A CONVENIENT PREPARATION OF C-TERMINAL PEPTIDE ALCOHOLS BY SOLID PHASE SYNTHESIS
A new method is described which allows ready access to C-terminal peptide alcohols via solid phase synthesis.The procedure involves coupling of a hemisuccinate derived from a N-protected β-aminoalcohol to a solid phase resin, elaboration of the desired pe
Swistok, J.,Tilley, J. W.,Danho, W.,Wagner, R.,Mulkerins, K.
p. 5045 - 5048
(2007/10/02)
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