On the public citation graph
Applications of asymmetric organocatalysis in medicinal chemistry
0 signed · 492 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/(sici)1521-3773(19990601)38:11<1583::aid-anie1583>3.0.co;2-eopenalex-snapshot
Asymmetric Phase-Transfer Catalysis
inferredcites →https://doi.org/10.1002/9783527622627openalex-snapshot
Asymmetric Phase Transfer Catalysis
inferredcites →https://doi.org/10.1002/9783527627844openalex-snapshot
Hydrogen Bonding in Organic Synthesis
inferredcites →https://doi.org/10.1002/adsc.200800812openalex-snapshot
Primary Amine‐Thioureas based on tert‐Butyl Esters of Natural Amino Acids as Organocatalysts for the Michael Reaction
inferredcites →https://doi.org/10.1002/adsc.201000287openalex-snapshot
Asymmetric Synthesis of Maraviroc (UK‐427,857)
inferredcites →https://doi.org/10.1002/adsc.201100288openalex-snapshot
Enantioselective Synthesis of Cyclic Thioureas via Mannich Reaction and Concise Synthesis of Highly Optically Active Methylthioimidazolines: Discovery of a More Potent Antipyretic Agent
inferredcites →https://doi.org/10.1002/adsc.201100488openalex-snapshot
The Growing Impact of Catalysis in the Pharmaceutical Industry
inferredcites →https://doi.org/10.1002/adsc.201100636openalex-snapshot
Primary Amine‐Thioureas with Improved Catalytic Properties for “Difficult” Michael Reactions: Efficient Organocatalytic Syntheses of (S)‐Baclofen, (R)‐Baclofen and (S)‐Phenibut
inferredcites →https://doi.org/10.1002/ange.200804883openalex-snapshot
High‐Yielding Synthesis of the Anti‐Influenza Neuramidase Inhibitor (−)‐Oseltamivir by Three “One‐Pot” Operations
inferredcites →https://doi.org/10.1002/anie.197104961openalex-snapshot
New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures
inferredcites →https://doi.org/10.1002/anie.200352136openalex-snapshot
Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3‐Dicarbonyl Compounds and α,β‐Unsaturated Ketones—A Highly Atom‐Economic Catalytic One‐Step Formation of Optically Active Warfarin Anticoagulant
inferredcites →https://doi.org/10.1002/anie.200400650openalex-snapshot
In the Golden Age of Organocatalysis
inferredcites →https://doi.org/10.1002/anie.200601025openalex-snapshot
Organocatalytic Conjugate Addition of Malonates to α,β‐Unsaturated Aldehydes: Asymmetric Formal Synthesis of (−)‐Paroxetine, Chiral Lactams, and Lactones
inferredcites →https://doi.org/10.1002/anie.200705523openalex-snapshot
Asymmetric Aminocatalysis—Gold Rush in Organic Chemistry
inferredcites →https://doi.org/10.1002/anie.200804883openalex-snapshot
High‐Yielding Synthesis of the Anti‐Influenza Neuramidase Inhibitor (−)‐Oseltamivir by Three “One‐Pot” Operations
inferredcites →https://doi.org/10.1002/anie.201001644openalex-snapshot
Organocatalytic Michael Addition of Aldehydes to Protected 2‐Amino‐1‐Nitroethenes: The Practical Syntheses of Oseltamivir (Tamiflu) and Substituted 3‐Aminopyrrolidines
inferredcites →https://doi.org/10.1002/anie.201100059openalex-snapshot
One‐Pot Reactions Accelerate the Synthesis of Active Pharmaceutical Ingredients
inferredcites →https://doi.org/10.1002/anie.201105415openalex-snapshot
N‐Heterocyclic Carbene Catalyzed Domino Reactions
inferredcites →https://doi.org/10.1002/anie.201201364openalex-snapshot
A Rotaxane‐Based Switchable Organocatalyst
inferredcites →https://doi.org/10.1002/cbic.201000432openalex-snapshot
Potent Inhibition of HIV‐1 Entry with a Chemically Programmed Antibody Aided by an Efficient Organocatalytic Synthesis
inferredcites →https://doi.org/10.1002/cctc.201200124openalex-snapshot
Organocatalytic Michael Reaction of Nitroenamine Derivatives with Aldehydes: Short and Efficient Asymmetric Synthesis of (−)‐Oseltamivir
inferredcites →https://doi.org/10.1002/chem.201001108openalex-snapshot
High‐Yielding Synthesis of the Anti‐Influenza Neuraminidase Inhibitor (−)‐Oseltamivir by Two “One‐Pot” Sequences
inferredcites →https://doi.org/10.1002/chem.201003694openalex-snapshot
Squaramides: Bridging from Molecular Recognition to Bifunctional Organocatalysis
inferredcites →https://doi.org/10.1002/ejoc.200600502openalex-snapshot
Norstatines from Aldehydes by Sequential Organocatalytic α‐Amination and Passerini Reaction
inferredcites →https://doi.org/10.1002/ejoc.200700032openalex-snapshot
Organocatalytic Synthesis of Drugs and Bioactive Natural Products
inferredcites →https://doi.org/10.1002/ejoc.200900664openalex-snapshot
New Phenylglycine‐Derived Primary Amine Organocatalysts for the Preparation of Optically Active Warfarin
inferredcites →https://doi.org/10.1002/ejoc.200900831openalex-snapshot
Organocatalytic Enantioselective Michael Addition of 4‐Hydroxycoumarin to α,β‐Unsaturated Ketones: A Simple Synthesis of Warfarin
inferredcites →https://doi.org/10.1002/ejoc.201000239openalex-snapshot
Chiral Ionic Liquids Bearing O‐Silylated α,α‐Diphenyl (S)‐ or (R)‐Prolinol Units: Recoverable Organocatalysts for Asymmetric Michael Addition of Nitroalkanes to α,β‐Enals
inferredcites →https://doi.org/10.1002/jlac.19606340103openalex-snapshot
Organische Katalysatoren, LXI. Asymmetrische Synthesen mit Ketenen, I. Alkaloid‐katalysierte asymmetrische Synthesen von α‐Phenyl‐propionsäureestern
inferredcites →https://doi.org/10.1002/prac.19640240311openalex-snapshot
Organische Katalysatoren. LXXI Asymmetrische Synthesen mit Ketenen. IV. Zusammenhänge zwischen dem räumlichen Bau einiger alkaloidartiger Katalysatoren und ihren stereospezifischen Wirkungen bei asymmetrischen Estersynthesen
inferredcites →https://doi.org/10.1007/978-1-59745-419-3_1openalex-snapshot
Peptide-Based Drug Design: Here and Now
inferredcites →https://doi.org/10.1016/j.bmc.2008.11.062openalex-snapshot
Organocatalyzed highly atom economic one pot synthesis of tetrahydropyridines as antimalarials
inferredcites →https://doi.org/10.1016/j.bmcl.2006.11.094openalex-snapshot
Synthesis and HIV-1 integrase inhibitory activity of spiroundecane(ene) derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2009.03.028openalex-snapshot
