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A New Copper Acetate-Bis(oxazoline)-Catalyzed, Enantioselective Henry Reaction
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0022-328x(88)83103-6openalex-snapshot
Comprehensive Coordination Chemistry
inferredcites →https://doi.org/10.1021/cr010297zopenalex-snapshot
Lanthanide Complexes in Multifunctional Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/ja00037a068openalex-snapshot
Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions
inferredcites →https://doi.org/10.1021/ja00037a069openalex-snapshot
New class of bridged diiron(III) complexes with a single hydroxo bridge. The preparation and structure of (.mu.-hydroxo)bis((octaethylporphinato)iron(III)) perchlorate
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Interface Nano-Engineering to Synthesize Functionalized Melamine-Based Gn-Dendron-Oms Hybrids as Highly-Efficient Catalysts for the Nitroaldol (Henry) Reaction
inferred← citeshttps://doi.org/10.1002/047084289x.rd346m.pub3openalex-snapshot
(S,S)-2,2′-(Dimethylmethylene)bis(4-tert-butyl-2-oxazoline)
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Enantioselective Nitroaldol (Henry) Reaction of p ‐Nitrobenzaldehyde and Nitromethane Using a Copper ( II ) Complex Derived from ( R,R )‐1,2‐Diaminocyclohexane: (1 S )‐1‐(4‐Nitrophenyl)‐2‐nitroethane‐1‐ol
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Chiral auxiliaries and catalysts
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Chiral auxiliaries and catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub4openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub5openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub6openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub7openalex-snapshot
Chiral Auxiliaries and Catalysts
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Nanocrystalline Magnesium Oxide for Asymmetric Organic Reactions
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Formation of Alcohols and Phenols by Alkylation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/9781118681299.ch3openalex-snapshot
Stabilized Carbanions, Enamines and Ylides
inferred← citeshttps://doi.org/10.1002/9781118846919.ch3openalex-snapshot
Asymmetric Multifunctional Catalysis
inferred← citeshttps://doi.org/10.1002/9783527635207.ch5openalex-snapshot
Chiral Bisoxazoline Ligands
inferred← citeshttps://doi.org/10.1002/9783527664573.ch11openalex-snapshot
Chiral Copper Lewis Acids in Asymmetric Transformations
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Catalyzed Henry Reaction by Compartmentalized Copper‐Pyrazolyl‐Complex Modified Microgels
inferred← citeshttps://doi.org/10.1002/adsc.200404051openalex-snapshot
The Catalytic Diastereo‐ and Enantioselective Claisen Rearrangement of 2‐Alkoxycarbonyl‐Substituted Allyl Vinyl Ether
inferred← citeshttps://doi.org/10.1002/adsc.200505148openalex-snapshot
Guanidine‐Thiourea Bifunctional Organocatalyst for the Asymmetric Henry (Nitroaldol) Reaction
inferred← citeshttps://doi.org/10.1002/adsc.200600531openalex-snapshot
Recyclable Copper Catalysts Based on Imidazolium‐Tagged Bis(oxazolines): A Marked Enhancement in Rate and Enantioselectivity for Diels–Alder Reactions in Ionic Liquid
inferred← citeshttps://doi.org/10.1002/adsc.200700064openalex-snapshot
Hydroxynitrile Lyase‐Catalyzed Enzymatic Nitroaldol (Henry) Reaction
inferred← citeshttps://doi.org/10.1002/adsc.200700377openalex-snapshot
Catalytic Asymmetric 1, 3‐Dipolar Cycloaddition Reaction of Nitrones with α′‐Phosphoric Enones by a Chiral Ligand‐ Copper(II) Triflate Complex
inferred← citeshttps://doi.org/10.1002/adsc.200900069openalex-snapshot
Versatile Supramolecular Copper(II) Complexes for Henry and Aza‐Henry Reactions
inferred← citeshttps://doi.org/10.1002/adsc.200900129openalex-snapshot
Combining Fluorous and Triazole Moieties for the Tagging of Chiral Azabis(oxazoline) Ligands
inferred← citeshttps://doi.org/10.1002/adsc.201000934openalex-snapshot
Charge‐Transfer Interactions: An Efficient Tool for Recycling Bis(oxazoline)‐Copper Complexes in Asymmetric Henry Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201100157openalex-snapshot
Diastereoselective and Highly Enantioselective Henry Reactions using C1‐Symmetrical Copper(II) Complexes
inferred← citeshttps://doi.org/10.1002/adsc.201200337openalex-snapshot
Copper Complex of Aminoisoborneol Schiff Base Cu2(SBAIB‐d)2: An Efficient Catalyst for Direct Catalytic Asymmetric Nitroaldol (Henry) Reaction
