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Meldrum’s Acids and 5-Alkylidene Meldrum’s Acids in Catalytic Carbon−Carbon Bond-Forming Processes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/3527604693openalex-snapshot
Modern Rhodium‐Catalyzed Organic Reactions
inferredcites →https://doi.org/10.1002/anie.198200961openalex-snapshot
Lewis Acid Induced α‐Alkylation of Carbonyl Compounds
inferredcites →https://doi.org/10.1002/anie.200351916openalex-snapshot
Organocatalytic Asymmetric Domino Knoevenagel/Diels–Alder Reactions: A Bioorganic Approach to the Diastereospecific and Enantioselective Construction of Highly Substituted Spiro[5,5]undecane‐1,5,9‐triones
inferredcites →https://doi.org/10.1002/anie.200462137openalex-snapshot
Enantioselective Copper‐Catalyzed Conjugate Addition to Trisubstituted Cyclohexenones: Construction of Stereogenic Quaternary Centers
inferredcites →https://doi.org/10.1002/anie.200604511openalex-snapshot
All‐Carbon Quaternary Stereogenic Centers by Enantioselective Cu‐Catalyzed Conjugate Additions Promoted by a Chiral N‐Heterocyclic Carbene
inferredcites →https://doi.org/10.1002/anie.200703702openalex-snapshot
Catalytic Enantioselective 1,6‐Conjugate Addition of Grignard Reagents to Linear Dienoates
inferredcites →https://doi.org/10.1002/anie.200800628openalex-snapshot
Catalytic Enantioselective Hosomi–Sakurai Conjugate Allylation of Cyclic Unsaturated Ketoesters
inferredcites →https://doi.org/10.1002/anie.200803735openalex-snapshot
Regiodivergent 1,4 versus 1,6 Asymmetric Copper‐Catalyzed Conjugate Addition
inferredcites →https://doi.org/10.1002/anie.200804446openalex-snapshot
Copper‐Catalyzed Asymmetric Michael Addition of Magnesium, Zinc, and Aluminum Organometallic Reagents: Efficient Synthesis of Chiral Molecules
inferredcites →https://doi.org/10.1007/bf00900577openalex-snapshot
�ber die Reaktion einiger substituierter Methylenmeldrums�uren mit 2,3-Dimethylbutadien
inferredcites →https://doi.org/10.1007/bf00904726openalex-snapshot
Zur Kenntnis cyclischer Acylale, 8. Mitt.
inferredcites →https://doi.org/10.1007/s11030-009-9136-xopenalex-snapshot
One hundred years of Meldrum’s acid: advances in the synthesis of pyridine and pyrimidine derivatives
inferredcites →https://doi.org/10.1016/0031-9422(95)00358-eopenalex-snapshot
Uncommon diterpenes with the skeleton of six-five-six fused-rings from Taiwania cryptomerioides
inferredcites →https://doi.org/10.1016/j.tet.2009.05.058openalex-snapshot
Scandium triflate-catalyzed intramolecular Friedel–Crafts acylation with Meldrum's acids: insight into the mechanism
inferredcites →https://doi.org/10.1016/j.tetasy.2006.11.009openalex-snapshot
Asymmetric Cu-catalyzed 1,6-conjugate addition of dialkylzinc reagents to 5-(3-aryl-2-propenylidene) Meldrum’s acids
inferredcites →https://doi.org/10.1016/j.tetlet.2007.08.012openalex-snapshot
A general and practical preparation of alkylidene Meldrum’s acids
inferredcites →https://doi.org/10.1016/j.tetlet.2009.06.007openalex-snapshot
Functionalization of Csp3–H bond—Sc(OTf)3-catalyzed domino 1,5-hydride shift/cyclization/Friedel–Crafts acylation reaction of benzylidene Meldrum’s acids
inferredcites →https://doi.org/10.1016/s0040-4039(00)71908-3openalex-snapshot
Meldrum's acid derivative as a useful dienophilic component; Synthesis of δ-damascone
inferredcites →https://doi.org/10.1016/s0040-4039(00)99406-1openalex-snapshot
Reaction of trimethylsilyl derivatives with Meldrum's acid : A new and easy monofunctionalization of malonic acid
inferredcites →https://doi.org/10.1016/s0040-4039(01)00978-9openalex-snapshot
Clean synthesis in water. Part 2: Uncatalysed condensation reaction of Meldrum's acid and aldehydes
inferredcites →https://doi.org/10.1016/s0040-4039(97)01566-9openalex-snapshot
An Efficient Method for Generation of α-Oxoketenes: Cycloreversion of Enolized Meldrum's Acid Derivatives
inferredcites →https://doi.org/10.1021/ar900048qopenalex-snapshot
Recent Advances in Our Mechanistic Understanding of SNV Reactions
inferredcites →https://doi.org/10.1021/ar990084kopenalex-snapshot
Phosphoramidites: Marvellous Ligands in Catalytic Asymmetric Conjugate Addition
inferredcites →https://doi.org/10.1021/ja01190a060openalex-snapshot
The Structure of Meldrum's Supposed β-Lactonic Acid
inferredcites →https://doi.org/10.1021/ja050800fopenalex-snapshot
Enantioselective Synthesis of Nitroalkanes Bearing All-Carbon Quaternary Stereogenic Centers through Cu-Catalyzed Asymmetric Conjugate Additions
inferredcites →https://doi.org/10.1021/ja052411ropenalex-snapshot
Catalytic, Enantioselective, Conjugate Alkyne Addition
inferredcites →https://doi.org/10.1021/ja054447popenalex-snapshot
Total Synthesis of (±)-Taiwaniaquinol B via a Domino Intramolecular Friedel−Crafts Acylation/Carbonyl α-tert-Alkylation Reaction
inferredcites →https://doi.org/10.1021/ja056692eopenalex-snapshot
Asymmetric Synthesis of All-Carbon Benzylic Quaternary Stereocenters via Cu-Catalyzed Conjugate Addition of Dialkylzinc Reagents to 5-(1-Arylalkylidene) Meldrum's Acids
inferredcites →https://doi.org/10.1021/ja061430dopenalex-snapshot
Rhodium-Catalyzed Asymmetric Construction of Quaternary Carbon Stereocenters: Ligand-Dependent Regiocontrol in the 1,4-Addition to Substituted Maleimides
inferredcites →https://doi.org/10.1021/ja710540sopenalex-snapshot
