Tian Pan-Pan, Cai Sai-Hu, Liang Qiu-Ju, Zhou Xing-Yi, Xu Yun-He, Loh Teck-Peng
†Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026, China.
‡Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.
Org Lett. 2015 Apr 3;17(7):1636-9. doi: 10.1021/acs.orglett.5b00272. Epub 2015 Mar 19.
An efficient Pd(II)-catalyzed difunctionalization reaction of internal alkynes is reported. In this reaction, various enynoates and electron-deficient alkenes were used for the syntheses of useful highly substituted pyrone derivatives via a 6-endo cyclization and subsequent alkenylation pathway. The corresponding products could be obtained in moderate to good yields under very mild reaction conditions. The high regioselectivity and wide compatibility with different functional groups found in the desired products demonstrate this method to be a general and useful tool for the synthesis of highly substituted pyrone derivatives.
报道了一种高效的钯(II)催化的内炔双官能化反应。在该反应中,各种烯炔酸酯和缺电子烯烃通过6-内型环化及随后的烯基化途径用于合成有用的高度取代的吡喃酮衍生物。在非常温和的反应条件下可获得中等至良好产率的相应产物。所需产物中发现的高区域选择性和与不同官能团的广泛兼容性表明该方法是合成高度取代的吡喃酮衍生物的通用且有用的工具。