Organocatalytic synthesis and sterol 14α-demethylase binding interactions of enantioriched 3-(1H-1,2,4-triazol-1-yl)butyl benzoates
inferredcites →https://doi.org/10.1016/j.bmcl.2010.01.139openalex-snapshot
Structure-based design and synthesis of novel P2/P3 modified, non-peptidic β-secretase (BACE-1) inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2012.01.128openalex-snapshot
Synthesis and comparative evaluation of 4-oxa- and 4-aza-podophyllotoxins as antiproliferative microtubule destabilizing agents
inferredcites →https://doi.org/10.1016/j.tetlet.2009.02.049openalex-snapshot
Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (−)-Paroxetine
inferredcites →https://doi.org/10.1016/s0960-894x(99)00693-9openalex-snapshot
4-Aza-2,3-dehydro-4-deoxypodophyllotoxins: simple aza-podophyllotoxin analogues possessing potent cytotoxicity
inferredcites →https://doi.org/10.1021/cc100003copenalex-snapshot
Regioselective Synthesis and in Vitro Anticancer Activity of 4-Aza-podophyllotoxin Derivatives Catalyzed by l -Proline
inferredcites →https://doi.org/10.1021/cr068373ropenalex-snapshot
Small-Molecule H-Bond Donors in Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/ja000092sopenalex-snapshot
New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder Reaction
inferredcites →https://doi.org/10.1021/ja000300gopenalex-snapshot
Design of Potent Inhibitors for Human Brain Memapsin 2 (β-Secretase)
inferredcites →https://doi.org/10.1021/ja00314a045openalex-snapshot
Efficient catalytic asymmetric alkylations. 1. Enantioselective synthesis of (+)-indacrinone via chiral phase-transfer catalysis
inferredcites →https://doi.org/10.1021/ja106349mopenalex-snapshot
A Unique Approach to the Concise Synthesis of Highly Optically Active Spirooxazolines and the Discovery of a More Potent Oxindole-Type Phytoalexin Analogue
inferredcites →https://doi.org/10.1021/jm0109309openalex-snapshot
Inotropic Activity of Hydroindene Amidinohydrazones
inferredcites →https://doi.org/10.1021/jm060051sopenalex-snapshot
Design, Synthesis, and Biological Evaluation of the Combinatorial Library with a New Spirodiketopiperazine Scaffold. Discovery of Novel Potent and Selective Low-Molecular-Weight CCR5 Antagonists
inferredcites →https://doi.org/10.1021/jm8006195openalex-snapshot
Antitumor Compounds Based on a Natural Product Consensus Pharmacophore
inferredcites →https://doi.org/10.1021/jo00925a003openalex-snapshot
Asymmetric synthesis of bicyclic intermediates of natural product chemistry
inferredcites →https://doi.org/10.1021/jo0523666openalex-snapshot
Efficient Synthesis of Novel NK1 Receptor Antagonists: Selective 1,4-Addition of Grignard Reagents to 6-Chloronicotinic Acid Derivatives
inferredcites →https://doi.org/10.1021/jo100017topenalex-snapshot
Substrate-Controlled and Organocatalytic Asymmetric Synthesis of Carbocyclic Amino Acid Dipeptide Mimetics
inferredcites →https://doi.org/10.1021/jo101446dopenalex-snapshot
Organocatalytic Asymmetric Tandem Michael Addition−Hemiacetalization: A Route to Chiral Dihydrocoumarins, Chromanes, and 4H-Chromenes
inferredcites →https://doi.org/10.1021/jo101704bopenalex-snapshot
Asymmetric Synthesis of Telcagepant, a CGRP Receptor Antagonist for the Treatment of Migraine
inferredcites →https://doi.org/10.1021/jo202020mopenalex-snapshot
One-Pot Enantioselective Synthesis of Functionalized Pyranocoumarins and 2-Amino-4 H -chromenes: Discovery of a Type of Potent Antibacterial Agent
inferredcites →https://doi.org/10.1021/jo901409dopenalex-snapshot
Organocatalytic Asymmetric Friedel−Crafts Alkylation/Cyclization Cascade Reaction of 1-Naphthols and α,β-Unsaturated Aldehydes: An Enantioselective Synthesis of Chromanes and Dihydrobenzopyranes
inferredcites →https://doi.org/10.1021/ol0485417openalex-snapshot
Direct Organocatalytic Asymmetric Aldol Reactions of α-Amino Aldehydes: Expedient Syntheses of Highly Enantiomerically Enriched anti-β-Hydroxy-α-amino Acids
inferredcites →https://doi.org/10.1021/ol062000vopenalex-snapshot
Substrate-Directed Stereoselectivity in Vicinal Diamine-Catalyzed Synthesis of Warfarin
inferredcites →https://doi.org/10.1021/ol200185hopenalex-snapshot
Asymmetric Aza-Mannich Addition: Synthesis of Modified Chiral 2-(Ethylthio)-thiazolone Derivatives with Anticancer Potency
inferredcites →https://doi.org/10.1021/ol3002514openalex-snapshot
Asymmetric Synthesis of γ-Nitroesters by an Organocatalytic One-Pot Strategy
inferredcites →https://doi.org/10.1021/ol800108uopenalex-snapshot
Organocatalytic Asymmetric Total Synthesis of (R)-Rolipram and Formal Synthesis of (3S,4R)-Paroxetine
inferredcites →https://doi.org/10.1021/op1000447openalex-snapshot
Pilot-Plant Preparation of 3,4-Dihydropyridin-2-one Derivatives, the Core Structures of P2X 7 Receptor Antagonists
inferredcites →https://doi.org/10.1021/op200381wopenalex-snapshot
Asymmetric and Diastereoselective Conjugate Addition Reactions: C–C Bond Formation at Large Scale
inferredcites →https://doi.org/10.1021/op700023hopenalex-snapshot
Practical Syntheses of Chiral α-Amino Acids and Chiral Half-Esters by Kinetic Resolution of Urethane-Protected α-Amino Acid N-Carboxyanhydrides and Desymmetrization of Cyclic meso-Anhydrides with New Modified Cinchona Alkaloid Catalysts
inferredcites →https://doi.org/10.1038/nchem.215openalex-snapshot
Concise synthesis of ricciocarpin A and discovery of a more potent analogue
inferredcites →https://doi.org/10.1038/nchem.539openalex-snapshot
Organocatalytic cascade reactions as a new tool in total synthesis
inferredcites →https://doi.org/10.1038/nrd2972openalex-snapshot
New medicines to improve control and contribute to the eradication of malaria
inferredcites →https://doi.org/10.1039/b107298fopenalex-snapshot
Metal-free organocatalysis through explicit hydrogen bonding interactions
inferredcites →https://doi.org/10.1039/b618984aopenalex-snapshot
