Chemical Engineering College, Nanjing University of Science and Technology , Nanjing 210094, China.
Org Lett. 2016 Dec 16;18(24):6424-6427. doi: 10.1021/acs.orglett.6b03324. Epub 2016 Dec 8.
Transition-metal-free radical access to 1,4-benzothiazine derivatives from o-aminobenzenethiols is disclosed. This procedure is available for various ketones including α,β-unsaturated, cyclic, linear, and fluoroalkyl ketones to generate a number of 1,4-benzothiazines, which exist in numerous bioactive and natural molecules, rendering this protocol attractive to both synthetic and medicinal chemistry.
本文公开了一种从邻氨基苯硫醇到 1,4-苯并噻嗪衍生物的过渡金属自由基方法。该方法适用于各种酮,包括α,β-不饱和、环状、直链和氟烷基酮,以生成许多 1,4-苯并噻嗪,这些化合物存在于许多生物活性和天然分子中,这使得该方法对合成化学和药物化学都具有吸引力。