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Applications of ortho-Quinone Methide Intermediates in Catalysis and Asymmetric Synthesis
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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/anie.201001597openalex-snapshot
Dynamic Cross‐Linking Is Retained in Duplex DNA after Multiple Exchange of Strands
inferredcites →https://doi.org/10.1002/jhet.232openalex-snapshot
Syntheses of chromenes and chromanes via o‐quinone methide intermediates
inferredcites →https://doi.org/10.1016/s0040-4020(02)00496-9openalex-snapshot
o-Quinone methides: intermediates underdeveloped and underutilized in organic synthesis
inferredcites →https://doi.org/10.1021/ar010105mopenalex-snapshot
Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals: A Structure−Reactivity Relationship
inferredcites →https://doi.org/10.1021/bi00260a005openalex-snapshot
Studies on interaction of anthracycline antibiotics and deoxyribonucleic acid: equilibrium binding studies on the interaction of daunomycin with deoxyribonucleic acid
inferredcites →https://doi.org/10.1021/ja00094a013openalex-snapshot
Novel Michael Additions to Phenols Promoted by Osmium(II): Convenient Stereoselective Syntheses of 2,4- and 2,5-Cyclohexadienones
inferredcites →https://doi.org/10.1021/ja00167a060openalex-snapshot
Synthesis and chemistry of a quinone methide model for anthracycline antitumor antibiotics
inferredcites →https://doi.org/10.1021/ja01522a052openalex-snapshot
Reaction of Phenolic Mannich Base Methiodides and Oxides with Various Nucleophiles
inferredcites →https://doi.org/10.1021/ja0579053openalex-snapshot
Palladium(II)-Catalyzed Aerobic Dialkoxylation of Styrenes: A Profound Influence of an o-Phenol
inferredcites →https://doi.org/10.1021/ja0585533openalex-snapshot
Palladium(II)-Catalyzed Aerobic Hydroalkoxylation of Styrenes Containing a Phenol
inferredcites →https://doi.org/10.1021/ja062948kopenalex-snapshot
Substituents on Quinone Methides Strongly Modulate Formation and Stability of Their Nucleophilic Adducts
inferredcites →https://doi.org/10.1021/ja070263uopenalex-snapshot
Palladium(II)-Catalyzed Enantioselective Aerobic Dialkoxylation of 2-Propenyl Phenols: A Pronounced Effect of Copper Additives on Enantioselectivity
inferredcites →https://doi.org/10.1021/ja103472aopenalex-snapshot
Synthesis and Preliminary Biological Studies of 3-Substituted Indoles Accessed by a Palladium-Catalyzed Enantioselective Alkene Difunctionalization Reaction
inferredcites →https://doi.org/10.1021/ja108106hopenalex-snapshot
Advancing the Mechanistic Understanding of an Enantioselective Palladium-Catalyzed Alkene Difunctionalization Reaction
inferredcites →https://doi.org/10.1021/ja904876qopenalex-snapshot
Quinone Methides Tethered to Naphthalene Diimides as Selective G-Quadruplex Alkylating Agents
inferredcites →https://doi.org/10.1021/ja909030copenalex-snapshot
Palladium-Catalyzed Enantioselective Addition of Two Distinct Nucleophiles across Alkenes Capable of Quinone Methide Formation
inferredcites →https://doi.org/10.1021/ja9802145openalex-snapshot
General Synthesis, First Crystal Structure, and Reactivity of Stable o-Quinone Methide Complexes of Cp*Ir
inferredcites →https://doi.org/10.1021/ja9937526openalex-snapshot
Structure−Reactivity Relationships and Intrinsic Reaction Barriers for Nucleophile Additions to a Quinone Methide: A Strongly Resonance-Stabilized Carbocation
inferredcites →https://doi.org/10.1021/ja994209sopenalex-snapshot
New Construction of Ortho Ring-Alkylated Phenols via Generation and Reaction of Assorted o-Quinone Methides
inferredcites →https://doi.org/10.1021/jm070828xopenalex-snapshot
BINOL−Amino Acid Conjugates as Triggerable Carriers of DNA-Targeted Potent Photocytotoxic Agents
inferredcites →https://doi.org/10.1021/jo0006627openalex-snapshot
Alkylation of Amino Acids and Glutathione in Water by o-Quinone Methide. Reactivity and Selectivity
inferredcites →https://doi.org/10.1021/jo001752eopenalex-snapshot
A Mild Anionic Method for Generating o-Quinone Methides: Facile Preparations of Ortho-Functionalized Phenols
inferredcites →https://doi.org/10.1021/jo01022a523openalex-snapshot
Quinone Methides. Base-Catalyzed Condensation Reactions of Hydroxybenzyl Alcohols and Ethers
inferredcites →https://doi.org/10.1021/jo01043a507openalex-snapshot
The Structures of Substituted o-Quinone Methide Trimers
inferredcites →https://doi.org/10.1021/jo01051a021openalex-snapshot
The Structure of o-Quinone Methide Trimer
inferredcites →https://doi.org/10.1021/jo020224vopenalex-snapshot
Rapid Syntheses of Benzopyrans from o-OBOC Salicylaldehydes and Salicyl alcohols: A Three-Component Reaction
inferredcites →https://doi.org/10.1021/jo048703copenalex-snapshot
Enantioselective [4 + 2] Cycloadditions of o-Quinone Methides: Total Synthesis of (+)-Mimosifoliol and Formal Synthesis of (+)-Tolterodine
inferredcites →https://doi.org/10.1021/jo060227yopenalex-snapshot
Photogenerated Quinone Methides as Useful Intermediates in the Synthesis of Chiral BINOL Ligands
inferredcites →https://doi.org/10.1021/jo062491xopenalex-snapshot
Mechanistic Insights into the PalladiumII-Catalyzed Hydroxyalkoxylation of 2-Allylphenols
inferredcites →https://doi.org/10.1021/jo801302mopenalex-snapshot
Photolabile Protection of Alcohols, Phenols, and Carboxylic Acids with 3-Hydroxy-2-Naphthalenemethanol
inferredcites →https://doi.org/10.1021/jo970539oopenalex-snapshot