The synthesis of chromenes, chromanes, coumarins and related heterocycles via tandem reactions of salicylic aldehydes or salicylic imines with α,β-unsaturated compounds
inferredcites →https://doi.org/10.1039/b807577hopenalex-snapshot
Binaphthol-derived phosphoric acid as a versatile catalyst for enantioselective carbon–carbon bond forming reactions
inferredcites →https://doi.org/10.1039/b924964hopenalex-snapshot
Asymmetric organocatalysis in total synthesis – a trial by fire
inferredcites →https://doi.org/10.1039/c0cs00200copenalex-snapshot
Squaramides: physical properties, synthesis and applications
inferredcites →https://doi.org/10.1039/c1cc14379dopenalex-snapshot
Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency
inferredcites →https://doi.org/10.1039/c1gc15118eopenalex-snapshot
Efficient “on water” organocatalytic protocol for the synthesis of optically pure warfarin anticoagulant
inferredcites →https://doi.org/10.1039/c1ob06133jopenalex-snapshot
Design, synthesis and biological evaluation of optically pure functionalized spiro[5,5]undecane-1,5,9-triones as HIV-1 inhibitors
inferredcites →https://doi.org/10.1039/c2cc17219dopenalex-snapshot
Discovery of 2-aminobuta-1,3-enynes in asymmetric organocascade catalysis: construction of drug-like spirocyclic cyclohexanes having five to six contiguous stereocenters
inferredcites →https://doi.org/10.1055/s-0029-1218699openalex-snapshot
Cinchona Alkaloids in Asymmetric Organocatalysis
inferredcites →https://doi.org/10.1055/s-0029-1218801openalex-snapshot
Chiral Phosphoric Acids as Versatile Catalysts for Enantioselective Transformations
inferredcites →https://doi.org/10.1055/s-0030-1260545openalex-snapshot
Metal-Free Chiral Phosphoric Acid or Chiral Metal Phosphate as Active Catalyst in the Activation of N-Acyl Aldimines
inferredcites →https://doi.org/10.1055/s-0031-1290396openalex-snapshot
Thiol-Free Synthesis of Oseltamivir and Its Analogues via Organocatalytic Michael Additions of Oxyacetaldehydes to 2-Acylaminonitroalkenes
inferredcites →https://doi.org/10.1055/s-2003-36265openalex-snapshot
Efficient Asymmetric Synthesis of β-Amino Acid BAY 10-8888/PLD-118, a Novel Antifungal for the Treatment of Yeast Infections
inferredcites →https://doi.org/10.1073/pnas.1017666108openalex-snapshot
Discovery of new antimalarial chemotypes through chemical methodology and library development
inferredcites →https://doi.org/10.1074/jbc.m109266200openalex-snapshot
Substrate and Inhibitor Profile of BACE (β-Secretase) and Comparison with Other Mammalian Aspartic Proteases
inferredcites →https://doi.org/10.1124/jpet.107.129973openalex-snapshot
Deletion of μ-Opioid Receptor in Mice Alters the Development of Acute Neuroinflammation
inferredcites →https://doi.org/10.1126/science.290.5489.150openalex-snapshot
Structure of the Protease Domain of Memapsin 2 (β-Secretase) Complexed with Inhibitor
inferredcites →https://doi.org/10.1128/aac.42.9.2197openalex-snapshot
Molecular Mode of Action of the Antifungal β-Amino Acid BAY 10-8888
inferredcites →https://doi.org/10.1246/bcsj.20090268openalex-snapshot
Chiral Phosphoric Acids as Versatile Catalysts for Enantioselective Carbon–Carbon Bond Forming Reactions
inferredcites →https://doi.org/10.1517/17460441.3.11.1345openalex-snapshot
CCR5 inhibitors in HIV-1 therapy
inferredcites →https://doi.org/10.2174/138161207779313560openalex-snapshot
Aspartic Proteases in Drug Discovery
inferredcites →https://doi.org/10.2174/138527211796150732openalex-snapshot
Enantioselective Carbon-Carbon Bond Forming Reactions Catalyzed by Chiral Phosphoric Acid Catalysts
inferredcites →https://doi.org/10.2174/138955707780619617openalex-snapshot
Chirality - A New Era of Therapeutics
inferredcites →https://doi.org/10.2174/1389557511209030210openalex-snapshot
New Targets, New Hope: Novel Drug Targets for Curbing Malaria
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.4673736openalex-extracted
Novel Porous Organic Polymer Supported Chloramphenicol Base Derived Catalysts: Overcoming the Reduced Enantioselectivity of Immobilized Organocatalysts
inferred← citeshttps://doi.org/10.1002/9781119015789.ch1openalex-snapshot
Introduction to Practical Functional Group Synthesis
inferred← citeshttps://doi.org/10.1002/9781394212767.ch17openalex-snapshot
New Trends in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/9783527834204.ch16openalex-snapshot
The Synthesis and Application of BINOL Derivatives as Effective Building Blocks for Catalysts Employed in Enantioselective Synthesis
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0212openalex-snapshot
Organocatalytic Allylic and Benzylic CH Bond Functionalization
inferred← citeshttps://doi.org/10.1002/9783527841943.ch9openalex-snapshot
Recent Achievements in Organic Reactions in Polyethylene Glycol
inferred← citeshttps://doi.org/10.1002/adma.201700296openalex-snapshot
Chiral Responsive Liquid Quantum Dots
inferred← citeshttps://doi.org/10.1002/adsc.201201099openalex-snapshot
An Asymmetric Organocatalytic Quadruple Cascade Initiated by a Friedel–Crafts‐Type Reaction with Electron‐Rich Arenes
inferred← citeshttps://doi.org/10.1002/adsc.201400404openalex-snapshot
Organocatalysis in Enantioselective α‐Functionalization of 2‐Cyanoacetates
inferred← citeshttps://doi.org/10.1002/adsc.201500375openalex-snapshot
Heterogeneous Dipeptide‐Catalyzed α‐Amination of Aldehydes in a Continuous‐Flow Reactor: Effect of Residence Time on Enantioselectivity
inferred← citeshttps://doi.org/10.1002/adsc.201500416openalex-snapshot
The Squaramide‐Catalyzed 1,3‐Dipolar Cycloaddition of Nitroalkenes with N‐2,2,2‐Trifluoroethylisatin Ketimines: An Approach for the Synthesis of 5′‐Trifluoromethyl‐spiro[pyrrolidin‐3,2′‐oxindoles]
inferred← citeshttps://doi.org/10.1002/adsc.201500862openalex-snapshot
Stereocontrolled Construction of 3,4‐Dihydrocoumarin Scaffolds with a Quaternary Amino Acid Moiety via Chiral Squaramide‐Catalyzed Cascade Michael Addition/Lactonization Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201600782openalex-snapshot
