Lewis acid-driven reaction pathways in synergistic cooperative catalysis over gold/palladium bimetallic nanoparticles for hydrogen autotransfer reaction between amide and alcohol

[1]  H. Miyamura,et al.  Integrated Process of Aerobic Oxidation–Olefination–Asymmetric CC Bond Formation Catalyzed by Robust Heterogeneous Gold/Palladium and Chirally Modified Rhodium Nanoparticles , 2015 .

[2]  Shuj Kobayashi,et al.  Chiral Metal Nanoparticle Systems as Heterogeneous Catalysts beyond Homogeneous Metal Complex Catalysts for Asymmetric Addition of Arylboronic Acids to α,β-Unsaturated Carbonyl Compounds. , 2015, Journal of the American Chemical Society.

[3]  H. Miyamura,et al.  Preparation of polymer incarcerated gold nanocluster catalysts (PI-Au) and their application to aerobic oxidation reactions of boronic acids, alcohols, and silyl enol ethers , 2014 .

[4]  H. Yoshimitsu,et al.  Reductive coupling reaction of aldehydes using indium(III) triflate as the catalyst , 2014 .

[5]  H. Miyamura,et al.  Tandem oxidative processes catalyzed by polymer-incarcerated multimetallic nanoclusters with molecular oxygen. , 2014, Accounts of chemical research.

[6]  H. Miyamura,et al.  Chiral metal nanoparticle-catalyzed asymmetric C-C bond formation reactions. , 2014, Chemical Society reviews.

[7]  M. Haruta,et al.  Size- and Structure-specificity in Catalysis by Gold Clusters , 2014 .

[8]  H. Miyamura,et al.  Direct amidation from alcohols and amines through a tandem oxidation process catalyzed by heterogeneous-polymer-incarcerated gold nanoparticles under aerobic conditions. , 2013, Chemistry, an Asian journal.

[9]  H. Miyamura,et al.  A heterogeneous layered bifunctional catalyst for the integration of aerobic oxidation and asymmetric C-C bond formation. , 2013, Chemical communications.

[10]  Xiaoyuan Zou,et al.  Tandem Synthesis of N‐Alkylated Amides from Aldoximes and Alcohols by Using a Ru/Ir Dual‐Catalyst System , 2013 .

[11]  S. H. Siddiki,et al.  Heterogeneous Ni Catalysts for N-Alkylation of Amines with Alcohols , 2013 .

[12]  Kangnian Fan,et al.  C-C cross-coupling of primary and secondary benzylic alcohols using supported gold-based bimetallic catalysts. , 2013, ChemSusChem.

[13]  Zhihui Shao,et al.  Combining transition metal catalysis and organocatalysis--an update. , 2013, Chemical Society reviews.

[14]  H. Miyamura,et al.  Selective Lactam Formation from Amino Alcohols Using Polymer‐Incarcerated Gold and Gold/Cobalt Nanoparticles as Catalysts under Aerobic Oxidative Conditions , 2012 .

[15]  H. Miyamura,et al.  A Cooperative Catalytic System of Platinum/Iridium Alloyed Nanoclusters and a Dimeric Catechol Derivative: An Efficient Synthesis of Quinazolines Through a Sequential Aerobic Oxidative Process , 2012 .

[16]  H. Miyamura,et al.  Polymer-incarcerated chiral Rh/Ag nanoparticles for asymmetric 1,4-addition reactions of arylboronic acids to enones: remarkable effects of bimetallic structure on activity and metal leaching. , 2012, Journal of the American Chemical Society.

[17]  H. Miyamura,et al.  α-Hydroxylation of 1,3-Dicarbonyl Compounds Catalyzed by Polymer-incarcerated Gold Nanoclusters with Molecular Oxygen , 2012 .

[18]  H. Miyamura,et al.  Discovery of a metalloenzyme-like cooperative catalytic system of metal nanoclusters and catechol derivatives for the aerobic oxidation of amines. , 2012, Journal of the American Chemical Society.

[19]  Yan Zhang,et al.  Nano-gold catalysis in fine chemical synthesis. , 2012, Chemical reviews.

[20]  G. Hutchings,et al.  Selective liquid phase oxidation with supported metal nanoparticles , 2012 .

[21]  J. Porco,et al.  Chemical Synthesis of Complex Molecules Using Nanoparticle Catalysis. , 2012, ACS catalysis.

[22]  D. MacMillan,et al.  Synergistic Catalysis: A Powerful Synthetic Strategy for New Reaction Development. , 2012, Chemical science.

[23]  N. T. Patil,et al.  A one-pot catalysis: the strategic classification with some recent examples. , 2012, Organic & biomolecular chemistry.

[24]  Shuj Kobayashi,et al.  Powerful amide synthesis from alcohols and amines under aerobic conditions catalyzed by gold or gold/iron, -nickel or -cobalt nanoparticles. , 2011, Journal of the American Chemical Society.

[25]  H. Miyamura,et al.  Aerobic Oxidation of Amines Catalyzed by Polymer-Incarcerated Au Nanoclusters: Effect of Cluster Size and Cooperative Functional Groups in the Polymer , 2011 .

[26]  M. Yus,et al.  Nickel nanoparticles in hydrogen transfer reactions. , 2011, Accounts of chemical research.

[27]  A. Corma,et al.  Gold-catalyzed carbon-heteroatom bond-forming reactions. , 2011, Chemical reviews.

[28]  H. Sakurai,et al.  Aerobic oxidations catalyzed by colloidal nanogold. , 2011, Chemistry, an Asian journal.

