Superacid-catalyzed tandem Meyer–Schuster rearrangement/intramolecular hydroamination of o-anilinopropargyl alcohols for the synthesis of 2,3-dihydro-4(1H)-quinolones-Reference-Cited by-同舟云学术

Superacid-catalyzed tandem Meyer–Schuster rearrangement/intramolecular hydroamination of o-anilinopropargyl alcohols for the synthesis of 2,3-dihydro-4(1H)-quinolones

Published:2016-07-22 Issue:15 Volume:46 Page:1249-1256
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Sun Guofeng¹,Cheng Fengkai¹,Tao Ruiheng¹,Sun Yuxing¹,Pan Jinpeng¹,Zhu Yaohua¹,Wang Zhonghua¹,Wu Fanhong¹,Yin Yan¹²

Affiliation:

1. School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai, China

2. Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China

Funder

National Natural Science Foundation of China

Shanghai Municipal Education Commission

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2016.1196293

Reference17 articles.

1. Azidotrimethylsilane-mediated Schmidt rearrangement of 2-aryl-1,2,3,4-tetrahydro-1-methylsulfonyl-4-quinolones: non-regioselectivity of carbon migration

2. 1-(Arylsulfonyl)-2,3-dihydro-1H-quinolin-4-one derivatives as 5-HT6 serotonin receptor ligands

3. Synthesis of quinolines and 2,3-dihydro-4(1h)-quinolones. Palladium catalysed reaction of o-iodoanilides with acetylenic carbinols

4. Ketene Dithioacetals in the Aza-Diels−Alder Reaction with N-Arylimines: A Versatile Approach to Tetrahydroquinolines, 2,3-Dihydro-4-quinolones, and 4-Quinolones

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3. One‐pot Synthesis of 3‐Aryliden‐2,3‐dihydro‐4‐quinolones from o ‐Anilinopropargyl Alcohols via Aldol Condensation of In Situ Generated 2,3‐Dihydroquinolin‐4‐ones and Aryl Aldehydes;Asian Journal of Organic Chemistry;2022-01-21

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