Squaramide‐Catalyzed Enantioselective Cascade Approach to Bispirooxindoles with Multiple Stereocenters
inferred← citeshttps://doi.org/10.1002/adsc.201700023openalex-snapshot
Diastereoselective Synthesis of Functionalized Angularly‐Fused Tetracycles via an Organocatalytic Quadruple Reaction Sequence
inferred← citeshttps://doi.org/10.1002/adsc.201700693openalex-snapshot
Asymmetric Stereoablative Aryloxylation of 3‐Bromooxindoles with Bifunctional Catalyst
inferred← citeshttps://doi.org/10.1002/adsc.201700927openalex-snapshot
Organocatalytic Asymmetric Synthesis of Six‐Membered Carbocycle‐Based Spiro Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201701164openalex-snapshot
(E)‐3‐(Alkoxycarbonyl‐2‐Alkyliden)‐2‐Oxindoles: Multidentate Pronucleophiles for the Organocatalytic, Vinylogous Michael Addition to Nitroolefins
inferred← citeshttps://doi.org/10.1002/adsc.201800636openalex-snapshot
Organocatalytic Asymmetric Four‐Component [5+1+1+1] Cycloadditions via a Quintuple Cascade Process
inferred← citeshttps://doi.org/10.1002/adsc.201801647openalex-snapshot
Organocatalytic Asymmetric Synthesis of Cyclic Compounds Bearing a Trifluoromethylated Stereogenic Center: Recent Developments
inferred← citeshttps://doi.org/10.1002/adsc.201900218openalex-snapshot
Asymmetric Synthesis of Spirooxindoles with Seven Stereocenters via Organocatalyzed One‐pot Three‐component Sequential Cascade Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202001507openalex-snapshot
Organocatalytic Deuteration Induced by the Dynamic Covalent Interaction of Imidazolium Cations with Ketones
inferred← citeshttps://doi.org/10.1002/adsc.202100635openalex-snapshot
Enantioselective Organocatalyzed aza‐Michael Addition Reaction of 2‐Hydroxybenzophenone Imines to Nitroolefins under Batch and Flow Conditions
inferred← citeshttps://doi.org/10.1002/adsc.202101019openalex-snapshot
Asymmetric Conjugate Addition of 3‐Hydroxychromen‐4‐Ones to Electron‐Deficient Olefins Catalyzed by Recyclable C2‐Symmetric Squaramide
inferred← citeshttps://doi.org/10.1002/adsc.202301394openalex-snapshot
Enantioselective Acyl‐Transfer/Protonation Reactions with Designed Chiral Thiourea‐Iminophosphorane Catalysts
inferred← citeshttps://doi.org/10.1002/advs.202309343openalex-snapshot
Innovative Arylimidazole‐Fused Phytovirucides via Carbene‐Catalyzed [3+4] Cycloaddition: Locking Viral Cell‐To‐Cell Movement by Out‐Competing Virus Capsid‐Host Interactions
inferred← citeshttps://doi.org/10.1002/ajoc.201800146openalex-snapshot
Asymmetric Organocatalytic Electrophilic Heterofunctionalization of Oxindoles
inferred← citeshttps://doi.org/10.1002/ajoc.202100216openalex-snapshot
Reversal Reactivity of β‐Alkylnitroalkenes as 1,3‐Binucleophiles: Application to Nitroarenes using Organocatalysis
inferred← citeshttps://doi.org/10.1002/ajoc.202100232openalex-snapshot
Sulfide‐Catalyzed Diastereoselective Spirocyclopropanation: Constructing Spiro‐cyclopropanyl‐pyrazolones From α‐Arylidenepyrazolones
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/ajoc.70551openalex-snapshot
Green Organocatalysis as a Sustainable Platform for Drug Synthesis: A Perspective
inferred← citeshttps://doi.org/10.1002/ange.201303247openalex-snapshot
NHC Organocatalytic Formal LUMO Activation of α,β‐Unsaturated Esters for Reaction with Enamides
inferred← citeshttps://doi.org/10.1002/ange.201400203openalex-snapshot
Organocatalytic Asymmetric Formation of Steroids
inferred← citeshttps://doi.org/10.1002/ange.201605790openalex-snapshot
γ′‐Selective Functionalization of Cyclic Enones: Construction of a Chiral Quaternary Carbon Center by [4+2] Cycloaddition/Retro‐Mannich Reaction with 3‐Substituted Maleimides
inferred← citeshttps://doi.org/10.1002/ange.201609390openalex-snapshot
Organocatalytic Friedel–Crafts Alkylation/Lactonization Reaction of Naphthols with 3‐Trifluoroethylidene Oxindoles: The Asymmetric Synthesis of Dihydrocoumarins
inferred← citeshttps://doi.org/10.1002/ange.201807134openalex-snapshot
The Hydrazine–O2 Redox Couple as a Platform for Organocatalytic Oxidation: Benzo[c]cinnoline‐Catalyzed Oxidation of Alkyl Halides to Aldehydes
inferred← citeshttps://doi.org/10.1002/ange.201912043openalex-snapshot
Enantioenriched Methylene‐Bridged Benzazocanes Synthesis by Organocatalytic and Superacid Activations
inferred← citeshttps://doi.org/10.1002/ange.202205633openalex-snapshot
Excitation‐Dependent Circularly Polarized Luminescence from Helical Assemblies Based on Tartaric Acid‐Derived Acylhydrazones
inferred← citeshttps://doi.org/10.1002/ange.202217724openalex-snapshot
Highly Enantioselective Construction of Multifunctional Silicon‐Stereogenic Silacycles by Asymmetric Enamine Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201303247openalex-snapshot
NHC Organocatalytic Formal LUMO Activation of α,β‐Unsaturated Esters for Reaction with Enamides
inferred← citeshttps://doi.org/10.1002/anie.201400203openalex-snapshot
Organocatalytic Asymmetric Formation of Steroids
inferred← citeshttps://doi.org/10.1002/anie.201605790openalex-snapshot
γ′‐Selective Functionalization of Cyclic Enones: Construction of a Chiral Quaternary Carbon Center by [4+2] Cycloaddition/Retro‐Mannich Reaction with 3‐Substituted Maleimides
inferred← citeshttps://doi.org/10.1002/anie.201609390openalex-snapshot
Organocatalytic Friedel–Crafts Alkylation/Lactonization Reaction of Naphthols with 3‐Trifluoroethylidene Oxindoles: The Asymmetric Synthesis of Dihydrocoumarins
inferred← citeshttps://doi.org/10.1002/anie.201807134openalex-snapshot
The Hydrazine–O 2 Redox Couple as a Platform for Organocatalytic Oxidation: Benzo[ c ]cinnoline‐Catalyzed Oxidation of Alkyl Halides to Aldehydes
inferred← citeshttps://doi.org/10.1002/anie.201912043openalex-snapshot
Enantioenriched Methylene‐Bridged Benzazocanes Synthesis by Organocatalytic and Superacid Activations
inferred← citeshttps://doi.org/10.1002/anie.202205633openalex-snapshot
