Ring closing metathesis as an efficient approach to branched cyclitols andaminocyclitols: a short synthesis of valiolamine

Citation
O. Sellier et al., Ring closing metathesis as an efficient approach to branched cyclitols andaminocyclitols: a short synthesis of valiolamine, TETRAHEDR L, 40(5), 1999, pp. 853-856
Citations number
20
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
5
Year of publication
1999
Pages
853 - 856
Database
ISI
SICI code
0040-4039(19990129)40:5<853:RCMAAE>2.0.ZU;2-L
Abstract
Ring closing metathesis of sugar-derived 1,6 dienes is the key step for the construction of highly functionnalized cyclohexenes, precursors of branche d cyclitols and aminocyclitols. The method has been used for a short synthe sis of valiolamine. (C) 1999 Elsevier Science Ltd. All rights reserved.