tert-butyl N-[(1S,3S)-1-[(2S,4
S)-4-isopropyl-5-oxo-tetrahydrofuran-2-yl]-3-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-pentyl]carbamate- 询价
- Elucigen
- 中国
- PBT0975
- 2025年07月12日
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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-[(1S,3S)-1-[(2S,4S)-4-isopropyl-5-oxo-tetrahydrofuran-2-yl]-3-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-pentyl]carbamate
- 供应商：
南京鼎石
- CAS号：
866030-35-5
- 规格：
10g///25g///50g///100g///250g///500g///1kg///5kg///15727kg
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文献和实验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 Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
3 ) Methyl O‐[tert‐butyl(dimethyl)silyl]‐(D )‐serinate ( S.6 b , see protocol 3 ) Isopropyl O‐[tert‐butyl(dimethyl)silyl]‐(L )‐serinate ( S.6 c , see protocol
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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