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Regioselective 1,2-carbosulfenylation of unactivated alkenes via directed nickel catalysis

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成果类型:
期刊论文
作者:
Zhu, Lin;Meng, Xiao;Xie, Leipeng;Shen, Qiuyang;Li, Wenyi;...
通讯作者:
Wang, C
作者机构:
[Zhang, Lanlan; Zhu, Lin; Wang, C; Wang, Chao; Xie, Leipeng; Shen, Qiuyang; Meng, Xiao] Tianjin Normal Univ, Coll Chem, Tianjin Key Lab Struct & Performance Funct Mol, Tianjin 300387, Peoples R China.
[Li, Wenyi] Hengyang Normal Univ, Coll Chem & Mat Sci, Hengyang 421000, Peoples R China.
通讯机构:
[Wang, C ] T
Tianjin Normal Univ, Coll Chem, Tianjin Key Lab Struct & Performance Funct Mol, Tianjin 300387, Peoples R China.
语种:
英文
期刊:
Organic Chemistry Frontiers
ISSN:
2052-4110
年:
2022
卷:
9
期:
11
页码:
3068-3074
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21901185, 22002037]; Tianjin Normal University
机构署名:
本校为其他机构
院系归属:
化学与材料科学学院
摘要:
A bidentate directing group-assisted Ni-catalyzed three component 1,2-carbosulfenylation of unactivated alkenes with aryl/alkenylboronic acids and disulfide electrophiles is reported. The reaction affords the desired products with high levels of chemo- and regioselectivity. A wide range of aryl groups and sulfur moieties can be simultaneously installed in both internal and terminal homoallylic amines with excellent functional group tolerance. Notably, the alkene substrates with a chiral center at the α-position furnish α,γ-dibranched thiolam...

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