English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/113980
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:

Crossed intramolecular Rauhut−Currier-type reactions via dienamine activation

AuthorsMarqués-López, Eugenia ; Herrera, Raquel P.; Marks, Timo; Jacobs, Wiebke C.; Könning, Daniel; Figueiredo, Renata M. de; Christmann, Mathias
Issue Date2009
PublisherAmerican Chemical Society
CitationOrganic Letters 11(18): 4116-4119 (2009)
AbstractThe intramolecular Rauhut−Currier reaction creates a carbon−carbon bond between two tethered Michael acceptors. Previous asymmetric versions have relied on 1,4-additions of chiral nucleophilic catalysts. Herein, we investigate a novel strategy that involves the formation of electron rich dienamines as key intermediates. Our methodology provides an efficient entry to the iridoid framework.
DescriptionTrabajo presentado como póster al 3.Tag der Chemie celebrado en Dortmund (Alemania) en 2010.
Publisher version (URL)http://dx.doi.org/10.1021/ol901614t
Identifiersdoi: 10.1021/ol901614t
issn: 1523-7060
e-issn: 1523-7052
Appears in Collections:(ICMA) Artículos
Files in This Item:
File Description SizeFormat 
Rauhut-Currier-Type.pdf171,94 kBAdobe PDFThumbnail
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.