REDUCTIVE ALKYLATION OF 9-AMINO-XANTHEN-3-YLOXYMETHYLPOLY(STYRENE) - A NOVEL PROCEDURE FOR THE SYNTHESIS OF PEPTIDYL N-ALKYL AMIDES BY FMOCBU(T) CHEMISTRY/

Authors
Citation
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
Citations number
22
Categorie Soggetti
Chemistry
ISSN journal
00224936
Issue
14
Year of publication
1995
Pages
1475 - 1477
Database
ISI
SICI code
0022-4936(1995):14<1475:RAO9-A>2.0.ZU;2-6
Abstract
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.