On the public citation graph
H-Bonding Additives Act Like Lewis Acid Catalysts
0 signed · 494 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-94-009-2464-2openalex-snapshot
Selectivities in Lewis Acid Promoted Reactions
inferredcites →https://doi.org/10.1016/0040-4020(94)00921-gopenalex-snapshot
Experimental and theoretical studies of substituent effects in hydrogen bond based molecular recognition of a zwitterion by substituted arylureas
inferredcites →https://doi.org/10.1016/0306-4549(89)90016-9openalex-snapshot
Density-functional theory of atoms and molecules
inferredcites →https://doi.org/10.1016/s0040-4039(00)97402-1openalex-snapshot
Diels-alder reactions: Rate acceleration promoted by a biphenylenediol
inferredcites →https://doi.org/10.1021/ar00172a005openalex-snapshot
Encoding and decoding hydrogen-bond patterns of organic compounds
inferredcites →https://doi.org/10.1021/j100165a007openalex-snapshot
Hydrogen bonds as design elements in organic chemistry
inferredcites →https://doi.org/10.1021/j100165a008openalex-snapshot
Excitation of iodine fluoride(B3.PI.(0+)) by metastable oxygen. 1. Studies involving iodine fluoride (X,v)
inferredcites →https://doi.org/10.1021/ja00052a016openalex-snapshot
Chemistry of synthetic receptors and functional group arrays. 18. Approaches to quantitative supramolecular chemistry. Hydrogen-bond-based molecular recognition phenomena and sigmoidal behavior in multicomponent mixtures
inferredcites →https://doi.org/10.1021/ja00052a017openalex-snapshot
Stereochemistry of base-catalyzed ring opening of 1,3,2-oxathiaphospholanes. Absolute configuration of 2-{N-[(Rc)-1-(.alpha.-naphthyl)ethyl]amino}-2-thiono-1,3,2-oxathiaphospholanes and O,S-dimethyl N-[(Rc)-1-(.alpha.-naphthyl)ethyl]phosphoramidothioates
inferredcites →https://doi.org/10.1021/ja00053a046openalex-snapshot
Effects of hydration on the Claisen rearrangement of allyl vinyl ether from computer simulations
inferredcites →https://doi.org/10.1021/ja00053a047openalex-snapshot
Cation radical probes. Development and application to metalloporphyrin-catalyzed epoxidation
inferredcites →https://doi.org/10.1021/ja00060a061openalex-snapshot
Diethylaluminum chloride complexes of an N-acyloxazolidinone: NMR investigation
inferredcites →https://doi.org/10.1021/ja00225a050openalex-snapshot
Depth sensitivity of wetting: monolayers of .omega.-mercapto ethers on gold
inferredcites →https://doi.org/10.1021/ja00313a048openalex-snapshot
Long-range proton-proton spin-spin couplings through the interglycosidic oxygen and the primary structure of oligosaccharides as studied by 2D-NMR
inferredcites →https://doi.org/10.1021/ja961380kopenalex-snapshot
An NMR Investigation of the Effect of Hydrogen Bonding on the Rates of Rotation about the C−N Bonds in Urea and Thiourea
inferredcites →https://doi.org/10.1021/ja972357hopenalex-snapshot
Calculated and Experimental Low-Energy Conformations of Cyclic Urea HIV Protease Inhibitors
inferredcites →https://doi.org/10.1021/jo00305a009openalex-snapshot
Tin tetrachloride chelation of an N-acyloxazolidinone: an NMR investigation
inferredcites →https://doi.org/10.1021/jo00305a010openalex-snapshot
A new macrobicyclic hard and soft ligand built on phenanthroline
inferredcites →https://doi.org/10.1021/jp972611sopenalex-snapshot
Theoretical Study on the Urea−Hydrogen Peroxide 1:1 Complexes
inferredcites →https://doi.org/10.1103/physreva.38.3098openalex-snapshot
Density-functional exchange-energy approximation with correct asymptotic behavior
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.4690931openalex-extracted
A Molecular Electron Density Theory Study of Hydrogen Bond Catalysed Polar Diels–Alder Reactions of a , B -Unsaturated Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/047084289x.rn01642openalex-snapshot
N,N′-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea
inferred← citeshttps://doi.org/10.1002/9781118604755.ch02openalex-snapshot
Activation Modes In Asymmetric Organocatalysis
inferred← citeshttps://doi.org/10.1002/9781118846919.ch3openalex-snapshot
Asymmetric Multifunctional Catalysis
inferred← citeshttps://doi.org/10.1002/9783527627844.ch3openalex-snapshot
Computational Studies of Organocatalytic Processes Based on Hydrogen Bonding
inferred← citeshttps://doi.org/10.1002/9783527652235.ch29openalex-snapshot
Bifunctional Thiourea Catalysts
inferred← citeshttps://doi.org/10.1002/9783527658862.ch12openalex-snapshot
Brønsted Acids: Chiral (Thio)urea Derivatives
inferred← citeshttps://doi.org/10.1002/9783527830664.ch1openalex-snapshot
From Anion Recognition to Organocatalytic Chemical Reactions
inferred← citeshttps://doi.org/10.1002/9783527830664.ch3openalex-snapshot
