articleTop 1% cited
Efficient Conversion of Aromatic Amines into Azides: A One-Pot Synthesis of Triazole Linkages
Organic Letters · 2007 · Vol. 9(9) · pp. 1809–1811
Karine Barral✉(University of London)Adam D. Moorhouse(University of London)John E. Moses(University of London)
Abstract
[reaction: see text] An efficient and improved procedure for the preparation of aromatic azides and their application in the Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition ("click reaction") is described. The synthesis of aromatic azides from the corresponding amines is accomplished under mild conditions with tert-butyl nitrite and azidotrimethylsilane. 1,4-Disubstituted 1,2,3-triazoles were obtained in excellent yields from a variety of aromatic amines without the need for isolation of the azide intermediates.
Click Chemistry and ApplicationsChemical Synthesis and AnalysisSynthesis and Catalytic ReactionsChemistryTriazoleCombinatorial chemistryOrganic chemistry
MeSH terms
AminesAzidesCross-Linking ReagentsTriazolesMolecular Structure
Citations
397
FWCI
13.48
field-weighted impact
References
7
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99%
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References
Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
The Journal of Organic Chemistry · 2002 · 8,416 citations
A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
Angewandte Chemie International Edition · 2002 · 11,380 citations
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Tetrahedron Letters · 1996 · 352 citations
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