Synthesis of L-xylose derived cyclohexenephosphonates - versatile precursors of sialidase inhibitor libraries

Citation
H. Streicher et al., Synthesis of L-xylose derived cyclohexenephosphonates - versatile precursors of sialidase inhibitor libraries, TETRAHEDRON, 57(42), 2001, pp. 8851-8859
Citations number
19
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
57
Issue
42
Year of publication
2001
Pages
8851 - 8859
Database
ISI
SICI code
0040-4020(20011015)57:42<8851:SOLDC->2.0.ZU;2-T
Abstract
L-xylo Configured cyclohexenephosphonates 1 and 2 have been synthesized as scaffolds for sialidase inhibitor libraries. These compounds were obtained by chain elongation and cyclization of suitably protected L-xylose. An unex pected phosphorylation was observed, however, the resulting phosphate could be removed in a final enzymatic step. Optimization of the reaction conditi ons avoided the undesired phosphorylation and opened the way to a purely ch emical synthesis. (C) 2001 Elsevier Science Ltd. All rights reserved.