E. Cros et al., Solid-phase synthesis of C-terminal peptide amides from N-tetrachlorophthaloyl protected amino acids, TETRAHEDR L, 42(35), 2001, pp. 6105-6107
A new strategy for solid-phase synthesis of C-terminal peptide amides based
on the use of N-tetrachlorophthaloyl protected amino acids with acid-labil
e side-chain protection is described. (C) 2001 Elsevier Science Ltd. All ri
ghts reserved.