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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
2,3-Dihydro-6-methoxy-5-(methoxymethoxy)- 1H-inden-1-one
- 库存：
1
- 供应商：
甄准生物
- CAS号：
1346604-60-1
- 保存条件：
Refrigerator
- 规格：
50mg / 500mg
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文献和实验Immunochemical Method for Ochratoxin A
Ochratoxin A (7-L-β-phenylalanylcarbonyl-5-chloro-8-hydroxy-3,4-dihydro-3-R-methylisocoumarin, Fig. 1 ) was first isolated in 1965 from A. ochraceus (1 ). Meanwhile several Aspergillus and Penicillium species are known to produce
Preparation of Unnatural Amino Acids with Ammonia-Lyases and 2,3-Aminomutases
of unnatural amino acids. Besides the synthesis of various unnatural α-amino acids with the aid of phenylalanine ammonia-lyases (PALs) utilizing the 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO) prosthetic groups, the biotransformations leading to various
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
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