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1-hydroxy-7-azabenzotriazole

Known as: 7-aza-1-hydroxybenzotriazole 
 
National Institutes of Health

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2 relations

Broader (2)

Aza CompoundsTriazoles

Papers overview

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2016
2016
Optimized Reaction Conditions for Amide Bond Formation in DNA-Encoded Combinatorial Libraries.
DNA-encoded combinatorial libraries are increasingly being used as tools for the discovery of small organic binding molecules to… Expand
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2010
2010
Reactivity and applications of new amine reactive cross-linkers for mass spectrometric detection of protein-protein complexes.
Chemical cross-linking of proteins permits the stabilization of noncovalent complexes through introduction of covalent bonds. A… Expand
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2010
2010
Sulfonate esters of 1-hydroxypyridin-2(1H)-one and ethyl 2-cyano-2-(hydroxyimino)acetate (oxyma) as effective peptide coupling reagents to replace 1-hydroxybenzotriazole and 1-hydroxy-7…
A new family of sulfonate ester-type coupling reagents is described which differs in its leaving group. The sulfonate ester… Expand
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2004
2004
Organophosphorus and nitro-substituted sulfonate esters of 1-hydroxy-7-azabenzotriazole as highly efficient fast-acting peptide coupling reagents.
Organophosphorus esters 9, 10, 14, and 15 prepared via reaction of diethyl- and diphenylphosphoryl chloride, di(o-tolyl… Expand
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2001
2001
The 5,6- and 4,5-benzo derivatives of 1-hydroxy-7-azabenzotriazole.
[structure: see text]. Syntheses of the two benzo derivatives of HOAt are described. Conversion of the two isomers to the… Expand
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1999
1999
Rapid esterification of nucleosides to solid-phase supports for oligonucleotide synthesis using uronium and phosphonium coupling reagents.
Nucleosides can be esterified to solid-phase supports using uronium or phosphonium coupling reagents and a coupling additive… Expand
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1998
1998
Protein and peptide labeling with (cyclopentadienyl)tricarbonyl rhenium and technetium.
A method for labeling proteins and peptides with (methoxycarbonyl cyclopentadienyl)tricarbonyl rhenium and technetium is… Expand
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1998
1998
Synthesis of peptides employing Fmoc-amino acid chlorides and commercial zinc dust
Abstract Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis of peptides is… Expand
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1997
1997
Occurrence and Minimization of Cysteine Racemization during Stepwise Solid-Phase Peptide Synthesis(1)(,)(2).
Contrary to the conventional wisdom of the peptide synthesis field, N,S-protected derivatives of cysteine can undergo substantial… Expand
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1996
1996
Cyclization of all-L-Pentapeptides by Means of 1-Hydroxy-7-azabenzotriazole-Derived Uronium and Phosphonium Reagents.
Due to their restricted conformational flexibility, cyclic peptides are of great interest in connection with structure-activity… Expand
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