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Aza‐Henry Reaction of Isatin Ketimines with Methyl 4‐Nitrobutyrate en Route to Spiro[piperidine‐3,3′‐oxindoles]
inferred← citeshttps://doi.org/10.1002/adsc.201600046openalex-snapshot
Trifunctional Squaramide Catalyst for Efficient Enantioselective Henry Reaction Activation
inferred← citeshttps://doi.org/10.1002/adsc.201800067openalex-snapshot
Asymmetric Brominative Dearomatization of Naphthols Catalyzed by Chiral Copper Complexes
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Synthesis of 3‐Nitroisoxazoles via Copper Acetate‐Mediated Reaction of Benzaldehydes with Nitromethane
inferred← citeshttps://doi.org/10.1002/adsc.201900421openalex-snapshot
Bis(imidazolidine)pyridine‐CoCl2: A Novel, Catalytically Active Neutral Complex for Asymmetric Michael Reaction of 1,3‐Carbonyl Compounds with Nitroalkenes
inferred← citeshttps://doi.org/10.1002/ange.200460506openalex-snapshot
Verbesserte Katalysatoren für die asymmetrische Nitroaldol‐Reaktion (Henry‐Reaktion)
inferred← citeshttps://doi.org/10.1002/ange.200463075openalex-snapshot
Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands
inferred← citeshttps://doi.org/10.1002/ange.200503724openalex-snapshot
Asymmetric Organocatalytic Henry Reaction
inferred← citeshttps://doi.org/10.1002/ange.200504230openalex-snapshot
Eine biokatalytische Henry‐Reaktion – die Hydroxynitrillyase aus Hevea brasiliensis katalysiert auch Nitroaldolreaktionen
inferred← citeshttps://doi.org/10.1002/ange.200602255openalex-snapshot
Direct Monitoring of the Asymmetric Induction of Solid‐Phase Catalysis Using Circular Dichroism: Diamine–CuI‐Catalyzed Asymmetric Henry Reaction
inferred← citeshttps://doi.org/10.1002/ange.200705344openalex-snapshot
Catalytic Enantioselective Aldol‐type Reaction of β‐Ketosters with Acetals
inferred← citeshttps://doi.org/10.1002/ange.200705617openalex-snapshot
A Heterobimetallic Pd/La/Schiff Base Complex for anti‐Selective Catalytic Asymmetric Nitroaldol Reactions and Applications to Short Syntheses of β‐Adrenoceptor Agonists
inferred← citeshttps://doi.org/10.1002/ange.200801373openalex-snapshot
Tandem Catalytic Asymmetric Friedel–Crafts/Henry Reaction: Control of Three Contiguous Acyclic Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.201105778openalex-snapshot
Asymmetric Synthesis of Chiral 1,3‐Diaminopropanols: Bisoxazolidine‐Catalyzed CC Bond Formation with α‐Keto Amides
inferred← citeshttps://doi.org/10.1002/ange.201107785openalex-snapshot
Urea/Transition‐Metal Cooperative Catalyst foranti‐Selective Asymmetric Nitroaldol Reactions
inferred← citeshttps://doi.org/10.1002/ange.201203092openalex-snapshot
Catalytic Asymmetric Claisen Rearrangement of Enolphosphonates: Construction of Vicinal Tertiary and All‐Carbon Quaternary Centers
inferred← citeshttps://doi.org/10.1002/ange.201612462openalex-snapshot
Enantioselektive Chemo‐ und Biokatalyse: Partner in der Retrosynthese
inferred← citeshttps://doi.org/10.1002/ange.201812244openalex-snapshot
Catalytic Enantioselective α‐Ketol Rearrangement
inferred← citeshttps://doi.org/10.1002/ange.201916129openalex-snapshot
Catalytic Enantioselective Direct Aldol Addition of Aryl Ketones to α‐Fluorinated Ketones
inferred← citeshttps://doi.org/10.1002/ange.202405876openalex-snapshot
Catalytic Aerobic Carbooxygenation for the Construction of Vicinal Tetrasubstituted Centers: Application to the Synthesis of Hexasubstituted γ‐Lactones
inferred← citeshttps://doi.org/10.1002/ange.202518342openalex-snapshot
Ligand‐Promoted Site‐Selective Regiodivergent Lactamization of Activated δ‐ versus Inert γ‐Methylene C(sp 3 )–H Bonds via Open‐Shell Copper(II) Nitrenoid Catalysis
inferred← citeshttps://doi.org/10.1002/ange.7009966openalex-snapshot
Halogen‐Bond‐Assisted Anti ‐Selective Henry Reaction Promoted by a Chiral Nickel Catalyst
inferred← citeshttps://doi.org/10.1002/anie.200460506openalex-snapshot
Unveiling Reliable Catalysts for the Asymmetric Nitroaldol (Henry) Reaction
inferred← citeshttps://doi.org/10.1002/anie.200463075openalex-snapshot
Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands
inferred← citeshttps://doi.org/10.1002/anie.200503724openalex-snapshot
Asymmetric Organocatalytic Henry Reaction
inferred← citeshttps://doi.org/10.1002/anie.200504230openalex-snapshot
A Biocatalytic Henry Reaction—The Hydroxynitrile Lyase from Hevea brasiliensis Also Catalyzes Nitroaldol Reactions