Excitation‐Dependent Circularly Polarized Luminescence from Helical Assemblies Based on Tartaric Acid‐Derived Acylhydrazones
inferred← citeshttps://doi.org/10.1002/anie.202217724openalex-snapshot
Highly Enantioselective Construction of Multifunctional Silicon‐Stereogenic Silacycles by Asymmetric Enamine Catalysis
inferred← citeshttps://doi.org/10.1002/asia.201301549openalex-snapshot
Synergy, Compatibility, and Innovation: Merging Lewis Acids with Stereoselective Enamine Catalysis
inferred← citeshttps://doi.org/10.1002/asia.201600013openalex-snapshot
Hydrogen‐Bonding Network Promoted [3+2] Cycloaddition: Asymmetric Catalytic Construction of Spiro‐pseudoindoxyl Derivatives
inferred← citeshttps://doi.org/10.1002/asia.201800608openalex-snapshot
Transition‐Metal‐Free Multicomponent Approach to Stereoenriched Cyclopentyl‐isoxazoles through C−C Bond Cleavage
inferred← citeshttps://doi.org/10.1002/asia.201801296openalex-snapshot
Organocatalysts Derived from Unnatural α‐Amino Acids: Scope and Applications
inferred← citeshttps://doi.org/10.1002/asia.202300370openalex-snapshot
Blossoming of Polyenamine Catalysis in Asymmetric Synthesis: Scope and Future Applications
inferred← citeshttps://doi.org/10.1002/cctc.201300399openalex-snapshot
Electrosteric Activation by using Ion‐Tagged Prolines: A Combined Experimental and Computational Investigation
inferred← citeshttps://doi.org/10.1002/cctc.201402973openalex-snapshot
Efficient Organocatalyst Supported on a Simple Ionic Liquid as a Recoverable System for the Asymmetric Diels–Alder Reaction in the Presence of Water
inferred← citeshttps://doi.org/10.1002/cctc.201500455openalex-snapshot
Recent Advances in Organocatalytic Kinetic Resolution for the Synthesis of Functionalized Products
inferred← citeshttps://doi.org/10.1002/cctc.201601527openalex-snapshot
Gold(I)‐Mediated Thiourea Organocatalyst Activation: A Synergic Effect for Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/cctc.201701975openalex-snapshot
Serendipitous Observation of Liquid‐Phase Size Selectivity inside a Mesoporous Silica Nanoreactor in the Reaction of Chromene with Formic Acid
inferred← citeshttps://doi.org/10.1002/cctc.201901129openalex-snapshot
From Immobilization to Catalyst Use: A Complete Continuous‐Flow Approach Towards the Use of Immobilized Organocatalysts
inferred← citeshttps://doi.org/10.1002/cctc.202000463openalex-snapshot
Synthesis of Polycyclic Spiro Pyrrolidone Derivatives via DBU‐Catalyzed Diastereoselective Vinylogous Aldol‐Michael Cascade Reaction
inferred← citeshttps://doi.org/10.1002/cctc.202400031openalex-snapshot
A C3‐Symmetric Amino Organocatalyst for Asymmetric Synthesis of Warfarin and Analogues: Mechanistic Insight from ESI‐MS Spectrometry and Computational Calculations
inferred← citeshttps://doi.org/10.1002/cctc.202402021openalex-snapshot
Enantioselective Preparation of Chiral Succinimide Derivatives by Mechanochemical Catalytic Michael Addition
inferred← citeshttps://doi.org/10.1002/celc.201600187openalex-snapshot
N‐Heterocyclic Carbenes and Parent Cations: Acidity, Nucleophilicity, Stability, and Hydrogen Bonding—Electrochemical Study and Ab Initio Calculations
inferred← citeshttps://doi.org/10.1002/celc.201700992openalex-snapshot
Electrogenerated N‐Heterocyclic Olefins: Stability and Catalytic Ability
inferred← citeshttps://doi.org/10.1002/chem.201302127openalex-snapshot
Organocatalytic Asymmetric Synthesis of Tetracyclic Pyridocarbazole Derivatives by Using a Diels–Alder/aza‐Michael/Aldol Condensation Domino Reaction
inferred← citeshttps://doi.org/10.1002/chem.201302220openalex-snapshot
Chiral Hypervalent Iodine Reagents: Synthesis and Reactivity
inferred← citeshttps://doi.org/10.1002/chem.201402373openalex-snapshot
Organocatalyzed Step‐Growth Polymerization through Desymmetrization of Cyclic Anhydrides: Synthesis of Chiral Polyesters
inferred← citeshttps://doi.org/10.1002/chem.201402947openalex-snapshot
One‐Pot Asymmetric Synthesis of Quaternary Pyrroloindolones through a Multicatalytic N‐Allylation/Hydroacylation Sequence
inferred← citeshttps://doi.org/10.1002/chem.201405038openalex-snapshot
Aminocatalysis: Beyond Steric Shielding and Hydrogen‐Bonding
inferred← citeshttps://doi.org/10.1002/chem.201500660openalex-snapshot
Dienamine and Friedel–Crafts One‐Pot Synthesis, and Antitumor Evaluation of Diheteroarylalkanals
inferred← citeshttps://doi.org/10.1002/chem.201503063openalex-snapshot
Core‐Scaffold‐Inspired Asymmetric Synthesis of Polysubstituted Chiral Hexahydropyridazines that Potently Inhibit Breast Cancer Cell Proliferation by Inducing Apoptosis
inferred← citeshttps://doi.org/10.1002/chem.201503352openalex-snapshot
Organocatalytic Asymmetric Conjugate Additions to Cyclopent‐1‐enecarbaldehyde: A Critical Assessment of Organocatalytic Approaches towards the Telaprevir Bicyclic Core
inferred← citeshttps://doi.org/10.1002/chem.201602884openalex-snapshot
Design of Selenium‐Based Chiral Chemical Probes for Simultaneous Enantio‐ and Chemosensing of Chiral Carboxylic Acids with Remote Stereogenic Centers by NMR Spectroscopy
inferred← citeshttps://doi.org/10.1002/chem.201705010openalex-snapshot
Chemo‐ and Stereoselective Cross Rauhut–Currier‐Type Reaction of Tri‐substituted Alkenes Containing Trifluoromethyl Groups
inferred← citeshttps://doi.org/10.1002/chem.201905704openalex-snapshot
Ambident Reactivity of Imidazolium Cations as Evidence of the Dynamic Nature of N‐Heterocyclic Carbene‐Mediated Organocatalysis
inferred← citeshttps://doi.org/10.1002/chem.202302764openalex-snapshot
Nucleophilicity of 4‐(Alkylthio)‐3‐imidazoline Derived Enamines
inferred← citeshttps://doi.org/10.1002/chin.201322216openalex-snapshot
ChemInform Abstract: Applications of Asymmetric Organocatalysis in Medicinal Chemistry
inferred← citeshttps://doi.org/10.1002/chir.22303openalex-snapshot
A Practical and Stereoselective Organocatalytic Alkylation of Aldehydes with Benzodithiolylium Tetrafluoroborate
inferred← citeshttps://doi.org/10.1002/chir.22794openalex-snapshot
