about
Carbohydrates as enantioinduction components in stereoselective catalysisFormation of Gas-Phase Formate in Thermal Reactions of Carbon Dioxide with Diatomic Iron Hydride Anions.Synthesis and structures of ruthenium-NHC complexes and their catalysis in hydrogen transfer reaction.Enhanced Activity of Supported Ni Catalysts Promoted by Pt for Rapid Reduction of Aromatic Nitro Compounds.A Decennary Journey towards the Efficient Asymmetric Hydrogenation of Highly Functionalized Ketones.The Langmuir-Hinshelwood approach for kinetic evaluation of cucurbit[7]uril-capped gold nanoparticles in the reduction of the antimicrobial nitrofurantoin.Recent advances in organocatalytic enantioselective transfer hydrogenation.Shuttle Catalysis-New Strategies in Organic Synthesis.Catalytic enantioselective OFF ↔ ON activation processes initiated by hydrogen transfer: concepts and challenges.The Development of Phosphine-Free "Tethered" Ruthenium(II) Catalysts for the Asymmetric Reduction of Ketones and Imines.Imino Transfer Hydrogenation Reductions.Transition-Metal-Catalyzed Asymmetric Hydrogenation and Transfer Hydrogenation: Sustainable Chemistry to Access Bioactive Molecules.A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst.Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes.Selective cobalt nanoparticles for catalytic transfer hydrogenation of N-heteroarenes.Enhancements in catalytic reactivity and selectivity of homobimetallic complexes containing heteroditopic ligands.Chemoselective Hydrazine-mediated Transfer Hydrogenation of Nitroarenes by Co3 O4 Nanoparticles Immobilized on an Al/Si-mixed Oxide Support.Comparative Study of Bifunctional Mononuclear and Dinuclear Amidoiridium Complexes with Chiral C-N Chelating Ligands for the Asymmetric Transfer Hydrogenation of Ketones.Iron-based nanocatalyst for the acceptorless dehydrogenation reactions.Homoleptic iron(ii) and cobalt(ii) bis(phosphoranimide) complexes for the selective hydrofunctionalization of unsaturated molecules.Photocatalytic alkene reduction by a B12-TiO2 hybrid catalyst coupled with C-F bond cleavage for gem-difluoroolefin synthesis.Hydrogenation and Transfer Hydrogenation Promoted by Tethered Ru-S Complexes: From Cooperative Dihydrogen Activation to Hydride Abstraction/Proton Release from Dihydrogen Surrogates.Catalytic (de)hydrogenation promoted by non-precious metals - Co, Fe and Mn: recent advances in an emerging field.Nickel-Catalyzed Enantioselective Reductive Amination of Ketones with Both Arylamines and Benzhydrazide.Cyclohexa-1,3-diene-based dihydrogen and hydrosilane surrogates in B(C6F5)3-catalysed transfer processes.Stereoselective Transfer Semi-Hydrogenation of Alkynes to E-Olefins with N-Heterocyclic Silylene-Manganese Catalysts.Orderly Layered Zr-Benzylphosphonate Nanohybrids for Efficient Acid-Base-Mediated Bifunctional/Cascade Catalysis.Small "Yaw" Angles, Large "Bite" Angles and an Electron-Rich Metal: Revealing a Stereoelectronic Synergy To Enhance Hydride-Transfer Activity.A ruthenium(ii) bis(phosphinophosphinine) complex as a precatalyst for transfer-hydrogenation and hydrogen-borrowing reactions.Highly Efficient Transition Metal Nanoparticle Catalysts in Aqueous Solutions.Molecularly Defined Manganese Pincer Complexes for Selective Transfer Hydrogenation of Ketones.C(sp(3) )-H Oxidative Addition and Transfer Hydrogenation Chemistry of a Titanium(II) Synthon: Mimicry of Late-Metal Type Reactivity.Rethinking the Claisen-Tishchenko Reaction.Diruthenium(ii)-NNN pincer complex catalysts for transfer hydrogenation of ketones.Catalytic applications of small bite-angle diphosphorus ligands with single-atom linkers.Supported gold nanoparticles catalyzed cis-selective semihydrogenation of alkynes using ammonium formate as the reductant.Iron-Catalyzed Regioselective Transfer Hydrogenative Couplings of Unactivated Aldehydes with Simple Alkenes.Base-Free Asymmetric Transfer Hydrogenation of 1,2-Di- and Monoketones Catalyzed by a (NH)2 P2 -Macrocyclic Iron(II) Hydride.Kinetic investigation into the chemoselective hydrogenation of α,β-unsaturated carbonyl compounds catalyzed by Ni(0) nanoparticles.Chelating N-heterocyclic carbene-carboranes offer flexible ligand coordination to IrIII, RhIII and RuII: effect of ligand cyclometallation in catalytic transfer hydrogenation.