inferred← citeshttps://doi.org/10.1002/anie.200602255openalex-snapshot
Direct Monitoring of the Asymmetric Induction of Solid‐Phase Catalysis Using Circular Dichroism: Diamine–CuI‐Catalyzed Asymmetric Henry Reaction
inferred← citeshttps://doi.org/10.1002/anie.200705344openalex-snapshot
Catalytic Enantioselective Aldol‐type Reaction of β‐Ketosters with Acetals
inferred← citeshttps://doi.org/10.1002/anie.200705617openalex-snapshot
A Heterobimetallic Pd/La/Schiff Base Complex for anti‐Selective Catalytic Asymmetric Nitroaldol Reactions and Applications to Short Syntheses of β‐Adrenoceptor Agonists
inferred← citeshttps://doi.org/10.1002/anie.200801373openalex-snapshot
Tandem Catalytic Asymmetric Friedel–Crafts/Henry Reaction: Control of Three Contiguous Acyclic Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.201105778openalex-snapshot
Asymmetric Synthesis of Chiral 1,3‐Diaminopropanols: Bisoxazolidine‐Catalyzed CC Bond Formation with α‐Keto Amides
inferred← citeshttps://doi.org/10.1002/anie.201107785openalex-snapshot
Urea/Transition‐Metal Cooperative Catalyst foranti‐Selective Asymmetric Nitroaldol Reactions
inferred← citeshttps://doi.org/10.1002/anie.201203092openalex-snapshot
Catalytic Asymmetric Claisen Rearrangement of Enolphosphonates: Construction of Vicinal Tertiary and All‐Carbon Quaternary Centers
inferred← citeshttps://doi.org/10.1002/anie.201612462openalex-snapshot
Enantioselective Chemo‐ and Biocatalysis: Partners in Retrosynthesis
inferred← citeshttps://doi.org/10.1002/anie.201812244openalex-snapshot
Catalytic Enantioselective α‐Ketol Rearrangement
inferred← citeshttps://doi.org/10.1002/anie.201916129openalex-snapshot
Catalytic Enantioselective Direct Aldol Addition of Aryl Ketones to α‐Fluorinated Ketones
inferred← citeshttps://doi.org/10.1002/anie.202405876openalex-snapshot
Catalytic Aerobic Carbooxygenation for the Construction of Vicinal Tetrasubstituted Centers: Application to the Synthesis of Hexasubstituted γ‐Lactones
inferred← citeshttps://doi.org/10.1002/anie.202518342openalex-snapshot
Ligand‐Promoted Site‐Selective Regiodivergent Lactamization of Activated δ‐ versus Inert γ‐Methylene C(sp 3 )–H Bonds via Open‐Shell Copper(II) Nitrenoid Catalysis
inferred← citeshttps://doi.org/10.1002/anie.7009966openalex-snapshot
Halogen‐Bond‐Assisted Anti ‐Selective Henry Reaction Promoted by a Chiral Nickel Catalyst
inferred← citeshttps://doi.org/10.1002/aoc.2969openalex-snapshot
Synthesis of novel thiophene‐based chiral ligands and their application in asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1002/aoc.3107openalex-snapshot
Asymmetric Henry reactions of aldehydes with various nitroalkanes catalyzed by copper(II) complexes of novel chiral N‐monoalkyl cyclohexane‐1,2‐diamines
inferred← citeshttps://doi.org/10.1002/aoc.3123openalex-snapshot
Asymmetric Henry reaction catalysed by L‐proline derivatives in the presence of Cu(OAc)2: isolation and characterization of an in situ formed Cu(II) complex
inferred← citeshttps://doi.org/10.1002/aoc.3347openalex-snapshot
Synthesis and applications in Henry reactions of novel chiral thiazoline tridentate ligands
inferred← citeshttps://doi.org/10.1002/aoc.3404openalex-snapshot
Binuclear Cu(II) chiral complexes: synthesis, characterization and application in enantioselective nitroaldol (Henry) reaction
inferred← citeshttps://doi.org/10.1002/aoc.3831openalex-snapshot
Carboxylate ion dependency in the Cu(II) catalysed asymmetric Henry reaction: Structural characterisation of a tridentate Schiff base complex containing a coordinated carboxylic acid
inferred← citeshttps://doi.org/10.1002/aoc.4955openalex-snapshot
Synthesis and structures of copper complexes bearing unsymmetric derivatives of (R,R)‐1,2‐diaminocyclohexane: An efficient catalyst for asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1002/asia.200700145openalex-snapshot
Organocatalytic Asymmetric Nitroaldol Reaction: Cooperative Effects of Guanidine and Thiourea Functional Groups
inferred← citeshttps://doi.org/10.1002/asia.200800339openalex-snapshot
Synthesis, Structure, and Application of Self‐Assembled Copper(II) Aqua Complex by H‐Bonding for Acceleration of the Nitroaldol Reaction on Water
inferred← citeshttps://doi.org/10.1002/asia.201200388openalex-snapshot
A Chiral Cu‐Salan Catalyst with a Rotatable Aromatic π‐Wall: Molecular Recognition‐Oriented Asymmetric Henry Transformation of Aromatic Aldehydes
