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  • 标题:Synthesis of cyclopentano-N-methylphosphatidylethanolamines: aminolysis during the use of methylamine.
  • 本地全文:下载
  • 作者:H Pajouhesh ; A J Hancock
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:1984
  • 卷号:25
  • 期号:3
  • 页码:310-312
  • 语种:English
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:Monomethylamine and N-benzyl-N-methylamine were used as nucleophiles in the amination of the bromoethylester of cyclopentano-phosphatidic acid. The former reagent led to extensive aminolysis and the quantitative formation of N-methylpalmitamide, rather than the desired cyclopentano-phosphatidyl-N-methylethanolamine. However, the method of Shapiro and Rabinsohn (1964. Biochemistry. 3:603-605), in which N-benzyl-N-methylamine was used as a nucleophile, was adapted for a successful synthesis.
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