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Stronger Brønsted Acids
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20001215)39:24<4518::aid-anie4518>3.0.co;2-jopenalex-snapshot
Catalytic Asymmetric Aziridination with Arylborate Catalysts Derived from VAPOL and VANOL Ligands
inferredcites →https://doi.org/10.1002/1521-3773(20011105)40:21<4077::aid-anie4077>3.0.co;2-1openalex-snapshot
Polystyrene-Bound Tetrafluorophenylbis(triflyl)methane as an Organic-Solvent-Swellable and Strong Brønsted Acid Catalyst The authors thank Mr. Shoichi Kondo for the single-crystal X-ray analysis. Sodium triflate was generously donated by Central Glass Co., Ltd., Japan. The authors also acknowledge…
inferredcites →https://doi.org/10.1002/ange.200503477openalex-snapshot
High Substrate/Catalyst Organocatalysis by a Chiral Brønsted Acid for an Enantioselective Aza‐Ene‐Type Reaction
inferredcites →https://doi.org/10.1002/anie.200353237openalex-snapshot
Copper( II )‐Catalyzed Highly Enantioselective Addition of Enamides to Imines: The Use of Enamides as Nucleophiles in Asymmetric Catalysis
inferredcites →https://doi.org/10.1002/anie.200353240openalex-snapshot
Enantioselective Mannich‐Type Reaction Catalyzed by a Chiral Brønsted Acid
inferredcites →https://doi.org/10.1002/anie.200461816openalex-snapshot
A Metal‐Free Transfer Hydrogenation: Organocatalytic Conjugate Reduction of α,β‐Unsaturated Aldehydes
inferredcites →https://doi.org/10.1002/anie.200503062openalex-snapshot
A Powerful Brønsted Acid Catalyst for the Organocatalytic Asymmetric Transfer Hydrogenation of Imines
inferredcites →https://doi.org/10.1002/anie.200503477openalex-snapshot
High Substrate/Catalyst Organocatalysis by a Chiral Brønsted Acid for an Enantioselective Aza‐Ene‐Type Reaction
inferredcites →https://doi.org/10.1002/anie.200504344openalex-snapshot
A Highly Enantioselective Brønsted Acid Catalyst for the Strecker Reaction
inferredcites →https://doi.org/10.1002/anie.200600191openalex-snapshot
A Highly Enantioselective Brønsted Acid Catalyzed Cascade Reaction: Organocatalytic Transfer Hydrogenation of Quinolines and their Application in the Synthesis of Alkaloids
inferredcites →https://doi.org/10.1002/anie.200600512openalex-snapshot
Asymmetric Counteranion‐Directed Catalysis
inferredcites →https://doi.org/10.1002/anie.200600529openalex-snapshot
Chiral Phosphoric Acids: Powerful Organocatalysts for Asymmetric Addition Reactions to Imines
inferredcites →https://doi.org/10.1002/anie.200601345openalex-snapshot
Chiral Brønsted Acid Catalyzed Enantioselective Aza‐Diels–Alder Reaction of Brassard's Diene with Imines
inferredcites →https://doi.org/10.1002/anie.200601832openalex-snapshot
Remarkably Low Catalyst Loading in Brønsted Acid Catalyzed Transfer Hydrogenations: Enantioselective Reduction of Benzoxazines, Benzothiazines, and Benzoxazinones
inferredcites →https://doi.org/10.1002/anie.200603199openalex-snapshot
Cooperative Coexistence: Effective Interplay of Two Brønsted Acids in the Asymmetric Synthesis of Isoquinuclidines
inferredcites →https://doi.org/10.1002/anie.200604809openalex-snapshot
Chiral Brønsted Acids in the Catalytic Asymmetric Nazarov Cyclization—The First Enantioselective Organocatalytic Electrocyclic Reaction
inferredcites →https://doi.org/10.1002/chin.200723161openalex-snapshot
Diastereo‐ and Enantioselective Synthesis of Nitroso Diels—Alder‐Type Bicycloketones Using Dienamine: Mechanistic Insight into Sequential Nitroso Aldol/Michael Reaction and Application for Optically Pure 1‐Amino‐3,4‐diol Synthesis.
inferredcites →https://doi.org/10.1002/tcr.10020openalex-snapshot
Chiral Proton Donor Reagents: Tin Tetrachloride—Coordinated Optically Active Binaphthol Derivatives
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(89)80016-xopenalex-snapshot
Stereochemical and spectroscopic studies on the reaction of allylstannanes with aldehydes
inferredcites →https://doi.org/10.1016/0040-4039(95)00065-kopenalex-snapshot
Silicon-directed cyclization of vinylsilanes bearing hydroxy group catalyzed by an acid
inferredcites →https://doi.org/10.1016/j.tetlet.2004.09.174openalex-snapshot
A new class of metal-free catalysts for direct diastereo- and regioselective Mannich reactions in aqueous media
inferredcites →https://doi.org/10.1016/j.tetlet.2006.11.017openalex-snapshot
On the mechanism of stereoselection in direct Mannich reaction catalyzed by BINOL-derived phosphoric acids
inferredcites →https://doi.org/10.1016/s0040-4020(01)00185-5openalex-snapshot
Triphenyl phosphonium perchlorate—an efficient catalyst for the imino Diels–Alder reaction of imines with electron rich dienophiles. Synthesis of pyranoquinoline, furoquinoline and phenanthridine derivatives
inferredcites →https://doi.org/10.1016/s0040-4020(01)00438-0openalex-snapshot
Recent developments in imino Diels–Alder reactions
inferredcites →https://doi.org/10.1016/s0040-4039(00)82208-xopenalex-snapshot
Role reversal in the cyclocondensation of cyclopentadiene with heterodienophiles derived from aryl amines and aldehydes: Synthesis of novel tetrahydroquinolines
inferredcites →https://doi.org/10.1016/s0040-4039(00)91783-0openalex-snapshot
Cyclic transition state in the acid catalyzed intramolecular allylstannane-aldehyde condensation
inferredcites →https://doi.org/10.1016/s0040-4039(01)86747-2openalex-snapshot
Regiospecific syntheses of quinones using vinylketene acetals derived from unsaturated esters
inferredcites →https://doi.org/10.1016/s0040-4039(99)00122-7openalex-snapshot
Trifluoromethane sulphonic acid: a Brönsted acid catalyst for the addition of allyltributylstannanes to carbonyl compounds in water
inferredcites →https://doi.org/10.1016/s0040-4039(99)00680-2openalex-snapshot
Chiral syntheses of 2,3,5-trisubstituted pyrrolidines by silicon-directed cyclization of allylsilanes bearing a sulfonamide moiety
inferredcites →https://doi.org/10.1016/s0040-4039(99)01630-5openalex-snapshot
Brønsted acid-catalyzed aza Diels-Alder reaction of Danishefsky's diene with aldimine generated in situ from aldehyde and amine in aqueous media
inferredcites →https://doi.org/10.1016/s0957-4166(00)80023-3openalex-snapshot
Asymmetric aza Diels-Alder reactions of amino acid ester imines with Brassard's diene
inferredcites →https://doi.org/10.1021/cr00022a010openalex-snapshot