(Thio)urea and Squaramide‐Catalyzed Anion‐Binding Catalysis with Halogen Anions
inferred← citeshttps://doi.org/10.1002/9783527832033.ch25openalex-snapshot
The Aryl‐Pyrrolidine‐tert‐Leucine Motif as a New Privileged Chiral Scaffold: The Role of Noncovalent Stabilizing Interactions
inferred← citeshttps://doi.org/10.1002/9783527832217.ch19openalex-snapshot
Computational Studies – A Useful Tool in Elucidation of Mechanisms of Organocatalytic Reactions
inferred← citeshttps://doi.org/10.1002/adsc.200404065openalex-snapshot
Planar Chiral PHANOLs as Double Hydrogen Bonding Donor Organocatalysts: Synthesis and Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.200404318openalex-snapshot
Organic Base‐Mediated Condensation of Pyridinecarboxaldehydes to Azachalcones
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.200900020openalex-snapshot
Hydrogen‐Bonding Catalysis: Mild and Highly Chemoselective Oxidation of Sulfides
inferred← citeshttps://doi.org/10.1002/adsc.200900787openalex-snapshot
Novel Cinchona‐Aminobenzimidazole Bifunctional Organocatalysts
inferred← citeshttps://doi.org/10.1002/adsc.201100408openalex-snapshot
Highly Enantioselective Co‐Catalytic Direct Aldol Reactions by Combination of Hydrogen‐Bond Donating and Acyclic Amino Acid Catalysts
inferred← citeshttps://doi.org/10.1002/adsc.201400780openalex-snapshot
Organocatalytic Diels–Alder Reaction of 2‐Vinylindoles with Methyleneindolinones: An Efficient Approach to Functionalized Carbazolespirooxindoles
inferred← citeshttps://doi.org/10.1002/adsc.201600110openalex-snapshot
Catalytic Enantioselective Addition of Pyrazol‐5‐ones to Trisubstituted Nitroalkenes with an N‐Sulfinylurea Organocatalyst
inferred← citeshttps://doi.org/10.1002/adsc.201600498openalex-snapshot
1,3‐Diamine‐Derived Bifunctional Organocatalyst Prepared from Camphor
inferred← citeshttps://doi.org/10.1002/adsc.201700158openalex-snapshot
Organocatalysis and Biocatalysis Hand in Hand: Combining Catalysts in One‐Pot Procedures
inferred← citeshttps://doi.org/10.1002/adsc.201700986openalex-snapshot
A Case Study of Thiourea‐Assisted Iminium Formation by Hydroxyl Anion Binding: Kinetic, Spectroscopic and Computational Evidences
inferred← citeshttps://doi.org/10.1002/adsc.201900061openalex-snapshot
Enantioselective Organocatalytic Enamine C−H Oxidation/Diels‐ Alder Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201901500openalex-snapshot
Chemodivergent Preparation of Various Heterocycles via Phase‐Transfer Catalysis: Enantioselective Synthesis of Functionalized Piperidines
inferred← citeshttps://doi.org/10.1002/adsc.202300455openalex-snapshot
L‐Proline Derived Thioamide Small Organic Molecule for the α‐Stereoselective Synthesis of 2‐Deoxyglycosides
inferred← citeshttps://doi.org/10.1002/adsc.202400067openalex-snapshot
Stereoselective Organocatalyzed Glycosylation of Glycosyl Trichloroacetimidate Donors: Thiouracil as Brønsted Acid Catalyst
inferred← citeshttps://doi.org/10.1002/adsc.202400255openalex-snapshot
Visible Light Induced Halogen Bond Assisted Friedel‐Crafts Reaction of Indole and Chalcones
inferred← citeshttps://doi.org/10.1002/ajoc.201800074openalex-snapshot
Stereoselective Construction of Cisoidal Bisspiroacetal Frameworks through Magnesium Coordination of the Bilateral Acetal Oxygen Atoms
inferred← citeshttps://doi.org/10.1002/ajoc.201900122openalex-snapshot
C(sp2)−H Hydrogen‐Bond Donor Groups in Chiral Small‐Molecule Organocatalysts
inferred← citeshttps://doi.org/10.1002/ajoc.70414openalex-snapshot
A Sustainable Approach to Synthesize Tetra‐ and Penta‐Substituted Pyrroles Under Three‐Component One‐Pot Synthesis Using Novel Thiourea‐Derived Organocatalysts
inferred← citeshttps://doi.org/10.1002/ange.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
inferred← citeshttps://doi.org/10.1002/ange.200400650openalex-snapshot
Im Goldenen Zeitalter der Organokatalyse
inferred← citeshttps://doi.org/10.1002/ange.200461442openalex-snapshot
Bifunktionale Organokatalysatoren auf Harnstoff‐Basis für die effiziente dynamische kinetische Racemattrennung von Azlactonen
inferred← citeshttps://doi.org/10.1002/ange.200500227openalex-snapshot
Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst
inferred← citeshttps://doi.org/10.1002/ange.200500459openalex-snapshot
Enantioselective Michael Addition to α,β‐Unsaturated Imides Catalyzed by a Bifunctional Organocatalyst
inferred← citeshttps://doi.org/10.1002/ange.200501721openalex-snapshot
Urea‐ and Thiourea‐Substituted Cinchona Alkaloid Derivatives as Highly Efficient Bifunctional Organocatalysts for the Asymmetric Addition of Malonate to Nitroalkenes: Inversion of Configuration at C9 Dramatically Improves Catalyst Performance.
