{"product_id":"9783527349029","title":"Supramolecular Catalysis : New Directions and Developments","description":"\u003cp\u003eSupramolecular Catalysis at its best! This book gathers the \"who-is-who\" in the field who are presenting the most important topics in this exciting field. Preface\n\u003cbr\u003eIntroduction\n\u003cbr\u003eLIGAND-LIGAND INTERACTIONS\n\u003cbr\u003eSupramolecular Construction of Bidentate Ligands through Self-assembly by Hydrogen Bonding\n\u003cbr\u003eSelf-Assembled bidentate ligands in transition metal catalysis; from fundamental invention to commercial application\n\u003cbr\u003eSELF-ASSEMBLED NANOSTRUCTURES AND MULTI-COMPONENT ASSEMBLIES\n\u003cbr\u003eAssembled Ionic Molecular Catalysts and Ligands\n\u003cbr\u003eSelf-Amplification of Enantioselectivity in Asymmetric Catalysis by Supramolecular Recognition and Stereodynamics\n\u003cbr\u003eInterlocked Molecules in Asymmetric Catalysis\n\u003cbr\u003eCatalytic Supramolecular Gels\n\u003cbr\u003eSupramolecular helical catalysts\n\u003cbr\u003eSelf-Assembled multi-component supramolecular catalysts for asymmetric reactions\n\u003cbr\u003eLIGAND-SUBSTRATE INTERACTIONS\n\u003cbr\u003eHarnessing non-covalent interactions for control of site-selectivity in transition metal-catalyzed C-H activation and cross-coupling\n\u003cbr\u003eSupramolecular interactions in distal C-H activation of (hetero)arenes\n\u003cbr\u003eTransition metal-catalyzed, site- and enantioselective oxygen and nitrogen transfer enabled by lactam hydrogen bonds\n\u003cbr\u003eSupramolecular substrate orientation as strategy to control selectivity in transition metal catalysis\n\u003cbr\u003ePhosphine Ligands with Acylguanidinium Groups as Substrate-directing Unit\n\u003cbr\u003eChemical reactions controlled by remote Zn...N interactions between substrates and catalysts\n\u003cbr\u003eCATALYSIS PROMOTED BY DISCRETE CAGES, CAPSULES AND OTHER CONFINED ENVIRONMENTS\n\u003cbr\u003eArtificial Enzymes Created Through Molecular Imprinting of Cross-Linked Micelles\n\u003cbr\u003eBioinspired catalysis using innately polarized Pd2L4 coordination cages\n\u003cbr\u003eSupramolecular catalysis with a cubic coordination cage: contributions from cavity and external-surface binding\n\u003cbr\u003eTransition metal catalysis in confined spaces\n\u003cbr\u003eCatalysis by Metal Organic Cages: A Computational Perspective\n\u003cbr\u003eN-heterocyclic carbene (NHC)-capped Cyclodextrins for cavity-controlled catalysis\n\u003cbr\u003eSupramolecular Catalysis by Metallohosts Based on Glycoluril\n\u003cbr\u003eCatalysis inside the hexameric resorcinare capsule: Towards addressing current challenges in synthetic organic chemistry\n\u003cbr\u003eSupramolecular Organocatalysis Within the Nanospace of Resorcinarene Capsule\n\u003cbr\u003eResorcin[4]arene hexamer: from nanocontainer to nanocatalyst\n\u003cbr\u003eSUPRAMOLECULAR ORGANOCATALYSIS AND NON-CLASSICAL INTERACTIONS\n\u003cbr\u003eThe Aryl-Pyrrolidine-tert-Leucine Motif as a New Privileged Chiral Scaffold: The Role of Non-Covalent Stabilizing Interactions\n\u003cbr\u003eChiral Triazole Foldamers in Enantioselective Anion-Binding Catalysis\n\u003cbr\u003eSupramolecular Catalysis via Organic Solids: Templates to Mechanochemistry to Cascades\n\u003cbr\u003eExploration of halogen bonding for the catalysis of organic reactions\n\u003cbr\u003eChalcogen-Bonding Catalysis\n\u003cbr\u003eAsymmetric Supramolecular Organocatalysis: the Fourth Pillar of Catalysis\n\u003cbr\u003eSUPRAMOLECULAR CATALYSIS IN WATER\n\u003cbr\u003eMetal Catalysis in Micellar Media\n\u003cbr\u003eSurfactant assemblies as nanoreactors for organic transformations\n\u003cbr\u003eCompartmentalized polymers for catalysis in aqueous media\n\u003cbr\u003ePhosphines modified by cyclodextrins for supramolecular catalysis in water\n\u003cbr\u003eWater-Soluble Yoctoliter Reaction Flasks\n\u003cbr\u003eChemical catalyst-promoted regioselective histone acylation \n\u003cbr\u003eProtein-substrate supramolecular interactions for the shape selective hydroformylation of long chain a-olefins\n\u003cbr\u003eSupramolecular assembly of DNA- and protein-based artificial metalloenzymes\n\u003cbr\u003eSUPRAMOLECULAR ALLOSTERIC CATALYSTS AND REPLICATORS\n\u003cbr\u003eSwitchable Catalysis Using Allosteric Effects\n\u003cbr\u003eSupramolecularly regulated enantioselective catalysts\n\u003cbr\u003eEmergent catalysis by self-replicating molecules\n\u003cbr\u003e Piet van Leeuwen worked at the Koninklijke Shell Laboratorium Amsterdam (1968-1994) heading the homogeneous catalysis group, he is emeritus professor of homogeneous catalysis of the University of Amsterdam (1989-2007) and the Eindhoven University of Technology (2001-2006), the Netherlands, he was Group leader in ICIQ, Tarragona, Spain (2004-2015), and had an IDEX Chair at LPCNO in INSA-Toulouse, France (2015-2020). \n\u003cbr\u003e \n\u003cbr\u003eMatthieu Raynal is a researcher at Sorbonne Université, Paris, France. His current research focuses on the development of supramolecular helical catalysts, the design of functional chiral assemblies, and the structure-property relationship of supramolecular polymers.\u003c\/p\u003e","brand":"Wiley-VCH","offers":[{"title":"Default Title","offer_id":49826009186552,"sku":"00000_00000_00000_00000","price":485.58,"currency_code":"AUD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0789\/8208\/6904\/files\/9783527349029-1.jpg?v=1783779672","url":"https:\/\/kinokuniya.com.au\/ja\/products\/9783527349029","provider":"Books Kinokuniya Australia","version":"1.0","type":"link"}