inferred← citeshttps://doi.org/10.1002/asia.201701384openalex-snapshot
Chemical Fixation of CO2 and Other Heterogeneous Catalytic Studies by Employing a Layered Cu‐Porphyrin Prepared Through Single‐Crystal to Single‐Crystal Exchange of a Zn Analogue
inferred← citeshttps://doi.org/10.1002/asia.201800389openalex-snapshot
Organocatalytic Strategies for the Synthesis of Cyclopenta‐Fused Arenes and Heteroarenes
inferred← citeshttps://doi.org/10.1002/asia.201800799openalex-snapshot
Copper(II) and Sodium(I) Complexes based on 3,7‐Diacetyl‐1,3,7‐triaza‐5‐phosphabicyclo[3.3.1]nonane‐5‐oxide: Synthesis, Characterization, and Catalytic Activity
inferred← citeshttps://doi.org/10.1002/cctc.201200551openalex-snapshot
Efficient Tertiary Amine/Weak Acid Bifunctional Mesoporous Silica Catalysts for Michael Addition Reactions
inferred← citeshttps://doi.org/10.1002/cctc.201200592openalex-snapshot
Biorelevant Metals in Sustainable Metal Catalysis—A Survey
inferred← citeshttps://doi.org/10.1002/chem.200601220openalex-snapshot
Rational Design of Sterically and Electronically Easily Tunable Chiral Bisimidazolines and Their Applications in Dual Lewis Acid/Brønsted Base Catalysis for Highly Enantioselective Nitroaldol (Henry) Reactions
inferred← citeshttps://doi.org/10.1002/chem.200601262openalex-snapshot
A New Copper(I)–Tetrahydrosalen‐Catalyzed Asymmetric Henry Reaction and Its Extension to the Synthesis of (S)‐Norphenylephrine
inferred← citeshttps://doi.org/10.1002/chem.200701085openalex-snapshot
Stereochemical Consequences of Threefold Symmetry in Asymmetric Catalysis: Distorting C3 Chiral 1,1,1‐Tris(oxazolinyl)ethanes (“Trisox”) in CuII Lewis Acid Catalysts
inferred← citeshttps://doi.org/10.1002/chem.200701439openalex-snapshot
A Library of Chiral Imidazoline–Aminophenol Ligands: Discovery of an Efficient Reaction Sphere
inferred← citeshttps://doi.org/10.1002/chem.200800069openalex-snapshot
New Highly Asymmetric Henry Reaction Catalyzed by CuII and a C1‐Symmetric Aminopyridine Ligand, and Its Application to the Synthesis of Miconazole
inferred← citeshttps://doi.org/10.1002/chem.200801958openalex-snapshot
A Secondary Amine Amide Organocatalyst for the Asymmetric Nitroaldol Reaction of α‐Ketophosphonates
inferred← citeshttps://doi.org/10.1002/chem.200900504openalex-snapshot
“Catalysis in a Tea Bag”: Synthesis, Catalytic Performance and Recycling of Dendrimer‐Immobilised Bis‐ and Trisoxazoline Copper Catalysts
inferred← citeshttps://doi.org/10.1002/chem.200901789openalex-snapshot
Chiral 2‐endo‐Substituted 9‐Oxabispidines: Novel Ligands for Enantioselective Copper(II)‐Catalyzed Henry Reactions
inferred← citeshttps://doi.org/10.1002/chem.201000650openalex-snapshot
A Highly syn‐Selective Nitroaldol Reaction Catalyzed by CuII–Bisimidazoline
inferred← citeshttps://doi.org/10.1002/chem.201000964openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201002915openalex-snapshot
Highly Enantioselective Henry Reactions in Water Catalyzed by a Copper Tertiary Amine Complex and Applied in the Synthesis of ( S )‐ N ‐ trans ‐Feruloyl Octopamine
inferred← citeshttps://doi.org/10.1002/chem.201102136openalex-snapshot
Synthesis of Chiral 1,3‐Diamines Derived from cis‐2‐Benzamidocyclohexanecarboxylic Acid and Their Application in the Cu‐Catalyzed Enantioselective Henry Reaction
inferred← citeshttps://doi.org/10.1002/chem.201201565openalex-snapshot
Highly Enantioselective Henry Reactions of Aromatic Aldehydes Catalyzed by an Amino Alcohol–Copper(II) Complex
inferred← citeshttps://doi.org/10.1002/chem.201201775openalex-snapshot
A Highly anti‐Selective Asymmetric Henry Reaction Catalyzed by a Chiral Copper Complex: Applications to the Syntheses of (+)‐Spisulosine and a Pyrroloisoquinoline Derivative
inferred← citeshttps://doi.org/10.1002/chem.201203254openalex-snapshot
Template Syntheses of Copper(II) Complexes from Arylhydrazones of Malononitrile and their Catalytic Activity towards Alcohol Oxidations and the Nitroaldol Reaction: Hydrogen Bond‐Assisted Ligand Liberation and E/Z Isomerisation
inferred← citeshttps://doi.org/10.1002/chem.201502090openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202302638openalex-snapshot
α‐Methylbenzylamine Functionalized Crown‐Ether‐Appended Calix[4]arene Phase Transfer Catalyst for Enantioselective Henry Reaction
inferred← citeshttps://doi.org/10.1002/chin.200407041openalex-snapshot
A New Copper Acetate‐bis(oxazoline)‐Catalyzed, Enantioselective Henry Reaction.