Synthesis and Chemistry of Quinone Methide Models for the Anthracycline Antitumor Antibiotics
inferredcites →https://doi.org/10.1021/ol062222topenalex-snapshot
Development of a General Pd(II)-Catalyzed Intermolecular Hydroalkoxylation Reaction of Vinylphenols by Using a Sacrificial Alcohol as the Hydride Source
inferredcites →https://doi.org/10.1021/ol200913ropenalex-snapshot
Palladium-Catalyzed Hydrofunctionalization of Vinyl Phenol Derivatives with Heteroaromatics
inferredcites →https://doi.org/10.1021/ol802029eopenalex-snapshot
Asymmetric Cycloadditions of o -Quinone Methides Employing Chiral Ammonium Fluoride Precatalysts
inferredcites →https://doi.org/10.1246/bcsj.20090245openalex-snapshot
Aryne, ortho-Quinone Methide, and ortho-Quinodimethane: Synthesis of Multisubstituted Arenes Using the Aromatic Reactive Intermediates
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781118560273.ch11openalex-snapshot
Addition Reactions: Polar Addition
inferred← citeshttps://doi.org/10.1002/adsc.201300830openalex-snapshot
A Streamlined Synthesis of 2,3‐Dihydrobenzofurans via the ortho‐Quinone Methides Generated from 2‐Alkyl‐Substituted Phenols
inferred← citeshttps://doi.org/10.1002/adsc.201600814openalex-snapshot
Bifunctional Amine‐Squaramide Catalyzed Friedel–Crafts Alkylation Based on ortho‐Quinone Methides in Oil‐Water Phases: Enantioselective Synthesis of Triarylmethanes
inferred← citeshttps://doi.org/10.1002/adsc.201601117openalex-snapshot
Ruthenium‐Catalyzed Aminomethylation and Methylation of Phenol Derivatives Utilizing Methanol as the C1 Source
inferred← citeshttps://doi.org/10.1002/adsc.201700487openalex-snapshot
Catalytic Asymmetric [4+1] Cyclization of ortho ‐Quinone Methides with 3‐Chlorooxindoles
inferred← citeshttps://doi.org/10.1002/adsc.201700825openalex-snapshot
Asymmetric Organocatalytic Conjugate Addition of Thiocarboxylic Acids to In Situ‐Generated ortho‐Quinomethanes in Oil‐Water Phases
inferred← citeshttps://doi.org/10.1002/adsc.201701333openalex-snapshot
Application of Homophthalic Anhydrides as 2C Building Blocks in Catalytic Asymmetric Cyclizations of ortho ‐Quinone Methides: Diastereo‐ and Enantioselective Construction of Dihydrocoumarin Frameworks
inferred← citeshttps://doi.org/10.1002/adsc.201800565openalex-snapshot
Scandium (III)‐Catalyzed Cycloaddition of in situ Generated ortho‐Quinone Methides with Vinyl Azides: An Efficient Access to Substituted 4H‐Chromenes
inferred← citeshttps://doi.org/10.1002/adsc.201801152openalex-snapshot
Asymmetric Phosphine‐Catalyzed [4+1] Annulations of o‐Quinone Methides with MBH Carbonates
inferred← citeshttps://doi.org/10.1002/adsc.201801509openalex-snapshot
Dearomative [4+2] Cycloaddition of Oxindole‐Embedded ortho‐Quinone Methides with 2,5‐Dialkylfurans
inferred← citeshttps://doi.org/10.1002/adsc.202200905openalex-snapshot
Metal‐Free Cascade 1,4‐Conjugate Addition/Selective Annulation Strategy for Divergent Synthesis of Polysubstituted Imidazoles and 4‐Alkenylquinazolines
inferred← citeshttps://doi.org/10.1002/adsc.70091openalex-snapshot
Organocatalytic Remote‐Controlled Enantioselective 1,10‐Additions of In Situ Generated Alkynyl 2,4′‐Biphenyl Quinone Methides
inferred← citeshttps://doi.org/10.1002/adsc.70449openalex-snapshot
Highly Diastereoselective (4 + 3)‐Cycloannulation of Carbonyl Ylides and 3‐Aryl‐1‐(2‐(1‐Arylvinyl)phenyl)prop‐2‐Yn‐1‐Ones Enabled by Silver Catalysis
inferred← citeshttps://doi.org/10.1002/ajoc.202100016openalex-snapshot
Synthesis of 1‐Naphthol‐based Unsymmetrical Triarylmethanes: Heck‐type Desulfitative Reaction of Arylsulfonyl Chlorides with Tetralone‐derived Chalcones
inferred← citeshttps://doi.org/10.1002/ajoc.202100141openalex-snapshot
Recent Advances in Organocatalytic Asymmetric Cycloaddition Reactions Through Ortho‐Quinone Methide Scaffolds
inferred← citeshttps://doi.org/10.1002/ajoc.202100363openalex-snapshot
Formal [4+1] Cyclization of ortho‐ or para‐Quinone Methides with 3‐Chlorooxindoles: Synthesis of 3,2′‐Tetrahydrofuryl Spirooxindoles
inferred← citeshttps://doi.org/10.1002/ajoc.202300390openalex-snapshot
Organocatalytic Diastereoselective Dearomative [4+2] Cyclodimerization of In‐situ Generated ortho‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/ajoc.202400370openalex-snapshot
Conjugate Addition of 3‐Aryl Oxindoles to In Situ Generated o–Quinone Methides Without Essential Electronic or Steric Groups
inferred← citeshttps://doi.org/10.1002/ajoc.202400380openalex-snapshot
Base‐Catalyzed Decarboxylative Amination of In‐Situ Generated Ortho‐Quinone Methides: Synthesis of Benzyl Amines
inferred← citeshttps://doi.org/10.1002/ajoc.202500047openalex-snapshot
Chiral Isoxazole‐Containing Triarylmethanes Through Enantioselective Nucleophilic Addition of 5‐Aminoisoxazoles to Ortho‐Quinone Methides and Their Antifungal Evaluation
inferred← citeshttps://doi.org/10.1002/ange.201204093openalex-snapshot
Development of an Alkaloid–Pyrone Annulation: Synthesis of Pleiomaltinine
inferred← citeshttps://doi.org/10.1002/ange.201303928openalex-snapshot
Asymmetric Catalytic 1,6‐Conjugate Addition/Aromatization of para‐Quinone Methides: Enantioselective Introduction of Functionalized Diarylmethine Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/ange.201403573openalex-snapshot
Brønsted‐Säure‐katalysierte konjugierte Addition von β‐Dicarbonylverbindungen an in situ erzeugte ortho‐Chinomethide – enantioselektive Synthese von 4‐Aryl‐4H‐chromenen
inferred← citeshttps://doi.org/10.1002/ange.201405252openalex-snapshot
