Gold-Catalyzed Regio- and Stereoselective Addition of Carboxylic Acids to Iodoalkynes: Access to (Z)-β-Iodoenol Esters and 1,4-Disubstituted (Z)-Enynyl Esters

详细信息    查看全文

• 作者：Pedro J. González-Liste ; Javier Francos ; Sergio E. García-Garrido ; Victorio Cadierno
• 刊名：Journal of Organic Chemistry
• 出版年：2017
• 出版时间：February 3, 2017
• 年：2017
• 卷：82
• 期：3
• 页码：1507-1516
• 全文大小：572K
• ISSN：1520-6904

文摘

In the presence of catalytic amounts of the Au(I) cation [Au(PPh₃)]⁺, a large variety of (Z)-β-iodoenol esters (39 examples) could be synthesized under mild reaction conditions through the regio- and stereospecific intermolecular addition of carboxylic acids to iodoalkynes. Sonogashira coupling of representative (Z)-β-iodoenol esters with terminal alkynes, alkynols, and 1,3-enynes allowed also the access to different 1,4-disubstituted (Z)-enynyl esters in excellent yields.