tert-butyl N-(14-hydroxy-3,6,9
,12-tetraoxatetradecan-1-yl)carbamate tert-butyl N-(14-hydroxy-3,6,9,12-tetraoxatetradecan-1-yl)carbamate nan 科研现货速达 ≥98% HPLC- 询价
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- 2025年07月14日
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
tert-butyl N-(14-hydroxy-3,6,9,12-tetraoxatetradecan-1-yl)carbamate
- 库存：
999
- 供应商：
智溯科ZSK
- CAS号：
N/A
- 规格：
100mg///1g
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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
Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
and lack sensitivity. GC methods based on the conversion into trimethylsilyl (4 ,5 ), neopentylidine (6 ), and N-trifluoroacetyl n -butyl ester (7 ) derivatives lack sensitivity, gives a tailing peak and requires anhydrous derivatization conditions
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