Selective reactions using allylic metals
inferredcites →https://doi.org/10.1021/cr010043dopenalex-snapshot
Recent Advances in the Baylis−Hillman Reaction and Applications
inferredcites →https://doi.org/10.1021/cr020020eopenalex-snapshot
Enantioselective Amino Acid Synthesis by Chiral Phase-Transfer Catalysis
inferredcites →https://doi.org/10.1021/cr941074uopenalex-snapshot
Stereochemical Control in Organic Synthesis Using Silicon-Containing Compounds
inferredcites →https://doi.org/10.1021/cr960433dopenalex-snapshot
Metal-Initiated Amination of Alkenes and Alkynes
inferredcites →https://doi.org/10.1021/cr980414zopenalex-snapshot
Catalytic Enantioselective Addition to Imines
inferredcites →https://doi.org/10.1021/ja00075a060openalex-snapshot
Highly chemoselective allylation of carbonyl compounds with tetraallyltin in acidic aqueous media
inferredcites →https://doi.org/10.1021/ja00103a052openalex-snapshot
Lewis Acid Assisted Chiral Bronsted Acid for Enantioselective Protonation of Silyl Enol Ethers and Ketene Bis(trialkylsilyl) Acetals
inferredcites →https://doi.org/10.1021/ja00191a079openalex-snapshot
Mechanistic and stereochemical divergence in the allylsilane-acetal addition reaction
inferredcites →https://doi.org/10.1021/ja00292a057openalex-snapshot
Aza Diels-Alder reactions in aqueous solution: cyclocondensation of dienes with simple iminium salts generated under Mannich conditions
inferredcites →https://doi.org/10.1021/ja00832a031openalex-snapshot
Useful diene for the Diels-Alder reaction
inferredcites →https://doi.org/10.1021/ja01101a514openalex-snapshot
The Mechanism of the Acid-catalyzed Hydration of Olefins1
inferredcites →https://doi.org/10.1021/ja016338qopenalex-snapshot
Dehydration Reactions in Water. Surfactant-Type Brønsted Acid-Catalyzed Direct Esterification of Carboxylic Acids with Alcohols in an Emulsion System
inferredcites →https://doi.org/10.1021/ja031906iopenalex-snapshot
Chiral Proton Catalysis: A Catalytic Enantioselective Direct Aza-Henry Reaction
inferredcites →https://doi.org/10.1021/ja037705wopenalex-snapshot
Asymmetric Morita−Baylis−Hillman Reactions Catalyzed by Chiral Brønsted Acids
inferredcites →https://doi.org/10.1021/ja0385282openalex-snapshot
The Brønsted Acid-Catalyzed Direct Aza-Darzens Synthesis of N-Alkyl cis-Aziridines
inferredcites →https://doi.org/10.1021/ja0444637openalex-snapshot
Brønsted Acid Catalysis of Achiral Enamine for Regio- and Enantioselective Nitroso Aldol Synthesis
inferredcites →https://doi.org/10.1021/ja046185hopenalex-snapshot
Organocatalytic Asymmetric Aza-Friedel−Crafts Alkylation of Furan
inferredcites →https://doi.org/10.1021/ja046259popenalex-snapshot
Highly Enantioselective Catalytic Acyl-Pictet−Spengler Reactions
inferredcites →https://doi.org/10.1021/ja046586xopenalex-snapshot
Brønsted Acid-Promoted Cyclizations of Siloxyalkynes with Arenes and Alkenes
inferredcites →https://doi.org/10.1021/ja0491533openalex-snapshot
Chiral Brønsted Acid-Catalyzed Direct Mannich Reactions via Electrophilic Activation
inferredcites →https://doi.org/10.1021/ja0500254openalex-snapshot
Bifunctional Organocatalysts for Enantioselective aza-Morita−Baylis−Hillman Reaction
inferredcites →https://doi.org/10.1021/ja051922aopenalex-snapshot
Organocatalytic Asymmetric Direct Alkylation of α-Diazoester via C−H Bond Cleavage
inferredcites →https://doi.org/10.1021/ja0533085openalex-snapshot
Brønsted Acid-Catalyzed Imine Amidation
inferredcites →https://doi.org/10.1021/ja053700iopenalex-snapshot
Proton-Catalyzed Hydroamination and Hydroarylation Reactions of Anilines and Alkenes: A Dramatic Effect of Counteranions on Reaction Efficiency
inferredcites →https://doi.org/10.1021/ja054171lopenalex-snapshot
Brønsted Acid-Catalyzed Allylboration: Short and Stereodivergent Synthesis of All Four Eupomatilone Diastereomers with Crystallographic Assignments
inferredcites →https://doi.org/10.1021/ja055735oopenalex-snapshot
Catalytic Asymmetric Reductive Michael Cyclization
inferredcites →https://doi.org/10.1021/ja056092fopenalex-snapshot
Highly Enantioseletive Biginelli Reaction Using a New Chiral Ytterbium Catalyst: Asymmetric Synthesis of Dihydropyrimidines
inferredcites →https://doi.org/10.1021/ja057222nopenalex-snapshot
Enantioselective Organocatalytic Reductive Amination
inferredcites →https://doi.org/10.1021/ja057444lopenalex-snapshot
Catalytic Asymmetric Pictet−Spengler Reaction
inferredcites →https://doi.org/10.1021/ja062508topenalex-snapshot
Design of Chiral N-Triflyl Phosphoramide as a Strong Chiral Brønsted Acid and Its Application to Asymmetric Diels−Alder Reaction
inferredcites →https://doi.org/10.1021/ja064676ropenalex-snapshot
Chiral Brønsted Acid-Catalyzed Inverse Electron-Demand Aza Diels−Alder Reaction
inferredcites →https://doi.org/10.1021/ja065267yopenalex-snapshot
Highly Enantioselective Organocatalytic Biginelli Reaction
inferredcites →https://doi.org/10.1021/ja065404ropenalex-snapshot
Catalytic Asymmetric Reductive Amination of Aldehydes via Dynamic Kinetic Resolution
inferredcites →https://doi.org/10.1021/ja065708dopenalex-snapshot
Highly Enantioselective Transfer Hydrogenation of α,β-Unsaturated Ketones
inferredcites →https://doi.org/10.1021/ja066037mopenalex-snapshot
Diastereo- and Enantioselective Synthesis of Nitroso Diels−Alder-Type Bicycloketones Using Dienamine: Mechanistic Insight into Sequential Nitroso Aldol/Michael Reaction and Application for Optically Pure 1-Amino-3,4-diol Synthesis
inferredcites →https://doi.org/10.1021/ja0673027openalex-snapshot
Enantioselective Reductive Coupling of 1,3-Enynes to Heterocyclic Aromatic Aldehydes and Ketones via Rhodium-Catalyzed Asymmetric Hydrogenation: Mechanistic Insight into the Role of Brønsted Acid Additives
inferredcites →https://doi.org/10.1021/ja067417aopenalex-snapshot
Highly Enantioselective Friedel−Crafts Reaction of Indoles with Imines by a Chiral Phosphoric Acid
inferredcites →https://doi.org/10.1021/ja0678166openalex-snapshot
Enantioselective Friedel−Crafts Reaction of Electron-Rich Alkenes Catalyzed by Chiral Brønsted Acid
inferredcites →https://doi.org/10.1021/ja068073ropenalex-snapshot
Chiral Proton Catalysis: Enantioselective Brønsted Acid Catalyzed Additions of Nitroacetic Acid Derivatives as Glycine Equivalents
inferredcites →https://doi.org/10.1021/ja068236bopenalex-snapshot
