Faculty of Pharmaceutical Sciences, Hokkaido University, Kita 12, Nishi 6, Kita-ku, Sapporo 060-0812 Japan.
J Org Chem. 2008 Dec 5;73(23):9494-6. doi: 10.1021/jo801915c.
A facile method for N-deallylation at the amide nitrogen of peptides is described. One-pot deallylation of a substrate through ruthenium hydride-catalyzed terminal olefin isomerization and subsequent ozonolysis gave the corresponding deallylated product under mild conditions.
描述了一种在肽的酰胺氮上进行 N-脱烯丙基化的简便方法。通过钌氢催化末端烯烃异构化和随后的臭氧化,在温和条件下一锅法脱烯丙基化底物,得到相应的脱烯丙基产物。