inferred← citeshttps://doi.org/10.1002/ange.200503132openalex-snapshot
Asymmetrische Katalyse durch chirale Wasserstoffbrückendonoren
inferred← citeshttps://doi.org/10.1002/ange.200603630openalex-snapshot
Katalytisch‐asymmetrische Acylcyanierung von Iminen
inferred← citeshttps://doi.org/10.1002/ange.200790070openalex-snapshot
Katalytisch‐asymmetrische Acylcyanierung von Iminen
inferred← citeshttps://doi.org/10.1002/ange.200802139openalex-snapshot
Eine hoch enantioselektive organokatalytische Carbonyl‐En‐Reaktion mit chiralen, stark aciden Brønsted‐Säuren als effizienten Katalysatoren
inferred← citeshttps://doi.org/10.1002/ange.201206881openalex-snapshot
Hydrogen‐Bond‐Mediated Supramolecular Iminium Ion Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201301351openalex-snapshot
Organokatalyse mit neutralen mehrzähnigen Halogenbrückendonoren
inferred← citeshttps://doi.org/10.1002/ange.201302158openalex-snapshot
Kooperative Katalyse bei der Glycosidierung mit O‐Glycosyltrichloracetimidaten als Glycosyldonoren
inferred← citeshttps://doi.org/10.1002/ange.201305644openalex-snapshot
Catalytic Enantioselective Synthesis of Tertiary Thiols From 5H‐Thiazol‐4‐ones and Nitroolefins: Bifunctional Ureidopeptide‐Based Brønsted Base Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201310532openalex-snapshot
Stereoselektive Metall‐freie Synthese von β‐Aminothioestern mit tertiären und quartären Stereozentren
inferred← citeshttps://doi.org/10.1002/ange.201402834openalex-snapshot
Catalytic Asymmetric Synthesis of 8‐Oxabicyclooctanes by Intermolecular [5+2] Pyrylium Cycloadditions
inferred← citeshttps://doi.org/10.1002/ange.201406971openalex-snapshot
Catalytic Enantioselective Addition of Thioacids to Trisubstituted Nitroalkenes
inferred← citeshttps://doi.org/10.1002/ange.201408613openalex-snapshot
Nitrimines as Reagents for Metal‐Free Formal C(sp2)–C(sp2) Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ange.201409004openalex-snapshot
Dekonstruktion kovalenter Organokatalyse
inferred← citeshttps://doi.org/10.1002/ange.201411350openalex-snapshot
Biomimetische Totalsynthese von Santalin Y
inferred← citeshttps://doi.org/10.1002/ange.201504454openalex-snapshot
[2+2] Photocycloaddition of Cinnamates in Flow and Development of a Thiourea Catalyst
inferred← citeshttps://doi.org/10.1002/ange.201703641openalex-snapshot
Electrophilic Activation of Iodonium Ylides by Halogen‐Bond‐Donor Catalysis for Cross‐Enolate Coupling
inferred← citeshttps://doi.org/10.1002/ange.201712726openalex-snapshot
Direct N‐Glycofunctionalization of Amides with Glycosyl Trichloroacetimidate by Thiourea/Halogen Bond Donor Co‐Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201811383openalex-snapshot
A Cooperative Hydrogen Bond Donor–Brønsted Acid System for the Enantioselective Synthesis of Tetrahydropyrans
inferred← citeshttps://doi.org/10.1002/ange.202204393openalex-snapshot
London Dispersion Favors Sterically Hindered Diarylthiourea Conformers in Solution
inferred← citeshttps://doi.org/10.1002/ange.202316364openalex-snapshot
Advances and Prospects in Understanding London Dispersion Interactions in Molecular Chemistry
inferred← citeshttps://doi.org/10.1002/ange.202316667openalex-snapshot
Exploiting π and Chalcogen Interactions for the β‐Selective Glycosylation of Indoles through Glycal Conformational Distortion
inferred← citeshttps://doi.org/10.1002/ange.202405706openalex-snapshot
Stereoselective Entry into α,α’‐C‐Oxepane Scaffolds through a Chalcogen Bonding Catalyzed Strain‐Release C‐Septanosylation Strategy
inferred← citeshttps://doi.org/10.1002/ange.202517553openalex-snapshot
Enhanced Selectivity of Chalcogen Bonding over Halogen Bonding Catalyzed C ‐glycosylation Through Differentiated Intermediate Activation
inferred← citeshttps://doi.org/10.1002/ange.4283917openalex-snapshot
Mechanically Interlocked Indigo Photoswitches
inferred← citeshttps://doi.org/10.1002/ange.8336123openalex-snapshot
Organocatalytic Enantioselective Addition of Malonates to Cyclic Imines: A Short Total Synthesis of Tetraponerine T‐1
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/anie.200400650openalex-snapshot
In the Golden Age of Organocatalysis
inferred← citeshttps://doi.org/10.1002/anie.200461442openalex-snapshot
Highly Efficient Dynamic Kinetic Resolution of Azlactones by Urea‐Based Bifunctional Organocatalysts
inferred← citeshttps://doi.org/10.1002/anie.200500227openalex-snapshot
Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst
inferred← citeshttps://doi.org/10.1002/anie.200500459openalex-snapshot
Enantioselective Michael Addition to α,β‐Unsaturated Imides Catalyzed by a Bifunctional Organocatalyst
inferred← citeshttps://doi.org/10.1002/anie.200501721openalex-snapshot
Urea‐ and Thiourea‐Substituted Cinchona Alkaloid Derivatives as Highly Efficient Bifunctional Organocatalysts for the Asymmetric Addition of Malonate to Nitroalkenes: Inversion of Configuration at C9 Dramatically Improves Catalyst Performance.
