Solid-Phase Synthesis of 1,2,3-Triazoles via 1,3-Dipolar Cycloaddition-Reference-Cited by-同舟云学术

Solid-Phase Synthesis of 1,2,3-Triazoles via 1,3-Dipolar Cycloaddition

Published:2003-08-26 Issue:6 Volume:5 Page:826-833
ISSN:1520-4766
Container-title:Journal of Combinatorial Chemistry
language:en
Short-container-title:J. Comb. Chem.

Author:

Harju Kirsi¹,Vahermo Mikko¹,Mutikainen Ilpo¹,Yli-Kauhaluoma Jari¹

Affiliation:

1. Viikki Drug Discovery Technology Center, Department of Pharmacy, P.O. Box 56, FIN-00014 University of Helsinki, Finland, and Department of Chemistry, Laboratory of Inorganic Chemistry, P.O. Box 55, FIN-00014 University of Helsinki, Finland

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cc030110c

Reference46 articles.

1. Benzylated 1,2,3-triazoles as anticoccidiostats

2. Cycloaddition of acetylenes to 7-acylamino-3-azidomethyl-3-cephem-4-carboxylic acids

3. Synthesis and .beta.-lactamase inhibitory properties of 2.beta.-[(1,2,3-triazol-1-yl)methyl]-2.alpha.-methylpenam-3.alpha.-carboxylic acid 1,1-dioxide and related triazolyl derivatives

4. Steric Effects on the Regioselectivity of an Azide-Alkyne Dipolar Cycloaddition Reaction: The Synthesis of Human Leukocyte Elastase Inhibitors

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