inferred← citeshttps://doi.org/10.1002/chin.200535078openalex-snapshot
Nitroaldol-reaction of aldehydes in the presence of non-activated Mg:Al 2:1 hydrotalcite; a possible new mechanism for the formation of 2-aryl-1,3-dinitropropanes
inferred← citeshttps://doi.org/10.1002/chir.20613openalex-snapshot
New adaptive chiral thiophene ligands for copper‐catalyzed asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1002/chir.20661openalex-snapshot
Asymmetric Henry reaction catalyzed by bifunctional copper‐based catalysts
inferred← citeshttps://doi.org/10.1002/chir.20934openalex-snapshot
Solvent‐free synthesis of chiral Schiff‐base ligands based on ferrocene under microwave irradiation and application to enantioselective nitroaldol (Henry) reaction
inferred← citeshttps://doi.org/10.1002/chir.22104openalex-snapshot
Noncovalent Immobilization of Ionic‐tagged Box‐Cu(OAc)2 Complex and Its Application in Asymmetric Henry Reaction
inferred← citeshttps://doi.org/10.1002/chir.22369openalex-snapshot
Synthesis of Novel Chiral Tridentate Schiff‐Base Ligands and Their Applications in Catalytic Asymmetric Henry Reaction
inferred← citeshttps://doi.org/10.1002/chir.22498openalex-snapshot
Copper‐Chiral Camphor β‐Amino Alcohol Complex Catalyzed Asymmetric Henry Reaction
inferred← citeshttps://doi.org/10.1002/cjce.23216openalex-snapshot
Preparation of a novel magnetically recoverable copper complex catalyst and its application in the Henry reaction
inferred← citeshttps://doi.org/10.1002/cplu.201300432openalex-snapshot
Effect of Nanospace Confinement on the Catalytic Activity and Stability of a Chiral Schiff Base Complex (CuL; L=C22H24N2O4): A Combined Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1002/cplu.201402200openalex-snapshot
Diastereoselective Nitroaldol Reaction Catalyzed by Binuclear Copper(II) Complexes in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/ejic.200700469openalex-snapshot
Methylation of a Terdentate Schiff Base Ligand NNO‐Coordinated to Palladium with Nitromethane
inferred← citeshttps://doi.org/10.1002/ejic.200900141openalex-snapshot
Synthesis, Structure and Catalysis of Tetranuclear Copper(II) Open Cubane for Henry Reaction on Water
inferred← citeshttps://doi.org/10.1002/ejoc.200600307openalex-snapshot
Diastereoselective and Enantioselective Henry (Nitroaldol) Reaction Utilizing a Guanidine‐Thiourea Bifunctional Organocatalyst
inferred← citeshttps://doi.org/10.1002/ejoc.200700021openalex-snapshot
Recent Advances in the Catalytic Asymmetric Nitroaldol (Henry) Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.200800570openalex-snapshot
Asymmetric Henry Reactions Catalyzed by Metal Complexes of Chiral Boron‐Bridged Bisoxazoline (borabox) Ligands
inferred← citeshttps://doi.org/10.1002/ejoc.201100579openalex-snapshot
Efficient Asymmetric Copper(I)‐Catalyzed Henry Reaction Using Chiral N‐Alkyl‐C1‐tetrahydro‐1,1′‐bisisoquinolines
inferred← citeshttps://doi.org/10.1002/ejoc.201100702openalex-snapshot
Heterogeneous Bisoxazoline/Copper Complex: A Green Catalyst for the Enantioselective Reaction of Nitromethane with Substituted Benzaldehydes
inferred← citeshttps://doi.org/10.1002/ejoc.201100824openalex-snapshot
Asymmetric Nitroaldol Reactions of Nitroalkanes with Isatins Catalyzed by Bifunctional Cinchona Alkaloid Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201100857openalex-snapshot
Asymmetric Copper(II)‐Catalysed Nitroaldol (Henry) Reactions Utilizing a Chiral C1‐Symmetric Dinitrogen Ligand
inferred← citeshttps://doi.org/10.1002/ejoc.201600033openalex-snapshot
Copper Catalyzed Assembly of N‐Aryloxazolidinones: Synthesis of Linezolid, Tedizolid, and Rivaroxaban
inferred← citeshttps://doi.org/10.1002/ejoc.201701289openalex-snapshot
Organocatalytic Asymmetric Tandem α‐Aminooxylation–Henry Reactions for the Synthesis of 1,2‐Diols: Total Synthesis of (–)‐ l ‐threo‐Sphinganine
inferred← citeshttps://doi.org/10.1002/ejoc.201701452openalex-snapshot
C1‐Symmetric 1,2‐Diaminobicyclo[2.2.2]octane Ligands in Copper‐Catalyzed Asymmetric Henry Reaction: Catalyst Development and DFT Studies
inferred← citeshttps://doi.org/10.1002/ejoc.201801443openalex-snapshot
Bimetallic Oriented (Au/Cu2O) vs. Monometallic 1.1.1 Au (0) or 2.0.0 Cu2O Graphene‐Supported Nanoplatelets as Very Efficient Catalysts for Michael and Henry Additions