Chiral Brønsted Acid-Catalyzed Direct Asymmetric Mannich Reaction
inferredcites →https://doi.org/10.1021/ja0684803openalex-snapshot
Chiral Brønsted Acid Catalyzed Enantioselective Mannich-Type Reaction
inferredcites →https://doi.org/10.1021/ja952018topenalex-snapshot
Synthesis, Resolution, and Determination of Absolute Configuration of a Vaulted 2,2‘-Binaphthol and a Vaulted 3,3‘-Biphenanthrol (VAPOL)
inferredcites →https://doi.org/10.1021/ja984064+openalex-snapshot
The First Enantioselective Biomimetic Cyclization of Polyprenoids
inferredcites →https://doi.org/10.1021/jo00002a003openalex-snapshot
Ruthenium-catalyzed allylation of primary alcohols by allylic acetates: a novel synthesis of .alpha.,.beta.-unsaturated ketones
inferredcites →https://doi.org/10.1021/jo00104a054openalex-snapshot
Effects of Olefin Geometry on the Stereochemistry of Lewis Acid Mediated Additions of Crotylstannanes to Aldehydes
inferredcites →https://doi.org/10.1021/jo981124lopenalex-snapshot
Spectrophotometric Acidity Scale of Strong Neutral Brønsted Acids in Acetonitrile
inferredcites →https://doi.org/10.1021/ol025659jopenalex-snapshot
Brønsted Acid-Catalyzed Intramolecular Hydroamination of Protected Alkenylamines. Synthesis of Pyrrolidines and Piperidines
inferredcites →https://doi.org/10.1021/ol034596hopenalex-snapshot
A General, Brønsted Acid-Catalyzed Hetero-Michael Addition of Nitrogen, Oxygen, and Sulfur Nucleophiles
inferredcites →https://doi.org/10.1021/ol0473391openalex-snapshot
Brønsted Acid-Catalyzed Highly Stereoselective Arene-Ynamide Cyclizations. A Novel Keteniminium Pictet−Spengler Cyclization in Total Syntheses of (±)-Desbromoarborescidines A and C
inferredcites →https://doi.org/10.1021/ol047341sopenalex-snapshot
Reversal of Chemoselectivity in Diels−Alder Reaction with α,β-Unsaturated Aldehydes and Ketones Catalyzed by Brønsted Acid or Lewis Acid
inferredcites →https://doi.org/10.1021/ol050695eopenalex-snapshot
Chiral Brønsted Acid Catalyzed Enantioselective Hydrophosphonylation of Imines: Asymmetric Synthesis of α-Amino Phosphonates
inferredcites →https://doi.org/10.1021/ol0515964openalex-snapshot
Enantioselective Brønsted Acid Catalyzed Transfer Hydrogenation: Organocatalytic Reduction of Imines
inferredcites →https://doi.org/10.1021/ol060939aopenalex-snapshot
Design of Brønsted Acid-Assisted Chiral Brønsted Acid Catalyst Bearing a Bis(triflyl)methyl Group for a Mannich-Type Reaction
inferredcites →https://doi.org/10.1021/ol0610035openalex-snapshot
Brønsted Acid Catalyzed Addition of Phenols, Carboxylic Acids, and Tosylamides to Simple Olefins
inferredcites →https://doi.org/10.1021/ol061174+openalex-snapshot
Hydroamination and Hydroalkoxylation Catalyzed by Triflic Acid. Parallels to Reactions Initiated with Metal Triflates
inferredcites →https://doi.org/10.1021/ol062499topenalex-snapshot
Enantioselective Direct Aza Hetero-Diels−Alder Reaction Catalyzed by Chiral Brønsted Acids
inferredcites →https://doi.org/10.1021/ol063112popenalex-snapshot
An Enantioselective Chiral Brønsted Acid Catalyzed Imino−Azaenamine Reaction
inferredcites →https://doi.org/10.1021/ol991113uopenalex-snapshot
Mannich-Type Reactions of Aldehydes, Amines, and Ketones in a Colloidal Dispersion System Created by a Brønsted Acid−Surfactant-Combined Catalyst in Water
inferredcites →https://doi.org/10.1021/ol991341oopenalex-snapshot
Acid-Catalyzed Cyclization of Vinylsilanes Bearing an Amino Group. Stereoselective Synthesis of Pyrrolidines1
inferredcites →https://doi.org/10.1038/214031a0openalex-snapshot
Substrate Specificity and Stereospecificity of Alcohol Dehydrogenases
inferredcites →https://doi.org/10.1038/424146aopenalex-snapshot
Single enantiomers from a chiral-alcohol catalyst
inferredcites →https://doi.org/10.1039/b304343fopenalex-snapshot
Mannich-type reactions in water using a hydrophobic polymer-supported sulfonic acid catalyst
inferredcites →https://doi.org/10.1039/b511216hopenalex-snapshot
Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors
inferredcites →https://doi.org/10.1039/b616143jopenalex-snapshot
An enantioselective Brønsted acid catalyzed enamine Mannich reaction
inferredcites →https://doi.org/10.1055/s-1997-1390openalex-snapshot
A Novel Synthesis of Deactivated Benzylic Triflones
inferredcites →https://doi.org/10.1055/s-1998-1888openalex-snapshot
Stereoselective Synthesis of 2,3,5-Substituted Tetrahydrofurans by Silicon-Directed Cyclization of Allylsilanes Bearing a Hydroxy Moiety
inferredcites →https://doi.org/10.1055/s-1999-2789openalex-snapshot
HBF4 Catalyzed Mannich-Type Reaction in Aqueous Media
inferredcites →https://doi.org/10.1055/s-1999-2871openalex-snapshot
A Brønsted Acid-Surfactant-Combined Catalyst for Mannich-Type Reactions of Aldehydes, Amines, and Silyl Enolates in Water
inferredcites →https://doi.org/10.1055/s-1999-2872openalex-snapshot
One-pot Mannich-Type Reaction In Water: HBF4 Catalyzed Condensation of Aldehydes, Amines, and Silyl Enolates for the Synthesis of β-Amino Carbonyl Compounds
inferredcites →https://doi.org/10.1055/s-2002-19329openalex-snapshot
Carbon-Carbon Bond Forming Reactions by using Bistrifluoromethanesulfonimide
inferredcites →https://doi.org/10.1055/s-2005-917098openalex-snapshot
Enantioselective Brønsted Acid Catalyzed Addition Reactions of Methyleneaminopyrrolidine to Imines
inferredcites →https://doi.org/10.1055/s-2005-922773openalex-snapshot
Enantioselective Aza-Diels-Alder Reaction Catalyzed by a Chiral Brønsted Acid: Effect of the Additive on the Enantioselectivity
inferredcites →https://doi.org/10.1055/s-2005-922783openalex-snapshot
Phosphorodiamidic Acid as a Novel Structural Motif of Brønsted Acid Catalysts for Direct Mannich Reaction ofN-Acyl Imines with 1,3-Dicarbonyl Compounds
inferredcites →https://doi.org/10.1246/cl.1978.267openalex-snapshot
ACID-CATALYZED [4+2]CYCLOADDITION BETWEEN ENAMINES AND BENZYLIDENEANILINES. SYNTHESIS OF 1,2,3,4-TETRAHYDROQUINOLINE DERIVATIVES
inferredcites →https://doi.org/10.1246/cl.2004.922openalex-snapshot
Synthesis of Aryl-substituted Quinoline Derivatives via Brønsted Acid-catalyzed [4+2] Aza Diels–Alder Reaction
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.4666632openalex-extracted
Exploring Green Solvents and Solvent-Free Conditions for Sustainable Organocatalysis