Steric Tuning of Silylacetylenes and Chiral Phosphine Ligands for Rhodium-Catalyzed Asymmetric Conjugate Alkynylation of Enones
inferredcites →https://doi.org/10.1021/ja710922hopenalex-snapshot
Asymmetric Ni-Catalyzed Conjugate Allylation of Activated Enones
inferredcites →https://doi.org/10.1021/ja806068hopenalex-snapshot
C−H Bond Functionalization via Hydride Transfer: Lewis Acid Catalyzed Alkylation Reactions by Direct Intramolecular Coupling of sp3 C−H Bonds and Reactive Alkenyl Oxocarbenium Intermediates
inferredcites →https://doi.org/10.1021/ja905336popenalex-snapshot
Enantioselective Rhodium-Catalyzed Conjugate Alkynylation of 5-Benzylidene Meldrum’s Acids with TMS-acetylene
inferredcites →https://doi.org/10.1021/ja9076815openalex-snapshot
Hydrogenolysis of Unstrained Carbon−Carbon σ Bonds: Stereoselective Entry into Benzylic Tertiary Centers
inferredcites →https://doi.org/10.1021/jo0483724openalex-snapshot
Meldrum's Acids as Acylating Agents in the Catalytic Intramolecular Friedel−Crafts Reaction
inferredcites →https://doi.org/10.1021/jo049456fopenalex-snapshot
Rationale for the Acidity of Meldrum's Acid. Consistent Relation of C−H Acidities to the Properties of Localized Reactive Orbital
inferredcites →https://doi.org/10.1021/jo052000topenalex-snapshot
Yb(OTf)3-Catalyzed Reactions of 5-Alkylidene Meldrum's Acids with Phenols: One-Pot Assembly of 3,4-Dihydrocoumarins, 4-Chromanones, Coumarins, and Chromones
inferredcites →https://doi.org/10.1021/jo0618876openalex-snapshot
Modular Synthesis of Tetrahydrofluorenones from 5-Alkylidene Meldrum's Acids
inferredcites →https://doi.org/10.1021/jo702590sopenalex-snapshot
Electrophilicity Parameters of 5-Benzylidene-2,2-dimethyl[1,3]dioxane-4,6-diones (Benzylidene Meldrum's Acids)
inferredcites →https://doi.org/10.1021/jo702591popenalex-snapshot
Synthesis of Fused 4,5-Disubstituted Indole Ring Systems by Intramolecular Friedel−Crafts Acylation of 4-Substituted Indoles
inferredcites →https://doi.org/10.1021/jo802311wopenalex-snapshot
Probing Persistent Intramolecular C−H···X (X = O, S, Br, Cl, and F) Bonding in Solution Using Benzyl Meldrum’s Acid Derivatives
inferredcites →https://doi.org/10.1021/jo900390dopenalex-snapshot
Lewis Base-Promoted Hydrosilylation of Cyclic Malonates: Synthesis of β-Substituted Aldehydes and γ-Substituted Amines
inferredcites →https://doi.org/10.1021/jo901559dopenalex-snapshot
Asymmetric Synthesis of All-Carbon Benzylic Quaternary Stereocenters via Conjugate Addition to Alkylidene and Indenylidene Meldrum’s Acids
inferredcites →https://doi.org/10.1021/ol035575qopenalex-snapshot
Asymmetric Conjugate Addition Reactions of Meldrum's Acid Derived Acceptors Employing Chiral Phosphoramidite Ligands
inferredcites →https://doi.org/10.1021/ol035817mopenalex-snapshot
Convenient Access to Polysubstituted 1-Indanones by Sc(OTf)3-Catalyzed Intramolecular Friedel−Crafts Acylation of Benzyl Meldrum's Acid Derivatives
inferredcites →https://doi.org/10.1021/ol702613fopenalex-snapshot
Sequential Rh(I)/Pd-Catalyzed 1,4-Addition/Intramolecular Allylation: Stereocontrolled Construction of γ-Butyrolactones and Cyclopropanes
inferredcites →https://doi.org/10.1021/ol8000359openalex-snapshot
Stereoselective Synthesis of Woody Fragrances Related to Georgyone and Arborone
inferredcites →https://doi.org/10.1021/ol800923qopenalex-snapshot
Asymmetric Synthesis of Carboxylic Acid Derivatives Having an All-Carbon α-Quaternary Center through Cu-Catalyzed 1,4-Addition of Dialkylzinc Reagents to 2-Aryl Acetate Derivatives
inferredcites →https://doi.org/10.1021/ol801830hopenalex-snapshot
Palladium-Catalyzed Conjugate Allylation Reactions of α,β-Unsaturated N-Acylpyrroles
inferredcites →https://doi.org/10.1021/ol9003959openalex-snapshot
Sc(OTf)3-Catalyzed Conjugate Allylation of Alkylidene Meldrum’s Acids
inferredcites →https://doi.org/10.1021/ol902216yopenalex-snapshot
Asymmetric Addition of Alkenylstannanes to Alkylidene Meldrum’s Acids
inferredcites →https://doi.org/10.1021/om9705113openalex-snapshot
Rhodium-Catalyzed Conjugate Addition of Aryl- or 1-Alkenylboronic Acids to Enones
inferredcites →https://doi.org/10.1039/b716020hopenalex-snapshot
Meldrum’s acid and related compounds in the synthesis of natural products and analogs
inferredcites →https://doi.org/10.1039/b816853aopenalex-snapshot
Recent advances in enantioselective copper-catalyzed 1,4-addition
inferredcites →https://doi.org/10.1039/c39880001382openalex-snapshot
1,2-Carbonyl migration along the allylic framework: synthesis of alkenylnaphthoquinones
inferredcites →https://doi.org/10.1039/ct9089300598openalex-snapshot
LIV.—A β-lactonic acid from acetone and malonic acid
inferredcites →https://doi.org/10.1055/s-2001-18057openalex-snapshot
Synthetic Applications of the Pyrolysis of Meldrum's Acid Derivatives
inferredcites →https://doi.org/10.1055/s-2005-837754openalex-snapshot
Four New 6-Nor-5(6→7)abeo-abietane Type Diterpenes and Antitumoral Cytotoxic Diterpene Constituents from the Bark ofTaiwania cryptomerioides
inferredcites →https://doi.org/10.1071/ch9751551openalex-snapshot
Methyleneketenes and methylenecarbenes. V. Condensation of ketones with isopropylidene malonate catalysed by titanium tetrachloride and synthesis of a dibenzofuran
inferredcites →https://doi.org/10.1071/ch9770179openalex-snapshot
Methyleneketenes and methylenecarbenes. VII. Evidence for the pyrolytic generation of methyleneketene (propadienone)
