Efficient Synthesis of N-2-Aryl-1,2,3-Triazole Fluorophores via Post-Triazole Arylation-Reference-Cited by-同舟云学术

Efficient Synthesis of N-2-Aryl-1,2,3-Triazole Fluorophores via Post-Triazole Arylation

Published:2008-11-01 Issue:23 Volume:10 Page:5389-5392
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Yuxiu¹,Yan Wuming¹,Chen Yunfeng¹,Petersen Jeffrey L.¹,Shi Xiaodong¹

Affiliation:

1. C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, West Virginia 26506, and Institute of Elemento-Organic Chemistry, Nankai University, Tianjin 200071, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol802246q

Reference35 articles.

1. Click Chemistry: Diverse Chemical Function from a Few Good Reactions

2. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

3. A Fluorogenic 1,3-Dipolar Cycloaddition Reaction of 3-Azidocoumarins and Acetylenes

4. 1,2,3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics

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