inferred← citeshttps://doi.org/10.1002/047084289x.rn00974openalex-snapshot
Dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin, 4-Hydroxy-2,6-diphenyl-, 4-Oxide, (11bR)- (Family of Reagents)
inferred← citeshttps://doi.org/10.1002/047084289x.rn00974.pub2openalex-snapshot
Dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin, 4-Hydroxy-2,6-diphenyl-, 4-Oxide, (11bR)- (Family of Reagents)
inferred← citeshttps://doi.org/10.1002/047084289x.rn01087openalex-snapshot
(11bR)-Dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin, 2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-hydroxy-, 4-Oxide
inferred← citeshttps://doi.org/10.1002/047084289x.rn01088openalex-snapshot
(11bR)-Dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin, 4-Hydroxy-2,6-di-2-naphthalenyl-, 4-Oxide
inferred← citeshttps://doi.org/10.1002/0471264229.os088.37openalex-snapshot
( R )‐3,3′‐bis(9‐Phenanthryl)‐1,1′‐Binaphthalene‐2,2′‐Diyl Hydrogen Phosphate
inferred← citeshttps://doi.org/10.1002/9780470584248.ch3openalex-snapshot
Chiral Lewis Acids and Brønsted Acids in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/9780470661345.smc156openalex-snapshot
Supramolecular Organocatalysis
inferred← citeshttps://doi.org/10.1002/9781118075647.ch1openalex-snapshot
Overview of Chirality and Chiral Drugs
inferred← citeshttps://doi.org/10.1002/9781118087992.ch14openalex-snapshot
Silicate‐Mediated Stereoselective Reactions Catalyzed by Chiral Lewis Bases
inferred← citeshttps://doi.org/10.1002/9781118158753.ch9openalex-snapshot
Ionic Liquids as (Co‐)Solvents and Co‐Catalysts for Organocatalytic Reactions
inferred← citeshttps://doi.org/10.1002/9781118356654.ch2openalex-snapshot
BRØNSTED ACID–CATALYZED CASCADE REACTIONS
inferred← citeshttps://doi.org/10.1002/9781118356654.ch3openalex-snapshot
APPLICATION OF ORGANOCATALYTIC CASCADE REACTIONS IN NATURAL PRODUCT SYNTHESIS AND DRUG DISCOVERY
inferred← citeshttps://doi.org/10.1002/9781118449400.ch2openalex-snapshot
Recent Advances in Green Chemistry
inferred← citeshttps://doi.org/10.1002/9781118604755.ch02openalex-snapshot
Activation Modes In Asymmetric Organocatalysis
inferred← citeshttps://doi.org/10.1002/9781118604755.ch15openalex-snapshot
Enantioselective Organocatalytic Reductions
inferred← citeshttps://doi.org/10.1002/9781118629871.ch9openalex-snapshot
Synthesis of Axially Chiral Aromatic Compounds via [2 + 2 + 2] Cycloaddition
inferred← citeshttps://doi.org/10.1002/9781118754085.ch10openalex-snapshot
Lignans, Lignins, and Resveratrols
inferred← citeshttps://doi.org/10.1002/9781118846919.ch3openalex-snapshot
Asymmetric Multifunctional Catalysis
inferred← citeshttps://doi.org/10.1002/9781119736424.ch2openalex-snapshot
ASYMMETRIC ACID ORGANOCATALYSIS
inferred← citeshttps://doi.org/10.1002/9781119736424.ch5openalex-snapshot
ASYMMETRIC PEPTIDE CATALYSIS
inferred← citeshttps://doi.org/10.1002/9781119953678.rad019openalex-snapshot
Stereoselective Radical Reactions
inferred← citeshttps://doi.org/10.1002/9783527345939.ch5openalex-snapshot
B rønsted Acid and Transition Metal Cooperative Catalysis
inferred← citeshttps://doi.org/10.1002/9783527626977.ch3openalex-snapshot
Addition to Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/9783527627325.ch8openalex-snapshot
Modern Arylations of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/9783527627844.ch5openalex-snapshot
Brønsted Acids, H‐Bond Donors, and Combined Acid Systems in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/9783527628698.hgc081openalex-snapshot
Synthesis Without Metals
inferred← citeshttps://doi.org/10.1002/9783527629541.ch3openalex-snapshot
Enantioselective Synthesis of Amines by Chiral Brønsted Acid Catalysts
inferred← citeshttps://doi.org/10.1002/9783527629541.ch5openalex-snapshot
Catalytic, Enantioselective, Vinylogous Mannich Reactions
inferred← citeshttps://doi.org/10.1002/9783527630554.ch4openalex-snapshot
Supported Organocatalysts as a Powerful Tool in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/9783527630554.ch6openalex-snapshot
Double Hydrogen Bonding in Asymmetric Organocatalysis: A Mechanistic Perspective
inferred← citeshttps://doi.org/10.1002/9783527633678.ch2openalex-snapshot
Design of Dynamic Salt Catalysts Based on Acid–Base Combination Chemistry
inferred← citeshttps://doi.org/10.1002/9783527634606.ch22openalex-snapshot
Bio‐Inspired Transfer Hydrogenations
inferred← citeshttps://doi.org/10.1002/9783527645824.ch8openalex-snapshot
Hydrogen Bonds as an Alternative Activation
inferred← citeshttps://doi.org/10.1002/9783527652235.ch11openalex-snapshot
Asymmetric Counteranion‐Directed Catalysis (ACDC)
inferred← citeshttps://doi.org/10.1002/9783527652235.ch32openalex-snapshot
Asymmetric C–C Bond Formation Using Chiral Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/9783527652235.ch7openalex-snapshot
Asymmetric Brønsted Acid Catalysis
inferred← citeshttps://doi.org/10.1002/9783527658862.ch11openalex-snapshot
Brønsted Acids: Chiral Phosphoric Acid Catalysts in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1002/9783527658862.ch28openalex-snapshot
Aldol and Mannich‐Type Reactions
inferred← citeshttps://doi.org/10.1002/9783527658862.ch44openalex-snapshot
Organocatalysis in Total Synthesis
inferred← citeshttps://doi.org/10.1002/9783527664801.ch10openalex-snapshot
The Proline‐Catalyzed Mannich Reaction and the Advent of Enamine Catalysis
inferred← citeshttps://doi.org/10.1002/9783527671304.ch10openalex-snapshot
Organocatalysis in Domino Processes
inferred← citeshttps://doi.org/10.1002/9783527678174.ch15openalex-snapshot
Chiral Phosphoric Acid‐Catalyzed Asymmetric Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/9783527681020.ch6openalex-snapshot
Cooperation of Transition Metals and Chiral Brønsted Acids in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/9783527681020.ch7openalex-snapshot
Cooperative Catalysis Involving Chiral Ion Pair Catalysts
inferred← citeshttps://doi.org/10.1002/9783527697014.ch7openalex-snapshot
One‐pot Multistep Regioselective Protection of Carbohydrates Catalyzed by Acids
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz02517openalex-snapshot
Brønsted acid‐base concept
inferred← citeshttps://doi.org/10.1002/9783527825172.ch10openalex-snapshot
Application for Axially Chiral Organocatalysts
inferred← citeshttps://doi.org/10.1002/9783527830664.ch4openalex-snapshot
