Functionalized platforms based on marine cyclopeptides: different pathwaysto the hexapeptide

Citation
C. Boss et al., Functionalized platforms based on marine cyclopeptides: different pathwaysto the hexapeptide, TETRAHEDR L, 41(33), 2000, pp. 6327-6331
Citations number
19
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
33
Year of publication
2000
Pages
6327 - 6331
Database
ISI
SICI code
0040-4039(20000812)41:33<6327:FPBOMC>2.0.ZU;2-2
Abstract
The synthesis of macrocyclic, roughly planar, exclusively syn-functionalize d hexapeptides, related to dolastatin I and bistratamide C from enantiomeri cally pure oxazole precursors is reported. The platforms can either be synt hesized in a stepwise procedure by final cyclization of the linear oxazole trimers or in a direct 'one-pot' reaction. The investigation on the couplin g of these building blocks into linear dimers and trimers with modern pepti de coupling reagents is reported. (C) 2000 Published by Elsevier Science Lt d.