An approach to the synthesis of furanoheliangolides through Diels-Alder reactions

dc.creatorCONSTANTINO, Mauricio Gomes
dc.creatorARAGAO, Valquiria
dc.creatorSILVA, Gil Valdo Jose da
dc.date.accessioned2012-10-19T14:19:11Z
dc.date.accessioned2018-07-04T15:02:39Z
dc.date.available2012-10-19T14:19:11Z
dc.date.available2018-07-04T15:02:39Z
dc.date.created2012-10-19T14:19:11Z
dc.date.issued2008
dc.identifierTETRAHEDRON LETTERS, v.49, n.8, p.1393-1395, 2008
dc.identifier0040-4039
dc.identifierhttp://producao.usp.br/handle/BDPI/21030
dc.identifier10.1016/j.tetlet.2007.12.079
dc.identifierhttp://dx.doi.org/10.1016/j.tetlet.2007.12.079
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1617808
dc.description.abstractThe 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.
dc.languageeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.relationTetrahedron Letters
dc.rightsCopyright PERGAMON-ELSEVIER SCIENCE LTD
dc.rightsclosedAccess
dc.subjectsynthesis
dc.subjectnatural products
dc.subjectfuranoheliangolides
dc.subjectDiels-Alder reactions
dc.titleAn approach to the synthesis of furanoheliangolides through Diels-Alder reactions
dc.typeArtículos de revistas


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