Chiral Ureas, Thioureas, and Squaramides in Anion‐Binding Catalysis with Co‐catalytic B rønsted/ L ewis Acids
inferred← citeshttps://doi.org/10.1002/9783527832217.ch1openalex-snapshot
New Developments in Enantioselective Brønsted Acid Catalysis with Strong Hydrogen Bond Donors
inferred← citeshttps://doi.org/10.1002/9783527832217.ch21openalex-snapshot
Mayr Linear Free Energy Relationship: A Powerful Tool for Understanding Aminocatalyzed Reactions
inferred← citeshttps://doi.org/10.1002/9783527832217.ch3openalex-snapshot
Asymmetric Phase‐Transfer Catalysis – From Classical Applications to New Concepts
inferred← citeshttps://doi.org/10.1002/9783527844258.ch2openalex-snapshot
Iron‐ and Ruthenium‐Catalyzed Atroposelective Synthesis of Axially Chiral Compounds
inferred← citeshttps://doi.org/10.1002/9783527844258.ch9openalex-snapshot
Binaphthyl‐Based Chiral DMAP Derivatives in Enantioselective Transformations
inferred← citeshttps://doi.org/10.1002/9783527846849.ch13openalex-snapshot
Asymmetric Organic Reactions in Water
inferred← citeshttps://doi.org/10.1002/adfm.202405401openalex-snapshot
Challenges and Opportunities for Proton Batteries: From Electrodes, Electrolytes to Full‐Cell Applications
inferred← citeshttps://doi.org/10.1002/adsc.200700521openalex-snapshot
Vinylogous Mannich‐Type Reaction Catalyzed by an Iodine‐Substituted Chiral Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/adsc.200800020openalex-snapshot
Asymmetric Counterion Pair Catalysis: An Enantioselective Brønsted Acid‐Catalyzed Protonation
inferred← citeshttps://doi.org/10.1002/adsc.200800239openalex-snapshot
Chiral Brønsted Acid‐Mediated Enantioselective Organocatalytic Three‐Component Reaction for the Construction of Trifluoromethyl‐Containing Molecules
inferred← citeshttps://doi.org/10.1002/adsc.200800314openalex-snapshot
Chiral Lithium Salts of Phosphoric Acids as Lewis Acid–Base Conjugate Catalysts for the Enantioselective Cyanosilylation of Ketones
inferred← citeshttps://doi.org/10.1002/adsc.200800523openalex-snapshot
Highly Enantioselective Friedel–Crafts Reaction of 4,7‐Dihydroindoles with β,γ‐Unsaturated α‐Keto Esters by Chiral Brønsted Acids
inferred← citeshttps://doi.org/10.1002/adsc.200800613openalex-snapshot
Origin of Enantioselectivity in the Organocatalytic Reductive Amination of α‐Branched Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.200800623openalex-snapshot
A Catalytic Asymmetric Electrocyclization‐Protonation Reaction
inferred← citeshttps://doi.org/10.1002/adsc.200900211openalex-snapshot
Phosphonium Salt Organocatalysis
inferred← citeshttps://doi.org/10.1002/adsc.200900746openalex-snapshot
Synthesis and Application of Polymer‐Supported Chiral Brønsted Acid Organocatalysts
inferred← citeshttps://doi.org/10.1002/adsc.200900851openalex-snapshot
Facile Creation of 3‐Indolyl‐3‐hydroxy‐2‐oxindoles by an Organocatalytic Enantioselective Friedel–Crafts Reaction of Indoles with Isatins
inferred← citeshttps://doi.org/10.1002/adsc.201000328openalex-snapshot
Enantioselective Organocatalytic Transfer Hydrogenation of α‐Imino Esters by Utilization of Benzothiazoline as Highly Efficient Reducing Agent
inferred← citeshttps://doi.org/10.1002/adsc.201000438openalex-snapshot
Second Generation CaSH (Camphor Sulfonyl Hydrazine) Organocatalysis. Asymmetric Diels–Alder Reactions and Isolation of the Catalytic Intermediate
inferred← citeshttps://doi.org/10.1002/adsc.201000510openalex-snapshot
Chiral Brønsted Acid‐Catalyzed Enantioselective Friedel–Crafts Reaction of 4,7‐Dihydroindoles with Trifluoromethyl Ketones
inferred← citeshttps://doi.org/10.1002/adsc.201000547openalex-snapshot
First Highly Enantioselective Synthesis of Benzodiazepinones by Catalytic Hydrogenation
inferred← citeshttps://doi.org/10.1002/adsc.201000608openalex-snapshot
Catalytic Asymmetric Inverse‐Electron‐Demand (IED) [4+2] Cycloaddition of Salicylaldimines: Preparation of Optically Active 4‐Aminobenzopyran Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201000754openalex-snapshot
Phosphoric Acid‐Catalyzed Enantioselective Transfer Hydrogenation of N‐Aryl‐ortho‐Hydroxybenzophenone Ketimines
inferred← citeshttps://doi.org/10.1002/adsc.201000952openalex-snapshot
Asymmetric Brønsted Acid‐Catalyzed Friedel–Crafts Reactions of Indoles with Cyclic Imines ‐ Efficient Generation of Nitrogen‐Substituted Quaternary Carbon Centers
inferred← citeshttps://doi.org/10.1002/adsc.201000981openalex-snapshot
Chiral Squaramide‐Catalyzed Highly Enantioselective Michael Addition of 2‐Hydroxy‐1,4‐naphthoquinones to Nitroalkenes
inferred← citeshttps://doi.org/10.1002/adsc.201100050openalex-snapshot
An Easy Entry to Optically Active Spiroindolinones: Chiral Brønsted Acid‐Catalysed Pictet–Spengler Reactions of Isatins
inferred← citeshttps://doi.org/10.1002/adsc.201100351openalex-snapshot
Organocatalytic Enantioselective Dipolar [3+2] Cycloadditions of Acetylenic Aldehydes with Nitrones for the Formation of Chiral 4‐Isoxazolines
inferred← citeshttps://doi.org/10.1002/adsc.201100379openalex-snapshot
Organocatalytic Asymmetric α‐Amination of Unprotected 3‐Aryl and 3‐Aliphatic Substituted Oxindoles using Di‐tert‐butyl Azodicarboxylate
inferred← citeshttps://doi.org/10.1002/adsc.201100714openalex-snapshot
Recent Developments in Asymmetric Organocatalytic Domino Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201100810openalex-snapshot
Chiral Phosphoric Acid‐Catalyzed Asymmetric Oxidation of Aryl Alkyl Sulfides and Aldehyde‐Derived 1,3‐Dithianes: Using Aqueous Hydrogen Peroxide as the Terminal Oxidant
inferred← citeshttps://doi.org/10.1002/adsc.201100849openalex-snapshot
Catalytic Asymmetric Synthesis of Dihydroquinazolinones from Imines and 2‐Aminobenzamides
inferred← citeshttps://doi.org/10.1002/adsc.201200251openalex-snapshot
Asymmetric Counteranion‐Directed Iron Catalysis: A Highly Enantioselective Sulfoxidation
inferred← citeshttps://doi.org/10.1002/adsc.201200293openalex-snapshot
Combining in situ Generated Chiral Silicon Lewis Acid and Chiral Brønsted Acid Catalysts for [3+2] Cycloadditions: Cooperative Catalysis as a Convenient Enantioselective Route to Pyrazolidines
inferred← citeshttps://doi.org/10.1002/adsc.201200456openalex-snapshot
The Synthesis of trans‐Perhydroindolic Acids and their Application in Asymmetric Domino Reactions of Aldehyde Esters with β,γ‐Unsaturated α‐Keto Esters