inferredcites →https://doi.org/10.1071/ch9790111openalex-snapshot
Synthetic Applications of Intramolecular Insertion in Arylcarbenes. III. Generation and Rearrangement of Aryloxycarbenes by Intramolecular Abstraction of Hydrogen
inferredcites →https://doi.org/10.1080/00397910802044272openalex-snapshot
Facile One-Pot Synthesis of 1,2,3,4-Tetrahydroquinoline-3-carboxylic Acids and Their Heterocyclic Analogs
inferredcites →https://doi.org/10.1080/00397918008065647openalex-snapshot
Monoalkylidene Derivatives of Meldrum's Acid
inferredcites →https://doi.org/10.1080/00397918708075747openalex-snapshot
The Reaction of Meldrum's Acid with Aldehydes and Phloroglucinol: A Synthesis of Dihydrocoumarins1
inferredcites →https://doi.org/10.2533/chimia.2008.461openalex-snapshot
Formation of All-Carbon Quaternary Centers by Copper-Catalyzed Asymmetric Conjugate Addition
inferredcites →https://doi.org/10.3891/acta.chem.scand.23-3003openalex-snapshot
The Acidity and General Base-Catalyzed Hydrolysis of Meldrum's Acid and Its Methyl Derivatives.
inferredcites →https://doi.org/10.3987/rev-90-422openalex-snapshot
Meldrum's Acid in Orgnaic Synthesis
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.4668249openalex-extracted
Oxygen Functional Groups in Carbon Material Obtained from Pyrolysis of Heterocyclic Compounds with Their Decomposition Mechanism
inferred← citeshttps://doi.org/10.1002/0471264229.os092.14openalex-snapshot
Asymmetric Synthesis of All‐Carbon Benzylic Quaternary Stereocenters via Conjugate Addition to Alkylidene Meldrum's Acids
inferred← citeshttps://doi.org/10.1002/0471264229.os092.19openalex-snapshot
Preparation of ( S )‐ tert ‐ ButylPyOx and Palladium‐Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/0471264229.os098.07openalex-snapshot
Discussion Addendum for: Preparation of ( S )‐ tert ‐ButylPyOx and Palladium‐Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids
inferred← citeshttps://doi.org/10.1002/9780470979525.ch9openalex-snapshot
Carbanions and Electrophilic Aliphatic Substitution
inferred← citeshttps://doi.org/10.1002/9781119941910.ch6openalex-snapshot
Electrophilic Aromatic Substitution
inferred← citeshttps://doi.org/10.1002/9781119941910.ch9openalex-snapshot
Carbanions and Electrophilic Aliphatic Substitution
inferred← citeshttps://doi.org/10.1002/adsc.201300465openalex-snapshot
Organocatalyzed Synthesis of Isoxazolidin‐5‐ones: The Meldrum’s Acid Approach
inferred← citeshttps://doi.org/10.1002/adsc.201701084openalex-snapshot
Direct Organocatalytic Multicomponent Synthesis of Enantiopure γ‐Butyrolactones via Tandem Knoevenagel‐Michael‐Lactonization Sequence
inferred← citeshttps://doi.org/10.1002/adsc.201801453openalex-snapshot
C5‐Disubstituted Meldrum's Acid Derivatives as Platform for the Organocatalytic Synthesis of C3‐Alkylated Dihydrocoumarins
inferred← citeshttps://doi.org/10.1002/adsc.202100559openalex-snapshot
Auto Tandem Catalysis: Asymmetric Vinylogous Cycloaddition/Kinetic Resolution Sequence for the Enantioselective Synthesis of Spiro‐Dihydropyranone from Benzylidene Meldrum's Acid
inferred← citeshttps://doi.org/10.1002/adsc.202100719openalex-snapshot
Multicomponent Catalytic Enantioselective Synthesis of Isoxazolidin‐5‐Ones
inferred← citeshttps://doi.org/10.1002/adsc.202300609openalex-snapshot
Alkylidene Meldrum′s Acid as Acceptor‐Donor‐Acceptor with Azomethine Ylide for Organocatalytic Asymmetric (3+2) Cycloaddition/Annulation: Synthesis of Chromeno[4,3‐b]pyrrolidine
inferred← citeshttps://doi.org/10.1002/ajoc.202200598openalex-snapshot
Design and Synthesis of Amino Acid Derivatives via Diethyl Acetadimalonate and Late‐Stage Modification by Chemical Methods
inferred← citeshttps://doi.org/10.1002/ange.201206186openalex-snapshot
Synthesis of Five‐ and Six‐Membered Benzocyclic Ketones through Intramolecular Alkene Hydroacylation Catalyzed by Nickel(0)/N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/ange.201206297openalex-snapshot
Effect of Multinuclear Copper/Aluminum Complexes in Highly Asymmetric Conjugate Addition of Trimethylaluminum to Acyclic Enones
inferred← citeshttps://doi.org/10.1002/ange.201303202openalex-snapshot
Formation of Quaternary Centers by Copper‐Catalyzed Asymmetric Conjugate Addition of Alkylzirconium Reagents
inferred← citeshttps://doi.org/10.1002/ange.201406247openalex-snapshot
Remarkable Enhancement of Enantioselectivity in the Asymmetric Conjugate Addition of Dimethylzinc to (Z)‐Nitroalkenes with a Catalytic [(MeCN)4Cu]PF6–Hoveyda Ligand Complex
inferred← citeshttps://doi.org/10.1002/ange.201500983openalex-snapshot
Synthesis and Characterization of Tricarbastannatranes and Their Reactivity in B(C 6 F 5 ) 3 ‐Promoted Conjugate Additions
inferred← citeshttps://doi.org/10.1002/ange.202014489openalex-snapshot
Alkylidene Meldrum's Acids as Platforms for the Vinylogous Synthesis of Dihydropyranones
inferred← citeshttps://doi.org/10.1002/ange.202214390openalex-snapshot
Donor‐Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor
inferred← citeshttps://doi.org/10.1002/ange.202422714openalex-snapshot
Reduktive Kohlenstoffmaterialien: Einstellung der chemischen und elektronischen Eigenschaften zur Verbesserung von Natrium‐Ionen‐Batterien
inferred← citeshttps://doi.org/10.1002/anie.201206186openalex-snapshot
Synthesis of Five‐ and Six‐Membered Benzocyclic Ketones through Intramolecular Alkene Hydroacylation Catalyzed by Nickel(0)/N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/anie.201206297openalex-snapshot
