Gold(I)-catalyzed Benzylation of (Hetero)aryl Boronic Acids with (Hetero)benzyl Bromides by the Strategy of a SN 2-type Reaction.
暂无分享,去创建一个
[1] Qi Sun,et al. Transition-Metal-Free Stereospecific Cross-Coupling with Alkenylboronic Acids as Nucleophiles. , 2016, Journal of the American Chemical Society.
[2] L. Wojtas,et al. Intermolecular Homopropargyl Alcohol Addition to Alkyne and a Sequential 1,6-Enyne Cycloisomerization with Triazole-Gold Catalyst. , 2016, Journal of the American Chemical Society.
[3] N. Ahlsten,et al. Au-Catalyzed Cross-Coupling of Arenes via Double C-H Activation. , 2015, Journal of the American Chemical Society.
[4] Maximilian Joost,et al. Reaktivität von Goldkomplexen in metallorganischen Elementarreaktionen , 2015 .
[5] D. Bourissou,et al. Reactivity of Gold Complexes towards Elementary Organometallic Reactions. , 2015, Angewandte Chemie.
[6] X. Ribas,et al. Oxidant-Free Au(I)-Catalyzed Halide Exchange and C(sp2)-O Bond Forming Reactions. , 2015, Journal of the American Chemical Society.
[7] J. Teles. Oxidative addition to gold(i): a new avenue in homogeneous catalysis with au. , 2015, Angewandte Chemie.
[8] J. Teles. Oxidative Additionen an Gold(I): neue Wege in der homogenen Katalyse mit Gold , 2015 .
[9] C. Jacobsen,et al. Stable Gold(III) Catalysts by Oxidative Addition of a Carbon-Carbon Bond , 2014, Nature.
[10] B. Xiao,et al. Cu-catalyzed Suzuki-Miyaura reactions of primary and secondary benzyl halides with arylboronates. , 2014, Chemical communications.
[11] F. Toste,et al. Gold-catalyzed allylation of aryl boronic acids: accessing cross-coupling reactivity with gold. , 2014, Angewandte Chemie.
[12] M. Kuriyama,et al. Palladium-catalyzed synthesis of heterocycle-containing diarylmethanes through Suzuki-Miyaura cross-coupling. , 2014, The Journal of organic chemistry.
[13] Kevin B. Smith,et al. Copper-catalyzed cross-coupling of boronic esters with aryl iodides and application to the carboboration of alkynes and allenes. , 2014, Angewandte Chemie.
[14] D. Bourissou,et al. Activation of aryl halides at gold(I): practical synthesis of (P,C) cyclometalated gold(III) complexes. , 2014, Journal of the American Chemical Society.
[15] W. J. Wolf,et al. Exceptionally Fast Carbon-Carbon Bond Reductive Elimination from Gold(III) , 2013, Nature chemistry.
[16] C. A. Russell,et al. Gold-Catalyzed Direct Arylation , 2012, Science.
[17] Peng Ren,et al. Copper-catalyzed cross-coupling of functionalized alkyl halides and tosylates with secondary and tertiary alkyl Grignard reagents. , 2012, Angewandte Chemie.
[18] T. Hatakeyama,et al. Iron-catalyzed alkyl-alkyl Suzuki-Miyaura coupling. , 2012, Angewandte Chemie.
[19] M. Zeller,et al. Arylgold(I) complexes from base-assisted transmetalation: structures, NMR properties, and density-functional theory calculations. , 2012, Inorganic chemistry.
[20] Lei Liu,et al. Copper-catalyzed cross-coupling of nonactivated secondary alkyl halides and tosylates with secondary alkyl Grignard reagents. , 2012, Journal of the American Chemical Society.
[21] R. O'hair,et al. Gold-mediated C-I bond activation of iodobenzene. , 2012, Angewandte Chemie.
[22] G. C. Fu,et al. New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles. , 2012, Journal of the American Chemical Society.
[23] Lei Liu,et al. Alkylboronic esters from copper-catalyzed borylation of primary and secondary alkyl halides and pseudohalides. , 2012, Angewandte Chemie.
[24] Magnus T. Johnson,et al. Reactivity of NHC Au(I)-C sigma-bonds with electrophiles. An investigation of their possible involvement in catalytic C-C bond formation , 2011 .
[25] W. Goddard,et al. Two metals are better than one in the gold catalyzed oxidative heteroarylation of alkenes. , 2011, Journal of the American Chemical Society.
[26] G. C. Fu,et al. Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings. , 2011, Journal of the American Chemical Society.
[27] Lei Liu,et al. Copper-catalyzed cross-coupling reaction of organoboron compounds with primary alkyl halides and pseudohalides. , 2011, Angewandte Chemie.
