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Direct α-acyloxylation of organic sulfides with the hypervalent (diacyloxyiodo)benzene/tetra-n-butylammonium bromide (TBAB) reagent combination
Dan Zhu; Denghu Chang; Shaoyan Gan and Lei Shi*
刊名RSC Advances
2016
卷号Vol.6 No.33页码:27983-27987
ISSN号2046-2069
URL标识查看原文
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/1863996
专题南开大学
作者单位1.a Shenzhen Graduate School, Harbin Institute of Technology, Shenzhen 518055, China E-mail: lshi@hit.edu.cn
2.State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China Web: http://homepage.hit.edu.cn/pages/shilei
3.Institute of Organic Chemistry, The Academy of Fundamental and Interdisciplinary Sciences, Harbin Institute of Technology, Harbin 150080, China
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Dan Zhu,Denghu Chang,Shaoyan Gan and Lei Shi*. Direct α-acyloxylation of organic sulfides with the hypervalent (diacyloxyiodo)benzene/tetra-n-butylammonium bromide (TBAB) reagent combination[J]. RSC Advances,2016,Vol.6 No.33:27983-27987.
APA Dan Zhu,Denghu Chang,&Shaoyan Gan and Lei Shi*.(2016).Direct α-acyloxylation of organic sulfides with the hypervalent (diacyloxyiodo)benzene/tetra-n-butylammonium bromide (TBAB) reagent combination.RSC Advances,Vol.6 No.33,27983-27987.
MLA Dan Zhu,et al."Direct α-acyloxylation of organic sulfides with the hypervalent (diacyloxyiodo)benzene/tetra-n-butylammonium bromide (TBAB) reagent combination".RSC Advances Vol.6 No.33(2016):27983-27987.
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