Enantioselective Formation of All‐Carbon Quaternary Stereocenters from Indoles and Tertiary Alcohols Bearing A Directing Group
inferred← citeshttps://doi.org/10.1002/ange.201406587openalex-snapshot
Enantio‐ and Diastereoselective Access to Distant Stereocenters Embedded within Tetrahydroxanthenes: Utilizing ortho‐Quinone Methides as Reactive Intermediates in Asymmetric Brønsted Acid Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201409850openalex-snapshot
Ortho‐Chinonmethide als reaktive Intermediate in asymmetrischen Brønsted‐Säure‐katalysierten Cycloadditionen mit Alkenen mittels exklusiver Aktivierung des Elektrophils
inferred← citeshttps://doi.org/10.1002/ange.201500215openalex-snapshot
Catalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction of In Situ Generated ortho‐Quinone Methides with 3‐Methyl‐2‐Vinylindoles
inferred← citeshttps://doi.org/10.1002/ange.201500219openalex-snapshot
Die organokatalytische asymmetrische Prins‐Cyclisierung
inferred← citeshttps://doi.org/10.1002/ange.201506701openalex-snapshot
Catalytic Asymmetric 1,6‐Conjugate Addition of para‐Quinone Methides: Formation of All‐Carbon Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.201509110openalex-snapshot
Phosphoric Acid Catalyzed Asymmetric 1,6‐Conjugate Addition of Thioacetic Acid topara‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/ange.201509247openalex-snapshot
Synergistic Rhodium/Phosphoric Acid Catalysis for the Enantioselective Addition of Oxonium Ylides to ortho‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/ange.201612149openalex-snapshot
Katalytisch‐asymmetrische intramolekulare [4+2]‐Cycloaddition von in situ generierten ortho‐Chinonmethiden
inferred← citeshttps://doi.org/10.1002/ange.201700437openalex-snapshot
Regioselective α‐Addition of Deconjugated Butenolides: Enantioselective Synthesis of Dihydrocoumarins
inferred← citeshttps://doi.org/10.1002/ange.201707523openalex-snapshot
Organocatalytic Intramolecular [4+2] Cycloaddition between In Situ Generated Vinylidene ortho‐Quinone Methides and Benzofurans
inferred← citeshttps://doi.org/10.1002/ange.201808197openalex-snapshot
Unterbrechung der Aromatizität mittels Aminokatalyse: Eine einfache Strategie für die asymmetrische Synthese
inferred← citeshttps://doi.org/10.1002/ange.201809692openalex-snapshot
Palladium‐Catalyzed Enantioselective Addition of Chiral Metal Enolates to In Situ Generated ortho ‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/ange.201901955openalex-snapshot
Catalytic Asymmetric (4+3) Cyclizations of In Situ Generated ortho‐Quinone Methides with 2‐Indolylmethanols
inferred← citeshttps://doi.org/10.1002/ange.201906954openalex-snapshot
Asymmetric Synthesis of Enantioenriched 2‐Aryl‐2,3‐Dihydrobenzofurans by a Lewis Acid Catalyzed Cyclopropanation/Intramolecular Rearrangement Sequence
inferred← citeshttps://doi.org/10.1002/ange.201913382openalex-snapshot
Difunctionalization of Alkenes Involving Metal Migration
inferred← citeshttps://doi.org/10.1002/ange.201913603openalex-snapshot
Kooperative Katalyse für die diastereo‐ und enantioselektive [4+3]‐Cycloanellierung von ortho‐Chinonmethiden und Carbonylyliden
inferred← citeshttps://doi.org/10.1002/ange.202000677openalex-snapshot
Divergent Biomimetic Total Syntheses of Ganocins A–C, Ganocochlearins C and D, and Cochlearol T
inferred← citeshttps://doi.org/10.1002/ange.202101682openalex-snapshot
Übergangsmetallfreie Synthese polyfunktioneller Triarylmethane und 1,1‐Diarylalkane durch sequentielle Kreuzkupplungen von Benzaldiacetaten mit Organozinkreagenzien
inferred← citeshttps://doi.org/10.1002/ange.202208174openalex-snapshot
Modular Construction of Heterobiaryl Atropisomers and Axially Chiral Styrenes via All‐Carbon Tetrasubstituted VQMs
inferred← citeshttps://doi.org/10.1002/ange.202315759openalex-snapshot
Catalytic Enantioselective [4+2] Cycloadditions of Salicylaldehyde Acetals with Enol Ethers
inferred← citeshttps://doi.org/10.1002/ange.202400143openalex-snapshot
Organocatalytic Enantioselective 1,12‐Addition of Alkynyl Biphenyl Quinone Methides Formed In Situ
inferred← citeshttps://doi.org/10.1002/anie.201204093openalex-snapshot
Development of an Alkaloid–Pyrone Annulation: Synthesis of Pleiomaltinine
inferred← citeshttps://doi.org/10.1002/anie.201303928openalex-snapshot
Asymmetric Catalytic 1,6‐Conjugate Addition/Aromatization of para ‐Quinone Methides: Enantioselective Introduction of Functionalized Diarylmethine Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/anie.201403573openalex-snapshot
Brønsted Acid Catalyzed, Conjugate Addition of β‐Dicarbonyls to In Situ Generated ortho‐Quinone Methides—Enantioselective Synthesis of 4‐Aryl‐4H‐Chromenes
inferred← citeshttps://doi.org/10.1002/anie.201405252openalex-snapshot
Enantioselective Formation of All‐Carbon Quaternary Stereocenters from Indoles and Tertiary Alcohols Bearing A Directing Group
inferred← citeshttps://doi.org/10.1002/anie.201406587openalex-snapshot
Enantio‐ and Diastereoselective Access to Distant Stereocenters Embedded within Tetrahydroxanthenes: Utilizing ortho‐Quinone Methides as Reactive Intermediates in Asymmetric Brønsted Acid Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201409850openalex-snapshot
Ortho‐Quinone Methides as Reactive Intermediates in Asymmetric Brønsted Acid Catalyzed Cycloadditions with Unactivated Alkenes by Exclusive Activation of the Electrophile
inferred← citeshttps://doi.org/10.1002/anie.201500215openalex-snapshot
Catalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction of In Situ Generated ortho‐Quinone Methides with 3‐Methyl‐2‐Vinylindoles
inferred← citeshttps://doi.org/10.1002/anie.201500219openalex-snapshot
The Organocatalytic Asymmetric Prins Cyclization
inferred← citeshttps://doi.org/10.1002/anie.201506701openalex-snapshot
Catalytic Asymmetric 1,6‐Conjugate Addition of para‐Quinone Methides: Formation of All‐Carbon Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.201509110openalex-snapshot
Phosphoric Acid Catalyzed Asymmetric 1,6‐Conjugate Addition of Thioacetic Acid topara‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/anie.201509247openalex-snapshot
Synergistic Rhodium/Phosphoric Acid Catalysis for the Enantioselective Addition of Oxonium Ylides to ortho‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/anie.201612149openalex-snapshot
Catalytic Asymmetric Intramolecular [4+2] Cycloaddition of In Situ Generated ortho‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/anie.201700437openalex-snapshot
Regioselective α‐Addition of Deconjugated Butenolides: Enantioselective Synthesis of Dihydrocoumarins
inferred← citeshttps://doi.org/10.1002/anie.201707523openalex-snapshot
Organocatalytic Intramolecular [4+2] Cycloaddition between In Situ Generated Vinylidene ortho‐Quinone Methides and Benzofurans
inferred← citeshttps://doi.org/10.1002/anie.201808197openalex-snapshot
Breaking Aromaticity with Aminocatalysis: A Convenient Strategy for Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201809692openalex-snapshot
Palladium‐Catalyzed Enantioselective Addition of Chiral Metal Enolates to In Situ Generated ortho‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/anie.201901955openalex-snapshot
Catalytic Asymmetric (4+3) Cyclizations of In Situ Generated ortho‐Quinone Methides with 2‐Indolylmethanols
inferred← citeshttps://doi.org/10.1002/anie.201906954openalex-snapshot
Asymmetric Synthesis of Enantioenriched 2‐Aryl‐2,3‐Dihydrobenzofurans by a Lewis Acid Catalyzed Cyclopropanation/Intramolecular Rearrangement Sequence
inferred← citeshttps://doi.org/10.1002/anie.201913382openalex-snapshot
Difunctionalization of Alkenes Involving Metal Migration
inferred← citeshttps://doi.org/10.1002/anie.201913603openalex-snapshot
Cooperative Catalysis for the Highly Diastereo‐ and Enantioselective [4+3]‐Cycloannulation of ortho ‐Quinone Methides and Carbonyl Ylides
inferred← citeshttps://doi.org/10.1002/anie.202000677openalex-snapshot
Divergent Biomimetic Total Syntheses of Ganocins A–C, Ganocochlearins C and D, and Cochlearol T
inferred← citeshttps://doi.org/10.1002/anie.202101682openalex-snapshot
Transition‐Metal‐Free Synthesis of Polyfunctional Triarylmethanes and 1,1‐Diarylalkanes by Sequential Cross‐Coupling of Benzal Diacetates with Organozinc Reagents
inferred← citeshttps://doi.org/10.1002/anie.202208174openalex-snapshot
Modular Construction of Heterobiaryl Atropisomers and Axially Chiral Styrenes via All‐Carbon Tetrasubstituted VQMs
inferred← citeshttps://doi.org/10.1002/anie.202315759openalex-snapshot
Catalytic Enantioselective [4+2] Cycloadditions of Salicylaldehyde Acetals with Enol Ethers
inferred← citeshttps://doi.org/10.1002/anie.202400143openalex-snapshot
Organocatalytic Enantioselective 1,12‐Addition of Alkynyl Biphenyl Quinone Methides Formed In Situ
inferred← citeshttps://doi.org/10.1002/aoc.5676openalex-snapshot
Selective synthesis of 2‐(5‐oxo‐1‐arylhex‐1‐yn‐3‐yl)phenyl benzoates via FeCl3‐mediated cascade reactions of propargylamines with β‐enamino ketones
inferred← citeshttps://doi.org/10.1002/asia.201900641openalex-snapshot
Catalyst‐Free Synthesis of α‐Functionalized 2H‐Chromenes in Water: A Tandem Self‐Promoted pseudo‐Substitution and Decarboxylation Process
inferred← citeshttps://doi.org/10.1002/asia.202000503openalex-snapshot
Catalytic Asymmetric Three‐component Hydroacyloxylation/ 1,4‐Conjugate Addition of Ynamides
inferred← citeshttps://doi.org/10.1002/asia.202000640openalex-snapshot
Highly Diastereoselective Synthesis of Polycyclic Indolines through Formal [4+2] Propargylic Cycloaddition of Indoles with Ethynyl Benzoxazinanones
inferred← citeshttps://doi.org/10.1002/cctc.201500176openalex-snapshot
para ‐Quinone Methide: a New Player in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201200619openalex-snapshot
ortho‐Quinone Methides in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/chem.201201144openalex-snapshot
Very Efficient Generation of Quinone Methides through Excited State Intramolecular Proton Transfer to a Carbon Atom
inferred← citeshttps://doi.org/10.1002/chem.201400038openalex-snapshot
Thermally Induced Twin Polymerization of 4H‐1,3,2‐Benzodioxasilines
inferred← citeshttps://doi.org/10.1002/chem.201406044openalex-snapshot
Brønsted Acid‐Catalyzed, Highly Enantioselective Addition of Enamides to In Situ‐Generated ortho‐Quinone Methides: A Domino Approach to Complex Acetamidotetrahydroxanthenes
inferred← citeshttps://doi.org/10.1002/chem.201500710openalex-snapshot
Catalytic Asymmetric Addition of Meldrum’s Acid, Malononitrile, and 1,3‐Dicarbonyls to ortho‐Quinone Methides Generated In Situ Under Basic Conditions
inferred← citeshttps://doi.org/10.1002/chem.201601227openalex-snapshot
Catalytic Asymmetric Cycloaddition of In Situ‐Generated ortho‐Quinone Methides and Azlactones by a Triple Brønsted Acid Activation Strategy
inferred← citeshttps://doi.org/10.1002/chem.201604088openalex-snapshot
Chiral N,N′‐Dioxide–Scandium(III) Complex‐Catalyzed Asymmetric Friedel–Crafts Alkylation Reaction of ortho‐Hydroxybenzyl Alcohols with C3‐Substituted N‐Protected Indoles
