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Boc-L-HAla(4-Br)-OtBu
Nom chimique: N-alpha-(t-butyloxycarbonyl)-L-(4-bromo)-homoalanine tert-butyl ester // Synonymes: N-alpha-(t-butyloxycarbonyl)-L-(4-bromo)-homoalanine t-butyl ester, Boc-L-(4-bromo)-homoalanine tert-butyl ester, Boc-L-(4-bromo)-homoalanine t-butyl ester, 1,1-Dimethylethyl(2S)-4-bromo-2-[[(1,1-di methylethoxy)carbonyl]amino]butanoate, Tert-butyl
- n° Art.:BAA4680
- n° CAS:163210-89-7
- Formule:C13H24BrNO4a
- Storage temperature:2-8°C
- Masse moléculaire:338,24 g/mol
- Pureté:min. 98%
- Pureté Énantiomérique:min. 99,7%
from 70,00 €
description
This brominated azidohomoalanine building block is reported as precursor for the synthesis of hydrocarbon-bridged diaminodiacids, as functionalized linker, as well as for nucleobase peptide synthesis.
references
Discovery of Nucleic Acid Binding Molecules from Combinatorial Biohybrid Nucleobase Peptide Libraries; S. Pomplun, Z. P. Gates, G. Zhang, A. J. Quartararo, B. L. Pentelute; J. Am. Chem. Soc. 2020; 142(46): 19642-19651. https://doi.org/10.1021/jacs.0c08964.
Inhibitors of nicotinamide N-methyltransferase designed to mimic the methylation reaction transition state; M. J. van Haren, R. Taig, J. Kuppens, J. S. Toraño, E. E. Moret, R. B. Parsons, D. Sartini, M. Emanuelli, N. I. Martin; Org. Biomol. Chem. 2017; 15: 6656-6657. https://doi.org/10.1039/c7ob01357d.
Efficient synthesis of hydrocarbon-bridged diaminodiacids through nickel-catalyzed reductive cross-coupling; T. Wang, Y.-F. Kong, Y. Xu, J. Fan, H.-J. Xu, D. Bierer, J. Wang, J. Shi, Y.-M. Li; Tetrahedron Lett. 2017; https://doi.org/10.1016/j.tetlet.2017.09.006.
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