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Rh( iii )-Catalyzed C–H bond activation/annulation reactions of arylacyl ammonium salts with 4-diazoisochroman-3-imines and 4-diazoisoquinolin-3-ones

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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.201900079openalex-snapshot

Rhodium/Gold Dual Catalysis in Carbene sp2 C−H Functionalization/Conia‐ene Cascade for the Stereoselective Synthesis of Diverse Spirocarbocycles

inferredcites →https://doi.org/10.1002/adsc.202000807openalex-snapshot

Radical‐Mediated Non‐Dearomative Strategies in Construction of Spiro Compounds

inferredcites →https://doi.org/10.1002/anie.200800924openalex-snapshot

Fluorescent Naphthyl‐ and Anthrylazoles from the Catalytic Coupling of Phenylazoles with Internal Alkynes through the Cleavage of Multiple CH Bonds

inferredcites →https://doi.org/10.1002/anie.201006222openalex-snapshot

Rhodium‐Catalyzed Oxidative Olefination of CH Bonds in Acetophenones and Benzamides

inferredcites →https://doi.org/10.1002/anie.201201273openalex-snapshot

Mild Rhodium(III)‐Catalyzed CH Activation and Intermolecular Annulation with Allenes

inferredcites →https://doi.org/10.1002/anie.201207204openalex-snapshot

Rhodium(III)‐Catalyzed Oxidative CH Functionalization of Azomethine Ylides

inferredcites →https://doi.org/10.1002/anie.201207995openalex-snapshot

Rhodium(III)‐Catalyzed Alkenyl CH Bond Functionalization: Convergent Synthesis of Furans and Pyrroles

inferredcites →https://doi.org/10.1002/anie.201300881openalex-snapshot

Rhodium(III)‐Catalyzed Redox‐Neutral Coupling of N‐Phenoxyacetamides and Alkynes with Tunable Selectivity

inferredcites →https://doi.org/10.1002/anie.201307174openalex-snapshot

N‐Oxide as a Traceless Oxidizing Directing Group: Mild Rhodium(III)‐Catalyzed CH Olefination for the Synthesis of ortho‐Alkenylated Tertiary Anilines

inferredcites →https://doi.org/10.1002/anie.201406747openalex-snapshot

Rhodium(III)‐Catalyzed CC and CO Coupling of Quinoline N‐Oxides with Alkynes: Combination of CH Activation with O‐Atom Transfer

inferredcites →https://doi.org/10.1002/chem.201303730openalex-snapshot

Rhodium‐Catalyzed Directed Sulfenylation of Arene CH Bonds

inferredcites →https://doi.org/10.1002/ejoc.201900675openalex-snapshot

Copper‐Catalyzed Dimerization of Sulfoxonium Ylides with 3‐Diazoindolin‐2‐imines: A Practical and Efficient Approach to Spiro[cyclopropane‐1,3′‐indolin]‐2′‐imines

inferredcites →https://doi.org/10.1016/0040-4020(80)80024-xopenalex-snapshot

Methodology for the construction of quaternary carbon centers

inferredcites →https://doi.org/10.1016/j.bmcl.2014.06.081openalex-snapshot

The use of spirocyclic scaffolds in drug discovery

inferredcites →https://doi.org/10.1016/j.ejmech.2010.04.001openalex-snapshot

Synthesis and biological evaluation of novel spiro 6-methoxytetralin-1,3′-pyrrolidine based organoselenocyanates against cadmium-induced oxidative and hepatic damage in mice

inferredcites →https://doi.org/10.1016/s0040-4020(99)00482-2openalex-snapshot

Stereocontrolled synthesis of spirocyclics

inferredcites →https://doi.org/10.1021/acs.joc.0c02204openalex-snapshot

Base Promoted Three-Component Annulation of 4-Diazoisochroman-3-imines with Dimethylsulfonium Ylides: Synthesis of Highly Functionalized Isochromeno[4,3-c]pyridazines

inferredcites →https://doi.org/10.1021/acs.joc.5b02824openalex-snapshot

Rh(III)-Catalyzed Redox-Neutral Annulation of Primary Benzamides with Diazo Compounds: Approach to Isoquinolinones

inferredcites →https://doi.org/10.1021/acs.joc.6b00264openalex-snapshot

Access to Isoquinolines and Isoquinolin-3-ols via Rh(III)-Catalyzed Coupling/Cyclization Cascade Reaction of Arylimidates and Diazo Compounds

