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Intramolecular Direct C-H Arylation via a Metallocenic Radical Pathway: Stereospecific Approach to Planar-Chiral Ferrocenes
被引:18
作者:

Liu, Yang
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机构: Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China

Xu, Jiancong
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机构: Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China

Zhang, Jinling
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机构: Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China

Xu, Xiaohua
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机构:
Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China

Jin, Zhong
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Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China
机构:
[1] Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China
基金:
中国国家自然科学基金;
关键词:
ENANTIOSELECTIVE SYNTHESIS;
ASYMMETRIC CATALYSIS;
COUPLING REACTIONS;
ELECTRON-TRANSFER;
CARBON-CARBON;
ARYL HALIDES;
LIGANDS;
BUTOXIDE;
PHENANTHRIDINONES;
ORGANOCATALYST;
D O I:
10.1021/acs.orglett.7b02995
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Transition metal-free synthesis of planar-chiral 1,2-fused ferrocenes via intramolecular direct C-H bond arylation was achieved. The C-H arylation reactions promoted by a catalytic amount of 1,10-phenanthroline highlighted a unique planar-chiral metallocenic radical intermediate, generated from iodoferrocenes via a single-electron transfer process.
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页码:5709 / 5712
页数:4
相关论文
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