Lewis Acid-Relayed Singlet Oxygen Reaction with Enamines: Selective Dimerization of Enamines to Pyrrolin-4-ones-Reference-Cited by-同舟云学术

Lewis Acid-Relayed Singlet Oxygen Reaction with Enamines: Selective Dimerization of Enamines to Pyrrolin-4-ones

Published:2022-09-01 Issue:36 Volume:144 Page:16667-16675
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Lei Tao¹²,Cheng Yuan-Yuan¹²,Han Xu¹²,Zhou Chao¹²,Yang Bing¹²,Fan Xiu-Wei¹²,Chen Bin¹²^ORCID,Tung Chen-Ho¹²^ORCID,Wu Li-Zhu¹²^ORCID

Affiliation:

1. Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, The Chinese Academy of Sciences, Beijing 100190, People’s Republic of China

2. School of Future Technology, University of Chinese Academy of Sciences, Beijing 100049, People’s Republic of China

Funder

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

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.2c07450

Reference75 articles.

1. Multicomponent reactions for the synthesis of pyrroles

2. Recent advances in the synthesis of pyrroles by multicomponent reactions

3. Iminium and enamine catalysis in enantioselective photochemical reactions

4. Visible-Light Induced and Oxygen-Promoted Oxidative Cyclization of Aromatic Enamines for the Synthesis of Quinolines Derivatives

5. Visible Light Initiated Hantzsch Synthesis of 2,5-Diaryl-Substituted Pyrroles at Ambient Conditions

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