Effect of Multinuclear Copper/Aluminum Complexes in Highly Asymmetric Conjugate Addition of Trimethylaluminum to Acyclic Enones
inferred← citeshttps://doi.org/10.1002/anie.201303202openalex-snapshot
Formation of Quaternary Centers by Copper‐Catalyzed Asymmetric Conjugate Addition of Alkylzirconium Reagents
inferred← citeshttps://doi.org/10.1002/anie.201406247openalex-snapshot
Remarkable Enhancement of Enantioselectivity in the Asymmetric Conjugate Addition of Dimethylzinc to (Z)‐Nitroalkenes with a Catalytic [(MeCN)4Cu]PF6–Hoveyda Ligand Complex
inferred← citeshttps://doi.org/10.1002/anie.201500983openalex-snapshot
Synthesis and Characterization of Tricarbastannatranes and Their Reactivity in B(C6F5)3‐Promoted Conjugate Additions
inferred← citeshttps://doi.org/10.1002/anie.202014489openalex-snapshot
Alkylidene Meldrum's Acids as Platforms for the Vinylogous Synthesis of Dihydropyranones
inferred← citeshttps://doi.org/10.1002/anie.202214390openalex-snapshot
Donor‐Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor
inferred← citeshttps://doi.org/10.1002/anie.202422714openalex-snapshot
Reductive Carbon Materials: Tailoring Chemistry and Electronic Properties to Improve Sodium‐Ion Batteries
inferred← citeshttps://doi.org/10.1002/cbdv.71611openalex-snapshot
Study on Synthesis, Antiproliferative Properties, Immunomodulatory Effects, and Anti‐Breast Cancer Activity of New Δ 2 ‐Pyrazoline‐1 H ‐1,2,3‐Triazole Derivatives
inferred← citeshttps://doi.org/10.1002/cctc.201600247openalex-snapshot
Meldrum's Acid: A Useful Platform in Asymmetric Organocatalysis
inferred← citeshttps://doi.org/10.1002/chem.201200694openalex-snapshot
Palladium‐Catalyzed Asymmetric Quaternary Stereocenter Formation
inferred← citeshttps://doi.org/10.1002/chem.201403161openalex-snapshot
Di‐ and Triarylmethylium Ions as Probes for the Ambident Reactivities of Carbanions Derived from 5‐Benzylated Meldrum’s Acid
inferred← citeshttps://doi.org/10.1002/chem.201603910openalex-snapshot
Enantioselective Phase‐Transfer Catalyzed α‐Sulfanylation of Isoxazolidin‐5‐ones: An Entry to β2,2‐Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/chem.201705714openalex-snapshot
A Unique (3+2) Annulation Reaction between Meldrum's Acid and Nitrones: Mechanistic Insight by ESI‐IMS‐MS and DFT Studies
inferred← citeshttps://doi.org/10.1002/chem.202001214openalex-snapshot
Organocatalytic Multicomponent Synthesis of α/β‐Dipeptide Derivatives
inferred← citeshttps://doi.org/10.1002/chem.202301311openalex-snapshot
An Organocatalytic and Stereoselective Vinylogous Domino Process towards Thiochromans
inferred← citeshttps://doi.org/10.1002/chin.200305241openalex-snapshot
Six-Membered Ring Systems: With O and/or S Atoms
inferred← citeshttps://doi.org/10.1002/ejoc.201700439openalex-snapshot
Design and Synthesis of Spirocycles
inferred← citeshttps://doi.org/10.1002/ejoc.201700472openalex-snapshot
A Meldrum's Acid Based Multicomponent Synthesis of N‐Fmoc‐isoxazolidin‐5‐ones: Entry to N‐Fmoc‐β‐amino Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201800331openalex-snapshot
Organocatalytic Enantioselective Decarboxylative Protonation Reaction of Meldrum's Acid Derivatives under PTC Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201901189openalex-snapshot
Expanding the Family of Fluorescent Coumarin[4]arenes: Improved Synthesis, π‐Extension, and Characterization
inferred← citeshttps://doi.org/10.1002/jhet.1941openalex-snapshot
Novel Synthesis of 6‐Substituted 2‐Picolines from Aryl/heteroaryl β‐Enaminones and Meldrum's Acid Using CeCl3.7H2O/NaI
inferred← citeshttps://doi.org/10.1002/jhet.2028openalex-snapshot
Thermal Decomposition of Carbamoyl Meldrum's Acids: A Starting Point for the Preparation of 1,3‐Oxazine Derivatives
inferred← citeshttps://doi.org/10.1002/jhet.2128openalex-snapshot
[4 + 2] Heterocyclization for Efficient Formation of Substituted Quinoxalines through Carbon–Oxygen Bonds Cleavage
inferred← citeshttps://doi.org/10.1002/pat.5910openalex-snapshot
Toward efficient functionalization of polystyrene backbone through ketene chemistry: Synthesis, characterization, and DFT study
inferred← citeshttps://doi.org/10.1002/pola.26797openalex-snapshot
The emerging utility of ketenes in polymer chemistry
inferred← citeshttps://doi.org/10.1002/slct.201601965openalex-snapshot
Solvent‐, and Catalyst–free Acylation of Anilines with Meldrum's Acids: ANeat Access to Anilides
inferred← citeshttps://doi.org/10.1002/slct.202302152openalex-snapshot
The Molecular Diversity Scope of Meldrum's Acid in Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/slct.202404787openalex-snapshot
Synthesis, Anti‐enzymatic Appraisal, In Silico, and SAR Analysis of 5‐Aryl/Heteroaryl‐2,2‐dimethyl‐1,3‐dioxane‐4,6‐dione Derivatives
inferred← citeshttps://doi.org/10.1002/slct.202503092openalex-snapshot
Exploring the Bioactive Potential of 2,2‐Dimethyl‐1,3‐Dioxane‐4,6‐Dione: A Comprehensive Computational Analysis
inferred← citeshttps://doi.org/10.1007/3418_2015_158openalex-snapshot
Formation of Quaternary Stereocentres by Copper-Catalysed Enantioselective Conjugate Addition Reaction
inferred← citeshttps://doi.org/10.1007/s11030-021-10240-4openalex-snapshot
Reverse orientation in the ultrasound-assisted [3 + 2]-cycloaddition reaction of nitrile imines with 3-formylchromone-Meldrum’s acid adducts
