Publication:
Pd(II)-catalyzed deprotection of acetals and ketals containing acid sensitive functional groups

dc.contributor.authorJuliá Hernández, Francisco
dc.contributor.authorArcas, Aurelia
dc.contributor.authorVicente, José
dc.contributor.departmentQuímica Inorgánica
dc.date.accessioned2025-01-07T11:38:19Z
dc.date.available2025-01-07T11:38:19Z
dc.date.issued2014-02-05
dc.description© 2014. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/.This document is the Accepted version of a Published Work that appeared in final form in Tetrahedron Letters. To access the final edited and published work see https://doi.org/10.1016/j.tetlet.2013.12.067
dc.description.abstractThe pincer complex [Pd(C1,O1,N1-L)(NCMe)]ClO4 (L = monoanionic ligand resulting from deprotonation of the acetyl group of the dimethyl monoketal of 2,6-diacetylpyridine) is used for the high-yield and selective catalytic hydrolysis of aliphatic, aromatic, cyclic and acyclic dimethyl-acetals, - ketals and dioxolanes, even in the presence of large substituents. Other protecting groups, as THP or TBDMS, or very acid-sensitive alcohols were not affected. The catalyst is easily prepared in high yield from Pd(AcO)2 and 2,6-diacetylpyridinium perchlorate stable to air and moisture, easily and fully recoverable and reusable.
dc.formatapplication/pdfes
dc.format.extent13es
dc.identifier.citationTetrahedron Letters 2014, 55, 1141-1144
dc.identifier.doihttps://doi.org/10.1016/j.tetlet.2013.12.067
dc.identifier.issnPrint: 0040-4039
dc.identifier.issnElectronic: 1873-3581
dc.identifier.urihttp://hdl.handle.net/10201/147930
dc.languageenges
dc.publisherElsevier
dc.relationMinisterio de Educación y Ciencia (Spain), FEDER (Grant CTQ2011-24016) and Fundación Séneca (Grants 04539/GERM/06 and 03059/PI/05) for financial support and a grant to F. J.-H.es
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0040403913021539?via%3Dihub
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAcetalses
dc.subjectCatalysises
dc.subjectHydrolysises
dc.subjectPalladiumes
dc.subjectAcetal deprotectiones
dc.subject.otherCDU::5 - Ciencias puras y naturaleses
dc.titlePd(II)-catalyzed deprotection of acetals and ketals containing acid sensitive functional groupses
dc.typeinfo:eu-repo/semantics/articlees
dspace.entity.typePublicationes
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
tetlett2014-accepted.pdf
Size:
271.77 KB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
2.26 KB
Format:
Item-specific license agreed upon to submission
Description:
Collections