Direct Intermolecular C–H Functionalization Triggered by 1,5-Hydride Shift: Access to N-Arylprolinamides via Ugi-Type Reaction-Reference-Cited by-同舟云学术

Direct Intermolecular C–H Functionalization Triggered by 1,5-Hydride Shift: Access to N-Arylprolinamides via Ugi-Type Reaction

Published:2017-03-14 Issue:7 Volume:19 Page:1566-1569
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhen Le¹,Wang Jiankun¹,Xu Qing-Long¹^ORCID,Sun Hongbin¹,Wen Xiaoan¹^ORCID,Wang Guangji¹

Affiliation:

1. Key Laboratory of Drug Metabolism and Pharmacokinetics and ‡Jiangsu Key Laboratory of Drug Discovery for Metabolic Diseases, China Pharmaceutical University, 24 Tongjia Xiang, Nanjing 210009, Jiangsu, China

Funder

Ministry of Education of the People's Republic of China

Ministry of Science and Technology of the People's Republic of China

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b00378

Reference37 articles.

1. Über ein neues Kondensations-Prinzip

2. Four-component condensation: a new versatile method for the synthesis of substituted prolyl peptides

3. Multicomponent Reactions with Isocyanides

4. Recent Developments in the Isonitrile‐Based Multicomponent Synthesis of Heterocycles

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