[28] R. Scopelliti,et al. A structure-activity study of Ni-catalyzed alkyl-alkyl Kumada coupling. Improved catalysts for coupling of secondary alkyl halides. , 2011, Journal of the American Chemical Society.
[29] G. C. Fu,et al. Asymmetric Suzuki cross-couplings of activated secondary alkyl electrophiles: arylations of racemic alpha-chloroamides. , 2010, Journal of the American Chemical Society.
[30] G. Lalic,et al. Catalytic SN2'-selective substitution of allylic chlorides with arylboronic esters. , 2010, Organic letters.
[31] H. Ohmiya,et al. Copper-catalyzed gamma-selective and stereospecific allyl-aryl coupling between (Z)-acyclic and cyclic allylic phosphates and arylboronates. , 2010, Organic letters.
[32] A. Gee,et al. Gold-catalyzed intramolecular oxidative cross-coupling of nonactivated arenes. , 2010, Chemistry.
[33] G. C. Fu,et al. Nickel/bis(oxazoline)-catalyzed asymmetric Kumada reactions of alkyl electrophiles: cross-couplings of racemic alpha-bromoketones. , 2010, Journal of the American Chemical Society.
[34] Liming Zhang,et al. Homogeneous gold-catalyzed oxidative carboheterofunctionalization of alkenes. , 2010, Journal of the American Chemical Society.
[35] A. Fürstner. Gold and platinum catalysis--a convenient tool for generating molecular complexity. , 2009, Chemical Society reviews.
[36] A. Echavarren. Gold catalysis: Carbene or cation? , 2009, Nature chemistry.
[37] Liming Zhang,et al. Gold-catalyzed homogeneous oxidative cross-coupling reactions. , 2009, Angewandte Chemie.
[38] G. C. Fu,et al. Nickel-catalyzed Negishi cross-couplings of secondary nucleophiles with secondary propargylic electrophiles at room temperature. , 2008, Angewandte Chemie.
[39] G. Evano,et al. Copper-mediated coupling reactions and their applications in natural products and designed biomolecules synthesis. , 2008, Chemical reviews.
[40] F Dean Toste,et al. Ligand effects in homogeneous Au catalysis. , 2008, Chemical reviews.
[41] A. Echavarren,et al. Gold-catalyzed cycloisomerizations of enynes: a mechanistic perspective. , 2008, Chemical reviews.
[42] Zigang Li,et al. Gold-catalyzed organic transformations. , 2008, Chemical reviews.
[43] G. C. Fu,et al. Enantioselective alkyl-alkyl Suzuki cross-couplings of unactivated homobenzylic halides. , 2008, Journal of the American Chemical Society.
[44] F. Diederich,et al. Metal-Catalyzed Cross-Coupling Reactions: Diederich/Metal , 2007 .
[45] A Stephen K Hashmi,et al. Gold-catalyzed organic reactions. , 2007, Chemical reviews.
[46] F. Dean Toste,et al. Relativistic effects in homogeneous gold catalysis , 2007, Nature.
[47] N. Kambe,et al. Copper-catalyzed cross-coupling reaction of grignard reagents with primary-alkyl halides: remarkable effect of 1-phenylpropyne. , 2007, Angewandte Chemie.
[48] M. R. Gagné,et al. A room temperature negishi cross-coupling approach to C-alkyl glycosides. , 2007, Journal of the American Chemical Society.
[49] M. Zeller,et al. Relativistic functional groups: aryl carbon-gold bond formation by selective transmetalation of boronic acids. , 2006, Angewandte Chemie.
[50] J. Hartwig,et al. Kumada coupling of aryl and vinyl tosylates under mild conditions. , 2005, The Journal of organic chemistry.
[51] G. C. Fu,et al. Asymmetric nickel-catalyzed Negishi cross-couplings of secondary alpha-bromo amides with organozinc reagents. , 2005, Journal of the American Chemical Society.
[52] A. Stephen K. Hashmi,et al. Highly Selective Gold-Catalyzed Arene Synthesis , 2000 .
[53] R. Tobias,et al. Synthesis of cationic dialkylgold(III) complexes: nature of the facile reductive elimination of alkane , 1976 .
[54] J. Kochi,et al. Catalytic mechanism involving oxidative addition in the coupling of alkylgold(I) with alkyl halides , 1972 .
[55] H. Schmidbaur,et al. Organogold-chemie IX. Versuche zur Oxydativen Addition an Organogold-Komplexen☆ , 1972 .
[56] Steven G. Bratsch,et al. Standard Electrode Potentials and Temperature Coefficients in Water at 298.15 K , 1989 .
[57] A. Tamaki,et al. アルキル金(I)とアルキルハライドのカップリングにおける酸化的付加を含んだ触媒的機作 , 1972 .