inferredcites →https://doi.org/10.1021/acs.orglett.0c00145openalex-snapshot

C(sp2)–H Bond Multiple Functionalization in Air for Construction of Tetrahydrocarbazoles with Continuous Quaternary Carbons and Polycyclic Diversification

inferredcites →https://doi.org/10.1021/acs.orglett.5b03669openalex-snapshot

Rh(III)-Catalyzed Synthesis of N-Unprotected Indoles from Imidamides and Diazo Ketoesters via C–H Activation and C–C/C–N Bond Cleavage

inferredcites →https://doi.org/10.1021/acs.orglett.7b01642openalex-snapshot

Synthesis of 2,3-Benzodiazepines via Rh(III)-Catalyzed C–H Functionalization of N-Boc Hydrazones with Diazoketoesters

inferredcites →https://doi.org/10.1021/acs.orglett.9b00779openalex-snapshot

Three-Component Coupling of Aldehydes, 2-Aminopyridines, and Diazo Esters via Rhodium(III)-Catalyzed Imidoyl C–H Activation: Synthesis of Pyrido[1,2-a]pyrimidin-4-ones

inferredcites →https://doi.org/10.1021/acs.orglett.9b03708openalex-snapshot

Preparation of 4-Diazoisoquinolin-3-ones via Dimroth Rearrangement and Their Extension to 4-Aryltetrahydroisoquinolin-3-ones

inferredcites →https://doi.org/10.1021/ar700137zopenalex-snapshot

Chiral Diphosphine and Monodentate Phosphorus Ligands on a Spiro Scaffold for Transition-Metal-Catalyzed Asymmetric Reactions

inferredcites →https://doi.org/10.1021/ja110932popenalex-snapshot

Immunosuppressive Polyketides from Mantis-Associated Daldinia eschscholzii

inferredcites →https://doi.org/10.1021/ja305771yopenalex-snapshot

Rh-Catalyzed Intermolecular Carbenoid Functionalization of Aromatic C–H Bonds by α-Diazomalonates

inferredcites →https://doi.org/10.1021/ja3099245openalex-snapshot

Rhodium(III)-Catalyzed N-Nitroso-Directed C–H Olefination of Arenes. High-Yield, Versatile Coupling under Mild Conditions

inferredcites →https://doi.org/10.1021/ja310153vopenalex-snapshot

Mild Rh(III)-Catalyzed C–H Activation and Annulation with Alkyne MIDA Boronates: Short, Efficient Synthesis of Heterocyclic Boronic Acid Derivatives

inferredcites →https://doi.org/10.1021/ja3104389openalex-snapshot

Rh(III)-Catalyzed Regioselective Synthesis of Pyridines from Alkenes and α,β-Unsaturated Oxime Esters

inferredcites →https://doi.org/10.1021/ja402274gopenalex-snapshot

A Coupling of Benzamides and Donor/Acceptor Diazo Compounds To Form γ-Lactams via Rh(III)-Catalyzed C–H Activation

inferredcites →https://doi.org/10.1021/ja405140fopenalex-snapshot

Rh(III)-Catalyzed C–H Activation and Double Directing Group Strategy for the Regioselective Synthesis of Naphthyridinones

inferredcites →https://doi.org/10.1021/ja406338ropenalex-snapshot

Rh(III)-Catalyzed Synthesis of Multisubstituted Isoquinoline and Pyridine N-Oxides from Oximes and Diazo Compounds

inferredcites →https://doi.org/10.1021/ja408541copenalex-snapshot

Rhodium(III)-Catalyzed Indole Synthesis Using N–N Bond as an Internal Oxidant

inferredcites →https://doi.org/10.1021/ja409861sopenalex-snapshot

Room-Temperature Synthesis of Trisubstituted Allenylsilanes via Regioselective C–H Functionalization

inferredcites →https://doi.org/10.1021/ja511796hopenalex-snapshot

Rhodium-Catalyzed C–H Activation of Phenacyl Ammonium Salts Assisted by an Oxidizing C–N Bond: A Combination of Experimental and Theoretical Studies

inferredcites →https://doi.org/10.1021/ja902762aopenalex-snapshot

Palladium-Catalyzed Alkenylation of Quinoline-N-oxides via C−H Activation under External-Oxidant-Free Conditions