inferred← citeshttps://doi.org/10.1002/chem.201605302openalex-snapshot
Chiral Primary Amine Catalyzed Asymmetric α‐Benzylation with In Situ Generated ortho ‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/chem.201800677openalex-snapshot
Multiple Hydrogen‐Bond Activation in Asymmetric Brønsted Acid Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201801543openalex-snapshot
Ultrafast Adiabatic Photodehydration of 2‐Hydroxymethylphenol and the Formation of Quinone Methide
inferred← citeshttps://doi.org/10.1002/chem.201901784openalex-snapshot
Enantioselective Catalytic [4+1]‐Cyclization of ortho ‐Hydroxy‐ para ‐Quinone Methides with Allenoates
inferred← citeshttps://doi.org/10.1002/chem.201904903openalex-snapshot
Asymmetric Catalytic [4+5] Annulation of ortho‐Quinone Methides with Vinylethylene Carbonates and its Extension to Stereoselective Tandem Rearrangement
inferred← citeshttps://doi.org/10.1002/chem.201905668openalex-snapshot
Benzazetidines and Related Compounds: Synthesis and Potential
inferred← citeshttps://doi.org/10.1002/chem.202002106openalex-snapshot
Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols
inferred← citeshttps://doi.org/10.1002/chem.202200224openalex-snapshot
Asymmetric Synthesis of Chromans Through Bifunctional Enamine‐Metal Lewis Acid Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202201112openalex-snapshot
Aza‐ Ortho ‐Quinone Methides as Reactive Intermediates: Generation and Utility in Contemporary Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/chem.202502375openalex-snapshot
Carbon and Heteroatom Activation via N ‐Heterocyclic Carbene‐Bound Dearomative Intermediates for Stereoselective Annulation Reactions
inferred← citeshttps://doi.org/10.1002/chin.201206230openalex-snapshot
ChemInform Abstract: Applications of ortho‐Quinone Methide Intermediates in Catalysis and Asymmetric Synthesis.
inferred← citeshttps://doi.org/10.1002/chir.22183openalex-snapshot
Planar Chiral Iridium Complexes with the Δ‐TRISPHAT Anion: Toward the First Enantiopure o‐Quinone Methide π‐Complex
inferred← citeshttps://doi.org/10.1002/cjoc.201400463openalex-snapshot
A Concise Synthesis of 2‐(2‐Hydroxyphenyl)acetonitriles via the o‐Quinone Methides Generated from 2‐(1‐Tosylalkyl)phenols
inferred← citeshttps://doi.org/10.1002/cjoc.201800330openalex-snapshot
Synthesis of Benzofuran‐fused 1,4‐Dihydropyridines via Bifunctional Squaramide‐catalyzed Formal [4+2] Cycloaddition of Azadienes with Malononitrile
inferred← citeshttps://doi.org/10.1002/cjoc.202200503openalex-snapshot
Design and Application of m‐Hydroxybenzyl Alcohols in Regioselective (3 + 3) Cycloadditions of 2‐Indolymethanols †
inferred← citeshttps://doi.org/10.1002/cssc.201900397openalex-snapshot
Palladium‐Catalyzed Oxidation Reactions of Alkenes with Green Oxidants
inferred← citeshttps://doi.org/10.1002/ejoc.201301018openalex-snapshot
Generation and Conjugate Additions of o‐Quinone Methides Under Mild Base Conditions: Rapid Synthesis of N‐Substituted Aryl Glycine Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201601186openalex-snapshot
Catalytic Asymmetric Synthesis of Chiral Dihydrobenzofurans through a Formal [4+1] Annulation Reaction of Sulfur Ylides and In Situ Generated ortho‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/ejoc.201700432openalex-snapshot
Concise Synthesis of Polycyclic Indoline Scaffolds through an In III ‐Catalyzed Formal [4+2] Annulation of 2,3‐Disubstituted Indoles with o ‐Aminobenzyl Alcohols
inferred← citeshttps://doi.org/10.1002/ejoc.201701183openalex-snapshot
Microwave‐Assisted Generation and Capture by Azoles of ortho‐Quinone Methide Intermediates under Aqueous Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201800013openalex-snapshot
Acid‐Promoted Cascade Cyclization to Produce 2‐(4′‐Alkoxyaryl)‐3,4‐Fused Tricyclic Dihydrobenzopyrans via a Vinylidene para‐Quinone Methide Intermediate
inferred← citeshttps://doi.org/10.1002/ejoc.201800396openalex-snapshot
Ferrocene‐Decorated Phenol Derivatives by Trapping ortho‐Quinone Methide Intermediates with Ferrocene
inferred← citeshttps://doi.org/10.1002/ejoc.201800679openalex-snapshot
Simultaneous Generation and Subsequent Cycloaddition of ortho‐Quinonemethides and Cyclic Enecarbamates Promoted by a Gold/Lewis Acid Catalytic System
inferred← citeshttps://doi.org/10.1002/ejoc.201900465openalex-snapshot
Advances in The Catalytic Synthesis of Triarylmethanes (TRAMs)
inferred← citeshttps://doi.org/10.1002/ejoc.201901796openalex-snapshot
para‐Quinone Methides as Acceptors in 1,6‐Nucleophilic Conjugate Addition Reactions for the Synthesis of Structurally Diverse Molecules
inferred← citeshttps://doi.org/10.1002/ejoc.202000295openalex-snapshot
CF3‐Containing para‐Quinone Methides for Organic Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.202500493openalex-snapshot
Palladium(II)‐Catalyzed Distal CH Functionalization of 8‐Aminoquinolinamides: Facile Synthesis of Triarylmethane Derivatives
inferred← citeshttps://doi.org/10.1002/med.70081openalex-snapshot
Current Development of Small Molecules Against Influenza A Virus by Targeting Hemagglutinin
inferred← citeshttps://doi.org/10.1002/slct.202003749openalex-snapshot
Approach to the Core Structure of Schweinfurthin B
inferred← citeshttps://doi.org/10.1002/tcr.201900020openalex-snapshot
Fluorinated Alcohols: Magic Reaction Medium and Promoters for Organic Synthesis
inferred← citeshttps://doi.org/10.1002/tcr.202100251openalex-snapshot
