Synthesis of Indenone-Fused Pyran Derivatives from Aryl Enaminones and Cyclopropenones through Unsymmetrical Relay C–H Bond Activation and Double C–C/C–O Bond Formation-Reference-Cited by-同舟云学术

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Synthesis of Indenone-Fused Pyran Derivatives from Aryl Enaminones and Cyclopropenones through Unsymmetrical Relay C–H Bond Activation and Double C–C/C–O Bond Formation

Published:2024-07-30 Issue:31 Volume:26 Page:6602-6607
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yang Chun¹,Li Bin¹,Zhang Xinying¹^ORCID,Fan Xuesen¹^ORCID

Affiliation:

1. State Key Laboratory of Antiviral Drugs, Pingyuan Laboratory, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, School of Chemistry and Chemical Engineering, School of Environment, Henan Normal University, Xinxiang, Henan 453007, China

Funder

Henan Normal University

Henan Postdoctoral Science Foundation

Henan Key Laboratory of Organic Functional Molecules and Drug Innovation

National Natural Science Foundation of China

Higher Education Discipline Innovation Project

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02197

Reference45 articles.

1. Indenone Synthesis via Transition‐Metal‐Catalyzed Annulation

2. Rhodium(III)‐Catalyzed Redox‐Neutral Synthesis of Indenones from 2‐Aryl‐3‐nitrosoindoles with Alkynes

3. The value of pyrans as anticancer scaffolds in medicinal chemistry

4. An overview of recent advances in the catalytic synthesis of substituted pyrans

5. Acid-mediated domino reaction of ortho -carbonylated alkynyl-substituted arylaldehydes with phenols: Rapid access to fused indeno[2,1- c ]chromen-7-one derivatives

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