The dihydropyrone Diels-Alder reaction: Development and application to thesynthesis of highly functionalized 1-oxa-4-decalones

Authors
Seth, PP Chen, DQ Wang, JQ Gao, XC Totah, NI
Citation
Pp. Seth et al., The dihydropyrone Diels-Alder reaction: Development and application to thesynthesis of highly functionalized 1-oxa-4-decalones, TETRAHEDRON, 56(52), 2000, pp. 10185-10195
Citations number
24
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
56
Issue
52
Year of publication
2000
Pages
10185 - 10195
Database
ISI
SICI code
0040-4020(200012)56:52<10185:TDDRDA>2.0.ZU;2-J
Abstract
A facile method for the synthesis of highly functionalized 1-oxadecalone de rivatives is described via the Diels-Alder reaction of 2,3-dihydro-4-pyrone dienophiles with electron rich dienes. By this process a variety of functi onal groups and substitution patterns can be incorporated into the oxadecal one framework. (C) 2000 Elsevier Science Ltd. All rights reserved.