inferred← citeshttps://doi.org/10.1002/ejoc.202000353openalex-snapshot
Enantioselective Synthesis of Clavaminol A, Xestoaminol C and their Stereoisomers Exhibiting Cytotoxic Activity
inferred← citeshttps://doi.org/10.1002/jcc.21422openalex-snapshot
DFT study of the asymmetric nitroaldol (Henry) reaction catalyzed by a dinuclear Zn complex
inferred← citeshttps://doi.org/10.1002/jhet.477openalex-snapshot
A facile and efficient synthesis of bis(oxazoline)s
inferred← citeshttps://doi.org/10.1002/jhet.669openalex-snapshot
Clay‐supported 2‐phenyl‐1H‐imidazole derivatives for heterogeneous catalysis of Henry reaction
inferred← citeshttps://doi.org/10.1002/slct.201600359openalex-snapshot
Copper Complex of Pinene based Schiff base [CuSBADBH] 2 : Synthesis and its Application in Catalytic Asymmetric Nitroaldol (Henry) Reaction
inferred← citeshttps://doi.org/10.1002/slct.201600547openalex-snapshot
Synthesis and Preliminary Results on the Catalytic Activity of Metal Complexes obtained from C 2 ‐Symmetric Ligands Derived from R ‐(+)‐Betti base
inferred← citeshttps://doi.org/10.1002/slct.201702689openalex-snapshot
Synthesis and Investigations of Chiral NNO Type Copper(II) Coordination Polymers
inferred← citeshttps://doi.org/10.1002/slct.201901078openalex-snapshot
Mono and Dinuclear Cu(II) Carboxylate Complexes with Pyridine and 1‐methylimidazole as Co–Ligands: Synthesis, Structure, Antibacterial Activity and Catalytic Nitroaldol Reactions
inferred← citeshttps://doi.org/10.1002/tcr.201500268openalex-snapshot
Copper(II)‐Catalyzed Nitroaldol (Henry) Reactions: Recent Developments
inferred← citeshttps://doi.org/10.1007/3418_2015_105openalex-snapshot
Iron-Catalyzed Cross-Dehydrogenative-Coupling Reactions
inferred← citeshttps://doi.org/10.1007/s10562-007-9169-7openalex-snapshot
Iodine Catalysis in Aqueous Medium: An Improved Reaction System for Knoevenagel and Nitroaldol Condensation
inferred← citeshttps://doi.org/10.1007/s10562-008-9595-1openalex-snapshot
Controlled Synthesis of the Henry Reaction Products: Nitroalcohol Versus Nitrostyrene by a Simple Change of Amino-Groups of Aminofunctionalized Nanoporous Catalysts
inferred← citeshttps://doi.org/10.1007/s10562-010-0443-8openalex-snapshot
Chiral Cu(II) Complexes as Recyclable Catalysts for Asymmetric Nitroaldol (Henry) Reaction in Ionic Liquids as Greener Reaction Media
inferred← citeshttps://doi.org/10.1007/s10562-021-03633-5openalex-snapshot
Controllable Preparation of Chiral Oxazoline-Cu(II) Catalyst as Nanoreactor for Highly Asymmetric Henry Reaction in Water
inferred← citeshttps://doi.org/10.1007/s10563-009-9071-yopenalex-snapshot
Dimeric & Polymeric Chiral Schiff Base Complexes and Supported BINOL Complexes as Potential Recyclable Catalysts in Asymmetric Kinetic Resolution and C–C Bond Formation Reactions
inferred← citeshttps://doi.org/10.1007/s11164-008-0008-2openalex-snapshot
Asymmetric Henry reaction catalyzed by oxazolinyl Cu(II) complexes
inferred← citeshttps://doi.org/10.1007/s11164-013-1262-5openalex-snapshot
One-pot synthesis of oxazolines and application to the cyanosilylation of prochiral aldehydes
inferred← citeshttps://doi.org/10.1007/s11172-012-0307-zopenalex-snapshot
Novel C 2-symmetric bis-oxazoline ligands
inferred← citeshttps://doi.org/10.1007/s11172-023-3827-9openalex-snapshot
Investigation of the possibility of complex formation of bidentate bispidine ligands with copper(ii) salts in solution by proton NMR spectroscopy
inferred← citeshttps://doi.org/10.1007/s11243-016-0072-1openalex-snapshot
Synthesis, crystal structures and catalytic activities of new palladium(II)–bis(oxazoline) complexes
inferred← citeshttps://doi.org/10.1007/s11243-019-00351-1openalex-snapshot
An efficient synthetic approach towards a single diastereomer of (2R,3R)-N2,N3-bis((S)-1-phenylethyl)butane-2,3-diamine via metalation and demetalation
inferred← citeshttps://doi.org/10.1007/s11705-013-1343-4openalex-snapshot
Synthesis of C 1-symmetric primary-secondary diamines and their application in the enantioselective Henry reaction
inferred← citeshttps://doi.org/10.1007/s12039-011-0107-2openalex-snapshot
Phenalenyl-based ligand for transition metal chemistry: Application in Henry reaction
inferred← citeshttps://doi.org/10.1007/s12039-024-02256-8openalex-snapshot
