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Direct Synthesis of 1,3-Diketones by Rh-Catalyzed Reductive α-Acylation of Enones

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What this work says

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

inferredcites →https://doi.org/10.1002/0471264229.os083.23openalex-snapshot

Trifluoromethylation at the α‐Position of α,β‐Unsaturated Ketones: 4‐Phenyl‐3‐(Trifluoromethyl)Butan‐2‐One

inferredcites →https://doi.org/10.1002/anie.200602950openalex-snapshot

Chemo‐ and Regioselective Preparation and Reaction of a Kinetic Zinc Enolate Formed from a Thiol Ester and Bis(iodozincio)methane

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/chin.200643140openalex-snapshot

1,3‐Diketones from Acid Chlorides and Ketones: A Rapid and General One‐Pot Synthesis of Pyrazoles.

inferredcites →https://doi.org/10.1002/jhet.5570270233openalex-snapshot

Synthesis of 4,4‐dimethyl‐3,4‐dihydro‐3,3,5‐trisubstituted‐2H‐pyrazoles and N‐benzoyl derivatives: Method for “Hydrolysis” of unreactive amides and carbamates

inferredcites →https://doi.org/10.1016/j.tet.2007.09.081openalex-snapshot

Rh-catalyzed novel α-fluoroalkylation of α,β-unsaturated ketones and its mechanism

inferredcites →https://doi.org/10.1016/j.tetlet.2005.10.036openalex-snapshot

Proline-catalyzed aldol reactions of acyl cyanides with acetone: an efficient and convenient synthesis of 1,3-diketones

inferredcites →https://doi.org/10.1016/s0040-4039(02)00432-xopenalex-snapshot

The regioselective preparation of 1,3-diketones

inferredcites →https://doi.org/10.1016/s0065-2725(08)60579-6openalex-snapshot

Progress in Pyrazole Chemistry

inferredcites →https://doi.org/10.1021/jo00028a079openalex-snapshot

Attempted synthesis of 1,2,3,4-tetraphenylfluoreno[1,9-gh]quinoline

inferredcites →https://doi.org/10.1021/jo00117a051openalex-snapshot

Reduction of 5-(Trifluoromethyl)isoxazoles with Lithium Aluminum Hydride: Synthesis of (2,2,2-Trifluoroethyl)aziridines

inferredcites →https://doi.org/10.1021/jo051087fopenalex-snapshot

γ,δ-Unsaturated β-Diketones by Acylation of Ketones

inferredcites →https://doi.org/10.1021/jo991878fopenalex-snapshot

Synthesis of β-Dicarbonyl Compounds Using 1-Acylbenzotriazoles as Regioselective C-Acylating Reagents

inferredcites →https://doi.org/10.1021/ol048134vopenalex-snapshot

Rhodium-Catalyzed Novel Trifluoromethylation at the α-Position of α,β-Unsaturated Ketones

inferredcites →https://doi.org/10.1021/ol060570popenalex-snapshot

1,3-Diketones from Acid Chlorides and Ketones: A Rapid and General One-Pot Synthesis of Pyrazoles

inferredcites →https://doi.org/10.1021/ol061948mopenalex-snapshot

Triethylgallium as a Nonnucleophilic Base to Generate Enolates from Ketones

inferredcites →https://doi.org/10.1021/ol701599vopenalex-snapshot

Direct Carbon−Carbon Bond Formation via Soft Enolization: A Facile and Efficient Synthesis of 1,3-Diketones

inferredcites →https://doi.org/10.1039/b201220kopenalex-snapshot

The regioselective preparation of 1,3-diketones within a micro reactor

inferredcites →https://doi.org/10.1139/v05-130openalex-snapshot

Synthesis and structure of new trichloromethyl-β-diketones 5-Trichloromethylisoxazole and 5-isoxazolecarboxylic acid derivatives

inferredcites →https://doi.org/10.15227/orgsyn.083.0177openalex-snapshot

TRIFLUOROMETHYLATION AT THE a-POSITION OF b,b-UNSATURATED KETONES: 4-PHENYL-3-(TRIFLUOROMETHYL)BUTAN-2-ONE

inferredcites →https://doi.org/10.2174/1385272033486134openalex-snapshot

Recent Advances in the Chemistry of 1,3-Diketones: Structural Modifications and Synthetic Applications

inferredcites →https://doi.org/10.2174/1385272033486233openalex-snapshot

Recent Advances in the Synthesis of 1,3-Diketones

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.4670490openalex-extracted

Generation and Radical-Radical Cross-Coupling of Alkenyloxy Radical: Ester and Ketone Synthesis

inferred← citeshttps://doi.org/10.1002/0471264229.os089.35openalex-snapshot

Discussion Addendum for: Trifluoromethylation at the α‐Position of α,β‐Unsaturated Ketones: 4‐Phenyl‐3‐Trifluoromethyl‐2‐Butanone

