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Cross-coupling reactions catalyzed by RuHCl(CO)(PPh 3 ) 3

https://doi.org/10.1039/d2cy01953a

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/adsc.200600638openalex-snapshot

Borrowing Hydrogen in the Activation of Alcohols

inferredcites →https://doi.org/10.1002/adsc.202200765openalex-snapshot

RuH‐Catalyzed Synthesis of 1,3‐Diaryl Ketones via Cross‐Coupling of Aromatic Enones with Aromatic Aldehydes and Mechanistic Insights

inferredcites →https://doi.org/10.1002/anie.200603794openalex-snapshot

Alcohols as Electrophiles in CC Bond‐Forming Reactions: The Hydrogen Autotransfer Process

inferredcites →https://doi.org/10.1002/anie.200701005openalex-snapshot

Ruthenium Hydride Catalyzed Regioselective Addition of Aldehydes to Enones To Give 1,3‐Diketones

inferredcites →https://doi.org/10.1002/anie.201802434openalex-snapshot

Metal‐Catalyzed Remote Functionalization of ω‐Ene Unsaturated Ethers: Towards Functionalized Vinyl Species

inferredcites →https://doi.org/10.1016/0022-328x(85)80446-0openalex-snapshot

Transformation of organic compounds in the presence of metal complexes

inferredcites →https://doi.org/10.1016/s0040-4039(00)71157-9openalex-snapshot

Stereoselective synthesis of tetrahydrofuran-3-carbaldehyde

inferredcites →https://doi.org/10.1016/s0040-4039(01)92103-3openalex-snapshot

Homogeneous rearrangement of unsaturated carbinols to saturated ketones catalyzed by ruthenium complexes

inferredcites →https://doi.org/10.1021/acs.chemrev.5b00203openalex-snapshot

The Golden Age of Transfer Hydrogenation

inferredcites →https://doi.org/10.1021/acs.joc.8b02123openalex-snapshot

RuHCl(CO)(PPh3)3-Catalyzed Direct Amidation of Arene C–H Bond with Azides

inferredcites →https://doi.org/10.1021/acscatal.0c01174openalex-snapshot

Alkene Isomerization through Allylmetals as a Strategic Tool in Stereoselective Synthesis

inferredcites →https://doi.org/10.1021/acscatal.1c02144openalex-snapshot

Kinetically Controlled Stereoselective Access to Branched 1,3-Dienes by Ru-Catalyzed Remote Conjugative Isomerization

inferredcites →https://doi.org/10.1021/acscentsci.1c00125openalex-snapshot

Borrowing Hydrogen for Organic Synthesis

inferredcites →https://doi.org/10.1021/ar9502341openalex-snapshot

Asymmetric Transfer Hydrogenation Catalyzed by Chiral Ruthenium Complexes

inferredcites →https://doi.org/10.1021/cr00013a015openalex-snapshot

Asymmetric hydrogen transfer reactions promoted by homogeneous transition metal catalysts

inferredcites →https://doi.org/10.1021/cr00066a003openalex-snapshot

Heterogeneous catalytic transfer hydrogenation and its relation to other methods for reduction of organic compounds

inferredcites →https://doi.org/10.1021/cr60291a003openalex-snapshot

Catalytic transfer hydrogenation

inferredcites →https://doi.org/10.1021/cr900202jopenalex-snapshot

Dehydrogenation as a Substrate-Activating Strategy in Homogeneous Transition-Metal Catalysis

inferredcites →https://doi.org/10.1021/ja512015wopenalex-snapshot

Alkyne Hydroacylation: Switching Regioselectivity by Tandem Ruthenium Catalysis

inferredcites →https://doi.org/10.1021/ja5130258openalex-snapshot

Ruthenium-Catalyzed C–C Coupling of Amino Alcohols with Dienes via Transfer Hydrogenation: Redox-Triggered Imine Addition and Related Hydroaminoalkylations

inferredcites →https://doi.org/10.1021/ja805356jopenalex-snapshot

Diene Hydroacylation from the Alcohol or Aldehyde Oxidation Level via Ruthenium-Catalyzed C−C Bond-Forming Transfer Hydrogenation: Synthesis of β,γ-Unsaturated Ketones

inferredcites →https://doi.org/10.1021/ja806929yopenalex-snapshot

Ruthenium Hydride-Catalyzed Addition of Aldehydes to Dienes Leading to β,γ-Unsaturated Ketones

inferredcites →https://doi.org/10.1021/jo01299a021openalex-snapshot

Isomerization of N-allylamides and -imides to aliphatic enamides by iron, rhodium, and ruthenium complexes

