Jc. Alfred et al., FACILE SYNTHESIS OF NEW AMINE HIGH-LOADED POLY(METH)ACRYLAMIDE-BASED RESINS FOR SOLID-PHASE PEPTIDE-SYNTHESIS, Macromolecular chemistry and physics, 197(1), 1996, pp. 389-401
Two methods for the ready preparation of some protected primary amine-
functionalized (meth)acrylamide derviatives from amino halides or amin
o alcohols are described. The (meth)acryloyl moiety is introduced eith
er in the last step from unsymmetrically N,N'-disubstituted diamines o
r, more simply, in the first step, but that demands a special work-up
of the reaction mixture in order to prevent polymerization. Both metho
ds are complementary. Reverse phase suspension polymerization of the t
itle compounds with N-acryloylpyrrolidine and N,N'-ethylenebis(acrylam
ide) directly affords new beaded, high-loaded amine-functionalized res
ins for solid phase peptide synthesis.