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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
Tert-Butyl (3-chloro-2-oxopropyl)carbamate
- 库存:
999
- 供应商:
智溯科ZSK
- CAS号:
137990-82-0
- 规格:
10mg/100mg/9777mg
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文献和实验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
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
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