inferred← citeshttps://doi.org/10.1002/anie.200503132openalex-snapshot
Asymmetric Catalysis by Chiral Hydrogen‐Bond Donors
inferred← citeshttps://doi.org/10.1002/anie.200603630openalex-snapshot
Catalytic Asymmetric Acylcyanation of Imines
inferred← citeshttps://doi.org/10.1002/anie.200790071openalex-snapshot
Catalytic Asymmetric Acylcyanation of Imines
inferred← citeshttps://doi.org/10.1002/anie.200802139openalex-snapshot
Highly Enantioselective Organocatalytic Carbonyl‐Ene Reaction with Strongly Acidic, Chiral Brønsted Acids as Efficient Catalysts
inferred← citeshttps://doi.org/10.1002/anie.201206881openalex-snapshot
Hydrogen‐Bond‐Mediated Supramolecular Iminium Ion Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201301351openalex-snapshot
Organocatalysis by Neutral Multidentate Halogen‐Bond Donors
inferred← citeshttps://doi.org/10.1002/anie.201302158openalex-snapshot
Cooperative Catalysis in Glycosidation Reactions with O‐Glycosyl Trichloroacetimidates as Glycosyl Donors
inferred← citeshttps://doi.org/10.1002/anie.201305644openalex-snapshot
Catalytic Enantioselective Synthesis of Tertiary Thiols From 5H‐Thiazol‐4‐ones and Nitroolefins: Bifunctional Ureidopeptide‐Based Brønsted Base Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201310532openalex-snapshot
Stereoselective Metal‐Free Synthesis of β‐Amino Thioesters with Tertiary and Quaternary Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/anie.201402834openalex-snapshot
Catalytic Asymmetric Synthesis of 8‐Oxabicyclooctanes by Intermolecular [5+2] Pyrylium Cycloadditions
inferred← citeshttps://doi.org/10.1002/anie.201406971openalex-snapshot
Catalytic Enantioselective Addition of Thioacids to Trisubstituted Nitroalkenes
inferred← citeshttps://doi.org/10.1002/anie.201408613openalex-snapshot
Nitrimines as Reagents for Metal‐Free Formal C(sp2)–C(sp2) Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.201409004openalex-snapshot
Deconstructing Covalent Organocatalysis
inferred← citeshttps://doi.org/10.1002/anie.201411350openalex-snapshot
Biomimetic Total Synthesis of Santalin Y
inferred← citeshttps://doi.org/10.1002/anie.201504454openalex-snapshot
[2+2] Photocycloaddition of Cinnamates in Flow and Development of a Thiourea Catalyst
inferred← citeshttps://doi.org/10.1002/anie.201703641openalex-snapshot
Electrophilic Activation of Iodonium Ylides by Halogen‐Bond‐Donor Catalysis for Cross‐Enolate Coupling
inferred← citeshttps://doi.org/10.1002/anie.201712726openalex-snapshot
Direct N‐Glycofunctionalization of Amides with Glycosyl Trichloroacetimidate by Thiourea/Halogen Bond Donor Co‐Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201811383openalex-snapshot
A Cooperative Hydrogen Bond Donor–Brønsted Acid System for the Enantioselective Synthesis of Tetrahydropyrans
inferred← citeshttps://doi.org/10.1002/anie.202204393openalex-snapshot
London Dispersion Favors Sterically Hindered Diarylthiourea Conformers in Solution
inferred← citeshttps://doi.org/10.1002/anie.202316364openalex-snapshot
Advances and Prospects in Understanding London Dispersion Interactions in Molecular Chemistry
inferred← citeshttps://doi.org/10.1002/anie.202316667openalex-snapshot
Exploiting π and Chalcogen Interactions for the β‐Selective Glycosylation of Indoles through Glycal Conformational Distortion
inferred← citeshttps://doi.org/10.1002/anie.202405706openalex-snapshot
Stereoselective Entry into α,α’‐ C ‐Oxepane Scaffolds through a Chalcogen Bonding Catalyzed Strain‐Release C ‐Septanosylation Strategy
inferred← citeshttps://doi.org/10.1002/anie.202517553openalex-snapshot
Enhanced Selectivity of Chalcogen Bonding over Halogen Bonding Catalyzed C ‐glycosylation Through Differentiated Intermediate Activation
inferred← citeshttps://doi.org/10.1002/anie.4283917openalex-snapshot
Mechanically Interlocked Indigo Photoswitches
inferred← citeshttps://doi.org/10.1002/anie.8336123openalex-snapshot
Organocatalytic Enantioselective Addition of Malonates to Cyclic Imines: A Short Total Synthesis of Tetraponerine T‐1
inferred← citeshttps://doi.org/10.1002/asia.200700327openalex-snapshot
The Catalytic Acylcyanation of Imines
inferred← citeshttps://doi.org/10.1002/asia.201000636openalex-snapshot
Oxazolones in Organocatalysis, New Tricks for an Old Reagent
inferred← citeshttps://doi.org/10.1002/asia.201300814openalex-snapshot
Enantioselective Reactions of N‐Acyliminium Ions Using Chiral Organocatalysts
inferred← citeshttps://doi.org/10.1002/cctc.201601144openalex-snapshot