[29]  A. Watson,et al.  Borrowing hydrogen methodology for amine synthesis under solvent-free microwave conditions. , 2011, The Journal of organic chemistry.

[30]  H. Miyamura,et al.  Polymer-incarcerated gold-palladium nanoclusters with boron on carbon: a mild and efficient catalyst for the sequential aerobic oxidation-Michael addition of 1,3-dicarbonyl compounds to allylic alcohols. , 2011, Journal of the American Chemical Society.

[31]  Youquan Deng,et al.  Organic ligand-free alkylation of amines, carboxamides, sulfonamides, and ketones by using alcohols catalyzed by heterogeneous Ag/Mo oxides. , 2011, Chemistry.

[32]  H. Miyamura,et al.  In situ coupled oxidation cycle catalyzed by highly active and reusable Pt-catalysts: dehydrogenative oxidation reactions in the presence of a catalytic amount of o-chloranil using molecular oxygen as the terminal oxidant. , 2010, Chemical communications.

[33]  H. Miyamura,et al.  Polymer-incarcerated metal(0) cluster catalysts. , 2010, Chemical record.

[34]  H. Miyamura,et al.  Remarkable effect of bimetallic nanocluster catalysts for aerobic oxidation of alcohols: combining metals changes the activities and the reaction pathways to aldehydes/carboxylic acids or esters. , 2010, Journal of the American Chemical Society.

[35]  A. Watson,et al.  The Give and Take of Alcohol Activation , 2010, Science.

[36]  H. Miyamura,et al.  Aerobic oxidative esterification of alcohols catalyzed by polymer-incarcerated gold nanoclusters under ambient conditions , 2010 .

[37]  M. Yus,et al.  Hydrogen autotransfer in the N-alkylation of amines and related compounds using alcohols and amines as electrophiles. , 2010, Chemical reviews.

[38]  R. Crabtree,et al.  Dehydrogenation as a substrate-activating strategy in homogeneous transition-metal catalysis. , 2010, Chemical reviews.

[39]  R. Matsubara,et al.  Addition reactions of sulfonylimidates with imines catalyzed by alkaline earth metals. , 2009, Angewandte Chemie.

[40]  K. Fujita,et al.  N-Alkylation of carbamates and amides with alcohols catalyzed by a Cp∗Ir complex , 2009 .

[41]  M. Whittlesey,et al.  Transition metal catalysed reactions of alcohols using borrowing hydrogen methodology. , 2009, Dalton transactions.

[42]  H. Miyamura,et al.  Aerobic oxidation of hydroquinone derivatives catalyzed by polymer-incarcerated platinum catalyst. , 2008, Angewandte Chemie.

[43]  H. Miyamura,et al.  Aerobic Oxidation of Alcohols under Mild Conditions Catalyzed by Novel Polymer‐Incarcerated, Carbon‐Stabilized Gold Nanoclusters , 2008 .

[44]  Avelino Corma,et al.  Supported gold nanoparticles as catalysts for organic reactions. , 2008, Chemical Society reviews.

[45]  H. Miyamura,et al.  Gold-platinum bimetallic clusters for aerobic oxidation of alcohols under ambient conditions. , 2008, Chemical communications.

[46]  A. Baiker,et al.  Asymmetric catalysis at chiral metal surfaces. , 2007, Chemical reviews.

[47]  Masatake Haruta,et al.  Gold catalysts: towards sustainable chemistry. , 2007, Angewandte Chemie.

[48]  Masatake Haruta,et al.  New generation of gold catalysts: nanoporous foams and tubes -- is unsupported gold catalytically active? , 2007, Chemphyschem : a European journal of chemical physics and physical chemistry.

[49]  Jonathan M. J. Williams,et al.  Borrowing hydrogen in the activation of alcohols , 2007 .

[50]  Masahiro Noji,et al.  Metal triflate-catalyzed cationic benzylation and allylation of 1,3-dicarbonyl compounds. , 2007, The Journal of organic chemistry.

[51]  H. Miyamura,et al.  Aerobic oxidation of alcohols at room temperature and atmospheric conditions catalyzed by reusable gold nanoclusters stabilized by the benzene rings of polystyrene derivatives. , 2007, Angewandte Chemie.

[52]  S. Saito,et al.  Highly anti-selective catalytic aldol reactions of amides with aldehydes. , 2006, Journal of the American Chemical Society.

[53]  M. Haruta.  Catalysis: Gold rush , 2005, Nature.

[54]  H. Shimizu,et al.  Bismuth triflate-chiral bipyridine complexes as water-compatible chiral Lewis acids. , 2005, Organic letters.

[55]  Masatake Haruta,et al.  When gold is not noble: catalysis by nanoparticles. , 2003, Chemical record.

[56]  S. Nagayama,et al.  A Novel Classification of Lewis Acids on the Basis of Activity and Selectivity , 2000 .

[57]  Naoki Toshima,et al.  Bimetallic nanoparticles—novel materials for chemical and physical applications , 1998 .

[58]  Masatake Haruta,et al.  Gold catalysts prepared by coprecipitation for low-temperature oxidation of hydrogen and of carbon monoxide , 1989 .

[59]  Hiroshi Sano,et al.  Novel Gold Catalysts for the Oxidation of Carbon Monoxide at a Temperature far Below 0 °C , 1987 .

[60]  Yoshihisa Watanabe,et al.  The Ruthenium Catalyzed N-Alkylation of Amides with Alcohols , 1983 .