English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/132515
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

Title

A robust and general protocol for the Lewis-base-catalysed reaction of alcohols and alkyl propiolates

AuthorsTejedor, David ; Álvarez-Méndez, Sergio J.; López-Soria, Juan M.; Martín, Víctor S.; García-Tellado, Fernando
KeywordsOrganocatalysis
Alkynes
­Amines
Alcohols
Vinyl ethers
Issue DateJan-2014
PublisherJohn Wiley & Sons
CitationEuropean Journal of Organic Chemistry: 198-205 (2014)
AbstractA general and practical protocol for the tertiary-amine-catalysed synthesis of β-alkoxyacrylates from primary, secondary, and tertiary alcohols is described. Of the currently used catalysts, DABCO proved to be the best one for this process. Three factors seem to influence the outcome of the reaction: (1) the nucleophilic strength of the catalyst, (2) the electrophilicity of the intermediate ammonium acrylate, and (3) the pKa/nucleophilicity of the alcohol/alkoxide nucleophile. Reactivity tuning enables the transformation of a range of tertiary alcohols into the corresponding β-alkoxyacrylate derivatives. Differences in the reactivity of different types of alcohol allow the selective transformation of diols containing two different hydroxy groups into the corresponding monoprotected derivatives. This protocol will aid other synthetic organic chemists to easily prepare such vinyl ethers under atom-economic, efficient, and bench-friendly reaction conditions. A practical protocol for the DABCO-catalysed synthesis of β-alkoxyacrylates is described. The protocol is efficient and economical, and it allows the transformation of a range of alcohols (including tertiary alcohols) into the corresponding β-alkoxyacrylate derivatives and the selective monoprotection of different diols (primary vs. secondary and tertiary). Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publisher version (URL)http://dx.doi.org/10.1002/ejoc.201301303
URIhttp://hdl.handle.net/10261/132515
DOI10.1002/ejoc.201301303
Identifiersissn: 1434-193X
e-issn: 1099-0690
Appears in Collections:(IPNA) Artículos
Files in This Item:
File Description SizeFormat 
accesoRestringido.pdf15,38 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.