Applications of Chiral Thiourea‐Amine/Phosphine Organocatalysts in Catalytic Asymmetric Reactions
inferred← citeshttps://doi.org/10.1002/cctc.201601583openalex-snapshot
Friedel–Crafts Alkylation of Indoles with Nitroalkenes through Hydrogen‐Bond‐Donating Metal–Organic Framework
inferred← citeshttps://doi.org/10.1002/cctc.201902219openalex-snapshot
Influence of Hydrogen Bond Donating Sites in UiO‐66 Metal‐Organic Framework for Highly Regioselective Methanolysis of Epoxides
inferred← citeshttps://doi.org/10.1002/cctc.202300953openalex-snapshot
Photoinduced Pyridine N‐oxides Catalyzed Carbon Radical Generation from Alkylboronic Acids
inferred← citeshttps://doi.org/10.1002/cctc.202401477openalex-snapshot
Engineering of Active Sites in Metal‐Organic Frameworks for Friedel–Crafts Alkylation
inferred← citeshttps://doi.org/10.1002/cctc.71070openalex-snapshot
Dual Functional Urea Tethered Al(III) MOF as a Robust Heterogeneous Platform for Hydrogen Bond Assisted Friedel‐Crafts Alkylation and Cu(II)‐Mediated Chan–Lam Coupling
inferred← citeshttps://doi.org/10.1002/chem.200390042openalex-snapshot
Metal‐Free, Noncovalent Catalysis of Diels–Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water
inferred← citeshttps://doi.org/10.1002/chem.200500735openalex-snapshot
Bifunctional‐Thiourea‐Catalyzed Diastereo‐ and Enantioselective Aza‐Henry Reaction
inferred← citeshttps://doi.org/10.1002/chem.200501076openalex-snapshot
Organocatalysis Mediated by (Thio)urea Derivatives
inferred← citeshttps://doi.org/10.1002/chem.200501639openalex-snapshot
Direct Asymmetric Intermolecular Aldol Reactions Catalyzed by Amino Acids and Small Peptides
inferred← citeshttps://doi.org/10.1002/chem.200800197openalex-snapshot
Edge‐to‐Face CH/π Aromatic Interaction and Molecular Self‐Recognition in epi‐Cinchona‐Based Bifunctional Thiourea Organocatalysis
inferred← citeshttps://doi.org/10.1002/chem.200900406openalex-snapshot
Bifunctional Catalysis by Natural Cinchona Alkaloids: A Mechanism Explained
inferred← citeshttps://doi.org/10.1002/chem.200900628openalex-snapshot
An Alternative Mechanism for Diels–Alder Reactions of Evans Auxiliary Derivatives
inferred← citeshttps://doi.org/10.1002/chem.200902430openalex-snapshot
Physical Organic Study of Structure–Activity–Enantioselectivity Relationships in Asymmetric Bifunctional Thiourea Catalysis: Hints for the Design of New Organocatalysts
inferred← citeshttps://doi.org/10.1002/chem.201003423openalex-snapshot
Organocatalytic Michael–Alkylation Cascade: The Enantioselective Nitrocyclopropanation of Oxindoles
inferred← citeshttps://doi.org/10.1002/chem.201003694openalex-snapshot
Squaramides: Bridging from Molecular Recognition to Bifunctional Organocatalysis
inferred← citeshttps://doi.org/10.1002/chem.201101492openalex-snapshot
Silanediol Hydrogen Bonding Activation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/chem.201201206openalex-snapshot
Transition Metal and Hydrogen Bond Donor Hybrids: Catalysts for the Activation of Alkylidene Malonates
inferred← citeshttps://doi.org/10.1002/chem.201201232openalex-snapshot
Metal‐Free Synthesis of 3,3‐Disubstituted Oxoindoles by Iodine(III)‐Catalyzed Bromocarbocyclizations
inferred← citeshttps://doi.org/10.1002/chem.201201583openalex-snapshot
Two‐Dimensional Infrared Spectroscopy Reveals the Structure of an Evans Auxiliary Derivative and Its SnCl4 Lewis Acid Complex
inferred← citeshttps://doi.org/10.1002/chem.201204573openalex-snapshot
A Cooperative Hydrogen‐Bond‐Promoted Organophotoredox Catalysis Strategy for Highly Diastereoselective, Reductive Enone Cyclization
inferred← citeshttps://doi.org/10.1002/chem.201303006openalex-snapshot
Asymmetric α‐Hydroxylation of Tetralone‐Derived β‐Ketoesters by Using a Guanidine–Urea Bifunctional Organocatalyst in the Presence of Cumene Hydroperoxide
inferred← citeshttps://doi.org/10.1002/chem.201602097openalex-snapshot
Towards an Observation of Active Conformations in Asymmetric Catalysis: Interaction‐Induced Conformational Preferences of a Chiral Thiourea Model Compound
inferred← citeshttps://doi.org/10.1002/chem.201602231openalex-snapshot
Bis‐Boron Compounds in Catalysis: Bidentate and Bifunctional Activation
inferred← citeshttps://doi.org/10.1002/chem.201603592openalex-snapshot
Harnessing the Lewis Acidity of HFIP through its Cooperation with a Calcium(II) Salt: Application to the Aza‐Piancatelli Reaction
