An approach to the synthesis of furanoheliangolides through Diels-Alder reactions
| Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
|---|---|
| Data(s) |
19/10/2012
19/10/2012
2008
|
| Resumo |
The core structure of the natural sesquiterpene lactones furanoheliangolides, an 11-oxabicyclo[6.2.1]undecane system, was synthesized through a pathway involving two Diels-Alder reactions. (c) 2007 Elsevier Ltd. All rights reserved. |
| Identificador |
TETRAHEDRON LETTERS, v.49, n.8, p.1393-1395, 2008 0040-4039 http://producao.usp.br/handle/BDPI/21030 10.1016/j.tetlet.2007.12.079 |
| Idioma(s) |
eng |
| Publicador |
PERGAMON-ELSEVIER SCIENCE LTD |
| Relação |
Tetrahedron Letters |
| Direitos |
closedAccess Copyright PERGAMON-ELSEVIER SCIENCE LTD |
| Palavras-Chave | #synthesis #natural products #furanoheliangolides #Diels-Alder reactions #SESQUITERPENE LACTONES #RING-SYSTEMS #(+)-EREMANTHOLIDE-A #FLAVONOIDS #ACID #Chemistry, Organic |
| Tipo |
article original article publishedVersion |