inferred← citeshttps://doi.org/10.1007/s11030-023-10610-0openalex-snapshot
Formation of bis-spiropyrrolidines from isatin, secondary amines, and alkylidene Meldrum’s acids
inferred← citeshttps://doi.org/10.1007/s11030-026-11469-7openalex-snapshot
Multicomponent reactions with Meldrum's acid and isocyanides as a valuable synthetic approach: An update
inferred← citeshttps://doi.org/10.1007/s11164-023-05168-3openalex-snapshot
Sonochemical synthesis of benzylidene derivatives of enolizable carbonyls and their analogues in aqueous ethanol
inferred← citeshttps://doi.org/10.1007/s11172-017-2010-6openalex-snapshot
One-pot three-component green synthesis of [1H-(1,2,3-triazol-5-yl)methylidene] heterocycles based on element-substituted propynals
inferred← citeshttps://doi.org/10.1007/s12013-026-02090-4openalex-snapshot
The Synthesis and Biological Activity of Series of New Polyfunctional Pyrroles with the Potential to Modulate Neuronal Viability
inferred← citeshttps://doi.org/10.1007/s13738-017-1129-6openalex-snapshot
Carbon-based leaving group capability of Meldrum’s acid in substitution reactions: a new strategy toward the synthesis of 4-phenyl-3, 4-dihydro-2H-benzo[g]chromene-2, 5, 10-triones
inferred← citeshttps://doi.org/10.1007/s13738-021-02224-wopenalex-snapshot
A green and efficient synthesis of novel caffeic acid derivatives with Meldrum’s acid moieties as potential antibacterial agents
inferred← citeshttps://doi.org/10.1007/s13738-024-03023-9openalex-snapshot
Chemoselective synthesis of multisubstituted pyrrolo[3,4-b]pyridine-2,5,7(6H)-trione through a cascade reaction
inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00015-2openalex-snapshot
Six-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14933-9openalex-snapshot
1,3-Dioxins, Oxathiins, Dithiins and Their Benzo Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-12-420160-6.00004-5openalex-snapshot
The Literature of Heterocyclic Chemistry, Part XII, 2010–2011
inferred← citeshttps://doi.org/10.1016/b978-0-444-63932-5.00008-5openalex-snapshot
Synthetic Advances in the Indane Natural Product Scaffolds as Drug Candidates
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.11.033openalex-snapshot
Facile synthesis and biological evaluation of 3,3-diphenylpropanoyl piperazines as T-type calcium channel blockers
inferred← citeshttps://doi.org/10.1016/j.cartre.2024.100333openalex-snapshot
Oxygen functionalized carbon obtained from pyrolysis of heterocyclic compounds with their decomposition mechanism
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.04.009openalex-snapshot
Rh(I)-catalyzed regio- and enantioselective allylic alkylation of Meldrum’s acid
inferred← citeshttps://doi.org/10.1016/j.cplett.2019.136908openalex-snapshot
A theoretical investigation on the nucleophilic behavior of Meldrum’s acid linked to experimental evidences
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.117174openalex-snapshot
Dihydrofolate reductase inhibitory potential of 1H-indole-based-meldrum linked 1H-1,2,3-triazoles as new anticancer derivatives: In-vitro and in-silico studies
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.117228openalex-snapshot
Novel antimalarial 3-substituted quinolones isosteres with improved pharmacokinetic properties
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2012.07.004openalex-snapshot
Boron difluoride complexes of carbamoyl Meldrum's acids
inferred← citeshttps://doi.org/10.1016/j.mcat.2023.113002openalex-snapshot
TFE assisted mechanochemical synthesis of new pyrazolones from Meldrum acid carbothioamides-Experimental and theoretical studies
inferred← citeshttps://doi.org/10.1016/j.tet.2010.12.046openalex-snapshot
Efficient synthesis of fluorinated α- and β-amino nitriles from fluoroalkylated α,β-unsaturated imines
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.022openalex-snapshot
New formal (3+3) cycloaddition of enaminones for forming tetracyclic indolo[2,3-b]quinolines under microwave irradiation
inferred← citeshttps://doi.org/10.1016/j.tet.2014.11.048openalex-snapshot
Synthesis of diverse β-quaternary ketones via palladium-catalyzed asymmetric conjugate addition of arylboronic acids to cyclic enones
inferred← citeshttps://doi.org/10.1016/j.tet.2015.05.040openalex-snapshot
Divergent total synthesis of crassalactones B and C and evaluation of their antiproliferative activity
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130573openalex-snapshot
A transition metal free expedient approach for the C C bond cleavage of arylidene Meldrum's acid and malononitrile derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2020.130967openalex-snapshot
Boron/zinc exchange for the conjugate arylation of unsaturated Meldrum’s acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133328openalex-snapshot
Facile synthesis of indole 3-acetic acid and azaindole 3-acetic acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.07.054openalex-snapshot
One-pot conversion of alkyl aldehydes into substituted propanoic acids via Knoevenagel condensation with Meldrum’s acid
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.08.018openalex-snapshot
‘Melen complexes’: a new family of Schiff base metal chelates derived from di-Meldrum’s acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.03.123openalex-snapshot
