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作 者:Qishun Liu Yufen Lv Ruisheng Liu Xiaohui Zhao Jiawen Wang Wei Wei
机构地区:[1]School of Chemistry and Chemical Engineering,Qufu Normal University,Qufu 273165,China [2]Qinghai Provincial Key Laboratory of Tibetan Medicine Research and Key Laboratory of Tibetan Medicine Research,Northwest Institute of Plateau Biology,Chinese Academy of Sciences,Qinghai 810008,China [3]College of Chemistry and Chemical Engineering,Shenyang Normal University,Shenyang 110034,China
出 处:《Chinese Chemical Letters》2021年第1期136-139,共4页中国化学快报(英文版)
基 金:supported by the International Cooperation Project of Qinghai Province(No.2018-HZ-806);the Youth Innovation and Technology Project of Higher School in Shandong Province(No.2019KJC021);the Natural Science Foundation of Shandong Province(No.ZR2018MB009);the Qinghai Key Laboratory of Tibetan Medicine Research(No.2017ZJ-Y11);CAS“Light of West China”Program 2018;Entrepreneurship Training Program for College Students(No.201910049)。
摘 要:A convenient and regioselective sulfonylation/cyclization of 1,6-enynes with arylazo sulfones has been developed to access a series of sulfonylated γ-butyrolactams.The present reaction could be efficiently conducted under catalyst-and additive-free conditions,in which C-S and C-C bonds were selectively constructed in one-pot procedure.
关 键 词:CATALYST-FREE Arylazo sulfones 1 6-Enynes Sulfonylatedγ-butyrolactams
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