Abstract
The preparation of amine and guanidine derivatives of phenylalaninamide and tryptophanamide as well as benzylamines from BAL, Rink-MBHA, and Rink resins has been performed. Cleavage of the target compound gave significant amounts of byproducts compounds in which the linker moiety was attached to the target unit. This side reaction can be avoided when the solid supports are prepared by anchoring the corresponding linker to an aminomethyl resin.
Original language | English |
---|---|
Pages (from-to) | 145-152 |
Number of pages | 8 |
Journal | QSAR and Combinatorial Science |
Volume | 23 |
Issue number | 2-3 |
Publication status | Published - Apr 2004 |
Keywords
- combinatorial chemistry
- handle
- AM linker
- side reaction
- solid-phase
- SOLID-PHASE SYNTHESIS
- TERMINAL PEPTIDE AMIDES
- MILD CONDITIONS
- COMBINATORIAL CHEMISTRY
- ORGANIC-SYNTHESIS
- ACID
- LINKAGE
- CLEAVAGE
- STRATEGY
- AMINES