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- CAS号:
2089245-28-1
- 规格:
0.1 g
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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
hydrolysis and sample extraction with tert-butyl-methylether, the residue is derivatized with 1,1,1,3,3,3-hexafluoroisopropanol and analyzed by HRGC-MS (detection limit 0.1 �g/L urine).
Uridine 2′‐Carbamates: Facile Tools for Oligonucleotide 2′‐Functionalization
1‐Pyrenemethylamine hydrochloride (Aldrich; for S.4d ) 2‐Aminomethyl‐15‐crown‐5 (for S.4e )
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