inferredcites →https://doi.org/10.1021/jo900396zopenalex-snapshot

Waste-Free Synthesis of Condensed Heterocyclic Compounds by Rhodium-Catalyzed Oxidative Coupling of Substituted Arene or Heteroarene Carboxylic Acids with Alkynes

inferredcites →https://doi.org/10.1021/ol402523xopenalex-snapshot

Traceless Directing Strategy: Efficient Synthesis of N-Alkyl Indoles via Redox-Neutral C–H Activation

inferredcites →https://doi.org/10.1021/ol402796mopenalex-snapshot

Synthesis of Isoquinolines via Rh(III)-Catalyzed C–H Activation Using Hydrazone as a New Oxidizing Directing Group

inferredcites →https://doi.org/10.1021/ol500345nopenalex-snapshot

Highly Functionalized Pyridines Synthesis from N-Sulfonyl Ketimines and Alkynes Using the N–S Bond as an Internal Oxidant

inferredcites →https://doi.org/10.1021/ol501483kopenalex-snapshot

Rh-Catalyzed Sequential Oxidative C–H and N–N Bond Activation: Conversion of Azines into Isoquinolines with Air at Room Temperature

inferredcites →https://doi.org/10.1021/ol9909280openalex-snapshot

Synthesis and DNA Binding of Spirocyclic Model Compounds Related to the Neocarzinostatin Chromophore

inferredcites →https://doi.org/10.1038/ncomms5610openalex-snapshot

A multitasking functional group leads to structural diversity using designer C–H activation reaction cascades

inferredcites →https://doi.org/10.1039/c1cs15156hopenalex-snapshot

Enantioselective methodologies for the synthesis of spiro compounds

inferredcites →https://doi.org/10.1039/c4cc01520gopenalex-snapshot

Rh( iii )-catalyzed synthesis of 1-aminoindole derivatives from 2-acetyl-1-arylhydrazines and diazo compounds in water

inferredcites →https://doi.org/10.1039/c4cs00288aopenalex-snapshot

Transition metal-catalyzed C–H functionalization of N-oxyenamine internal oxidants

inferredcites →https://doi.org/10.1039/c4ob00512kopenalex-snapshot

Rhodium( iii )-catalyzed formal oxidative [4 + 1] cycloaddition of benzohydroxamic acids and α-diazoesters. A facile synthesis of functionalized benzolactams

inferredcites →https://doi.org/10.1039/c6cs00825aopenalex-snapshot

New development in the enantioselective synthesis of spiro compounds

inferredcites →https://doi.org/10.1039/c7cc00603aopenalex-snapshot

Convenient preparation of 4-diazoisochroman-3-imines and 3-subsituted 3,5-dihydroisochromeno[3,4-d][1,2,3]triazoles

inferredcites →https://doi.org/10.1039/d0qo01515fopenalex-snapshot

Recent advances in the synthesis of indole embedded heterocycles with 3-diazoindolin-2-imines

inferredcites →https://doi.org/10.1055/s-1978-24682openalex-snapshot

Synthesis of Carbocyclic Spiro Compounds via Cycloaddition Routes

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.4650920openalex-extracted

inferred← citeshttps://doi.org/10.1016/j.catcom.2024.106862openalex-snapshot

Magnetically retractable tea extract stabilized palladium nanoparticles for denitrogenative cross-coupling of aryl bromides with arylhydrazines under green conditions: An alternate route for the biaryls synthesis

inferred← citeshttps://doi.org/10.1016/j.tet.2023.133392openalex-snapshot

Rh(III)-catalyzed cascade annulation of 4-diazoisoquinolin-3-ones with benzoic acids to access spiro[isobenzofuran-1,4′-isoquinoline]-3,3′-diones

inferred← citeshttps://doi.org/10.1021/acs.joc.3c00117openalex-snapshot

Rh(III)-Catalyzed Spiroannulation Reaction of N-Aryl Nitrones with 2-Diazo-1,3-indandiones: Synthesis of Spirocyclic Indole-N-oxides and Their 1,3-Dipolar Cycloaddition with Maleimides

inferred← citeshttps://doi.org/10.1039/d2ob01400aopenalex-snapshot

Rh( ii )-catalyzed synthesis of 5 H -isochromeno[3,4- b ]indolizines from 4-diazoisochroman-3-imines and pyridines

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