inferred← citeshttps://doi.org/10.1002/chem.201804023openalex-snapshot
Multifaceted Study on a Cytochalasin Scaffold: Lessons on Reactivity, Multidentate Catalysis, and Anticancer Properties
inferred← citeshttps://doi.org/10.1002/chem.201804230openalex-snapshot
How Do Substrates Bind to a Bifunctional Thiourea Catalyst? A Vibrational CD Study on Carboxylic Acid Binding
inferred← citeshttps://doi.org/10.1002/chem.202002637openalex-snapshot
N,N‐Diacylaminals as Emerging Tools in Synthesis: From Peptidomimetics to Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202004496openalex-snapshot
Bifunctional Hydrogen Bond Donor‐Catalyzed Diels–Alder Reactions: Origin of Stereoselectivity and Rate Enhancement
inferred← citeshttps://doi.org/10.1002/chem.202005188openalex-snapshot
Characterization of the Simplest Thiolimine: The Higher Energy Tautomer of Thioformamide
inferred← citeshttps://doi.org/10.1002/chem.202400188openalex-snapshot
A Tandem Hydroformylation‐Organocatalyzed Friedel‐Crafts Reaction for the Synthesis of Diindolylmethanes
inferred← citeshttps://doi.org/10.1002/chem.202402310openalex-snapshot
Secondary Sphere Lewis Acid Activated Heme Superoxo Adducts Mimic Crucial Non‐Covalent Interactions in IDO/TDO Heme Dioxygenases
inferred← citeshttps://doi.org/10.1002/chin.200644235openalex-snapshot
Chiral Ureas and Thioureas in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/chin.200646032openalex-snapshot
Pyrrolidine—Thiourea as a Bifunctional Organocatalyst: Highly Enantioselective Michael Addition of Cyclohexanone to Nitroolefins.
inferred← citeshttps://doi.org/10.1002/chir.21999openalex-snapshot
Synthesis and structural elucidation of novel camphor‐derived thioureas
inferred← citeshttps://doi.org/10.1002/chir.22035openalex-snapshot
Synthesis of 2‐(3‐(3,5‐bis(trifluoromethyl)phenyl)thioureido)‐3‐((dimethylamino)methyl)camphor organocatalysts
inferred← citeshttps://doi.org/10.1002/chir.23424openalex-snapshot
New bifunctional 1,3‐diamine organocatalysts derived from (+)‐camphoric acid for asymmetric Michael addition of 1,3‐dicarbonyl compounds to nitroolefins
inferred← citeshttps://doi.org/10.1002/cphc.200900848openalex-snapshot
Oriented Electric Fields Accelerate Diels–Alder Reactions and Control the endo/exo Selectivity
inferred← citeshttps://doi.org/10.1002/ejoc.200200635openalex-snapshot
A C 2 ‐Chiral Bis(amidinium) Catalyst for a Diels−Alder Reaction Constituting the Key Step of the Quinkert−Dane Estrone Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.200300543openalex-snapshot
Development of Thiourea‐Based Ligands for the Palladium‐Catalyzed Bis(methoxycarbonylation) of Terminal Olefins
inferred← citeshttps://doi.org/10.1002/ejoc.200801102openalex-snapshot
DFT Studies on Double Hydrogen Bond Catalysis of Reactions of Distinct Polarity
inferred← citeshttps://doi.org/10.1002/ejoc.201001439openalex-snapshot
Synthesis and NMR Binding Studies towards Rational Design of a Series of Electron‐Withdrawing Diamide Receptors/Organocatalysts
inferred← citeshttps://doi.org/10.1002/ejoc.201101765openalex-snapshot
Asymmetric Michael Addition Reactions between 3‐Substituted Benzofuran‐2(3H)‐ones and 1,1‐Bis(phenylsulfonyl)ethylene Catalyzed by Bifunctional Catalysts Containing Tertiary Amine and Thiourea Groups
inferred← citeshttps://doi.org/10.1002/ejoc.201200118openalex-snapshot
Design and Development of Bioinspired Guanine‐Based Organic Catalyst for Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.201200739openalex-snapshot
Hydrogen‐Bonding Thiourea Organocatalysts: The Privileged 3,5‐Bis(trifluoromethyl)phenyl Group
inferred← citeshttps://doi.org/10.1002/ejoc.201400035openalex-snapshot
Design Strategies for Enhanced Hydrogen‐Bond Donor Catalysts
inferred← citeshttps://doi.org/10.1002/ejoc.201402871openalex-snapshot
31P NMR Spectroscopically Quantified Hydrogen‐Bonding Strength of Thioureas and Their Catalytic Activity in Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201500585openalex-snapshot
Asymmetric Aldol Reaction of α,α‐Disubstituted Acetaldehydes Catalyzed by Diphenylprolinol Silyl Ether for the Construction of Quaternary Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/ejoc.201600062openalex-snapshot
A Concise One‐Pot Organo‐ and Biocatalyzed Preparation of Enantiopure Hexahydrofuro[2,3‐b]furan‐3‐ol: An Approach to the Synthesis of HIV Protease Inhibitors
inferred← citeshttps://doi.org/10.1002/ejoc.201600147openalex-snapshot
