(Me3Si)3SiH-mediated intermolecular radical perfluoroalkylation reactions of olefins in water

Figure presented. Perfluoroalkyl-substituted compounds are regarded as important components of fluorophors and for the introduction of fluorous tags into organic substrates. Their syntheses in organic solvents are achieved through different methods, among which, the addition of perfluoroalkyl radica...

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Autor principal: Barata-Vallejo, S.
Otros Autores: Postigo, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2010
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Acceso en línea:Registro en Scopus
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LEADER 12880caa a22018977a 4500
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024 7 |2 scopus  |a 2-s2.0-77956542116 
024 7 |2 cas  |a carbon, 7440-44-0; cyanide, 57-12-5; oxygen, 7782-44-7; silane, 7803-62-5; water, 7732-18-5; Alkenes; Free Radicals; Hydrocarbons, Fluorinated; Silicones; Water, 7732-18-5 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JOCEA 
100 1 |a Barata-Vallejo, S. 
245 1 0 |a (Me3Si)3SiH-mediated intermolecular radical perfluoroalkylation reactions of olefins in water 
260 |c 2010 
270 1 0 |m Postigo, A.; Faculty of Science, University of Belgrano, Villanueva 1324 CP, 1426-Buenos Aires, Argentina; email: alberto.postigo@ub.edu.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a Figure presented. Perfluoroalkyl-substituted compounds are regarded as important components of fluorophors and for the introduction of fluorous tags into organic substrates. Their syntheses in organic solvents are achieved through different methods, among which, the addition of perfluoroalkyl radicals to unsaturated bonds represents a convenient choice. On the other hand, intermolecular radical reactions in water have attracted the attention of synthetic chemists as a strategic route to carbon-carbon bond formation reactions. In this paper we undertook the intermolecular addition of perfluoroalkyl radicals on electron rich alkenes and alkenes with electron withdrawing groups in water, mediated by silyl radicals, and obtained perfluoroalkyl-substituted compounds in fairly good yields. The radical triggering events employed consist of the thermal decomposition of an azo compound and the dioxygen initiation. Our results indicate that for intermolecular carbon-carbon bond formation reactions mediated by (Me 3Si)3SiH, the decomposition of the azo compound 1,1′-azobis(cyclohexanecarbonitrile) (ACCN) is the best radical initiator. We also found that water exerts a relevant solvent effect on the rates of perfluoroalkyl radical additions onto double bonds and the H atom abstraction from the silane. Our account provides a versatile and convenient method to achieve perfluoroalkylation reactions of alkenes in water to render perfluoroalkylated alkanes as key intermediates in the synthesis of fluorophors and other fluorinated materials. This is the first report where perfluoroalkyl-substituted alkanes are synthesized through intermolecular radical carbon-carbon bond formation reactions in water, mediated by silyl radicals. © 2010 American Chemical Society.  |l eng 
593 |a Faculty of Science, University of Belgrano, Villanueva 1324 CP, 1426-Buenos Aires, Argentina 
593 |a Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón 2, 3er piso, CP 1428-Buenos Aires, Argentina 
690 1 0 |a AZO COMPOUND 
690 1 0 |a CARBON-CARBON BOND FORMATION REACTIONS 
690 1 0 |a DIOXYGENS 
690 1 0 |a DOUBLE BONDS 
690 1 0 |a ELECTRON WITHDRAWING GROUP 
690 1 0 |a ELECTRON-RICH ALKENES 
690 1 0 |a FLUORINATED MATERIALS 
690 1 0 |a FLUOROPHORS 
690 1 0 |a FLUOROUS 
690 1 0 |a GOOD YIELD 
690 1 0 |a H-ATOM ABSTRACTION 
690 1 0 |a INTERMOLECULAR ADDITIONS 
690 1 0 |a ORGANIC SUBSTRATE 
690 1 0 |a PERFLUOROALKYL RADICALS 
690 1 0 |a PERFLUOROALKYLATION 
690 1 0 |a RADICAL CARBON 
690 1 0 |a RADICAL INITIATORS 
690 1 0 |a RADICAL REACTIONS 
690 1 0 |a SILYL RADICAL 
690 1 0 |a SOLVENT EFFECTS 
690 1 0 |a SUBSTITUTED COMPOUNDS 
690 1 0 |a SYNTHETIC CHEMISTS 
690 1 0 |a THERMAL DECOMPOSITIONS 
690 1 0 |a UNSATURATED BONDS 
690 1 0 |a CHEMICAL BONDS 
690 1 0 |a OLEFINS 
690 1 0 |a ORGANIC SOLVENTS 
690 1 0 |a PARAFFINS 
690 1 0 |a PYROLYSIS 
690 1 0 |a REACTION INTERMEDIATES 
690 1 0 |a REACTION KINETICS 
690 1 0 |a ADDITION REACTIONS 
690 1 0 |a 1,1' AZOBIS(CYCLOHEXANECARBONITRILE) 
690 1 0 |a ALKANE DERIVATIVE 
690 1 0 |a ALKENE DERIVATIVE 
690 1 0 |a ALKYL GROUP 
690 1 0 |a BORANE DERIVATIVE 
690 1 0 |a CYANIDE 
690 1 0 |a OXYGEN 
690 1 0 |a PERFLUOROALKYL 
690 1 0 |a SILANE 
690 1 0 |a SILYLHYDROBORANE 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a WATER 
690 1 0 |a ALKENE 
690 1 0 |a FLUORINATED HYDROCARBON 
690 1 0 |a FREE RADICAL 
690 1 0 |a SILICONE DERIVATIVE 
690 1 0 |a WATER 
690 1 0 |a ALKYLATION 
690 1 0 |a ARTICLE 
690 1 0 |a CHEMICAL BOND 
690 1 0 |a PERFLUOROALKYLATION 
690 1 0 |a STRUCTURE ANALYSIS 
690 1 0 |a SUBSTITUTION REACTION 
690 1 0 |a SYNTHESIS 
690 1 0 |a CHEMICAL STRUCTURE 
690 1 0 |a CHEMISTRY 
690 1 0 |a STEREOISOMERISM 
690 1 0 |a ALKENES 
690 1 0 |a ALKYLATION 
690 1 0 |a FREE RADICALS 
690 1 0 |a HYDROCARBONS, FLUORINATED 
690 1 0 |a MOLECULAR STRUCTURE 
690 1 0 |a SILICONES 
690 1 0 |a STEREOISOMERISM 
690 1 0 |a WATER 
650 1 7 |2 spines  |a CARBON 
700 1 |a Postigo, A. 
773 0 |d 2010  |g v. 75  |h pp. 6141-6148  |k n. 18  |p J. Org. Chem.  |x 00223263  |w (AR-BaUEN)CENRE-337  |t Journal of Organic Chemistry 
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856 4 0 |u https://doi.org/10.1021/jo100901z  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00223263_v75_n18_p6141_BarataVallejo  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v75_n18_p6141_BarataVallejo  |y Registro en la Biblioteca Digital 
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