are reviewed in this pa-per.

Key words: 2(5H)-furanone, metal-catalyzed, coupling reaction, Sonogashira reaction, Suzuki reaction, Michael addition reaction

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金属催化的2(5H)-呋喃酮反应研究进展

2(5H)-呋喃酮|金属催化|偶联反应|Sonogashira反应|Suzuki反应|Michael加成反应

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