- ￥89
- 源叶
- 中国
- Y80363-100mg
- 2025年10月29日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
RT
- 库存：
99
- 供应商：
上海源叶生物科技有限公司
- CAS号：
535170-20-8
- 规格：
100mg
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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
Enzymes Acting on d-Amino Acid Containing Peptides
aminopeptidase and endopeptidase activities. The enzyme was active toward (d -Phe) n , Boc-(d -Phe) n , (d -Phe) n methyl ester, d -Phe-NH2 , Boc-(d -Phe) n methyl ester, and Boc-(d -Phe) n tert -butyl ester, but not toward (d -Ala) n (n = 2–4), (d
Synthesis and Application of Highly Reactive Amino Linkers for Functional Oligonucleotides
are functionalized by conjugation with a variety of molecules, and aliphatic amino linkers have been frequently used as a tether for their modifications. This unit describes the syntheses and applications of novel amino linkers having a carbamate structure
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