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Please use this identifier to cite or link to this item: http://uvadoc.uva.es/handle/10324/28947
Title: Recyclable Chiral Bifunctional Thioureas Derived from [60]Fullerene and Their Use as Highly Efficient Organocatalysts for the Asymmetric Nitro-Michael Reaction
Authors: Andrés García, José María
González, Miguel
Maestro Fernández, Alicia
Naharro, Daniel
Pedrosa Sáez, Rafael
Issue Date: 2017
Publisher: Wiley
Description: Producción Científica
Citation: European Journal of Organic Chemistry, 2017, Volume 2017, Issue 19, Pages 2683–2691
Abstract: Three novel fullerothioureas derived from natural valine, phenylalanine, and tert-leucine have been prepared by Prato's reaction of [60]fullerene and the corresponding aldehydes. These hybrids have been used as organocatalysts in a typical stereoselective nitro-Michael addition reaction under homogeneous and neat conditions. The catalysts are easily recoverable by filtration, and are recyclable for at least five times. The addition products were obtained in excellent yields and stereoselectivities by using catalyst loadings of as low as 0.5 mol-%.
Keywords: Catálisis
Química orgánica
ISSN: 1434-193X
Peer Review: SI
DOI: 10.1002/ejoc.201601640
Sponsor: Ministerio de Economía, Industria y Competitividad (Project CTQ2014-59870-P)
Publisher Version: http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201601640/full
Language: eng
URI: http://uvadoc.uva.es/handle/10324/28947
Rights: info:eu-repo/semantics/openAccess
Appears in Collections:CINQUIMA - Artículos de revista
DEP67 - Artículos de revista

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