inferred← citeshttps://doi.org/10.1002/adsc.201201008openalex-snapshot
Chiral Phosphoric Acid‐Catalyzed Enantioselective Aza‐Friedel–Crafts Alkylation of Indoles with γ‐Hydroxy‐γ‐lactams
inferred← citeshttps://doi.org/10.1002/adsc.201201095openalex-snapshot
Relay Catalysis: Enantioselective Synthesis of Cyclic Benzo‐Fused Homoallylic Alcohols by Chiral Brønsted Acid‐Catalyzed Allylboration/Ring Closing Metathesis
inferred← citeshttps://doi.org/10.1002/adsc.201300001openalex-snapshot
Catalytic Asymmetric Five‐Component Tandem Reaction: Diastereo‐ and Enantioselective Synthesis of Densely Functionalized Tetrahydropyridines with Biological Importance
inferred← citeshttps://doi.org/10.1002/adsc.201300255openalex-snapshot
Chemo‐, Regio‐ and Stereoselective Tricyclohexylphosphine‐Catalyzed [3+2] Cycloaddition of Enynes with [60]Fullerene Initiated by 1,4‐Michael Addition: Synthesis of Cyclopenteno[60]fullerenes and their Electrochemical Properties
inferred← citeshttps://doi.org/10.1002/adsc.201300352openalex-snapshot
Chemo‐ and Enantioselective Brønsted Acid‐Catalyzed Reduction of α‐Imino Esters with Catecholborane
inferred← citeshttps://doi.org/10.1002/adsc.201300366openalex-snapshot
Catalytic Asymmetric 1,3‐Dipolar Cycloadditions of Alkynes with Isatin‐Derived Azomethine Ylides: Enantioselective Synthesis of Spiro[indoline‐3,2′‐pyrrole] Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201300392openalex-snapshot
Asymmetric Synthesis of β‐Substituted α‐Methylenebutyro‐ lactones via TRIP‐Catalyzed Allylation: Mechanistic Studies and Application to the Synthesis of ( S )‐(−)‐Hydroxymatairesinol
inferred← citeshttps://doi.org/10.1002/adsc.201300576openalex-snapshot
Asymmetric Organocatalytic Tandem Cyclization/Transfer Hydrogenation: A Synthetic Strategy for Enantioenriched Nitrogen Heterocycles
inferred← citeshttps://doi.org/10.1002/adsc.201400091openalex-snapshot
Chiral Octahedral Complexes of Cobalt(III) as “Organic Catalysts in Disguise” for the Asymmetric Addition of a Glycine Schiff Base Ester to Activated Olefins
inferred← citeshttps://doi.org/10.1002/adsc.201400093openalex-snapshot
Chiral Phosphoric Acid‐Catalyzed Enantioselective Three‐ Component Aza‐Diels–Alder Reactions of Aminopyrroles and Aminopyrazoles
inferred← citeshttps://doi.org/10.1002/adsc.201400095openalex-snapshot
Enantioselective Construction of the Biologically Significant Dibenzo[1,4]diazepine Scaffold via Organocatalytic Asymmetric Three‐Component Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201400611openalex-snapshot
Enantioselective Synthesis of Chiral Biaryl Chlorides/Iodides by a Chiral Phosphoric Acid Catalyzed Sequential Halogenation Strategy
inferred← citeshttps://doi.org/10.1002/adsc.201400851openalex-snapshot
Construction of Chiral 2‐Substituted Octahydroindoles from Cyclic Ketones and Nitroolefins Bearing only One α‐Substituent
inferred← citeshttps://doi.org/10.1002/adsc.201401003openalex-snapshot
Bifunctional Amine‐Squaramides: Powerful Hydrogen‐Bonding Organocatalysts for Asymmetric Domino/Cascade Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201401016openalex-snapshot
Organocatalytic Reactions of Indoles with Quinone Imine Ketals: An Alternative Metal‐Free Approach to Bioactive meta‐Indolylanilines
inferred← citeshttps://doi.org/10.1002/adsc.201401155openalex-snapshot
Brønsted Acid‐Catalyzed Enantioselective Synthesis of Isatin‐ Derived N,S‐Acetals
inferred← citeshttps://doi.org/10.1002/adsc.201401189openalex-snapshot
2,6‐Bis(amido)benzoic Acid with Internal Hydrogen Bond as Brønsted Acid Catalyst for Friedel–Crafts Reaction of Indoles
inferred← citeshttps://doi.org/10.1002/adsc.201500901openalex-snapshot
Catalytic Enantioselective Arylative Dearomatization of 3‐Methyl‐2‐vinylindoles Enabled by Reactivity Switch
inferred← citeshttps://doi.org/10.1002/adsc.201501063openalex-snapshot
Intermediate‐Dependent Unusual [4+3], [3+2] and Cascade Reactions of 3‐Indolylmethanols: Controllable Chemodivergent and Stereoselective Synthesis of Diverse Indole Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201501175openalex-snapshot
The Application of N‐Protected 3‐Vinylindoles in Chiral Phosphoric Acid‐Catalyzed [3+2] Cyclization with 3‐Indolylmethanols: Monoactivation of the Catalyst to Vinyliminium
inferred← citeshttps://doi.org/10.1002/adsc.201600270openalex-snapshot
Organocatalytic [3+2] Cycloadditions of Barbiturate‐Based Olefins with 3‐Isothiocyanato Oxindoles: Highly Diastereoselective and Enantioselective Synthesis of Dispirobarbiturates
inferred← citeshttps://doi.org/10.1002/adsc.201600472openalex-snapshot
Concise Asymmetric Total Synthesis of ent‐Ancistrocladinium A
inferred← citeshttps://doi.org/10.1002/adsc.201600508openalex-snapshot
Enantioselective Construction of Cyclic Enaminone‐Based 3‐Substituted 3‐Amino‐2‐oxindole Scaffolds via Catalytic Asymmetric Additions of Isatin‐Derived Imines
inferred← citeshttps://doi.org/10.1002/adsc.201600931openalex-snapshot
Catalytic Asymmetric [3+2] Cycloadditions of C‐3 Unsubstituted 2‐Indolylmethanols: Regio‐, Diastereo‐ and Enantioselective Construction of the Cyclopenta[b]indole Framework
inferred← citeshttps://doi.org/10.1002/adsc.201700187openalex-snapshot
Catalytic Asymmetric 1,2‐Difunctionalization of Indolenines with α‐(Benzothiazol‐2‐ylsulfonyl) Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201700190openalex-snapshot
Rapid Access to Indeno[1,2‐c]quinolines via Brønsted Acid‐ Catalyzed Cascade Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201700203openalex-snapshot
Catalytic Asymmetric [3+3] Cycloaddition of Azomethine Ylides with C3‐Substituted 2‐Indolylmethanols
inferred← citeshttps://doi.org/10.1002/adsc.201700621openalex-snapshot
An Enantioselective Multicomponent Carbonyl Allylation of Aldehydes with Dienes and Alkynyl Bromides Enabled by Chiral Palladium Phosphate
inferred← citeshttps://doi.org/10.1002/adsc.201701354openalex-snapshot
Chiral Phosphoric Acid Catalyzed Enantioselective Friedel‐Crafts Reaction of N‐Protected 4‐Aminoindoles with β,γ‐Unsaturated α‐Ketimino Esters
inferred← citeshttps://doi.org/10.1002/adsc.201701484openalex-snapshot
Catalytic Enantioselective Povarov Reactions of Ferrocenecarbaldehyde‐Derived Imines – Brønsted Acid Catalysis at Parts‐Per‐Million Level Loading