A novel light induced Knoevenagel condensation of Meldrum’s acid with aromatic aldehydes in aqueous ethanol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.101openalex-snapshot
Bifunctional AgOAc/ThioClickFerrophos complex-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with aryl- and alkylidene malonates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.10.064openalex-snapshot
Friedel-Crafts alkylation of benzo[b]furan with activated cyclopropanes catalyzed by a calcium(II) complex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.12.013openalex-snapshot
Acyl/aroyl Meldrum’s acid as an enol surrogate for the direct organocatalytic synthesis of α,β-unsaturated ketones
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02538openalex-snapshot
Synthesis of 1-(Difluoromethyl)alk-1-enes via Palladium-Catalyzed SN2′-Type Substitution Reaction of Difluoromethylated Allylic Phosphates with 1,3-Dicarbonyl Compounds and Imides
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02690openalex-snapshot
Overcoming Kinetic and Thermodynamic Challenges of Classic Cope Rearrangements
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00252openalex-snapshot
The Catalytic Regio- and Stereoselective Synthesis of 1,6-Diazabicyclo[4.3.0]nonane-2,7-diones
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02403openalex-snapshot
Rigidified Bis(sulfonyl)ethylenes as Effective Michael Acceptors for Asymmetric Catalysis: Application to the Enantioselective Synthesis of Quaternary Hydantoins
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01881openalex-snapshot
Ruthenium-Catalyzed Chemo-Selective Carbene Insertion into C–H Bond of Styrene over Cyclopropanation: C–C Bond Formation
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01636openalex-snapshot
Base-Promoted One-Pot Four-Component Domino Strategy Involving Aldehydes and Ketones to Access Multifunctionalized Dihydropyridinones
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01173openalex-snapshot
Substrate-Controlled Divergent Syntheses of Polycyclic Tetrahydropyrimidin-4-ones and 1,3-Oxazinane-4,6-diones from Dihydroisoquinolines and Meldrum’s Acid
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02159openalex-snapshot
Radical-Stimulated Nucleophile Release
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02978openalex-snapshot
Stereoselective Sequential Spirocyclopropanation/Cloke–Wilson Rearrangement Reactions for Synthesis of trans-β,γ-Disubstituted γ-Butyrolactones Using Alkylidene Meldrum’s Acid and Benzyl Halides
inferred← citeshttps://doi.org/10.1021/acs.jpca.7b11796openalex-snapshot
Enhanced Proton Loss from Neutral Free Radicals: Toward Carbon-Centered Superacids
inferred← citeshttps://doi.org/10.1021/acs.macromol.3c01250openalex-snapshot
Hemiacetal Esters: Synthesis, Properties, and Applications of a Versatile Functional Group
inferred← citeshttps://doi.org/10.1021/acs.macromol.5c03430openalex-snapshot
Accessing Diverse Polymer Architectures through Meldrum’s Acid-Functionalized Polysiloxane Precursors
inferred← citeshttps://doi.org/10.1021/acs.oprd.5b00169openalex-snapshot
Palladium-Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids to α,β-Unsaturated Cyclic Electrophiles
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02504openalex-snapshot
5-Carbonyl-1,3-oxazine-2,4-diones from N-Cyanosulfoximines and Meldrum’s Acid Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03982openalex-snapshot
Synthesis of Cyclopentadienes for Cyclopentadienyl Ligands via Cp*RhIII-Catalyzed Formal sp3 C–H Activation/Spiroannulations
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02755openalex-snapshot
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01567openalex-snapshot
Multicomponent Domino Synthesis of Cyclopenta[b]furan-2-ones
inferred← citeshttps://doi.org/10.1021/acsmacrolett.8b00166openalex-snapshot
Vitrimeric Silicone Elastomers Enabled by Dynamic Meldrum’s Acid-Derived Cross-Links
inferred← citeshttps://doi.org/10.1021/acsomega.3c01291openalex-snapshot
Meldrum-Based-1 H -1,2,3-Triazoles as Antidiabetic Agents: Synthesis, In Vitro α-Glucosidase Inhibition Activity, Molecular Docking Studies, and In Silico Approach
inferred← citeshttps://doi.org/10.1021/acssuschemeng.4c01790openalex-snapshot
A One-Pot Two-Step Three-Component Stereoselective Mechanosynthesis of Ester-Functionalized Multisubstituted Δ2-Pyrazolines and Their Application in the Detection of Fluoride Ions
inferred← citeshttps://doi.org/10.1021/bk-2016-1239.ch005openalex-snapshot
Development of an Efficient Asymmetric Synthesis of the Chiral Quaternary 5-Lipoxygenase Activating Protein Inhibitor
inferred← citeshttps://doi.org/10.1021/cr3005263openalex-snapshot
Ketenes and Other Cumulenes as Reactive Intermediates
inferred← citeshttps://doi.org/10.1021/ja200664xopenalex-snapshot
Palladium-Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids to Five-, Six-, and Seven-Membered β-Substituted Cyclic Enones: Enantioselective Construction of All-Carbon Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1021/ja207635fopenalex-snapshot
Reactive, Multifunctional Polymer Films through Thermal Cross-linking of Orthogonal Click Groups
inferred← citeshttps://doi.org/10.1021/ja401713gopenalex-snapshot
Mechanism and Enantioselectivity in Palladium-Catalyzed Conjugate Addition of Arylboronic Acids to β-Substituted Cyclic Enones: Insights from Computation and Experiment
inferred← citeshttps://doi.org/10.1021/jacs.7b00363openalex-snapshot
