Synthesis of new triazole-based trifluoromethyl scaffolds
Open Access
- 29 May 2008
- journal article
- Published by Beilstein Institut in Beilstein Journal of Organic Chemistry
- Vol. 4 (1), 19
- https://doi.org/10.3762/bjoc.4.19
Abstract
Synthesis of new triazole-based trifluoromethyl scaffoldsKeywords
This publication has 33 references indexed in Scilit:
- Stereoselective Access to Substituted [(E)‐ or (Z)‐1‐(Trifluoromethyl)allyl]aminesEuropean Journal of Organic Chemistry, 2008
- Solution- and Solid-Phase Synthesis of Triazole Oligomers That Display Protein-Like FunctionalityThe Journal of Organic Chemistry, 2007
- Introduction of a Triazole Amino Acid into a Peptoid Oligomer Induces Turn Formation in Aqueous SolutionOrganic Letters, 2007
- CuI‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic PerspectiveEuropean Journal of Organic Chemistry, 2005
- Structural basis for the GSK-3β binding affinity and selectivity against CDK-2 of 1-(4-aminofurazan-3yl)-5-dialkylaminomethyl-1H-[1,2,3] triazole-4-carboxylic acid derivativesBioorganic & Medicinal Chemistry Letters, 2005
- Nonpeptidic Foldamers from Amino Acids: Synthesis and Characterization of 1,3-Substituted Triazole OligomersJournal of the American Chemical Society, 2005
- A One‐Pot Synthesis of Doubly Unsaturated Trifluoromethyl Amines:Easy Access to CF3‐Substituted PiperidinesEuropean Journal of Organic Chemistry, 2005
- Analogues of Key Precursors of Aspartyl Protease Inhibitors: Synthesis of Trifluoromethyl Amino EpoxidesThe Journal of Organic Chemistry, 2004
- Copper(I)-Catalyzed Synthesis of Azoles. DFT Study Predicts Unprecedented Reactivity and IntermediatesJournal of the American Chemical Society, 2004
- A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal AlkynesAngewandte Chemie-International Edition, 2002