inferred← citeshttps://doi.org/10.1002/adsc.201701521openalex-snapshot
Design of C3‐Alkenyl‐Substituted 2‐Indolylmethanols for Catalytic Asymmetric Interrupted Nazarov‐Type Cyclization
inferred← citeshttps://doi.org/10.1002/adsc.201800150openalex-snapshot
Application of 7‐Indolylmethanols in Catalytic Asymmetric Arylations with Tryptamines: Enantioselective Synthesis of 7‐indolylmethanes
inferred← citeshttps://doi.org/10.1002/adsc.201800829openalex-snapshot
Catalytic Asymmetric [4+2] Cyclization of para‐Quinone Methide Derivatives with 3‐Alkyl‐2‐vinylindoles
inferred← citeshttps://doi.org/10.1002/adsc.201801080openalex-snapshot
Enantioselective Allenylation of Aldehydes via Brønsted Acid Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.201801329openalex-snapshot
Asymmetric Syntheses of Spirooxindole‐dihydroquinazolinones by Cyclization Reactions between N‐substituted Anthranilamides and Isatins
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.201900377openalex-snapshot
C7‐Functionalization of Indoles via Organocatalytic Enantioselective Friedel‐Crafts Alkylation of 4‐Amino‐ indoles with 2‐Butene‐1,4‐diones and 3‐Aroylacrylates
inferred← citeshttps://doi.org/10.1002/adsc.201900665openalex-snapshot
Catalytic Mechanism Study on the 1,2‐ and 1,4‐Transfer Hydrogenation of Ketimines and β‐Enamino Esters Catalyzed by Axially Chiral Biscarboline‐Based Alcohols
inferred← citeshttps://doi.org/10.1002/adsc.201900710openalex-snapshot
Enantioselective Addition of Enamides to Cyclic Ketimines: Access to Chiral 3,3‐Disubstituted Isoindolin‐1‐Ones
inferred← citeshttps://doi.org/10.1002/adsc.201901035openalex-snapshot
Catalytic Asymmetric Dearomative [3+2] Cyclisation of 1,4‐Quinone with 2,3‐Disubstituted Indoles
inferred← citeshttps://doi.org/10.1002/adsc.202000210openalex-snapshot
Recent Developments in Enantioselective Multicatalyzed Tandem Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202000520openalex-snapshot
Enantioselective Construction of Sulfur‐Containing Tetrasubstituted Stereocenters via Asymmetric Functionalizations of α‐Sulfanyl Cyclic Ketones
inferred← citeshttps://doi.org/10.1002/adsc.202000540openalex-snapshot
Catalytic Strategies for the Asymmetric Construction of Cyclic Frameworks with a Halogenated Tetrasubstituted Stereocenter
inferred← citeshttps://doi.org/10.1002/adsc.202000848openalex-snapshot
Asymmetric Fluorination Reactions promoted by Chiral Hydrogen Bonding‐based Organocatalysts
inferred← citeshttps://doi.org/10.1002/adsc.202001051openalex-snapshot
Kinetic Resolution of 2‐N‐Acylamido Tertiary Allylic Alcohols: Asymmetric Synthesis of Oxazolines
inferred← citeshttps://doi.org/10.1002/adsc.202001128openalex-snapshot
Catalytic Enantioselective Synthesis of N,N‐Acetals from α‐Dicarbonyl Compounds Using Chiral Imidazoline‐Phosphoric Acid Catalysts
inferred← citeshttps://doi.org/10.1002/adsc.202001570openalex-snapshot
Cascade Chan‐Lam C−O Coupling/[3,3]‐Rearrangement of Arylhydroxylamines with Arylboronic Acids Toward NOBIN Analogues
inferred← citeshttps://doi.org/10.1002/adsc.202100037openalex-snapshot
Asymmetric Allylation Catalyzed by Chiral Phosphoric Acids: Stereoselective Synthesis of Tertiary Alcohols and a Reagent‐Based Switch in Stereopreference
inferred← citeshttps://doi.org/10.1002/adsc.202100039openalex-snapshot
Organocatalytic Enantioselective Aza‐Michael Addition of Arylamines to 7‐Methide‐7H‐Indoles
inferred← citeshttps://doi.org/10.1002/adsc.202100313openalex-snapshot
Organocatalytic Enantioselective Friedel‐Crafts Alkylation Reactions of Pyrroles
inferred← citeshttps://doi.org/10.1002/adsc.202100600openalex-snapshot
Organocatalytic Enantioselective Construction of Acyclic N,N‐Acetals via Aza‐Addition of Arylamines to Ketimines
inferred← citeshttps://doi.org/10.1002/adsc.202101011openalex-snapshot
Chiral Phosphoric Acid‐Catalyzed Enantioselective Synthesis of Pyrazole‐Based Unnatural α‐Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.202200161openalex-snapshot
Chiral Phosphoric Acid‐Catalyzed Enantioselective Formal [4+2] Cycloaddition Between Dienecarbamates and 2‐Benzothioazolimines
inferred← citeshttps://doi.org/10.1002/adsc.202201077openalex-snapshot
Chiral Phosphoric Acid‐Catalyzed Chemo‐ and Enantioselective N‐Alkylation of Indoles with Imines
inferred← citeshttps://doi.org/10.1002/adsc.202401173openalex-snapshot
Organocatalytic Dearomatization of β‐Naphthols through a 1,6‐Conjugated Addition of Alkynyl 7‐Methylene‐7H‐indoles Formed In Situ
inferred← citeshttps://doi.org/10.1002/adsc.202401458openalex-snapshot
Understanding Chiral Proton Catalysis Using Cinchonium Derivatives in aza‐Michael Additions
inferred← citeshttps://doi.org/10.1002/adsc.70236openalex-snapshot
Enantioselective α‐Aminoxylation of Ketones Catalyzed by a Chiral Brønsted Acid
inferred← citeshttps://doi.org/10.1002/adsc.70254openalex-snapshot
Asymmetric Synthesis of Atropisomeric Amines via Transaminase‐Catalyzed Dynamic Kinetic Resolution
inferred← citeshttps://doi.org/10.1002/ajoc.201300097openalex-snapshot
Recent Advances in the Use of Chiral Brønsted Acids as Cooperative Catalysts in Cascade and Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/ajoc.201300174openalex-snapshot
Enantioselective Transfer Hydrogenation of Difluoromethyl Ketimines Using Benzothiazoline as a Hydrogen Donor in Combination with a Chiral Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/ajoc.201300250openalex-snapshot
Kinetic Resolution of Diols via Etherification Catalyzed by a Chiral Phosphoric Acid: Concise Synthesis of (+)‐Sacidumlignan D
inferred← citeshttps://doi.org/10.1002/ajoc.201300256openalex-snapshot
Chiral 1,1′‐Binaphthyl‐2,2′‐Disulfonic Acid (BINSA) and Its Derivatives for Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/ajoc.201300285openalex-snapshot
Stereoselective NH Insertion‐Arylation Reactions of Nitrodiazoesters
inferred← citeshttps://doi.org/10.1002/ajoc.201400026openalex-snapshot
Imidazolium Salt‐Catalyzed Friedel–Crafts‐Type Conjugate Addition of Indoles: Analysis of Indole/Imidazolium Complex by High Level ab Initio Calculations
inferred← citeshttps://doi.org/10.1002/ajoc.201402005openalex-snapshot
Chiral β‐Lactam Synthesis through the Enantioselective Reduction of Iminocyclobutenones and the Thermal Rearrangement of Aminocyclobutenones
