Side-chain Modifications of Highly Functionalized 3(2H)-Furanones

dc.creatorNardini, Viviani
dc.creatorRodrigues, Shirley Muniz Machado
dc.creatorConstantino, Mauricio Gomes
dc.creatorSilva, Gil Valdo Jose da
dc.date.accessioned2013-10-21T11:16:12Z
dc.date.accessioned2018-07-04T16:26:21Z
dc.date.available2013-10-21T11:16:12Z
dc.date.available2018-07-04T16:26:21Z
dc.date.created2013-10-21T11:16:12Z
dc.date.issued2012
dc.identifierMOLECULES, BASEL, v. 17, n. 10, supl. 1, Part 1, pp. 12151-12162, OCT, 2012
dc.identifier1420-3049
dc.identifierhttp://www.producao.usp.br/handle/BDPI/35286
dc.identifier10.3390/molecules171012151
dc.identifierhttp://dx.doi.org/10.3390/molecules171012151
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1635849
dc.description.abstractA series of 3(2H)-furanones, based on side-chain modifications of a parent 3(2H)-furanone, was synthesized in good yield. The parent compound was prepared by hydrogenolysis, and subsequent acid hydrolysis, of isoxazole derivatives. The isoxazole was prepared by a [3+2] 1,3-dipolar cycloaddition reaction between 3-butyn-2-ol and nitrile oxide.
dc.languageeng
dc.publisherMDPI AG
dc.publisherBASEL
dc.relationMOLECULES
dc.rightsCopyright MDPI AG
dc.rightsopenAccess
dc.subject3(2H)-FURANONE
dc.subjectISOXAZOLE
dc.subjectNATURAL PRODUCTS
dc.subjectSIDE-CHAIN MODIFICATIONS
dc.titleSide-chain Modifications of Highly Functionalized 3(2H)-Furanones
dc.typeArtículos de revistas


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