Multicomponent Reactions (MCRs) with o‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/tcr.202300152openalex-snapshot
Organocatalytic (1+4)‐Annulations of MBH Adducts with Electron‐Deficient Systems
inferred← citeshttps://doi.org/10.1007/s00044-017-1927-5openalex-snapshot
Synthesis, in vitro antiproliferative activity, antioxidant activity and molecular modeling studies of new carbazole Mannich bases
inferred← citeshttps://doi.org/10.1007/s10812-014-9880-2openalex-snapshot
Rotational Isomers, Intramolecular Hydrogen Bond, and IR Spectra of o-Vinylphenol
inferred← citeshttps://doi.org/10.1007/s11172-014-0688-2openalex-snapshot
Spatial structure of 2-(2´-hydroxyphenyl)-4-methylchromanes and some specific features of intramolecular hydrogen bond
inferred← citeshttps://doi.org/10.1007/s11426-018-9359-4openalex-snapshot
Synthesis of 4H-chromenes by silver (I)-catalyzed cycloaddition of ortho-quinone methides with N-allenamides
inferred← citeshttps://doi.org/10.1016/b978-0-12-812522-9.00006-3openalex-snapshot
Metabolic Activation and Toxicities of bis-Benzylisoquinoline Alkaloids
inferred← citeshttps://doi.org/10.1016/bs.armc.2023.10.001openalex-snapshot
Chemical evolution of natural product structure for drug discovery
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.04.001openalex-snapshot
The unexplored potential of quinone methides in chemical biology
inferred← citeshttps://doi.org/10.1016/j.bmcl.2024.129877openalex-snapshot
Synthesis and biological evaluation of novel penindolone derivatives as potential antiproliferative agents against SCLC in vitro
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109322openalex-snapshot
Beyond 1,4-addition of in-situ generated (aza-)quinone methides and indole imine methides
inferred← citeshttps://doi.org/10.1016/j.gresc.2021.10.004openalex-snapshot
Diastereoselective synthesis of spiro[chromane-3,3′-indolines] and spiro[chromane-3,2′-indenes] via DBU promoted formal [4 + 2]cycloaddition reaction
inferred← citeshttps://doi.org/10.1016/j.gresc.2024.01.002openalex-snapshot
Controlled generation of ortho-quinone methides and (4+3) cyclization with 2-indolylalcohols by dual photoredox/Brønsted acid relay catalysis
inferred← citeshttps://doi.org/10.1016/j.jcat.2019.01.014openalex-snapshot
A cascade mechanism for a simple reaction: The gas-phase methylation of phenol with methanol
inferred← citeshttps://doi.org/10.1016/j.mcat.2017.08.017openalex-snapshot
Mechanisms and stereoselectivities of NHC-catalyzed [4 + 2] cycloaddition reaction between phenylacetic acid and o-quinone methide: A computational investigation
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.070openalex-snapshot
N-Tosylhydrazine-mediated deoxygenative hydrogenation of aldehydes and ketones catalyzed by Pd/C
inferred← citeshttps://doi.org/10.1016/j.tet.2014.09.076openalex-snapshot
Indium catalyzed solvent-free multicomponent synthesis of cytotoxic dibenzo[a,h]anthracenes from aldehydes, 2-hydroxy-1,4-naphthoquinone, and 2-naphthol
inferred← citeshttps://doi.org/10.1016/j.tet.2014.11.020openalex-snapshot
Intramolecular cyclization of β-nitroso-o-quinone methides. A theoretical endoscopy of a potentially useful innate ‘reclusive’ reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.063openalex-snapshot
Alternative routes to the acylphloroglucinol rhodomyrtone
inferred← citeshttps://doi.org/10.1016/j.tet.2015.12.011openalex-snapshot
A one-pot oxidation/cycloaddition cascade synthesis of 2,4-diaryl chromans via ortho-quinone methides
inferred← citeshttps://doi.org/10.1016/j.tet.2016.10.027openalex-snapshot
One step synthesis of 2-alkenylchromanes via inverse electron-demand Hetero-Diels–Alder reaction of o -quinone methide with unactivated dienes
inferred← citeshttps://doi.org/10.1016/j.tet.2017.06.060openalex-snapshot
Synthesis and detailed conformational analysis of new naphthoxazino[2,3-a]benz[c]azepine and naphthoxazino[2,3-a]thieno[3,2-c]pyridine derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132459openalex-snapshot
o-Quinone methide with overcrowded olefinic core as a catalytically-active surrogate of triarylmethylium salt for dehydridative oxidation of benzylic alcohols under aerobic photoirradiation conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133655openalex-snapshot
Recent advances in the cyclization of para-quinone methides
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.03.002openalex-snapshot
Chiral Brønsted acid-catalyzed alkylation of C3-substituted indoles with o-hydroxybenzyl alcohols: highly enantioselective synthesis of diarylindol-2-ylmethanes and evaluation on their cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.03.049openalex-snapshot
Efficient synthesis of rottlerin and its two subunits
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.006openalex-snapshot
Organocatalytic annulation of aldehydes and o-quinone methides: A facile access to dihydrocoumarins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.02.007openalex-snapshot
Construction of 9-functionalized xanthenes via Diels-Alder reaction of stable ortho-quinone methides and arynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.03.069openalex-snapshot
Organocatalytic stereoselective conjugate addition of 3-substituted oxindoles with in situ generated ortho-quinone methides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.03.090openalex-snapshot
