In Situ-Generated Formamidine as a Carbon/Nitrogen Source for Enaminone Formation: One-Pot Synthesis of Functionalized 4-Acyl-1,2,3-triazoles-Reference-Cited by-同舟云学术

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In Situ-Generated Formamidine as a Carbon/Nitrogen Source for Enaminone Formation: One-Pot Synthesis of Functionalized 4-Acyl-1,2,3-triazoles

Published:2024-08-19 Issue:17 Volume:89 Page:12170-12175
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lin Jia-Xin¹,Chen You-Xin¹,Chien Min-Cheng¹,Chen Hsiang-Jou¹,Lai Chian-Hui²^ORCID,Liang Chien-Fu¹^ORCID

Affiliation:

1. Department of Chemistry, National Chung Hsing University, Taichung 402, Taiwan

2. Graduate Institute of Biomedical Engineering, National Chung Hsing University, Taichung 402, Taiwan

Funder

National Chung-Hsing University

National Science and Technology Council

Ministry of Education, Taiwan

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c01054

Reference31 articles.

1. Cu-Catalyzed Click Reaction in Carbohydrate Chemistry

2. Bioactive 1,2,3‐Triazoles: An Account on their Synthesis, Structural Diversity and Biological Applications

3. Reactions of metallocarbenes derived from N-sulfonyl-1,2,3-triazoles

4. 1,2,3,-Triazole-Based Catalysts: From Metal- to Supramolecular Organic Catalysis

5. 1-Phenyl-4-benzoyl-1H-1,2,3-triazoles as Orally Bioavailable Transcriptional Function Suppressors of Estrogen-Related Receptor α

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