Enhancing catalytic activity of UiO-66 through CuO nanoparticles incorporation: a study on Henry reaction and one-pot allylic C-H bond oxidation of olefins
inferred← citeshttps://doi.org/10.1007/s40684-019-00093-6openalex-snapshot
Hybrid Manufacturing of Oxidation Resistant Cellulose Nanocrystals-Copper-Graphene Nanoplatelets Based Electrodes
inferred← citeshttps://doi.org/10.1007/s41061-026-00540-4openalex-snapshot
Earth-Abundant Transition Metals Catalyzed Alkylation, Alkenylation, and Alkynylation of Arenes via Cross Dehydrogenative Coupling (CDC): Synthetic Strategies and Mechanistic Pathways
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00411-0openalex-snapshot
4.12 Direct C–C Bond Formation (Henry, aza-Henry)
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00214-7openalex-snapshot
2.13 The Henry (Nitroaldol) Reaction
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00009-0openalex-snapshot
Synthesis of Nitroso, Nitro, and Related Compounds
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00111-3openalex-snapshot
The Henry (Nitroaldol) Reaction
inferred← citeshttps://doi.org/10.1016/j.apcata.2012.02.044openalex-snapshot
Recyclable copper catalysts based on ionic-tagged C2-symmetric Indabox ligands and their application in asymmetric Henry reactions
inferred← citeshttps://doi.org/10.1016/j.apcata.2012.05.010openalex-snapshot
Design of zeolite catalysts for nitroaldol reaction under mild condition
inferred← citeshttps://doi.org/10.1016/j.apcata.2012.06.042openalex-snapshot
Recyclable Cu(II)-macrocyclic salen complexes catalyzed nitroaldol reaction of aldehydes: A practical strategy in the preparation of (R)-phenylephrine
inferred← citeshttps://doi.org/10.1016/j.apcata.2013.03.032openalex-snapshot
Chiral recyclable Cu(II)-catalysts in nitroaldol reaction of aldehydes with various nitroalkanes and its application in the synthesis of a valuable drug (R)-isoproterenol
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.03.097openalex-snapshot
Enantioselective Henry (nitroaldol) reaction catalyzed by axially chiral guanidines
inferred← citeshttps://doi.org/10.1016/j.carres.2015.01.023openalex-snapshot
Synthesis of novel Schiff base ligands from gluco- and galactochloraloses for the Cu(II) catalyzed asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1016/j.catcom.2010.05.003openalex-snapshot
4,4′BOX based catalysts: Synthesis, structure and catalytic application
inferred← citeshttps://doi.org/10.1016/j.catcom.2012.03.021openalex-snapshot
Choline chloride based eutectic solvents: Magical catalytic system for carbon–carbon bond formation in the rapid synthesis of β-hydroxy functionalized derivatives
inferred← citeshttps://doi.org/10.1016/j.cclet.2012.04.018openalex-snapshot
Mn(OAc)2/Schiff base as a new efficient catalyst system for the Henry reaction of nitroalkanes with aldehydes
inferred← citeshttps://doi.org/10.1016/j.cclet.2017.10.001openalex-snapshot
Recent progress in copper catalyzed asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.11.007openalex-snapshot
Metal-bis(oxazoline) complexes: From coordination chemistry to asymmetric catalysis
inferred← citeshttps://doi.org/10.1016/j.ccr.2016.10.005openalex-snapshot
Synthesis and application of dynamic self-supported enantioselective catalysts
inferred← citeshttps://doi.org/10.1016/j.ccr.2017.11.030openalex-snapshot
Multidentate unsymmetrically-substituted Schiff bases and their metal complexes: Synthesis, functional materials properties, and applications to catalysis
inferred← citeshttps://doi.org/10.1016/j.cherd.2022.03.001openalex-snapshot
Kinetics of Henry reaction catalyzed by fluorapatite
inferred← citeshttps://doi.org/10.1016/j.cplett.2017.01.066openalex-snapshot
The new chemical insight for understanding the mechanism of Henry reaction over Cu(II) catalyst
inferred← citeshttps://doi.org/10.1016/j.crci.2014.03.014openalex-snapshot
Catalytic asymmetric Henry reaction using copper(II) chiral tridentate Schiff-base complexes and their polymer-supported complexes
inferred← citeshttps://doi.org/10.1016/j.electacta.2005.01.053openalex-snapshot
Stereoselective synthesis of optically active 2-alkylpiperidines utilizing electrochemical oxidation as a key step
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e39911openalex-snapshot
Chiral amido-oxazoline functionalized MCM-41: A sustainable heterogeneous catalyst for enantioselective Kharasch–Sosnovsky and Henry reactions
