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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
Methyl2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate
- 库存:
999
- 供应商:
智溯科ZSK
- CAS号:
69942-12-7
- 规格:
10mg///100mg///200mg
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文献和实验(HPLC) (9 –32 ), GC-mass spectrometry (GC-MS) (33 ,34 ), liquid chromatography-mass spectrometry (LC-MS) (35 ), and capillary zone electrophoresis (CZE) (36 –38 ). However, isotachophoresis and AAA methods are nonselective for sulfur amino acids
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
the selective functionalization of the 4?amino group of the cytosine base at pH 7 or the 2?amino group of the guanine base at pH 9.4 or at pH 7.4 in the presence of NiCl2 . In particular, the functionality?transfer reaction (FTR) under the alkaline conditions
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