High‐performance liquid chromatographic enantioseparation of N‐aryl‐thioureidoalkylphosphonates and thiourylenedi(alkylphosphonates) on polysaccharide‐based chiral stationary phases
inferred← citeshttps://doi.org/10.1002/chir.23137openalex-snapshot
Chiral Imidazolidin‐4‐one with catalytic amount of Dicationic ionic liquid act as a recoverable and reusable Organocatalyst for asymmetric Diels‐Alder reaction
inferred← citeshttps://doi.org/10.1002/chir.23633openalex-snapshot
Chiral measure of chiral polyhedrons
inferred← citeshttps://doi.org/10.1002/cjoc.201400836openalex-snapshot
One‐Pot Synthesis of Aliphatic Nitro Compounds by Michael/retro‐Claisen Fragmentation Domino Reaction
inferred← citeshttps://doi.org/10.1002/cmdc.202200104openalex-snapshot
Design, Synthesis, and Biological Evaluation of Tetrahydro‐α‐carbolines as Akt1 Inhibitors That Inhibit Colorectal Cancer Cell Proliferation
inferred← citeshttps://doi.org/10.1002/cphc.201501063openalex-snapshot
Catalysts Encapsulated in Molecular Machines
inferred← citeshttps://doi.org/10.1002/cplu.201600062openalex-snapshot
A pH‐Responsive Soluble‐Polymer‐Based Homogeneous Ruthenium Catalyst for Highly Efficient Asymmetric Transfer Hydrogenation (ATH)
inferred← citeshttps://doi.org/10.1002/cssc.201902500openalex-snapshot
Valorization of Waste: Sustainable Organocatalysts from Renewable Resources
inferred← citeshttps://doi.org/10.1002/ejoc.201300331openalex-snapshot
Bifunctional Primary Amine‐Squaramide Catalyzed Enantioselective Intramolecular Michael Addition of Keto‐enones: A Convenient Process to the Stereocontrolled Construction of trans‐Dihydrobenzofuran Skeletons
inferred← citeshttps://doi.org/10.1002/ejoc.201402243openalex-snapshot
Highly Enantioselective Michael Addition of Malonates to β‐CF3‐β‐(3‐Indolyl)nitroalkenes: Construction of Trifluoromethylated All‐Carbon Quaternary Stereogenic Centres
inferred← citeshttps://doi.org/10.1002/ejoc.201403180openalex-snapshot
Cinchona‐Derived Picolinamides: Effective Organocatalysts for Stereoselective Imine Hydrosilylation
inferred← citeshttps://doi.org/10.1002/ejoc.201500616openalex-snapshot
Construction of Diverse and Functionalized 2H‐Chromenes by Organocatalytic Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201501618openalex-snapshot
Enantioselective Catalytic Domino Aza‐Michael–Henry Reactions: One‐Pot Asymmetric Synthesis of 3‐Nitro‐1,2‐dihydroquinolines via Iminium Activation
inferred← citeshttps://doi.org/10.1002/ejoc.201601357openalex-snapshot
Organocatalyst Efficiency in the α‐Aminoxylation and α‐Hydrazination of Carbonyl Derivatives in Aqueous Media or in a Ball‐Mill
inferred← citeshttps://doi.org/10.1002/ejoc.201700133openalex-snapshot
Chiral Imidazolium Ionic Liquids Derived from (S)‐Prolinamine as Organocatalysts in the Asymmetric Michael Reaction and Michael‐Aldol Cascade Reaction under Solvent‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201800236openalex-snapshot
Organocatalytic Enantioselective Synthesis of Tetrahydropyridines
inferred← citeshttps://doi.org/10.1002/ejoc.201800746openalex-snapshot
Divergent Synthesis of Quinazolines Using Organocatalytic Domino Strategies under Aerobic Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201801339openalex-snapshot
Synthesis of a New N‐Diaminophosphoryl‐N′‐[(2S)‐2‐pyrrolidinylmethyl]thiourea as a Chiral Organocatalyst for the Stereoselective Michael Addition of Cyclohexanone to Nitrostyrenes and Chalcones – Application in Cascade Processes for the Synthesis of Polycyclic Systems
inferred← citeshttps://doi.org/10.1002/ejoc.201901344openalex-snapshot
Hydrogen Bonding and Internal or External Lewis or Brønsted Acid Assisted (Thio)urea Catalysts
inferred← citeshttps://doi.org/10.1002/ejoc.202000235openalex-snapshot
Synthesis of Chiral 3,4‐Disubstituted Pyrrolidines with Antibacterial Properties
inferred← citeshttps://doi.org/10.1002/ejoc.202100502openalex-snapshot
Organocatalytic Desymmetrization of Meso‐Aziridines Via Asymmetric Intramolecular Rearrangement
inferred← citeshttps://doi.org/10.1002/ejoc.202101042openalex-snapshot
Asymmetric Organocatalysis Accelerated via Self‐Assembled Minimal Structures
inferred← citeshttps://doi.org/10.1002/ejoc.202101171openalex-snapshot
Enantioselective Povarov Reactions: An Update of a Powerful Catalytic Synthetic Methodology
inferred← citeshttps://doi.org/10.1002/ejoc.202200962openalex-snapshot
Fast Transition Metal‐Free Synthesis of Functionalized Oxindoles and Dihydroquinoline‐2‐ones Under Microwave Irradiation
inferred← citeshttps://doi.org/10.1002/ejoc.202400373openalex-snapshot
2‐Methylene‐1,2‐dihydropyridines (2‐pyNHOs): Highly Nucleophilic Enamines
inferred← citeshttps://doi.org/10.1002/ejoc.202401048openalex-snapshot
Synthetic Approaches for the Construction of Chiral Aziridines
inferred← citeshttps://doi.org/10.1002/ejoc.202500338openalex-snapshot
A C 3 ‐Symmetric Diphenylethylendiamine‐Based Catalyst in the Asymmetric Michael Addition of α,β‐Unsaturated Ketones with 4‐Hydroxycoumarin and 4‐Hydroxyquinolin‐2‐One
inferred← citeshttps://doi.org/10.1002/ejoc.70549openalex-snapshot
Redox Properties of Catalytically Generated Iminium Ions From α,β‐Unsaturated Aldehydes and Chiral Secondary Amines
inferred← citeshttps://doi.org/10.1002/elps.70061openalex-snapshot
Mirror‐Image β‐ l ‐Cyclodextrin as a Chiral Pseudophase in Capillary Electrophoresis
inferred← citeshttps://doi.org/10.1002/slct.201601165openalex-snapshot
Phenyl (2‐quinolyl) methanol: A Valuable Reagent for Metal‐Free Reduction of Aromatic Nitro Compounds and Imines
inferred← citeshttps://doi.org/10.1002/slct.201601213openalex-snapshot
Short Synthesis of Novel Recyclable Chiral Bifunctional Thioureas from Aminoalkyl Polystyrene and their use as Organocatalysts in Stereoselective aza‐Henry Reaction.
inferred← citeshttps://doi.org/10.1002/slct.201601859openalex-snapshot
Recyclable Silica‐Supported Proline Sulphonamide Organocatalysts for Asymmetric Direct Aldol Reaction.