Exploration of the Bis(thio)urea‐Catalyzed Atropselective Synthesis of Marinopyrrole A
inferred← citeshttps://doi.org/10.1002/ejoc.201600801openalex-snapshot
Thiourea‐Catalyzed Cross‐Dehydrogenative Coupling of C(sp3)–H with Diethyl Phosphite
inferred← citeshttps://doi.org/10.1002/ejoc.201601524openalex-snapshot
Schreiner's Thiourea Promoted [2+2] Cycloaddition of Captodative Azetidinones and Nitroolefins
inferred← citeshttps://doi.org/10.1002/ejoc.201701502openalex-snapshot
Asymmetric Organocatalytic Synthesis of Bisindoles – Scope and Derivatizations
inferred← citeshttps://doi.org/10.1002/ejoc.201800844openalex-snapshot
A DFT Perspective on Diels–Alder Organocatalysts Based on Substituted Phosphoramides
inferred← citeshttps://doi.org/10.1002/ejoc.202001501openalex-snapshot
Novel, Chiral, and Enantiopure C2‐Symmetric Thioureas Promote Asymmetric Protio‐Pictet‐Spengler Reactions by Anion‐Binding Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.202201254openalex-snapshot
Progress in (Thio)urea‐ and Squaramide‐Based Brønsted Base Catalysts with Multiple H‐Bond Donors
inferred← citeshttps://doi.org/10.1002/ijch.201100082openalex-snapshot
[2.2]Paracyclophane‐Derived Planar‐Chiral Hydrogen‐Bond Receptors
inferred← citeshttps://doi.org/10.1002/jhet.70100openalex-snapshot
Collective Synthesis of Indole‐Derived Natural Products via Halogen Bond Donor Catalysis: Efficient Access to Arundine, Turbomycin B, and Arsindoline A Through 3,3′‐Bis(Indolyl)methane Assembly
inferred← citeshttps://doi.org/10.1002/poc.4069openalex-snapshot
Structural considerations for charge‐enhanced Brønsted acid catalysts
inferred← citeshttps://doi.org/10.1002/slct.202003336openalex-snapshot
Novel Access to Known and Unknown Thiourea Catalyst via a Multicomponent‐Reaction Approach
inferred← citeshttps://doi.org/10.1002/slct.202201314openalex-snapshot
Growing Impact of Carbohydrate‐Based Organocatalysts
inferred← citeshttps://doi.org/10.1007/128_2011_248openalex-snapshot
Thiourea Based Fluorous Organocatalyst
inferred← citeshttps://doi.org/10.1007/978-3-642-02815-1_3openalex-snapshot
Noncovalent Organocatalysis Based on Hydrogen Bonding: Elucidation of Reaction Paths by Computational Methods
inferred← citeshttps://doi.org/10.1007/b136352openalex-snapshot
Chiral Ureas and Thiroureas in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1007/s00706-009-0239-yopenalex-snapshot
Addition of allylzinc to α-amino acid-derived imines: synthesis of diamino alcohols by hydroboration
inferred← citeshttps://doi.org/10.1007/s00706-022-02991-zopenalex-snapshot
A novel synthesis of functionalized sulfonamide derivatives using the reaction of substituted thiourea or oxime derivatives with N-(2,3-dibromopropyl)-aryl(alkyl)sulfonamides
inferred← citeshttps://doi.org/10.1007/s10562-009-9936-8openalex-snapshot
Pd[tBuNH(S)NHP(O)(OiPr)2-S]2Cl2 Complex as Air- and Moisture-Stable Catalyst for Palladium Catalyzed Suzuki Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1007/s10562-017-2061-1openalex-snapshot
Organocatalytic Approach for Transfer Hydrogenation of Quinolines, Benzoxazines and Benzothiazines
inferred← citeshttps://doi.org/10.1007/s10870-026-01121-5openalex-snapshot
Crystallographic and Computational Studies of Conformationally Controlled 1,3-Bis(benzo[b]selenophen-2-yl)thiourea by Chalcogen-Bonding Interactions
inferred← citeshttps://doi.org/10.1007/s11030-016-9681-zopenalex-snapshot
Multicomponent synthesis of diverse pyrano-fused benzophenazines using bifunctional thiourea-based organocatalyst in aqueous medium
inferred← citeshttps://doi.org/10.1007/s11244-009-9423-xopenalex-snapshot
Urea and Thiourea-Functionalized Mesoporous Silica Nanoparticle Catalysts with Enhanced Catalytic Activity for Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1007/s11426-010-4179-5openalex-snapshot
Synthesis and antiviral bioactivities of novel chiral bis-thiourea-type derivatives containing α-aminophosphonate moiety
inferred← citeshttps://doi.org/10.1016/b978-0-323-91729-2.00021-5openalex-snapshot
Carbohydrate-based chiral organocatalysts
inferred← citeshttps://doi.org/10.1016/b978-0-443-19204-3.00004-8openalex-snapshot
Synthesis of azetidines by cycloaddition of imines to aromatic acetyl chloride moiety
inferred← citeshttps://doi.org/10.1016/b978-0-444-53349-4.00119-9openalex-snapshot
Organocatalyzed Ring-Opening Polymerizations
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.05.014openalex-snapshot