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Rhodium Enolate Complexes as Synthons and Catalysts in Organic Chemistry

inferred← citeshttps://doi.org/10.1002/9780471264194.fos02718.pub3openalex-snapshot

Chlorotris(triphenylphosphine)rhodium( I ) ( W ilkinson's catalyst)

inferred← citeshttps://doi.org/10.1002/9780471264194.fos02718.pub4openalex-snapshot

Chlorotris(triphenylphosphine)rhodium( I )

inferred← citeshttps://doi.org/10.1002/9780471264194.fos02718.pub5openalex-snapshot

Chlorotris(triphenylphosphine)rhodium( I )

inferred← citeshttps://doi.org/10.1002/9780471264194.fos02718.pub6openalex-snapshot

Chlorotris(triphenylphosphine)rhodium( I )

inferred← citeshttps://doi.org/10.1002/adsc.201100463openalex-snapshot

Reductive Reformatsky–Honda Reaction of α,β‐Unsaturated Esters: Facile Formation of 1,3‐Dicarbonyl Compounds and β‐Hydroxy Esters

inferred← citeshttps://doi.org/10.1002/adsc.202500007openalex-snapshot

Photoredox Assisted Net‐Neutral Radical‐Polar Crossover α ‐Acylation of Enol Acetates with Acyl Chlorides: Access to 1,3‐Diketones

inferred← citeshttps://doi.org/10.1002/ange.201107494openalex-snapshot

Palladium‐Catalyzed Carbonylative α‐Arylation for Accessing 1,3‐Diketones

inferred← citeshttps://doi.org/10.1002/ange.202421872openalex-snapshot

Kationische, Iod(III)‐vermittelte und dirigierte diastereoselektive Oxidation inerter C−H‐Bindungen in cyclischen Kohlenwasserstoffen

inferred← citeshttps://doi.org/10.1002/anie.201107494openalex-snapshot

Palladium‐Catalyzed Carbonylative α‐Arylation for Accessing 1,3‐Diketones

inferred← citeshttps://doi.org/10.1002/anie.202421872openalex-snapshot

Cationic, Iodine(III)‐Mediated and Directed Diastereoselective Oxidation of Inert C−H Bonds in Cyclic Hydrocarbons

inferred← citeshttps://doi.org/10.1002/aoc.4786openalex-snapshot

Ball milling: a green mechanochemical approach for synthesis of Ni (II), Co (II) and Cu (II) complexes

inferred← citeshttps://doi.org/10.1002/chem.201001068openalex-snapshot

Rhodium‐Catalyzed Synthesis of γ‐Pyrones by Three Consecutive Redox–Aldol Reactions of Allylic Alcohols with α,β‐Unsaturated Aldehydes

inferred← citeshttps://doi.org/10.1002/chem.201303384openalex-snapshot

Pd‐Catalyzed Carbonylative α‐Arylation of Aryl Bromides: Scope and Mechanistic Studies

inferred← citeshttps://doi.org/10.1002/chin.200845087openalex-snapshot

ChemInform Abstract: Direct Synthesis of 1,3‐Diketones by Rh‐Catalyzed Reductive α‐Acylation of Enones.

inferred← citeshttps://doi.org/10.1002/ejic.201101014openalex-snapshot

Synthesis of β‐Hydroxy and β‐Amino Ketones from Allylic Alcohols Catalyzed by Ru(η5‐C5Ph5)(CO)2Cl

inferred← citeshttps://doi.org/10.1002/ejoc.202001041openalex-snapshot

Reductive Carbon–Carbon Bond Forming Reactions with Carbonyls Mediated by Rh–H Complexes

inferred← citeshttps://doi.org/10.1002/mrc.2668openalex-snapshot

Synthesis and characterization of 1‐ and 2‐cinnamoyloxyacetonaphthones

inferred← citeshttps://doi.org/10.1007/s10870-010-9923-3openalex-snapshot

Synthesis and X-Ray Crystal Structure of 1- and 2-Cinnamoyaloxy Acetonaphthones

inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00822-3openalex-snapshot

8.20 Partial Reduction of Enones, Styrenes, and Related Systems

inferred← citeshttps://doi.org/10.1016/j.cclet.2019.12.016openalex-snapshot

Hetero diacylation of 1,1-diborylalkanes: Practical synthesis of 1,3-diketones

inferred← citeshttps://doi.org/10.1016/j.rechem.2024.101860openalex-snapshot

The chemical organic reactions of β-diketones to prepare different β-diketone derivatives, their properties and its applications: A review

inferred← citeshttps://doi.org/10.1016/j.saa.2014.12.040openalex-snapshot

Synthesis, spectroscopic, thermal and antimicrobial studies of neodymium(III) and samarium(III) complexes derived from tetradentate ligands containing N and S donor atoms

inferred← citeshttps://doi.org/10.1016/j.tet.2017.09.017openalex-snapshot

Mitsunobu C-alkylation of β -alkoxycarbonyl 2-nitrobenzenesulfones and its use for the rapid synthesis of novel benzothiazine derivatives

