SYNTHESIS OF A BRANCHED CYCLIC PEPTIDE USING A STRATEGY EMPLOYING FMOC CHEMISTRY AND 2 ADDITIONAL ORTHOGONAL PROTECTING GROUPS

Authors
BLOOMBERG GB ASKIN D GARGARO AR TANNER MJA
Citation
Gb. Bloomberg et al., SYNTHESIS OF A BRANCHED CYCLIC PEPTIDE USING A STRATEGY EMPLOYING FMOC CHEMISTRY AND 2 ADDITIONAL ORTHOGONAL PROTECTING GROUPS, Tetrahedron letters, 34(29), 1993, pp. 4709-4712
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
29
Year of publication
1993
Pages
4709 - 4712
Database
ISI
SICI code
0040-4039(1993)34:29<4709:SOABCP>2.0.ZU;2-G
Abstract
A novel branched cyclic peptide has been made by solid-phase synthesis (Fmoc/t-Bu chemistry) using two additional orthogonal strategies (All yl and Dde) and resin-bound cyclization.