Efficient access to peptidyl ketones and peptidyl diketones via Calkylations and Cacylations of polymersupported phosphorus ylides followed by hydrolytic andor oxidative cleavage

Autor: ElDahshan, Adeeb, Ahsanullah, Rademann, Jörg
Zdroj: Peptide Science; 2010, Vol. 94 Issue: 2 p220-228, 9p
Abstrakt: Novel syntheses of peptidyl ketones and peptidyl diketones on polymer support are described. Peptidyl phosphoranylidene acetates were prepared via Cacylation of polymersupported phosphorus ylides. Selective alkylation of the ylide carbon with various alkyl halides, such as methyl iodide and benzyl bromide was established. Peptidyl diketones were obtained by oxidative cleavage. Peptidyl ketones were furnished by hydrolysis of the peptidyl phosphorus ylides under either basic or acidic conditions. © 2010 Wiley Periodicals, Inc. Biopolymers Pept Sci 94: 220–228, 2010.
Databáze: Supplemental Index