Department of Chemistry, School of Sciences, Gujarat University, Ahmedabad, Gujarat, 380009, India.
Mol Divers. 2017 Nov;21(4):1011-1020. doi: 10.1007/s11030-017-9756-5. Epub 2017 Jun 15.
Herein, we report a facile method for the alkenylation of a 4-thiazolidinone motif without using external acid and high-pressure gas, which are required in conventional Fujiwara-Moritani reactions. Mild reaction conditions, one-pot synthesis, and utilization of an oxidant made this process more feasible in comparison with previously reported methods. Functionalization of the slightly more acidic [Formula: see text] C-H bond with the less acidic [Formula: see text] C-H bond yielded the alkenylated motif. This pathway opens new possibilities for organic synthesis.
在此,我们报告了一种无需使用传统 Fujiwara-Moritani 反应所需的外部酸和高压气体的简便方法,用于 4-噻唑烷酮基序的烯基化反应。与之前报道的方法相比,温和的反应条件、一锅合成和氧化剂的使用使该过程更具可行性。与稍酸性的[化学式:见正文]C-H 键相比,利用酸性较弱的[化学式:见正文]C-H 键进行功能化,生成了烯基化基序。这条途径为有机合成开辟了新的可能性。