inferred← citeshttps://doi.org/10.1002/slct.201904059openalex-snapshot
Amino‐Acid‐Mediated Aerobic Oxidation of Organoborons for the Synthesis of Phenolic Derivatives Using Single Electron Transfer
inferred← citeshttps://doi.org/10.1002/slct.202002765openalex-snapshot
Recent Advances in Pyridine‐Based Organocatalysis and its Application towards Valuable Chemical Transformations
inferred← citeshttps://doi.org/10.1002/slct.202100679openalex-snapshot
Recent Advances in Organocatalytic Asymmetric Michael Addition Reactions to α, β‐Unsaturated Nitroolefins
inferred← citeshttps://doi.org/10.1002/slct.202300204openalex-snapshot
The Importance of Organocatalysis (Asymmetric and Non‐Asymmetric) in Agrochemicals
inferred← citeshttps://doi.org/10.1002/slct.202403964openalex-snapshot
Dipeptidic Proline Amide–Isothiouronium Salt Organocatalysts for Enantiodivergent Conjugate Addition Reactions Between Aldehydes and Nitroolefins
inferred← citeshttps://doi.org/10.1002/tcr.201500286openalex-snapshot
Harnessing the Versatility of Continuous-Flow Processes: Selective and Efficient Reactions
inferred← citeshttps://doi.org/10.1002/tcr.201800047openalex-snapshot
Organocatalytic Asymmetric Cascade Reactions Based on Gamma‐Nitro Carbonyl Compound
inferred← citeshttps://doi.org/10.1002/tcr.201800190openalex-snapshot
Organocatalyzed Asymmetric Friedel‐Crafts Reactions: An Update
inferred← citeshttps://doi.org/10.1002/tcr.201800199openalex-snapshot
Catalytic Asymmetric Synthesis of Spiropyrazolones and their Application in Medicinal Chemistry
inferred← citeshttps://doi.org/10.1007/7355_2021_119openalex-snapshot
Organocatalysis in Continuous Flow for Drug Discovery
inferred← citeshttps://doi.org/10.1007/s00044-016-1589-8openalex-snapshot
POM analyses and evaluation of in vitro antimicrobial, antitumor activity of 4H-pyrimido[2,1-b]benzothiazole derivatives
inferred← citeshttps://doi.org/10.1007/s00253-026-13717-0openalex-snapshot
Highly enantioselective reduction of benzophenones by engineered Geotrichum candidum alcohol dehydrogenase
inferred← citeshttps://doi.org/10.1007/s00706-015-1486-8openalex-snapshot
Optimization of stereoselective Michael addition of 2-(pentan-3-yloxy)acetaldehyde to N-[(Z)-2-nitroethenyl]acetamide with the aid of design of experiments
inferred← citeshttps://doi.org/10.1007/s10562-017-2015-7openalex-snapshot
A New Type of Magnetically-Recoverable Heteropolyacid Nanocatalyst Supported on Zirconia-Encapsulated Fe3O4 Nanoparticles as a Stable and Strong Solid Acid for Multicomponent Reactions
inferred← citeshttps://doi.org/10.1007/s11164-015-2249-1openalex-snapshot
Recyclable task-specific acidic ionic liquid [NMP]H2PO4: Microwave-assisted, efficient one-pot, two-step tandem synthesis of fused thiazolo[2,3-b]quinazolinone and thiazolo[2,3-b]quinazoline derivatives
inferred← citeshttps://doi.org/10.1007/s11164-020-04361-yopenalex-snapshot
Synthesis of a novel acidic ionic liquid catalyst and its application for preparation of pyridines via a cooperative vinylogous anomeric-based oxidation
inferred← citeshttps://doi.org/10.1007/s11164-025-05635-zopenalex-snapshot
Chiral guanidine-functionalized chloramphenicol base: a novel ultra-low-loading bifunctional organocatalyst for highly enantioselective alcoholysis of meso-cyclic anhydride
inferred← citeshttps://doi.org/10.1007/s11172-021-3163-xopenalex-snapshot
Novel C2-symmetric phenylglycine derivatives as organocatalysts of the Michael reaction between nitroalkenes and ketones
inferred← citeshttps://doi.org/10.1007/s11237-022-09710-zopenalex-snapshot
Modern Approaches to Synthetic Design of Chiral α-Tertiary Amines Based on Trifluoromethylcontaining Ketimines: A Review
inferred← citeshttps://doi.org/10.1007/s13738-017-1157-2openalex-snapshot
Magnetic nanoparticles grafted l-carnosine dipeptide: remarkable catalytic activity in water at room temperature
inferred← citeshttps://doi.org/10.1016/b978-0-12-813594-5.00010-2openalex-snapshot
Nanomagnetic-Supported Catalysts
inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00025-5openalex-snapshot
Organic synthetic methodology-based new scaffolds in drug discovery
inferred← citeshttps://doi.org/10.1016/bs.acat.2025.10.003openalex-snapshot
Homogeneous catalysis in continuous flow. Metal and organo-catalysis
inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.04.002openalex-snapshot
The Literature of Heterocyclic Chemistry, Part XIII, 2012–2013
inferred← citeshttps://doi.org/10.1016/j.catcom.2013.08.015openalex-snapshot
1,4-Michael additions of cyclic-β-ketoesters catalyzed by DNA in aqueous media
inferred← citeshttps://doi.org/10.1016/j.chroma.2014.04.080openalex-snapshot
Enantiomeric separation of biaryl atropisomers using cyclofructan based chiral stationary phases
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.12.002openalex-snapshot
Synthesis and biological evaluation of cyanoaziridine phosphine oxides and phosphonates with antiproliferative activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.115009openalex-snapshot
Discovery of tetrahydrofuranyl spirooxindole-based SMYD3 inhibitors against gastric cancer via inducing lethal autophagy
inferred← citeshttps://doi.org/10.1016/j.jcat.2013.05.010openalex-snapshot
Potassium fluoride: A convenient, non-covalent support for the immobilization of organocatalysts through strong hydrogen bonds
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115366openalex-snapshot
Novel porous organic polymer supported chloramphenicol base derivatives: A highly enantioselective, recyclable heterogeneous organocatalyst for asymmetric desymmetrization reaction
inferred← citeshttps://doi.org/10.1016/j.jcou.2020.01.024openalex-snapshot
Carboxylative cyclization of propargylic alcohols with carbon dioxide: A facile and Green route to α-methylene cyclic carbonates
inferred← citeshttps://doi.org/10.1016/j.jiec.2015.03.035openalex-snapshot
Sustainable alternative protocols for the multicomponent synthesis of spiro-4H-pyrans catalyzed by 4-dimethylaminopyridine
inferred← citeshttps://doi.org/10.1016/j.matchemphys.2019.122298openalex-snapshot
Graphene-based recyclable and bifunctional heterogeneous chiral catalyst for direct asymmetric aldol reaction
inferred← citeshttps://doi.org/10.1016/j.mcat.2017.03.003openalex-snapshot
9-Amino(9-deoxy)epi-cinchona alkaloid-tethered aluminium phosphonate architectures for heterogeneous cooperative catalysis: asymmetric aldol and double-Michael cascade reaction
inferred← citeshttps://doi.org/10.1016/j.mcat.2019.110744openalex-snapshot
Knoevenagel-Doebner condensation promoted by chitosan as a reusable solid base catalyst
inferred← citeshttps://doi.org/10.1016/j.mcat.2020.110814openalex-snapshot
Innovative catalysis in Michael addition reactions for C-X bond formation
inferred← citeshttps://doi.org/10.1016/j.mcat.2020.111071openalex-snapshot
Co-catalyst and solvent free nitrogen rich triazole based organocatalysts for cycloaddition of CO2 into epoxide
inferred← citeshttps://doi.org/10.1016/j.mencom.2015.11.001openalex-snapshot
Novel approaches to pharmacology-oriented and energy rich organic nitrogen–oxygen systems
inferred← citeshttps://doi.org/10.1016/j.mencom.2016.09.001openalex-snapshot
Challenges in the development of organic and hybrid molecular systems
inferred← citeshttps://doi.org/10.1016/j.mencom.2017.11.001openalex-snapshot
Recent advances in synthesis of organic nitrogen–oxygen systems for medicine and materials science
inferred← citeshttps://doi.org/10.1016/j.molcata.2016.03.013openalex-snapshot
Weakly bounded intermediates as a previous step towards highly-enantioselective iminium type additions of β-keto-sulfoxides and -sulfones
inferred← citeshttps://doi.org/10.1016/j.nantod.2013.07.002openalex-snapshot
Superhydrophobic, chiral, and mesoporous TsDPEN copolymer coordinated to ruthenium species as an efficient catalyst for asymmetric transfer hydrogenation
inferred← citeshttps://doi.org/10.1016/j.nantod.2026.103136openalex-snapshot
Nanocarbons as organocatalysts for asymmetric reactions: A critical evaluation against conventional catalysis
inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103825openalex-snapshot
Unravelling the mechanism of thiourea-enabled N-heterocyclic carbene catalysis in dihydrocoumarin synthesis: A theoretical investigation
inferred← citeshttps://doi.org/10.1016/j.supflu.2015.11.004openalex-snapshot
