Selective Kumada biaryl cross-coupling reaction enabled by an iron(III) alkoxide-N-heterocyclic carbene catalyst system.
暂无分享,去创建一个
[1] Richard L. Lord,et al. Reductive coupling of azides mediated by an iron(II) bis(alkoxide) complex. , 2013, Inorganic chemistry.
[2] P. Knochel,et al. Efficient chromium(II)-catalyzed cross-coupling reactions between Csp2 centers. , 2013, Journal of the American Chemical Society.
[3] P. Knochel,et al. Ligand-accelerated iron- and cobalt-catalyzed cross-coupling reactions between N-heteroaryl halides and aryl magnesium reagents. , 2013, Angewandte Chemie.
[4] J. Schläfer,et al. Heterobi- and trimetallic cerium(IV) tert-butoxides with mono-, di-, and trivalent metals (M = K(I), Ge(II), Sn(II), Pb(II), Al(III), Fe(III)). , 2013, Inorganic chemistry.
[5] D. Nocera,et al. Iron in a trigonal tris(alkoxide) ligand environment. , 2013, Inorganic chemistry.
[6] Jean-Baptiste Sortais,et al. N‐Heterocyclic Carbene Ligands and Iron: An Effective Association for Catalysis , 2013 .
[7] B. R. Rad,et al. Highly chemoselective cobalt-catalyzed biaryl coupling reactions , 2013 .
[8] P. Knochel,et al. Iron-catalyzed cross-coupling of N-heterocyclic chlorides and bromides with arylmagnesium reagents. , 2012, Organic letters.
[9] M. Ingleson,et al. N-Heterocyclic carbene chemistry of iron: fundamentals and applications. , 2012, Chemical communications.
[10] A. J. von Wangelin,et al. Chlorostyrenes in iron-catalyzed biaryl coupling reactions. , 2012, Angewandte Chemie.
[11] Allan M Jordan,et al. The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates. , 2011, Journal of medicinal chemistry.
[12] Javier Magano,et al. Large-scale applications of transition metal-catalyzed couplings for the synthesis of pharmaceuticals. , 2011, Chemical reviews.
[13] A. Corma,et al. Iron-Catalysed Regio- and Stereoselective Head-to-Tail Dimerisation of Styrenes , 2010 .
[14] E. Nakamura,et al. Low-valent iron-catalyzed C-C bond formation-addition, substitution, and C-H bond activation. , 2010, The Journal of organic chemistry.
[15] Matthew E Welsch,et al. Privileged scaffolds for library design and drug discovery. , 2010, Current opinion in chemical biology.
[16] R. Kellogg,et al. Practical Aspects of Carbon−Carbon Cross-Coupling Reactions Using Heteroarenes , 2010 .
[17] T. Skrydstrup,et al. Heteroaromatic sulfonates and phosphates as electrophiles in iron-catalyzed cross-couplings. , 2009, Organic letters.
[18] T. Hatakeyama,et al. Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: a new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides. , 2009, Journal of the American Chemical Society.
[19] J. Cvengroš,et al. Coming of age: sustainable iron-catalyzed cross-coupling reactions. , 2009, ChemSusChem.
[20] A. Fürstner. From oblivion into the limelight: iron (domino) catalysis. , 2009, Angewandte Chemie.
[21] P. T. Wolczanski. Structure and reactivity studies of transition metals ligated by tBuSi3X (X = O, NH, N, S, and CC). , 2009, Chemical communications.
[22] Alois Fürstner,et al. The promise and challenge of iron-catalyzed cross coupling. , 2008, Accounts of chemical research.
[23] Matthias Beller,et al. Sustainable metal catalysis with iron: from rust to a rising star? , 2008, Angewandte Chemie.
[24] T. Hatakeyama,et al. Iron-catalyzed selective biaryl coupling: remarkable suppression of homocoupling by the fluoride anion. , 2007, Journal of the American Chemical Society.
[25] A. Gaumont,et al. Metal-Catalyzed Cross-Coupling Reactions , 2007 .
[26] J. S. Carey,et al. Analysis of the reactions used for the preparation of drug candidate molecules. , 2006, Organic & biomolecular chemistry.
[27] M. Darabantu,et al. Aryl‐aryl bonds formation in pyridine and diazine series. Diazines part 41 , 2005 .
[28] P. Power. Some highlights from the development and use of bulky monodentate ligands , 2004 .
[29] L. Zani,et al. Iron-catalyzed reactions in organic synthesis. , 2004, Chemical reviews.
[30] I. Cepanec. Synthesis of biaryls , 2004 .
[31] M. Kusserow,et al. Alkoxo-Verbindungen des dreiwertigen Eisen: Synthese und Charakterisierung von [Fe2(OtBu)6], [Fe2Cl2(OtBu)4], [Fe2Cl4(OtBu)2] und [N(nBu)4]2[Fe6OCl6(OMe)12] , 2003 .
[32] A. Fürstner,et al. Iron-catalyzed cross-coupling reactions. , 2002, Journal of the American Chemical Society.
[33] R. Hocquemiller,et al. Iron-catalysed arylation of heteroaryl halides by Grignard reagents , 2002 .
[34] A. Fürstner,et al. Iron-Catalyzed Cross-Coupling Reactions of Alkyl-Grignard Reagents with Aryl Chlorides, Tosylates, and Triflates , 2002 .
[35] M. Hillmyer,et al. Rapid and controlled polymerization of lactide by structurally characterized ferric alkoxides. , 2001, Journal of the American Chemical Society.
[36] E. Nakamura,et al. Iron-Catalyzed Olefin Carbometalation , 2000 .
[37] P. T. Wolczanski. Chemistry of electrophilic metal centres coordinated by silox (tBu3SiO), tritox (tBu3CO) and related binfunctional ligands , 1995 .