Enantioselective Alkyne Conjugate Addition Enabled by Readily Tuned Atropisomeric P , N -Ligands
inferred← citeshttps://doi.org/10.1021/jo4017524openalex-snapshot
Scandium Triflate-Catalyzed Nucleophilic Additions to Indolylmethyl Meldrum’s Acid Derivatives via a Gramine-Type Fragmentation: Synthesis of Substituted Indolemethanes
inferred← citeshttps://doi.org/10.1021/jo502075popenalex-snapshot
Selective Perfluoro- and Polyfluoroarylation of Meldrum’s Acid
inferred← citeshttps://doi.org/10.1021/jp5029245openalex-snapshot
Persistent Intramolecular C–H···X (X = O or S) Hydrogen-Bonding in Benzyl Meldrum’s Acid Derivatives
inferred← citeshttps://doi.org/10.1021/mz300250bopenalex-snapshot
Cyclopolymerization To Synthesize Conjugated Polymers Containing Meldrum's Acid as a Precursor for Ketene Functionality
inferred← citeshttps://doi.org/10.1021/mz300497mopenalex-snapshot
Ketene-Based Route to rigid Cyclobutanediol Monomers for the Replacement of BPA in High Performance Polyesters
inferred← citeshttps://doi.org/10.1021/ol302848mopenalex-snapshot
Cu(II)-Catalyzed Aerobic Hydroperoxidation of Meldrum’s Acid Derivatives and Application in Intramolecular Oxidation: A Conceptual Blueprint for O2/H2Dihydroxylation
inferred← citeshttps://doi.org/10.1021/ol401276bopenalex-snapshot
A Csp3–Csp3 Bond Forming Reductive Condensation of α-Keto Esters and Enolizable Carbon Pronucleophiles
inferred← citeshttps://doi.org/10.1021/ol402130topenalex-snapshot
A Practical and Convenient Protocol for the Synthesis of (E)-α,β-Unsaturated Acids
inferred← citeshttps://doi.org/10.1021/ol502811jopenalex-snapshot
Expedient Synthesis of Complex γ-Butyrolactones from 5-(1-Arylalkylidene) Meldrum’s Acids via Sequential Conjugate Alkynylation/Ag(I)-Catalyzed Lactonization
inferred← citeshttps://doi.org/10.1038/nprot.2012.034openalex-snapshot
Selective synthesis of 3-hydroxy acids from Meldrum's acids using SmI2-H2O
inferred← citeshttps://doi.org/10.1038/nprot.2013.169openalex-snapshot
Copper-catalyzed asymmetric conjugate addition of alkylzirconium reagents to cyclic enones to form quaternary centers
inferred← citeshttps://doi.org/10.1038/s41598-023-50535-0openalex-snapshot
Meldrum’s acid assisted formation of tetrahydroquinolin-2-one derivatives a short synthetic pathway to the biologically useful scaffold
inferred← citeshttps://doi.org/10.1039/c0cc02309dopenalex-snapshot
Metal-catalyzed asymmetric conjugate addition reaction: formation of quaternary stereocenters
inferred← citeshttps://doi.org/10.1039/c1cc14055hopenalex-snapshot
An energy efficient and facile synthesis of high molecular weight polyesters using ketenes
inferred← citeshttps://doi.org/10.1039/c2sc00841fopenalex-snapshot
Low-temperature ketene formation in materials chemistry through molecular engineering
inferred← citeshttps://doi.org/10.1039/c3cc47695bopenalex-snapshot
Organocatalysed decarboxylative protonation process from Meldrum's acid: enantioselective synthesis of isoxazolidinones
inferred← citeshttps://doi.org/10.1039/c3ob40666kopenalex-snapshot
A novel domino strategy for forming poly-substituted quaternary imidazoles through a Cs2CO3-promoted aryl migration process
inferred← citeshttps://doi.org/10.1039/c4cc03216kopenalex-snapshot
Mechanistic investigation of the selective reduction of Meldrum's acids to β-hydroxy acids using SmI 2 and H 2 O
inferred← citeshttps://doi.org/10.1039/c4cc04852kopenalex-snapshot
Organocatalysed multicomponent synthesis of pyrazolidinones: Meldrum's acid approach
inferred← citeshttps://doi.org/10.1039/c4ob00618fopenalex-snapshot
Synthesis of functionalized chromones through sequential reactions in aqueous media
inferred← citeshttps://doi.org/10.1039/c5cc02382copenalex-snapshot
Utilization of a Meldrum's acid towards functionalized fluoropolymers possessing dual reactivity for thermal crosslinking and post-polymerization modification
inferred← citeshttps://doi.org/10.1039/c5ra08792aopenalex-snapshot
Modified multicomponent Biginelli–Atwal reaction towards a straightforward construction of 5,6-dihydropyrimidin-4-ones
inferred← citeshttps://doi.org/10.1039/c6nj00884dopenalex-snapshot
The stereoselective formation of β-lactams with acyl ketenes generated from 5-acyl-Meldrum's acids
inferred← citeshttps://doi.org/10.1039/c6qo00034gopenalex-snapshot
Diastereoselective and regiodivergent oxa-[3 + 2] cycloaddition of Achmatowicz products and cyclic 1,3-dicarbonyl compounds
inferred← citeshttps://doi.org/10.1039/c6sc02811jopenalex-snapshot
Acyclic quaternary centers from asymmetric conjugate addition of alkylzirconium reagents to linear trisubstituted enones
inferred← citeshttps://doi.org/10.1039/c7ob00086copenalex-snapshot
Sc(OTf) 3 -catalyzed synthesis of anhydrides from twisted amides
inferred← citeshttps://doi.org/10.1039/c8ob02473aopenalex-snapshot
Multicomponent synthesis of pyroglutamic acid derivatives via Knoevenagel–Michael-hydrolysis-lactamization-decarboxylation (KMHL-D) sequence
inferred← citeshttps://doi.org/10.1039/c8py01173gopenalex-snapshot
Self-crosslinkable and modifiable polysiloxanes possessing Meldrum's acid groups
inferred← citeshttps://doi.org/10.1039/c8sc03057jopenalex-snapshot
Transient [3,3] Cope rearrangement of 3,3-dicyano-1,5-dienes: computational analysis and 2-step synthesis of arylcycloheptanes
inferred← citeshttps://doi.org/10.1039/d0qo00770fopenalex-snapshot