Asymmetric catalytic synthesis of functionalized tetrahydroquinolines in supercritical fluids
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.116openalex-snapshot
Asymmetric Michael addition of 4H-thiopyran-4-one to nitroolefins catalyzed by diamine mono-N-sulfonamide and its application to concise synthesis of enantiopure multiring heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2013.10.033openalex-snapshot
Task-specific ionic liquid incorporating anionic heteropolyacid-catalyzed Hantzsch and Mannich multicomponent reactions. Ionic liquid effect probed by ESI-MS(/MS)
inferred← citeshttps://doi.org/10.1016/j.tet.2013.12.007openalex-snapshot
tert-Butyl esters of tripeptides based on Pro-Phe as organocatalysts for the asymmetric aldol reaction in aqueous or organic medium
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.016openalex-snapshot
Evaluation of mono- and dipeptides as organocatalysts for enantioselective aldol reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2014.07.023openalex-snapshot
Organocatalytic transformations of alkynals, alkynones, propriolates, and related electron-deficient alkynes
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.078openalex-snapshot
tert-Butyl ester or benzylamide of the dipeptide Pro-Gly as organocatalysts for the asymmetric aldol reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2016.07.067openalex-snapshot
Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients
inferred← citeshttps://doi.org/10.1016/j.tet.2018.03.054openalex-snapshot
Combining prolinamides with 2-pyrrolidinone: Novel organocatalysts for the asymmetric aldol reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2018.06.015openalex-snapshot
Recent advances in the asymmetric catalytic synthesis of chiral 3-hydroxy and 3-aminooxindoles and derivatives: Medicinally relevant compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2018.07.043openalex-snapshot
Recyclable C2-symmetric tertiary amine-squaramide organocatalysts: Design and application to asymmetric synthesis of γ-nitrocarbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2018.08.038openalex-snapshot
Proline dipeptides containing fluorine moieties as oganocatalysts for the asymmetric aldol reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2018.11.052openalex-snapshot
Phosphinoyl-aziridines as a new class of chiral catalysts for enantioselective Michael addition
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132143openalex-snapshot
Recent developments in next generation (S)-proline-derived chiral organocatalysts
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134112openalex-snapshot
Novel centratherin derivatives: Molecular docking design, asymmetric synthesis, and antitumoral activity
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134129openalex-snapshot
Some contributions to three relevant areas in organic stereochemistry during the last decade: (1) conformational effects, (2) asymmetric organocatalysis, and (3) mechanoenzymatic processes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.03.002openalex-snapshot
Organocatalytic asymmetric synthesis of 3-amino-2-oxindole derivatives bearing a tetra-substituted stereocenter
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.06.009openalex-snapshot
Enantioselective Michael addition of α,α-disubstituted aldehydes to nitroolefins catalyzed by a pyrrolidine-pyrazole
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.07.005openalex-snapshot
Asymmetric Michael addition of aldehydes to nitroolefins catalyzed by a pyrrolidine–pyrazole
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.10.014openalex-snapshot
Pyrrolidine-oxyimides: new chiral catalysts for enantioselective Michael addition of ketones to nitroolefins in water
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.12.007openalex-snapshot
tert-Butyl esters of peptides as organocatalysts for the asymmetric aldol reaction
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.04.010openalex-snapshot
A highly enantio- and diastereoselective direct aldol reaction in aqueous medium catalyzed by thiazolidine-based compounds
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.07.009openalex-snapshot
Pyrrolidine–oxyimide catalyzed asymmetric Michael addition of α,α-disubstituted aldehydes to nitroolefins
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.08.006openalex-snapshot
Pyrrolidine-HOBt: an oxytriazole catalyst for the enantioselective Michael addition of cyclohexanone to nitroolefins in water
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.02.005openalex-snapshot
Enantioselective Michael addition of aldehydes to nitroolefins catalyzed by pyrrolidine-HOBt
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.02.006openalex-snapshot
Evolution of synthetic routes towards homochiral Tapentadol
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.03.002openalex-snapshot
Solvent free, fast and asymmetric Michael additions of ketones to nitroolefins using chiral pyrrolidine–pyridone conjugate bases as organocatalysts
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.09.006openalex-snapshot
Thermal racemization of biaryl atropisomers
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.068openalex-snapshot
p-tert-Butylcalix[8]arene catalysed synthesis of 3,5-dinitrothiophene scaffolds: antiproliferative effect of some representative compounds on selective anticancer cell lines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.07.075openalex-snapshot
Catalytic asymmetric reactions in alkaloid and terpenoid syntheses
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.053openalex-snapshot
Organocatalytic aldol addition reaction of cyclic hemiacetals to aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.05.012openalex-snapshot
The impact of asymmetric organocatalysis in dearomatization and aromatization of carbocycles: increasing molecular complexity and diversity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.05.053openalex-snapshot
Enantioselective organocatalytic approach to δ-lactones bearing a fused cyclohexanone scaffold
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.07.020openalex-snapshot
Asymmetric synthesis and antiviral activity of novel chiral amino-pyrimidine derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.05.065openalex-snapshot
Recent applications of mechanochemistry in enantioselective synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151131openalex-snapshot
N-Heterocyclic carbene as a Brønsted base catalyst for the amination of naphthol derivatives and alcoholysis of glutaric anhydrides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152792openalex-snapshot
Polysulfonate supported chiral diamine-nickel catalysts: Synthesis and applications
inferred← citeshttps://doi.org/10.1016/j.trechm.2021.12.010openalex-snapshot
Recent advances towards organocatalytic enantioselective desymmetrizing reactions
inferred← citeshttps://doi.org/10.1021/acs.accounts.9b00549openalex-snapshot
Organocatalytic Asymmetric Synthesis of Indole-Based Chiral Heterocycles: Strategies, Reactions, and Outreach
inferred← citeshttps://doi.org/10.1021/acs.chemmater.8b02884openalex-snapshot
Hierarchically Porous Single Nanocrystals of Bimetallic Metal–Organic Framework for Nanoreactors with Enhanced Conversion
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00156openalex-snapshot
Enantioselective Organocatalyzed Transformations of β-Ketoesters
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00657openalex-snapshot
Organocatalysis in Inert C–H Bond Functionalization
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00183openalex-snapshot
The Hitchhiker’s Guide to Flow Chemistry
inferred← citeshttps://doi.org/10.1021/acs.chemrev.9b00338openalex-snapshot
Chiral Hypervalent Iodines: Active Players in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02081openalex-snapshot
Organocatalyzed Sulfa-Michael Addition of Thiophenols on Trisubstituted α-Fluoroacrylates, a Straightforward Access to Chiral Fluorinated Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00124openalex-snapshot
Asymmetric 1,4-Michael Addition in Aqueous Medium Using Hydrophobic Chiral Organocatalysts
showing the first 200 of 399 · page through all 399
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.