Temperature-controlled divergent synthesis of 4-alkoxy- or 4-alkenyl-chromanes via inverse electron-demand cycloaddition with in situ generated ortho-quinone methides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.05.016openalex-snapshot
A general asymmetric route to enantio-enriched isoflavanes via an organocatalytic annulation of o-quinone methides and aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151187openalex-snapshot
An efficient approach to isoquinoline via AgNO3-promoted 6-endo-dig cyclization followed by oxidative elimination of o-alkynylarylaldimines and its application in fluoride recognition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.152862openalex-snapshot
Enantioselective synthesis of hetero-triarylmethanes by chiral phosphoric acid-catalyzed 1,4-addition of 3-substituted indoles with azadienes
inferred← citeshttps://doi.org/10.1016/s1872-2067(19)63396-6openalex-snapshot
Chiral Brønsted acid-catalyzed conjugate addition of indoles to azadienes: Enantioselective synthesis of hetero-triarylmethanes
inferred← citeshttps://doi.org/10.1021/acs.energyfuels.6b00238openalex-snapshot
Compositional Changes to Low Water Content Bio-oils during Aging: An NMR, GC/MS, and LC/MS Study
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.0c00312openalex-snapshot
Chemoreactive-Inspired Discovery of Influenza A Virus Dual Inhibitor to Block Hemagglutinin-Mediated Adsorption and Membrane Fusion
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00119openalex-snapshot
Diastereo- and Enantioselective Construction of Biologically Important Chiral 1,3-Dioxolochroman Frameworks via Catalytic Asymmetric [4+2] Cycloaddition
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00215openalex-snapshot
Hetero-Diels–Alder Reactions of Quinone Methides: The Origin of the α-Regioselectivity of 3-Methylene-1,2,4-naphthotriones
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01375openalex-snapshot
Phosphoric Acid Catalyzed Formation of Hydrogen-Bonded o-Quinone Methides. Enantioselective Cycloaddition with β-Dicarbonyl Compounds toward Benzannulated Oxygen Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02908openalex-snapshot
o-Quinone Methides and o-Quinone Sulfides via Arynes: Synthesis of Ortho-Disubstituted Arenes and Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.joc.0c03029openalex-snapshot
Copper-Catalyzed Cascade 1,4-Addition/Annulation/Hydrolysis of Propargylamines with 2-Hydroxynaphthalene-1,4-diones: Direct Formation of 12-Phenacyl-11H-benzo[b]xanthenes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00435openalex-snapshot
Organocatalytic Asymmetric Addition of Aromatic α-Cyanoketones to o-Quinone Methides: Synthesis of 3,4-Dihydrocoumarins and Tetrasubstituted Chromans
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00672openalex-snapshot
TfOH-Catalyzed [4 + 1] Annulation of p-Quinone Methides with α-Aryl Diazoacetates: Straightforward Access to Highly Functionalized 2,3-Dihydrobenzofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02202openalex-snapshot
TEMPO-Mediated Synthesis of Indolyl/Imidazo[1,2-a]pyridinyl-Substituted para-Quinone Methides from Butylated Hydroxytoluene
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02939openalex-snapshot
Brønsted Acid Catalyzed Friedel–Crafts Alkylation of Naphthols with In Situ Generated Naphthol-Derived ortho-Quinone Methides: Synthesis of Chiral and Achiral Xanthene Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00213openalex-snapshot
Lewis Acid-Catalyzed 1,4-Addition and Annulation of 4-Hydroxy-coumarins with o-Hydroxyphenyl Propargyl Amines: Entry to Regio-Selective Synthesis of Furano[3,2-c]coumarins and Pyrano[3,2-c]coumarins
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00239openalex-snapshot
Base-Mediated Cascade Lactonization/1,3-Dipolar Cycloaddition Pathway for the One-Pot Assembly of Coumarin-Functionalized Pyrrolo[2,1-a]isoquinolines
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01613openalex-snapshot
Catalytic Chemo-, E/Z-, and Enantioselective Cyclizations of o-Hydroxybenzyl Alcohols with Dimedone-Derived Enaminones
inferred← citeshttps://doi.org/10.1021/acs.joc.5c03236openalex-snapshot
Ambiphilic p -Quinone Methides and α-Imino Ketones: Ca(II)-Catalyzed, One-Pot, Three-Component Synthesis of Benzoxazines
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00078openalex-snapshot
Merging Chiral Brønsted Acid/Base Catalysis: An Enantioselective [4 + 2] Cycloaddition of o-Hydroxystyrenes with Azlactones
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01309openalex-snapshot
Synthesis, Structure, and Unusual Reactivity of a Stable 3-(Oxazolidin-2-ylidene)thiophen-2-one
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01367openalex-snapshot
Emerging Roles of in Situ Generated Quinone Methides in Metal-Free Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00367openalex-snapshot
Asymmetric Synthesis of cis-3,4-Dihydrocoumarins via [4 + 2] Cycloadditions Catalyzed by Amidine Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02533openalex-snapshot
Catalytic Asymmetric [4+2] Cycloaddition of in Situ Generated o-Quinone Methide Imines with o-Hydroxystyrenes: Diastereo- and Enantioselective Construction of Tetrahydroquinoline Frameworks
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02769openalex-snapshot
Thermal Hetero-Diels–Alder Reaction of Benzocyclobutenones with Isatins To Form 2-Oxindole Spirolactones
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02897openalex-snapshot
