Zhao J.-F, * Zhang X.-H, Ding Y.-J, Yang Y.-S, Bi X.-B, Liu C.-F. * Nanyang Technological
University, Singapore
Facile Synthesis of Peptidyl Salicylaldehyde Esters and Its Use in Cyclic Peptide
Synthesis.
Org. Lett. 2013;
15: 5182-5185
Key words
cyclic peptides - solid-phase peptide synthesis - cyclization - salicylaldehyde esters
Significance
A protocol for the solid-phase synthesis of cyclopeptides was described. Starting
from MBHA resin and 1, peptide 3 was prepared in 50–90% purity utilizing Boc-SPPS. Ozonolysis of 3 afforded a salicylaldehyde ester peptide 4 in 55% yield (other 15 examples: 42–89% yield). The reaction of 4 in the mixture of pyridine, acetic acid and 2,2,2-trifluoroethanol (1:1:2) followed
by TFA treatment gave mahafacyclin B in 56% yield over two steps (other 7 examples:
29–65% yield).
Comment
The present cyclization of salicylaldehyde ester peptides bearing a Thr or Ser N-terminal
residue (5) proceeds via the formation of salicylidene N,O-acetals 6. Li’s group reported a similar approach on the cyclic peptide synthesis independently
(C. T. T. Wong et al. Angew. Chem. Int. Ed. 2013, 52, 10212).