P2860
Q28072011-2136ED4A-52F8-4CBF-A461-CC47C8273784Q36291312-9F0E0B5C-20B3-4444-9191-82BC85BE2F0AQ36322202-4A9FF704-54C1-4FC6-B59B-D03B3C6C786EQ37636348-07323349-DB22-41D7-BDE7-F33919961060Q38559648-3E3DC42A-C38F-4891-84A3-6C0EDDD06754Q38675844-FEF12E10-A098-4319-8C69-AD8089CF8C09Q38754364-A1157522-1805-41FB-B35B-1C1776FEC675Q38765611-DA336B94-B0B2-4CA9-A961-6CB5DA6549FFQ38844938-9A6CD665-84A0-425C-9EE3-6CFE5633D95CQ38927774-A0CC3412-13DD-4A6E-A1E7-9E9E72BCA5CDQ38940186-66B2BDA7-A8D5-4472-9A71-100418FEFA51Q38971756-82B166A9-FB73-499B-8760-10FCF924DE76Q39533886-D227A7CC-7C70-40E0-9433-81887B6776DAQ41175405-EDCC46E1-8D54-48ED-9B64-C76D3398710CQ42279116-64CB96E1-8939-4829-9CF2-87795E5AF6DDQ46358639-9B0A1FEE-0051-495F-BAE2-86048B0AA92FQ46399712-C71551E5-C23B-4933-B4B0-1E524A4FBDC4Q46476059-6A4B911C-8A58-4969-8EB3-5FB5A1968F6EQ47094346-DAB738F2-6F19-4AEA-9339-C4BC6B392A3FQ47769377-E6FCA611-5DBA-44FC-A660-94F8CDB45462Q47811039-445EE320-6174-4D94-B24E-8A4E2F6AC392Q48042046-C5EDBECC-C797-4A2D-ABD0-38C7D328E9D1Q48042952-3C96C000-71FF-445D-9609-3BE8A9C15C94Q48090407-AC63DD8D-5621-4109-9451-866645348CFBQ48122344-88CD9698-2F87-4264-85FD-F949E1C0EDD2Q48140672-053414A4-4664-4BF2-B6C5-4B100F76FD1EQ48183395-5C86259B-EDD2-41AC-9DF6-5F3B8C4A2581Q48186065-9CA256D0-80E1-46D9-835A-847613935CF8Q48241304-2354C58F-0404-4E80-88CF-7C0D58650EDEQ48251741-1913C6ED-A981-454A-8987-F3535596B4FBQ48267725-82F9E77B-331E-414A-BE9B-D2DDDE8F89E1Q48269412-6B2F89AD-B142-49D0-A989-21964469EA2BQ48373336-523D8FA8-9697-4E60-83E2-EE0ADD92269FQ48959624-DD4B225B-FB77-4947-A9B8-E82DAF442460Q50085853-D31CA662-8B1D-4BAD-AE0E-ED7177D01D59Q50230081-7E3CABBA-F3E9-407D-85FF-AB4C8519A753Q51373469-266316E6-84CB-4E1E-852A-0F0FF7342ED2Q52561251-49BDB0CF-027F-4DA3-A763-5FB80EEDE6B6Q52693818-223BC880-2352-432A-B70A-4C3A38BB93EFQ52815210-741FFC78-1B53-4799-A4C7-58B85C28BA02
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
The golden age of transfer hydrogenation.
@en
type
label
The golden age of transfer hydrogenation.
@en
prefLabel
The golden age of transfer hydrogenation.
@en
P1433
P1476
The golden age of transfer hydrogenation.
@en
P2093
P304
P356
10.1021/ACS.CHEMREV.5B00203
P577
2015-06-10T00:00:00Z