Synthesis of Fullerotetrahydroquinolines via [4 + 2] Cycloaddition Reaction of [60]Fullerene with in Situ Generated Aza-o-quinone Methides
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02942openalex-snapshot
[4 + 2] Cyclization of para-Quinone Methide Derivatives with Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00234openalex-snapshot
Asymmetric Formal [4 + 2] Annulation of o-Quinone Methides with β-Keto Acylpyrazoles: A General Approach to Optically Active trans-3,4-Dihydrocoumarins
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01390openalex-snapshot
Application of Naphthylindole-Derived Phosphines as Organocatalysts in [4 + 1] Cyclizations of o-Quinone Methides with Morita–Baylis–Hillman Carbonates
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02186openalex-snapshot
Metal-Catalyzed Oxa-[4+2] Cyclizations of Quinone Methides with Alkynyl Benzyl Alcohols
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03260openalex-snapshot
Formal [4 + 2] Annulation of Oxindole-Embedded ortho-Quinone Methides with 1,3-Dicarbonyls: Synthesis of Spiro[Chromen-4,3′-Oxindole] Scaffolds
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00710openalex-snapshot
Catalytic Asymmetric Conjugate Addition of Indoles to para-Quinone Methide Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00860openalex-snapshot
Brønsted Acid-Catalyzed, Diastereo- and Enantioselective, Intramolecular Oxa-Diels–Alder Reaction of ortho-Quinone Methides and Unactivated Dienophiles
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01085openalex-snapshot
Formation of Quinone Methides by Ultrafast Photodeamination: A Spectroscopic and Computational Study
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02058openalex-snapshot
Mild, Modular, and Convergent Synthesis of Helical Naphtho[2,1-c]chromenes via a Multistep Cyclization/Aromatization Cascade Sequence
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02206openalex-snapshot
Total Synthesis of (−)-Phomoarcherin C
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02971openalex-snapshot
Increasing Structural Diversity of Natural Products by Michael Addition with ortho-Quinone Methide as the Acceptor
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03302openalex-snapshot
Catalytic Asymmetric [4 + 2] Cycloaddition of ortho-Alkenyl Naphthols/Phenols with ortho-Quinone Methides: Highly Stereoselective Synthesis of Chiral 2,3,4-Trisubstituted Chromans
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03479openalex-snapshot
Regio- and Enantioselective Friedel–Crafts Benzhydrylation of Indoles in Carbocyclic Ring with ortho-Quinomethanes: Access to Chiral Diarylindolylmethanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01261openalex-snapshot
Substituted Benzothietes: Synthesis and a Quantum Chemical Investigation of Their Cycloreversion Properties
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00588openalex-snapshot
Cooperative Photoinduced/Brønsted Acid Catalyzed Cycloaddition of Transient Thioaldehydes and ortho -Quinone Methides toward a Synthesis of Benzo[ e ][1,3]oxathiines
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02268openalex-snapshot
Nonenzymatic Self-Assembly Access to Diverse ortho-Quinone Methide-Based Pseudonatural Products
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03850openalex-snapshot
p-Quinone Methide-Mediated Nonenzymatic Formation of Chalcane-Containing Dimers in Dragon’s Blood
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c04070openalex-snapshot
Organocatalytic Enantioselective Nucleophilic Addition of Indole Imine 5-Methides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00972openalex-snapshot
Michael Additions of Highly Basic Enolates toortho-Quinone Methides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01030openalex-snapshot
Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization–Extended Conjugate Addition Approach
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01177openalex-snapshot
Oxidative Inter-/Intermolecular Alkene Diamination of Hydroxy Styrenes with Electron-Rich Amines
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01419openalex-snapshot
Total Syntheses of (−)-Spirooliganones A and B and Their Diastereoisomers: Absolute Stereochemistry and Inhibitory Activity against Coxsackie Virus B3
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02902openalex-snapshot
Total Synthesis of Peniphenones A–D via Biomimetic Reactions of a Common o-Quinone Methide Intermediate
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02954openalex-snapshot
Enantioselective Multicomponent Condensation Reactions of Phenols, Aldehydes, and Boronates Catalyzed by Chiral Biphenols
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03072openalex-snapshot
Organocatalytic Asymmetric Nucleophilic Addition to o-Quinone Methides by Alcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03707openalex-snapshot
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01856openalex-snapshot
A Palladium-Catalyzed Cascade Double Annulation Strategy for Modular Access to Dihydrocyclopenta[b]chromenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00404openalex-snapshot
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01368openalex-snapshot
Regioselective Intermolecular Diamination and Aminooxygenation of Alkenes with Saccharin
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01736openalex-snapshot
A Total Synthesis of Paeoveitol
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