REDUCTIVE ALKYLATION OF 9-AMINO-XANTHEN-3-YLOXYMETHYLPOLY(STYRENE) - A NOVEL PROCEDURE FOR THE SYNTHESIS OF PEPTIDYL N-ALKYL AMIDES BY FMOCBU(T) CHEMISTRY/
Wc. Chan et Sl. Mellor, REDUCTIVE ALKYLATION OF 9-AMINO-XANTHEN-3-YLOXYMETHYLPOLY(STYRENE) - A NOVEL PROCEDURE FOR THE SYNTHESIS OF PEPTIDYL N-ALKYL AMIDES BY FMOCBU(T) CHEMISTRY/, Journal of the Chemical Society, Chemical Communications, (14), 1995, pp. 1475-1477
Reductive N-alkylation of the 'amide' anchor resin, 9-amino-xanthen-3-
yloxymethyl poly(styrene) 1, by sequential treatment with alkyl aldehy
des under mild acidic conditions followed by NaBH4 in MeOH-DMF, and th
en followed by optimised Fmoc/Bu(t) solid-phase peptide synthetic proc
edures afforded an unique class of peptidyl N-alkyl amides in excellen
t yields.