dc.creatorCoelho F.
dc.creatorVeronese D.
dc.creatorPavam C.H.
dc.creatorde Paula V.I.
dc.creatorBuffon R.
dc.date2006
dc.date2015-06-30T18:06:47Z
dc.date2015-11-26T14:23:00Z
dc.date2015-06-30T18:06:47Z
dc.date2015-11-26T14:23:00Z
dc.date.accessioned2018-03-28T21:24:56Z
dc.date.available2018-03-28T21:24:56Z
dc.identifier
dc.identifierTetrahedron. , v. 62, n. 18, p. 4563 - 4572, 2006.
dc.identifier404020
dc.identifier10.1016/j.tet.2006.02.045
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-33646112175&partnerID=40&md5=0fd3d505908f17aa8236c1062c34d456
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/103115
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/103115
dc.identifier2-s2.0-33646112175
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1244986
dc.descriptionA palladium-mediated carbonylative cyclization reaction of Baylis-Hillman adducts is disclosed. This simple, efficient and straightforward sequence leads to the formation of an array of 3-alkenylphthalides with different substitution patterns on the aromatic ring, with good chemical yields and selectivities. © 2006 Elsevier Ltd. All rights reserved.
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dc.languageen
dc.publisher
dc.relationTetrahedron
dc.rightsfechado
dc.sourceScopus
dc.titlePalladium-catalyzed Carbonylative Cyclization Of Baylis-hillman Adducts. An Efficient Approach For The Stereoselective Synthesis Of 3-alkenyl Phthalides
dc.typeArtículos de revistas


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