[3+3] Annulation Reaction of 2‐Amino‐4 H ‐chromen‐4‐ones with Cinnamaldehydes or Aromatic Aldehydes and Ethanal in One Pot: Access to 2‐Aryl‐5 H ‐Chromeno[2,3‐ b ]pyridin‐5‐ones-Reference-Cited by-同舟云学术

[3+3] Annulation Reaction of 2‐Amino‐4 H ‐chromen‐4‐ones with Cinnamaldehydes or Aromatic Aldehydes and Ethanal in One Pot: Access to 2‐Aryl‐5 H ‐Chromeno[2,3‐ b ]pyridin‐5‐ones

Published:2022-09-20 Issue:10 Volume:11 Page:
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J Org Chem

Author:

Gan Jianbo¹,Xin Junhu¹,Xue Yuhang¹,Wang Cunde¹^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering Yangzhou University 180 Siwangting Street Yangzhou 225002 P. R. China

Funder

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajoc.202200435

Reference68 articles.

2. Synthesis and cytotoxic activity of some new azapyranoxanthenone aminoderivatives

3. A. Semov G. Pietrzynski V. Alakhov Method of treating tumors with azaxanthones Supratek Pharma Inc US Pat. US7772255B2 2010;

4. Toxicological and pharmacological evaluation, antioxidant, ADMET and molecular modeling of selected racemic chromenotacrines {11-amino-12-aryl-8,9,10,12-tetrahydro-7H-chromeno[2,3-b]quinolin-3-ols} for the potential prevention and treatment of Alzheimer's disease

5. Fatty Acid Amide Hydrolase (FAAH), Acetylcholinesterase (AChE), and Butyrylcholinesterase (BuChE): Networked Targets for the Development of Carbamates as Potential Anti-Alzheimer’s Disease Agents

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