EVALUATION OF MONOMETHOXYTRITYL AND DIMETHOXYTRITYL AS ORTHOGONAL AMINO PROTECTING GROUPS IN FMOC SOLID-PHASE PEPTIDE-SYNTHESIS

Citation
S. Matysiak et al., EVALUATION OF MONOMETHOXYTRITYL AND DIMETHOXYTRITYL AS ORTHOGONAL AMINO PROTECTING GROUPS IN FMOC SOLID-PHASE PEPTIDE-SYNTHESIS, Tetrahedron letters, 39(13), 1998, pp. 1733-1734
Citations number
4
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
39
Issue
13
Year of publication
1998
Pages
1733 - 1734
Database
ISI
SICI code
0040-4039(1998)39:13<1733:EOMADA>2.0.ZU;2-X
Abstract
Amino acid derivatives protected at the alpha- or side chain amino fun ction with mono- as well as dimethoxytrityl were successfully prepared by a one-step procedure. These derivatives were evaluated for their u tilization in solid phase peptide synthesis (SPPS), particularly with respect to the selective detritylation in the presence of other acid l abile protecting groups to allow for the preparation of multiple, bran ched or cyclized peptide structures as well as for site specific post- assembly manipulations. (C) 1998 Elsevier Science Ltd. All rights rese rved.