(2-[(tert-丁氧羰基)氨基]咪唑[1,2-a]吡啶-
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
(2-((tert-butoxycarbonyl)amino)imidazo1,2-apyridin-6-yl)boronic acid pinacol ester
- 库存：
999
- 供应商：
智溯科ZSK
- CAS号：
2304634-51-1
- 规格：
10mg///100mg///200mg
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文献和实验Synthesis of Peptides Using Tert-Butyloxycarbonyl (Boc) as the -Amino Protection Group
The use of the tert -butyloxycarbonyl (Boc) as the N α-amino protecting group in peptide synthesis can be advantageous in several cases, such as synthesis of hydrophobic peptides and peptides containing ester and thioester moieties
Synthesis of Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
‐Ethyldiisopropylamine, (DIEA; Alfa Aesar), freshly distilled over KOH Amino acids or dipeptide: Methyl N ‐(tert ‐butoxycarbonyl
The determination of sulfur amino acids, glutathione (GSH), and related aminothiols has been carried out by isotachophoresis (1 ), amino acid analyzer (AAA) (2 ,3 ), gas chromatography (GC) (4 –8 ), high-performance liquid chromatography
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