Zemlicka J, Owens J
Biochim Biophys Acta. 1976 Aug 2;442(1):71-5. doi: 10.1016/0005-2787(76)90177-5.
The title compound and the corresponding diacyl derivative has been prepared by the reaction of 5'-O-(4-methoxytrityl)adenosine with L-(O-methyl-3-phenyl)lactic acid in the presence of dicyclohexylcarbodiimide in pyridine and subsequent detritylation in 80% acetic acid. Neither compound accepted the N-acetyl-L-phenylalanyl residue from N-acetyl-L-phenylalanyl-tRNA in an Escherichia coli ribosomal system nor did either inhibit the puromycin reaction in the same system.
标题化合物及相应的二酰基衍生物是通过使5'-O-(4-甲氧基三苯甲基)腺苷与L-(O-甲基-3-苯基)乳酸在二环己基碳二亚胺存在下于吡啶中反应,随后在80%乙酸中脱三苯甲基而制备的。在大肠杆菌核糖体系统中,这两种化合物既不接受来自N-乙酰-L-苯丙氨酰-tRNA的N-乙酰-L-苯丙氨酰残基,也不在同一系统中抑制嘌呤霉素反应。