inferredcites →https://doi.org/10.1021/jo9918753openalex-snapshot

Isomerization Reaction of Olefin Using RuClH(CO)(PPh3)3

inferredcites →https://doi.org/10.1021/ol302145aopenalex-snapshot

RuHCl(CO)(PPh3)3-Catalyzed α-Alkylation of Ketones with Primary Alcohols

inferredcites →https://doi.org/10.1021/ol902289ropenalex-snapshot

Synthesis of 2-Hydroxymethyl Ketones by Ruthenium Hydride-Catalyzed Cross-Coupling Reaction of α,β-Unsaturated Aldehydes with Primary Alcohols

inferredcites →https://doi.org/10.1021/om00036a051openalex-snapshot

Catalytic transfer hydrogenation of benzaldehyde in a microwave oven

inferredcites →https://doi.org/10.1021/om049646gopenalex-snapshot

Isomerism of [Ru(η3-allyl)Cl(CO)(PPh3)2]

inferredcites →https://doi.org/10.1038/nchem.2445openalex-snapshot

Remote functionalization through alkene isomerization

inferredcites →https://doi.org/10.1039/b602103dopenalex-snapshot

An unusual dimerization of primary unsaturated alcohols catalyzed by RuHCl(CO)(PPh3)3

inferredcites →https://doi.org/10.1039/b813383bopenalex-snapshot

Transition metal catalysed reactions of alcohols using borrowing hydrogen methodology

inferredcites →https://doi.org/10.1039/b912850fopenalex-snapshot

Hydroruthenation triggered catalytic conversion of dialdehydes and keto aldehydes to lactones

inferredcites →https://doi.org/10.1039/c3ra42834fopenalex-snapshot

Ruthenium hydride/nitrogen tridentate ligand-catalyzed α-alkylation of acetamides with primary alcohols

inferredcites →https://doi.org/10.1039/d0cs00449aopenalex-snapshot

Transition metal-catalyzed alkene isomerization as an enabling technology in tandem, sequential and domino processes

inferredcites →https://doi.org/10.1246/cl.130465openalex-snapshot

Synthesis of Alkylated Nitriles by [RuHCl(CO)(PPh3)3]-catalyzed Alkylation of Acetonitrile Using Primary Alcohols

inferredcites →https://doi.org/10.1246/cl.1981.1435openalex-snapshot

1,3-O- TO C-ALKYL MIGRATION OF 1-ALKENYL ALKYL ACETALS CATALYZED BY BORON TRIFLUORIDE. A NOVEL CROSS ALDOL TYPE REACTION

inferredcites →https://doi.org/10.1246/cl.2008.1102openalex-snapshot

Formation of C–C Bonds via Ruthenium-catalyzed Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation Level

inferredcites →https://doi.org/10.1246/cl.2011.1453openalex-snapshot

Diaryl Ketone Synthesis by [RuHCl(CO)(PPh3)3]-catalyzed Coupling Reaction of Arylboronic Acids with Aryl Aldehydes

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4673734openalex-extracted

Triphenylphosphine-Derived Ligands for Rhodium-Catalyzed High Olefin Hydroformylations: From Traditional Molecules to Modern Cage Ligands

inferred← citeshttps://doi.org/10.1002/9783527841448.ch4openalex-snapshot

Polyacylation for Ion Exchange Membrane Preparation

inferred← citeshttps://doi.org/10.1002/adsc.202201394openalex-snapshot

RuHCl(CO)(PPh3)3‐Catalyzed Isomerization of Homoallyl Silyl Ethers and Carbonates to Allyl Silyl Ethers and Carbonates

inferred← citeshttps://doi.org/10.1002/cctc.202500100openalex-snapshot

Synthesis of 16‐Electron RuHCl(CO)(PPh3)2 Catalyst Rendering Superior C═C Double Bond Isomerization Activity

inferred← citeshttps://doi.org/10.1002/marc.202500171openalex-snapshot

Green and Sustainable Chemistry Approaches on Azide‐Based Click Reactions in Polymer Science

inferred← citeshttps://doi.org/10.1021/acscatal.3c02209openalex-snapshot

Intermolecular Metal-Catalyzed C–C Coupling of Unactivated Alcohols or Aldehydes for Convergent Ketone Construction beyond Premetalated Reagents

inferred← citeshttps://doi.org/10.1039/d4dt02627fopenalex-snapshot

Modular synthesis of triphenylphosphine-derived cage ligands for rhodium-catalyzed hydroformylation applications

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