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Please use this identifier to cite or link to this item: http://uvadoc.uva.es/handle/10324/21720
Title: Diamine Catalyzed Addition of ZnEt2 to PhC(O)CF3: Two Mechanisms and Autocatalytic Asymmetric Enhancement
Authors: Calvillo Barahona, Mercedes
Casares González, Juan Ángel
Cordovilla, Carlos
Genov, Miroslav N.
Martínez de Ilarduya, Jesús María
Espinet Rubio, Pablo
Issue Date: 2014
Publisher: Wiley
Description: Producción Científica
Citation: Chemistry - A European Journal, 2014, vol. 20, Issue 45, p. 14800–14806
Abstract: NMR studies of the catalytic addition reaction of ZnEt2 to PhC(O)CF3 in the presence of three very efficient catalysts [TMEDA, tBuBOX, and L; where L is a chiral diamine synthesized from optically pure (R,R)-1,2-diphenylethylenediamine and (S)-2,2'-bis-(bromomethyl)-1,1'-binaphthalene] reveal large differences in their behavior. For the ligands TMEDA and tBuBOX, the catalysis shows no unusual features and proceeds via [(N?N)Zn(Et){OC(CF3 )(Et)Ph}]. For N?N?L, the observation of autocatalytic asymmetric enhancement during the catalysis, and unusual inverse concentration dependence on the reaction rate, indicate the participation of an additional novel catalytic cycle that goes through a dinuclear intermediate containing one ZnEt2 and one ZnEt fragment connected by N?N and OR bridges. Interestingly, the (19) F NMR signals of the main product of the reaction ([Zn(Et){OC*(CF3 )(Et)Ph}]2 ) allowed us to assess the enantioselectivity of the processes in situ without the assistance of chiral chromatography.
Keywords: Catalyst
ISSN: 0947-6539
Peer Review: SI
DOI: 10.1002/chem.201403648
Sponsor: Ministerio de Economía, Industria y Competitividad (CTQ2013-48406-P)
Junta de Castilla y León (programa de apoyo a proyectos de investigación – Ref. GR169 and VA256U13)
Language: eng
URI: http://uvadoc.uva.es/handle/10324/21720
Rights: info:eu-repo/semantics/openAccess
Appears in Collections:CINQUIMA - Artículos de revista
DEP63 - Artículos de revista

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