Ring closing metathesis of sterically hindered 1,6-dienes: A new approach to 5-membered branched cyclitols

Authors
Sellier, O Van de Weghe, P Eustache, J
Citation
O. Sellier et al., Ring closing metathesis of sterically hindered 1,6-dienes: A new approach to 5-membered branched cyclitols, TETRAHEDR L, 40(32), 1999, pp. 5859-5860
Citations number
9
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
32
Year of publication
1999
Pages
5859 - 5860
Database
ISI
SICI code
0040-4039(19990806)40:32<5859:RCMOSH>2.0.ZU;2-Q
Abstract
A sterically hindered 1,6-dienic system underwent clean ring-closing metath esis using Schrock's catalyst. The product was converted into new 5-membere d branched cyclitols and is a potential precursor of other biologically rel evant aminocyclitols. (C) 1999 Published by Elsevier Science Ltd. All right s reserved.