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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
tert-butyl (3S,6S)-3-[tert-butyl(dimethyl)silyl]oxy-6-hydroxy-azepane-1-carboxylate
- 库存:
期货
- 供应商:
上海阿拉丁生化科技股份有限公司
- CAS号:
2865073-15-8
- 规格:
T638189-1g
设定黄金标准,在阿拉丁,我们不仅相信保持质量,而且相信质量。 我们的目标是定义它。 我们的质量管理理念为业界研究试剂建立了高质量的标准。 当您听到阿拉丁这个名字时,就会知道它是各个方面坚定不移品质的灯塔。
中文名:tert-butyl (3S,6S)-3-[tert-butyl(dimethyl)silyl]oxy-6-hydroxy-azepane-1-carboxylate
英文名:tert-butyl (3S,6S)-3-[tert-butyl(dimethyl)silyl]oxy-6-hydroxy-azepane-1-carboxylate
纯度:≥97%
cas号:2865073-15-8
存储温度:-
运输条件:常规运输
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文献和实验Synthesis of Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
to 200 mesh, 1% cross‐linked, typical loading 1.0 to 1.8 mmol/g; Aldrich) Methyl O‐[tert‐butyl(dimethyl)silyl]‐(L )‐serinate ( S.6 a , see protocol
RNA Synthesis Using 2-O-(Tert-Butyldimethylsilyl) Protection
This chapter enables the reader to carry out the solid-phase synthesis of ribonucleic acid (RNA) using β-cyanoethyl phosphoramidite chemistry combined with tert -butyldimethylsilyl protection of the ribose 2′-hydroxyl group. Phosphoramidite
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
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