dc.creatorOliveira C.C.
dc.creatorCorreia C.R.D.
dc.date2014
dc.date2015-06-25T17:54:40Z
dc.date2015-11-26T14:36:09Z
dc.date2015-06-25T17:54:40Z
dc.date2015-11-26T14:36:09Z
dc.date.accessioned2018-03-28T21:39:43Z
dc.date.available2018-03-28T21:39:43Z
dc.identifier9780124171855
dc.identifierStrategies And Tactics In Organic Synthesis. Academic Press Inc., v. 10, n. , p. 1 - 32, 2014.
dc.identifier18746004
dc.identifier10.1016/B978-0-12-417185-5.00001-6
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84904282782&partnerID=40&md5=aa7cc2bdd2f98fa669faf602cc8a90ee
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/86739
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/86739
dc.identifier2-s2.0-84904282782
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1248606
dc.descriptionThe Heck arylation of olefins by the substrate-directed Heck-Matsuda strategy using arenediazonium salts, especially the tetrafluoroborates, constitutes an effective way to synthesize functionalized olefins, thus making them more valuable intermediates in organic synthesis. The basic principle of the method relies on the complexation of a cationic δ-aryl-palladium species to a nearby functional group on the substrate in which structural and electronic arrangement governs the arylation process in a regio- and stereoselective manner. The present review highlights this strategy focusing on some selected syntheses accomplished in our laboratory. The synthetic strategy includes the directed arylation of allylic acetates, allylamine derivatives, and functionalized cyclopentene substrates. Illustrative syntheses include the kavalactones yangonine, methysticin, and dehydromethysticin, the antifungal drug naftifine, the phytohormones abamine and abamine SG, the drug cinacalcet, and the muscle relaxant alverine. Moreover, the method was also applied to the successful total synthesis of the sphingosine 1-phosphate agonist VPC01091, a promising drug for the treatment of multiple sclerosis. The examples presented herein demonstrate the substrate-directed strategy method as a general one applicable to metal-catalyzed processes other than the palladium-catalyzed Heck reaction. © 2014 Elsevier Ltd.
dc.description10
dc.description
dc.description1
dc.description32
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dc.languageen
dc.publisherAcademic Press Inc.
dc.relationStrategies and Tactics in Organic Synthesis
dc.rightsfechado
dc.sourceScopus
dc.titleSubstrate-directed Heck-matsuda Arylations: From Curiosity To A Valuable Synthetic Tool
dc.typeArtículos de revistas


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