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Copper‐Catalyzed Asymmetric Radical 1,2‐Alkylesterification of 1,3‐Dienes with Cycloalkyl Hydroperoxides and Acids

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成果类型:
期刊论文
作者:
Li, Tian-Tian;Cheng, Ying;Xiao, Wen-Jing;Shi, De-Qing*;Chen, Jia-Rong
通讯作者:
Shi, De-Qing;Chen, JR
作者机构:
[Cheng, Ying; Xiao, Wen-Jing; Chen, Jia-Rong; Shi, De-Qing; Li, Tian-Tian; Chen, JR] Cent China Normal Univ, Coll Chem, Engn Res Ctr Photoenergy Utilizat Pollut Control &, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China.
[Xiao, Wen-Jing] Shanghai Inst Organ Chem, State Key Lab Organometall Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China.
通讯机构:
[Shi, DQ; Chen, JR ] C
Cent China Normal Univ, Coll Chem, Engn Res Ctr Photoenergy Utilizat Pollut Control &, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China.
语种:
英文
关键词:
copper catalysis;C-O coupling;alkyl hydroperoxides;radical reaction;1,3-dienes
期刊:
ChemCatChem
ISSN:
1867-3880
年:
2023
卷:
15
期:
23
页码:
e202301068-
基金类别:
<italic>We are grateful to the financial support from the Nation Key Ramp;D Program of China (2022YFA1506100), the National Natural Science Foundation of China (21971081, 22171099, 21820102003, 91956201, 22203034, 22271111, and 92256301), the Region Joint [2022YFA1506100]; Nation Key Ramp;D Program of China [21971081, 22171099, 21820102003, 91956201, 22203034, 22271111, 92256301]; National Natural Science Foundation of China [U21 A20384]; Region Joint Funds of the National Natural Science Foundation of China [jxsq2023102004]; Double-Thousand Talents Plan of Jiangxi Province [2021YB02, B17019]; Open Research Fund of School of Chemistry and Chemical Engineering, Henan Normal University
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
Radical Cross‐CouplingA copper‐catalyzed enantioselective three‐component radical relay 1,2‐alkylesterification of 1,3‐dienes using cycloalkyl hydroperoxides and carboxylic acids was reported. This protocol features broad substrate scope and good functional group tolerance with respect to each component, providing practical access to a variety of distally keto‐functionalized chiral allylic esters with high enantioselectivity under mild and redox‐neutral conditions. Abstract Transition‐metal‐catalyzed radical relay cross‐coupling react...

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