Oxidative [4+2] Cycloaddition of α-(N-Arylamino) Carbonyls with Aryl Alkenes by Multiple C–H Functionalizations and [1,2]-Aryl Shifts-Reference-Cited by-同舟云学术

Oxidative [4+2] Cycloaddition of α-(N-Arylamino) Carbonyls with Aryl Alkenes by Multiple C–H Functionalizations and [1,2]-Aryl Shifts

Published:2019-08-01 Issue:16 Volume:21 Page:6285-6288
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wei Wen-Ting¹²,Teng Fan¹,Li Yang¹,Song Ren-Jie¹^ORCID,Li Jin-Heng¹²³^ORCID

Affiliation:

1. Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang 330063, China

2. Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Ministry of Education), Hunan Normal University, Changsha 410081, China

3. State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China

Funder

National Natural Science Foundation of China

Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research, Hunan Normal University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02169

Reference59 articles.

1. Quinoline, quinazoline and acridone alkaloids

2. Quinolines and structurally related heterocycles as antimalarials

3. Quinoline as a Privileged Scaffold in Cancer Drug Discovery

4. Quinoline Drug–Heme Interactions and Implications for Antimalarial Cytostatic versus Cytocidal Activities

5. In Vivo and In Vitro Optimization of Screening Antimalarial Hits toward Lead Molecules for Preclinical Development

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