inferred← citeshttps://doi.org/10.1016/j.heliyon.2026.e45450openalex-snapshot
Chiral Betti base immobilized on UiO-66-NH2: Synthesis and catalytic application in the asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1016/j.ica.2007.08.003openalex-snapshot
Synthesis, structure, and catalytic activity of chiral Cu(II) and Ag(I) complexes with (S,S)-1,2-diaminocyclohexane-based N4-donor ligands
inferred← citeshttps://doi.org/10.1016/j.ica.2008.07.019openalex-snapshot
Synthesis of new chiral cis-3-aminoazetidines and their use in catalytic asymmetric reactions
inferred← citeshttps://doi.org/10.1016/j.ica.2010.11.023openalex-snapshot
Synthesis, structure, and catalytic activity of chiral silver(I) and copper(II) complexes with biaryl-based nitrogen-containing ligands
inferred← citeshttps://doi.org/10.1016/j.ica.2011.04.033openalex-snapshot
Synthesis, crystal structure, and catalytic studies on dinuclear copper(II) mesocates
inferred← citeshttps://doi.org/10.1016/j.ica.2018.11.014openalex-snapshot
Chiral 1,8-naphthyridine based ligands: Syntheses and characterization of Di- and tetranuclear copper (I) and silver (I) complexes
inferred← citeshttps://doi.org/10.1016/j.ica.2021.120492openalex-snapshot
Application of asymmetric Henry reaction by copper(II) complexes containing (R,R)-1,2-diaminocyclohexane with naphthyl and thiophenyl substituents
inferred← citeshttps://doi.org/10.1016/j.inoche.2012.03.020openalex-snapshot
Crystal structures of chiral mono- and dinuclear salan–Cu(II) complexes and the application to catalytic asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1016/j.inoche.2017.06.027openalex-snapshot
Synthesis, crystal structure of copper(II) complexes comprising 2-(biphenylazo)phenol and 1-(biphenylazo)naphthol ligands and their catalytic activity in nitroaldol reaction
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2011.03.011openalex-snapshot
Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous–organic biphasic system
inferred← citeshttps://doi.org/10.1016/j.jcat.2019.06.001openalex-snapshot
High-nitrogen containing covalent triazine frameworks as basic catalytic support for the Cu-catalyzed Henry reaction
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115566openalex-snapshot
Functionalized melamine-based Dendron-OMS hybrids as highly-efficient catalysts for the nitroaldol (Henry) reaction
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2013.09.014openalex-snapshot
Fluorous chiral bis(oxazolines): Synthesis and application in asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.01.056openalex-snapshot
Copper(II) complexes containing chiral substituted 2-(4-isopropyl-4-methyl-4,5-dihydro-1H-imidazol-5-one-2-yl)pyridine ligands: Synthesis, X-ray structural studies and asymmetric catalysis
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.04.039openalex-snapshot
Highly enantioselective introduction of bis(alkoxycarbonyl)methyl group into the 2-position of piperidine skeleton
inferred← citeshttps://doi.org/10.1016/j.mcat.2017.03.017openalex-snapshot
Chiral N-arylated diamine – Copper complexes catalyzed asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1016/j.micromeso.2021.111392openalex-snapshot
Mixed valent copper oxide nanocatalyst on Zeolite-Y for mechanochemical oxidation, reduction and C–C bond formation reaction
inferred← citeshttps://doi.org/10.1016/j.molcata.2005.08.045openalex-snapshot
Chiral lanthanum–lithium–binaphthol complex covalently bonded to silica and MCM-41 for enantioselective nitroaldol (Henry) reaction
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.04.018openalex-snapshot
Siliceous mesocellular foam-supported chiral bisoxazoline: Application to asymmetric cyclopropanation
inferred← citeshttps://doi.org/10.1016/j.molcata.2010.03.013openalex-snapshot
Cu(II) homogeneous and heterogeneous catalysts for the asymmetric Henry reaction
inferred← citeshttps://doi.org/10.1016/j.molcata.2011.03.018openalex-snapshot
Nanocrystalline MgO catalysts for the Henry reaction of benzaldehyde and nitromethane
inferred← citeshttps://doi.org/10.1016/j.molcata.2013.06.008openalex-snapshot
Synthesis and application of new iminopyridine ligands to enantioselective copper(II)-catalyzed Henry reaction
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