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.06.009openalex-snapshot

Rhodium-catalyzed hydroaroylation of α,β-unsaturated esters using aroyl chlorides and Et2MeSiH

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.08.109openalex-snapshot

Reductive aldol-type reaction of α,β-unsaturated esters with aldehydes or ketones in the presence of Rh catalyst and Et2Zn

inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.10.006openalex-snapshot

Direct synthesis of 1,3-dicarbonyl compounds via radical coupling of aldehydes with ketones under metal-free conditions

inferred← citeshttps://doi.org/10.1021/acs.joc.6b02575openalex-snapshot

Room-Temperature Coupling/Decarboxylation Reaction of α-Oxocarboxylates with α-Bromoketones: Solvent-Controlled Regioselectivity for 1,2- and 1,3-Diketones

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00627openalex-snapshot

Generation and Radical–Radical Cross-Coupling of Alkenyloxy Radical

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01501openalex-snapshot

Synthesis of Unnatural 2-Substituted Quinolones and 1,3-Diketones by a Member of Type III Polyketide Synthases from Huperzia serrata

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02320openalex-snapshot

Stereoselective Multicomponent Reactions Using Zincate Nucleophiles: β-Dicarbonyl Synthesis and Functionalization

inferred← citeshttps://doi.org/10.1021/ol501619wopenalex-snapshot

Csp3–Csp3 Homocoupling Reaction of Benzyl Halides Catalyzed by Rhodium

inferred← citeshttps://doi.org/10.1039/c2cc32787bopenalex-snapshot

Iridium-catalyzed reaction of enones with alcohols affording 1,3-diketones

inferred← citeshttps://doi.org/10.1039/c8ob01861hopenalex-snapshot

An effective preparation of both 1,3-diketones and nitriles from alkynones with oximes as hydroxide sources

inferred← citeshttps://doi.org/10.1039/c9ob00494gopenalex-snapshot

Facile access to 1,3-diketones by gold( i )-catalyzed regioselective hydration of ynones

inferred← citeshttps://doi.org/10.1039/d1gc02856aopenalex-snapshot

Formal metal-free γ-arylation of 1,3-dicarbonyl compounds via an isomerisation/1,4-addition/[3,3]-sigmatropic rearrangement sequence

inferred← citeshttps://doi.org/10.1039/d5qo00827aopenalex-snapshot

Visible-light or sunlight-driven copper catalysis for base-free synthesis of β-diketones via radical acylation of enol silyl ethers

inferred← citeshttps://doi.org/10.1107/s1600536811028820openalex-snapshot

[2-(4-Methylbenzoyl)phenyl](4-methylphenyl)methanone

inferred← citeshttps://doi.org/10.1107/s1600536811047131openalex-snapshot

(Biphenyl-4-yl)[2-(4-methylbenzoyl)phenyl]methanone

inferred← citeshttps://doi.org/10.1107/s1600536813000032openalex-snapshot

1-Cyclopropyl-2-(2-fluorophenyl)-5-(4-fluorophenyl)-3-phenylpentane-1,5-dione

inferred← citeshttps://doi.org/10.1107/s1600536813001050openalex-snapshot

8,8-Dimethyl-8,9-dihydro-7H-chromeno[2,3-b]quinoline-10,12-dione

inferred← citeshttps://doi.org/10.1107/s1600536813001062openalex-snapshot

2-Chloro-8,8-dimethyl-8,9-dihydro-7H-chromeno[2,3-b]quinoline-10,12-dione

inferred← citeshttps://doi.org/10.1107/s1600536813001074openalex-snapshot

5-(4-Chlorophenyl)-1-cyclopropyl-2-(2-fluorophenyl)-3-phenylpentane-1,5-dione

inferred← citeshttps://doi.org/10.1107/s1600536813011276openalex-snapshot

3-(4-Chlorophenyl)-1-cyclopropyl-2-(2-fluorophenyl)-5-phenylpentane-1,5-dione

inferred← citeshttps://doi.org/10.1134/s1070428015060019openalex-snapshot

1,3-Diketones. Synthesis and properties

inferred← citeshttps://doi.org/10.1134/s1070428024070091openalex-snapshot

One-Pot Synthesis of 1,3-Diketones from Alkynones with the Assistance of Imidazole

inferred← citeshttps://doi.org/10.3762/bjoc.18.176openalex-snapshot

Rhodium-catalyzed intramolecular reductive aldol-type cyclization: Application for the synthesis of a chiral necic acid lactone

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