Four Pathways in Radical Alkylation of Isocyanide with Simple Alcohol-Reference-Cited by-同舟云学术

Four Pathways in Radical Alkylation of Isocyanide with Simple Alcohol

Published:2019-05-09 Issue:13 Volume:361 Page:3086-3093
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Liu Shuai¹²,Fan Fenghua³,Wang Nengyong¹,Yuan Dandan¹,Wang Yaxin¹,Luo Zaigang²,Liu Zhong‐Quan¹³

Affiliation:

1. State Key Laboratory Cultivation Base for TCM Quality and Efficacy, College of PharmacyNanjing University of Chinese Medicine Nanjing 210023 People's Republic of China

2. College of Chemical EngineeringAnhui University of Science and Technology, Huainan Anhui 232001 People's Republic of China

3. State Key Laboratory of Applied Organic ChemistryLanzhou University Lanzhou 730000 People's Republic of China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201900221

Reference44 articles.

1. For reviews on selective functionalization of α-hydroxy C−H bond in alcohol see:

2. Direct Sp3α-C–H activation and functionalization of alcohol and ether

3. Recent Advances in Free-Radical-Promoted Selective Activation of Alcohol/Etherα-O-C(sp3)-H Bond

5. A Reaction for sp3−sp3 C−C Bond Formation via Cooperation of Lewis Acid-Promoted/Rh-Catalyzed C−H Bond Activation

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