A thermal decarboxylative Cloke–Wilson rearrangement of dispirocyclopropanes derived from para -quinone methides and bromo-Meldrum's acids: an approach to synthesize spirobutyrolactone para -dienones
inferred← citeshttps://doi.org/10.1039/d1cc06212copenalex-snapshot
Synthesis of fluorenes and their related compounds from biaryls and Meldrum's acid derivatives
inferred← citeshttps://doi.org/10.1039/d1cs00193kopenalex-snapshot
Dissociations of free radicals to generate protons, electrophiles or nucleophiles: role in DNA strand breaks
inferred← citeshttps://doi.org/10.1039/d1ob00395jopenalex-snapshot
Selected applications of Meldrum's acid – a tutorial
inferred← citeshttps://doi.org/10.1039/d4ob00233dopenalex-snapshot
Vinylogous and stereoselective domino synthesis of pyrano[2,3- c ]pyrroles from alkylidene meldrum's acids
inferred← citeshttps://doi.org/10.1039/d5cc01032bopenalex-snapshot
Recent advances of asymmetric catalytic transformations of alkylidene Meldrum's acid derivatives
inferred← citeshttps://doi.org/10.1039/d6ob00287kopenalex-snapshot
HTE-enabled discovery of palladium-catalysed (hetero)arylation of barbituric and meldrum's acid
inferred← citeshttps://doi.org/10.1055/a-1638-5783openalex-snapshot
Regio- and Stereoselective Addition of Brønsted Acids to Yndiamides: Synthesis of N,O,N- and N,S,N-Trisubstituted Ketene Acetals
inferred← citeshttps://doi.org/10.1055/a-2722-9900openalex-snapshot
Iron-Catalyzed One-Pot Four-Component Synthesis of Dihydropyridinones from Benzyl Alcohols and Ketones
inferred← citeshttps://doi.org/10.1055/s-0041-1738758openalex-snapshot
Practical Synthesis of 7-Azaserotonin and 7-Azamelatonin
inferred← citeshttps://doi.org/10.1070/rc2014v083n07abeh004441openalex-snapshot
Acyl Meldrum's acid derivatives: application in organic synthesis
inferred← citeshttps://doi.org/10.1080/00268976.2025.2603621openalex-snapshot
Cu-, Zn-melophen or salophen complexes? Comparative prediction of the first-order molecular hyperpolarizability based on a DFT approach
inferred← citeshttps://doi.org/10.1080/00397911.2017.1383432openalex-snapshot
New thiourea organocatalysts and their application for the synthesis of 5-(1H-indol-3-yl)methyl-2,2-dimethyl-1,3-dioxane-4,6-diones a source of chiral 3-indoylmethyl ketenes
inferred← citeshttps://doi.org/10.1080/00397911.2024.2413165openalex-snapshot
Sequential Knoevenagel condensation/cyclization reaction using Meldrum’s acid
inferred← citeshttps://doi.org/10.1134/s1063774513080038openalex-snapshot
Synthesis, crystal structure and DFT studies of N-(4-acetyl-5,5-dimethyl-4,5-dihydro-1,3,4-thiadiazol-2-yl)acetamide
inferred← citeshttps://doi.org/10.15227/orgsyn.098.0117openalex-snapshot
Discussion Addendum for: Preparation of (S)-tert-ButylPyOx and Palladium-Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10499390/v1openalex-snapshot
Molecular Length and conjugation Influence on the Binding of Meldrum’s Acid Derivatives to β-Lactoglobulin
inferred← citeshttps://doi.org/10.2139/ssrn.5358490openalex-snapshot
The Synthesis and Biological Activity of Series of Polyfunctional Pyrroles with Potential Antioxidant Activity in Neuronal Cells
inferred← citeshttps://doi.org/10.22215/etd/2022-14840openalex-snapshot
New Derivatization Strategies for Installation of Fixed, Permanent Charges onto Analytes of Biological and Environmental Concern
inferred← citeshttps://doi.org/10.3184/174751917x14839766277251openalex-snapshot
Reaction of Meldrum's Acid with an Aminomethylating Agent and Nitroalkanes
inferred← citeshttps://doi.org/10.3390/catal9020131openalex-snapshot
Enantioselective Catalytic Transformations of Barbituric Acid Derivatives
inferred← citeshttps://doi.org/10.3390/ijms222011119openalex-snapshot
Development of Novel Quinoline-Based Sulfonamides as Selective Cancer-Associated Carbonic Anhydrase Isoform IX Inhibitors
inferred← citeshttps://doi.org/10.3390/molecules30173534openalex-snapshot
Disubstituted Meldrum’s Acid: Another Scaffold with SuFEx-like Reactivity
inferred← citeshttps://doi.org/10.3390/molecules31010083openalex-snapshot
4,5-Dihydro-2H-pyridazin-3-ones as a Platform for the Construction of Chiral 4,4-Disubstituted-dihydropyridazin-3-ones
inferred← citeshttps://doi.org/10.3390/ph16020281openalex-snapshot
Synthesis, Characterization, and Biological Evaluation of Meldrum’s Acid Derivatives: Dual Activity and Molecular Docking Study
inferred← citeshttps://doi.org/10.3762/bjoc.16.90openalex-snapshot
Copper-catalysed alkylation of heterocyclic acceptors with organometallic reagents
inferred← citeshttps://doi.org/10.3987/com-13-12766openalex-snapshot
NOVEL NITENPYRAM ANALOGUES WITH TETRAHYDROPYRIDONE FIXED CIS-CONFIGURATION: SYNTHESIS, INSECTICIDAL ACTIVITIES, AND MOLECULAR DOCKING STUDIES
inferred← citeshttps://doi.org/10.3987/com-14-13026openalex-snapshot
Multicomponent and Regioselective Synthesis of Dihydropyrazolo[1,5-a]pyrimidines from Aromatic Aldehydes, Meldrum’s Acid, and Aminopyrazole CAN508
inferred← citeshttps://doi.org/10.4236/ijoc.2013.34039openalex-snapshot
Solvent-Free Synthesis of 5-Alkenyl-2,2-butylidene-1, 3-dioxane-4,6-diones under Ultrasonic Irradiation with o-Phthalimide-N-Sulfonic Acid as Catalyst
inferred← citeshttps://doi.org/10.70675/ae68aebcz3b7cz42fdza373z98920f9f5a98openalex-snapshot
Développement de ligands anticlastogéniques des prohibitines
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