Pinacol Rearrangement and Direct Nucleophilic Substitution of Allylic Alcohols Promoted by Graphene Oxide and Graphene Oxide CO2H

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Title: Pinacol Rearrangement and Direct Nucleophilic Substitution of Allylic Alcohols Promoted by Graphene Oxide and Graphene Oxide CO2H
Authors: Gómez-Martínez, Melania | Baeza, Alejandro | Alonso, Diego A.
Research Group/s: Catálisis Estereoselectiva en Síntesis Orgánica (CESO) | Nuevos Materiales y Catalizadores (MATCAT)
Center, Department or Service: Universidad de Alicante. Departamento de Química Orgánica | Universidad de Alicante. Instituto Universitario de Síntesis Orgánica
Keywords: Allylic compounds | Carbocations | Graphene | Green chemistry | Rearrangement
Knowledge Area: Química Orgánica
Issue Date: 20-Mar-2017
Publisher: Wiley-VCH Verlag GmbH & Co. KGaA
Citation: ChemCatChem. 2017, 9(6): 1032-1039. doi:10.1002/cctc.201601362
Abstract: Graphene oxide (GO) and carboxylic acid functionalized GO (GO–CO2H) have been found to efficiently promote the heterogeneous and environmentally friendly pinacol rearrangement of 1,2-diols and the direct nucleophilic substitution of allylic alcohols. In general, high yields and regioselectivities are obtained in both reactions using 20 wt % of catalyst loading and mild reaction conditions.
Sponsor: Financial support from the University of Alicante (UAUSTI16-03, VIGROB-173), and Spanish Ministerio de Economía y Competitividad (CTQ2015-66624-P) is acknowledged.
URI: http://hdl.handle.net/10045/64767
ISSN: 1867-3880 (Print) | 1867-3899 (Online)
DOI: 10.1002/cctc.201601362
Language: eng
Type: info:eu-repo/semantics/article
Rights: © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Peer Review: si
Publisher version: http://dx.doi.org/10.1002/cctc.201601362
Appears in Collections:INV - MATCAT - Artículos de Revistas
INV - CESO - Artículos de Revistas
INV - AMIC - Artículos de Revistas

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