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Amino Acids  >  Unusual Amino Acids  >  Azide and Alkyne containing Amino Acids  >>  TBTA, Tris[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl] amine

Product Name TBTA, Tris[(1 - benzyl - 1H - 1,2,3 - triazol - 4 - yl)methyl] amine
CAS 510758-28-8
Size 500 mg
Catalog # AS-63360-500
US$ $523

A ligand used in the synthesis of a Cu(I) catalyst for the synthesis of N-sulfonylazetidin-2-imines.1,2

Detailed Information Material Safety Data Sheets (MSDS)
Storage -20 °C
References 1. Whiting, M.; Forkin, V. V. Copper-catalyzed reaction cascade: direct conversion of alkynes into N-sulfonylazetidin-2-imines.Angew. Chem. Int. Ed.2006 (45) 3157-3161.
2. Yoo, E. J.; Chang, S. Copper-Catalyzed Multicomponent Reactions: Securing a Catalytic Route to Ketenimine Intermediates and their Reactivities.Curr. Org. Chem.2009 (13) 1766-1776.
Molecular Weight 530.6
Solvent System DMF
Product Citations Al-Shareffi, E. et al. (2013). 6-Alkynyl fucose is a bioorthogonal analog for O-fucosylation of epidermal growth factor-like repeats and thrombospondin Type-1 repeats by protein O-fucosyltransferases 1 and 2. Glycobiol 23, 188. doi: 10.1093/glycob/cws140.

Zaro, BW. et al. (2013). Incorporation of unnatural sugars for the identification of glycoproteins. Mass Spectrom Glycoproteins 951, 57.

Codreanu, SG. et al. (2012). Biotinylated probes for the analysis of protein modification by electrophiles. Chem Proteomics 803, 77.

Hannoush, RN. (2012). Profiling cellular myristoylation and palmitoylation using ω-alkynyl fatty acids. Chem Genomics Proteomics 800, 85.

Yang, J. et al. (2012). Activity-based probes linked with laser-cleavable mass tags for signal amplification in imaging mass spectrometry: analysis of serine hydrolase enzymes in mammalian tissue. Anal Chem doi:10.1021/ac300203v.

Hudalla, GA. and WL. Murphy (2009). Using “click” chemistry to prepare SAM substrates to study stem cell adhesion. Langmuir 25, 5737. doi: 10.1021/la804077t.

MacKinnon, AL. et al. (2009). Target identification by Diazirine photo-cross-linking and click chemistry. Curr Protocols Chem Biol doi: 10.1002/9780470559277.ch090167.
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