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- 英文名：
tert-Butyl 3,3-Difluoro-4-(hydroxymethyl)piperidine-1-carboxylate
- 库存：
100+
- 供应商：
上海维亦特生物
- CAS号：
1303974-47-1
tert-Butyl 3,3-Difluoro-4-(hydroxymethyl)piperidine-1-carboxylate
1303974-47-1
C₁₁H₁₉NO₃F₂
251.27
No Data Available
No Data Available
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文献和实验tert-Butyl 3,3-Difluoro-4-(hydroxymethyl)piperidine-1-carboxylate
1303974-47-1
C₁₁H₁₉NO₃F₂
251.27
No Data Available
No Data Available
Solid-Phase Synthesis of Neuropeptides by Fmoc Strategies
is used to protect the α-amino group of each residue. Those residues that have potentially reactive side chains are protected with acid-labile groups such as t-butyl. After removal of the Fmoc group with piperidine, the next protected amino
Synthesis of Peptide‐Oligonucleotide Conjugates by Diels‐Alder Cycloaddition in Water
) N α ‐(9‐Fluorenylmethoxycarbonyl)‐protected amino acids (Fmoc‐aa‐OH; Novabiochem, Bachem): e.g., for sequences illustrated here, Arg(Pbf), Gly, Leu, Phe, Ser(t Bu), and Tyr(t Bu) (t Bu: tert ‐butyl; Pbf
Disulfide Conjugation of Peptides to Oligonucleotides and Their Analogs
5 ), oligonucleotide synthesis ( appendix 3C ), and amino acid analysis (optional; see unit 4.22 ) NOTE: Amino acid protecting groups are t Bu, tert ‐butyl; Boc, tert ‐butyloxycarbonyl; Fmoc, 9‐fluorenylmethoxycarbonyl
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