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Redox-triggered hydroarylation of o-(hydroxyalkyl)arylalkynes with arylsulfonyl chlorides using visible light catalysis

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成果类型:
期刊论文
作者:
Song, Renjie;Xia, Jiadong;Yu, Jiangxi*;Li, Jinheng*
通讯作者:
Yu, Jiangxi;Li, Jinheng
作者机构:
[Song, Renjie; Li, Jinheng; Yu, Jiangxi; Xia, Jiadong; Yu, JX; Li, JH] State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China.
[Song, Renjie; Li, Jinheng; Yu, Jiangxi; Xia, Jiadong; Yu, JX; Li, JH] Hunan Univ, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China.
[Yu, Jiangxi] Coll Hunan Prov, Key Lab Funct Organometall Mat, Hengyang 421008, Peoples R China.
[Yu, Jiangxi] Hengyang Normal Univ, Coll Chem & Mat Sci, Hengyang 421008, Peoples R China.
通讯机构:
[Yu, JX; Li, JH] S
[Yu, JX; Li, JH; Yu, Jiangxi] H
[Yu, Jiangxi] C
State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China.
Hunan Univ, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China.
语种:
英文
关键词:
hydroarylation;redox;visible light catalysis;alkynes;arylsulfonyl chlorides
关键词(中文):
氧化还原引发;芳基磺酰氯;羟烷基;光催化;氧化还原反应;合成方法;催化方法;自由基
期刊:
中国科学:化学英文版
ISSN:
1674-7291
年:
2016
卷:
59
期:
2
页码:
184-189
基金类别:
This work was supported by the National Natural Science Foundation of China (21402046, 21172060, 21472039), and the Fundamental Research Funds for the Central Universities. Dr. Renjie Song also thanks the Fundamental Research Funds for the Central Universities.
机构署名:
本校为通讯机构
院系归属:
化学与材料科学学院
摘要:
A new radical-mediated method for the synthesis of 1-(2-(1,2-diarylvinyl)phenyl)ethan-1-ones by the redox hydroarylation of o-(hydroxyalkyl)arylalkynes with arylsulfonyl chlorides is described. This visible light catalysis method proceeds via a sequence of the radical addition of aryl group across the C-C triple bond, protonation and redox reaction, and represents a new redox transformation ...
摘要(中文):
为 1-(2-(1,2-diarylvinyl ) 苯基) 的合成的一个新调停激进分子的方法由 o-(hydroxyalkyl ) 的氧化还原作用 hydroarylation 的 ethan-1-ones 有 arylsulfonyl 氯化物的 arylalkynes 被描述。这个可见轻催化作用方法越过 C-C 三倍的契约, protonation 和氧化还原作用反应经由芳基组的激进的增加的一个序列继续,并且代表一个附近的氢氧根组指导的新氧化还原作用转变反应。

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