Thiourea-based non-nucleoside inhibitors of HIV reverse transcriptase as bifunctional organocatalysts in the asymmetric Strecker synthesis
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.08.063openalex-snapshot
Highly efficient selective oxidation of alcohols to carbonyl compounds catalyzed by ruthenium (III) meso-tetraphenylporphyrin chloride in the presence of molecular oxygen
inferred← citeshttps://doi.org/10.1016/j.bpc.2019.106280openalex-snapshot
Functional changes of biomolecules and organocatalysts as a probe for pressure effects in solution
inferred← citeshttps://doi.org/10.1016/j.carres.2025.109470openalex-snapshot
Organocatalyzed O-glycosylation of glycosyl trichloroacetimidates donors: l-prolinethioamide as brønsted acid catalyst
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.01.046openalex-snapshot
Camphor-derived thioureas: Synthesis and application in asymmetric Kabachnik-Fields reaction
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2022.129103openalex-snapshot
Surfactant regulated synthesis of ZIF-8 crystals as carbonic anhydrase-mimicking nanozyme
inferred← citeshttps://doi.org/10.1016/j.compositesb.2014.11.001openalex-snapshot
New glass fiber/bismaleimide composites with significantly improved flame retardancy, higher mechanical strength and lower dielectric loss
inferred← citeshttps://doi.org/10.1016/j.comptc.2012.07.022openalex-snapshot
DFT analysis of a key step in the cinchona-mediated organocatalytic Michael-addition of nitromethane to 1,3-diphenylpropenone
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2016.11.027openalex-snapshot
A perspective approach to sustainable routes for non-isocyanate polyurethanes
inferred← citeshttps://doi.org/10.1016/j.jcat.2020.09.026openalex-snapshot
Catalysis in polymerization of cyclic esters. Catalyst and initiator in one molecule. Polymerization of ε-caprolactone
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2011.05.026openalex-snapshot
A recyclable fluorous thiourea organocatalyst for the chemoselective oxidation of sulfides
inferred← citeshttps://doi.org/10.1016/j.mcat.2018.03.009openalex-snapshot
Applications of biological urea-based catalysts in chemical processes
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114628openalex-snapshot
Application of a new porous bimetallic H-bond catalyst in the preparation of biological henna-based pyrazolo[3,4-b]quinolines via a cooperative vinylogous anomeric based oxidation
inferred← citeshttps://doi.org/10.1016/j.molliq.2019.111829openalex-snapshot
CF3-groups critically enhance the binding of thiourea catalysts to ketones – a NMR and FT-IR study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.134174openalex-snapshot
The Pd(0) and Pd(II) SBA‐TU‐anchored catalysts in the Mizoroki-Heck and Suzuki-Miyaura cross-coupling reactions: A comparative catalytic study
inferred← citeshttps://doi.org/10.1016/j.poly.2015.08.047openalex-snapshot
Synthesis, single crystal structure and efficient catalysis for alcohol oxidation of a novel Ru(II) complex with both a N,N,N-tridentate ligand and a pyridinedicarboxylate
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100064openalex-snapshot
A molecular electron density theory study of hydrogen bond catalysed polar Diels–Alder reactions of α,β-unsaturated carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2005.09.079openalex-snapshot
Acid-free, organocatalytic acetalization
inferred← citeshttps://doi.org/10.1016/j.tet.2005.11.029openalex-snapshot
Regioselective electrophilic substitutions of fulvenes with ethyl glyoxylate and subsequent Diels–Alder reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2006.03.037openalex-snapshot
A DFT study of the Diels–Alder reaction between methyl acrolein derivatives and cyclopentadiene. Understanding the effects of Lewis acids catalysts based on sulfur containing boron heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2008.07.087openalex-snapshot
Thiourea-catalyzed Morita–Baylis–Hillman reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2010.02.053openalex-snapshot
Thiourea catalyzed aminolysis of epoxides under solvent free conditions. Electronic control of regioselective ring opening
inferred← citeshttps://doi.org/10.1016/j.tet.2011.12.021openalex-snapshot
Chiral 2-aminobenzimidazole bifunctional organocatalysts: effect of di-CF3 and TFA on catalytic mechanisms
showing the first 200 of 474 · page through all 474
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.