Department of Chemistry , The University of Texas at San Antonio , San Antonio , Texas 78249 , United States.
J Am Chem Soc. 2018 Jul 11;140(27):8434-8438. doi: 10.1021/jacs.8b05421. Epub 2018 Jun 26.
Conjugated dienes and polyenes are typically synthesized by sequential introduction of C═C bonds. Here, we report a practical and scalable, catalytic dienylation that is highly regio- and stereoselective for both C═C bonds. The reaction is enabled by a stereoselective palladium-catalyzed cross-coupling that is preceded by a regioselective base-induced ring opening of readily available sulfolenes. The dienylation reaction is particularly useful for the synthesis of synthetically challenging dienes containing cis double bonds. We also show that the reaction can serve as a synthetic platform for the construction of conjugated polyenes.
共轭二烯和多烯通常通过顺序引入 C═C 键来合成。在这里,我们报告了一种实用且可扩展的催化二烯化反应,该反应对两个 C═C 键具有高度的区域和立体选择性。该反应是通过立体选择性钯催化交叉偶联来实现的,该偶联反应之前是通过区域选择性碱诱导的易得的砜的开环反应。该二烯化反应对于含有顺式双键的合成具有挑战性的二烯的合成特别有用。我们还表明,该反应可以作为构建共轭多烯的合成平台。