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![(2S)-4-tert-butoxy-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-4-oxo-butanoic acid](https://img1.dxycdn.com/p/s14/2025/0410/042/8254548921414120191.jpg!wh200)
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Recommended Refrigeration Conditions (2℃-8℃) for storage
- 英文名：
tert-butyl N-(4-acetylnorbornan-1-yl)carbamate
- 供应商：
南京鼎石
- CAS号：
2423978-43-0
- 规格：
10g///25g///50g///100g///250g///500g///1kg///5kg///25057kg
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文献和实验Over the past 20 years, amino acid analysis methods based on precolumn derivatization procedures have become a popular alternative to the traditional postcolumn derivatization techniques based on ion-exchange separation of the underivatized
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
N‐/purin‐6‐yl/pyridinium salts. Nucleic Acids Res. 13:2989‐3003. Allerson, C.R., Chen, S.L., and Verdine, G.L. 1997. A chemical method for site‐specific modification
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