inferred← citeshttps://doi.org/10.1002/ajoc.201600021openalex-snapshot
Chiral Brønsted Acid Catalyzed Kinetic Resolutions
inferred← citeshttps://doi.org/10.1002/ajoc.201600185openalex-snapshot
Rational Design of Amine Nucleophiles for Dynamic Kinetic Resolution of Azlactones Leading to Highly Enantioselective Synthesis of Bisamides
inferred← citeshttps://doi.org/10.1002/ajoc.201800359openalex-snapshot
Catalytic Stereoselective SN1‐Type Reactions Promoted by Chiral Phosphoric Acids as Brønsted Acid Catalysts
inferred← citeshttps://doi.org/10.1002/ajoc.201900239openalex-snapshot
Asymmetric syn‐1,3‐Dioxane Construction via Kinetic Resolution of Secondary Alcohols Using Chiral Phosphoric Acid Catalysts
inferred← citeshttps://doi.org/10.1002/ajoc.202000603openalex-snapshot
Reusable Silica‐Supported Ammonium BINSate Catalysts for Enantio‐ and Diastereoselective Friedel–Crafts‐Type Double Aminoalkylation of N‐Alkylpyrroles with Aldimines
inferred← citeshttps://doi.org/10.1002/ajoc.202100091openalex-snapshot
Recent Advances in (Dynamic) Kinetic Resolution and Desymmetrization Catalyzed by Chiral Phosphoric Acids
inferred← citeshttps://doi.org/10.1002/ajoc.202100180openalex-snapshot
Organocatalytic Enantioselective Desymmetrization of Prochiral 2,2‐Disubstituted Cyclic 1,3‐Diones
inferred← citeshttps://doi.org/10.1002/ajoc.202300198openalex-snapshot
α‐Alkylation of Mono‐Carbonyl Compounds with N‐Allylamines through Cooperative Actions of Lewis Acids and a Brønsted Base
inferred← citeshttps://doi.org/10.1002/ajoc.202300231openalex-snapshot
Brønsted Acid–Catalyzed Tandem Reaction of 1,4‐Enediones with 2‐Naphthols: Synthesis of 2‐Furylmethylnaphthalenes
inferred← citeshttps://doi.org/10.1002/ajoc.202300360openalex-snapshot
TfOH‐Catalyzed Highly Regioselective Synthesis of Conjugated Enones by Coupling of Alkynes and Aldehydes
inferred← citeshttps://doi.org/10.1002/ajoc.202500299openalex-snapshot
C 3 ‐Symmetric Chiral Cage‐Shaped Phosphates: Synthesis and Application as Organocatalysts in Asymmetric Iodolactonizations
inferred← citeshttps://doi.org/10.1002/ange.200705300openalex-snapshot
Organocatalytic Asymmetric Three‐Component Cyclization of Cinnamaldehydes and Primary Amines with 1,3‐Dicarbonyl Compounds: Straightforward Access to Enantiomerically Enriched Dihydropyridines
inferred← citeshttps://doi.org/10.1002/ange.200705932openalex-snapshot
Chiral Brønsted Acid Catalyzed Asymmetric Baeyer–Villiger Reaction of 3‐Substituted Cyclobutanones by Using Aqueous H2O2
inferred← citeshttps://doi.org/10.1002/ange.200800103openalex-snapshot
Enantioselektive, Brønsted‐Säure‐katalysierte, vinyloge Mannich‐ Reaktion
inferred← citeshttps://doi.org/10.1002/ange.200800232openalex-snapshot
Enantioselective Activation of Aldehydes by Chiral Phosphoric Acid Catalysts in an Aza‐ene‐type Reaction between Glyoxylate and Enecarbamate
inferred← citeshttps://doi.org/10.1002/ange.200800381openalex-snapshot
A Highly Stereoselective Hydrogen‐Bond‐Mediated Michael–Michael Cascade Process through Dynamic Kinetic Resolution
inferred← citeshttps://doi.org/10.1002/ange.200800770openalex-snapshot
Chiral Phosphoric Acid Catalyzed Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes: Cooperative Effect of 3 Å Molecular Sieves
inferred← citeshttps://doi.org/10.1002/ange.200801173openalex-snapshot
Direkte katalytische asymmetrische Kabachnik‐Fields‐ Dreikomponentenreaktion
inferred← citeshttps://doi.org/10.1002/ange.200801354openalex-snapshot
Asymmetrische Brønsted‐Säure‐katalysierte Synthese von Isoindolinen: Steigerung des Enantiomerenverhältnisses durch stereoablative kinetische Racematspaltung
inferred← citeshttps://doi.org/10.1002/ange.200801435openalex-snapshot
Eine hoch enantioselektive Brønsted‐Säure‐katalysierte Reaktionskaskade
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.200803610openalex-snapshot
Katalytische asymmetrische Aminoallylierung von Aldehyden – eine katalytische enantioselektive Aza‐Cope‐Umlagerung
inferred← citeshttps://doi.org/10.1002/ange.200803731openalex-snapshot
Organocatalytic Asymmetric α‐Aminoxylation/Aza‐Michael Reactions for the Synthesis of Functionalized Tetrahydro‐1,2‐oxazines
inferred← citeshttps://doi.org/10.1002/ange.200804353openalex-snapshot
Characterization of Key Intermediates in a Complex Organocatalytic Cascade Reaction Using Mass Spectrometry
inferred← citeshttps://doi.org/10.1002/ange.200805385openalex-snapshot
Activation of Hemiaminal Ethers by Chiral Brønsted Acids for Facile Access to Enantioselective Two‐Carbon Homologation Using Enecarbamates
inferred← citeshttps://doi.org/10.1002/ange.200901127openalex-snapshot
Enantioselective Robinson‐Type Annulation Reaction Catalyzed by Chiral Phosphoric Acids
inferred← citeshttps://doi.org/10.1002/ange.200901768openalex-snapshot
A Powerful Chiral Counteranion Motif for Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/ange.200901771openalex-snapshot
Triflic Acid Catalyzed Synthesis of Spirocycles via Acetylene Cations
inferred← citeshttps://doi.org/10.1002/ange.200902084openalex-snapshot
Axial Chirality Control of Gold(biphep) Complexes by Chiral Anions: Application to Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/ange.200902385openalex-snapshot
Brønsted Acid Catalyzed Enantioselective Three‐Component Reaction Involving the α Addition of Isocyanides to Imines
inferred← citeshttps://doi.org/10.1002/ange.200903462openalex-snapshot
Asymmetric Construction of Polycyclic Indoles through Olefin Cross‐Metathesis/Intramolecular Friedel–Crafts Alkylation under Sequential Catalysis
inferred← citeshttps://doi.org/10.1002/ange.200903765openalex-snapshot
Asymmetrische reduktive Aminierung durch kombinierte Brønsted‐Säure‐ und Übergangsmetallkatalyse
inferred← citeshttps://doi.org/10.1002/ange.200904565openalex-snapshot
Brønsted Acid Catalyzed Enantioselective Semipinacol Rearrangement for the Synthesis of Chiral Spiroethers
inferred← citeshttps://doi.org/10.1002/ange.200904828openalex-snapshot
Protonierung oder Alkylierung? Stereoselektive Brønsted‐Säure‐katalysierte C‐C‐Verknüpfungen mit Diazoalkanen
inferred← citeshttps://doi.org/10.1002/ange.200905035openalex-snapshot
Eine katalytische asymmetrische 6π‐Elektrocyclisierung: enantioselektive Synthese von 2‐Pyrazolinen
inferred← citeshttps://doi.org/10.1002/ange.200905271openalex-snapshot
Chiral Phosphoric Acid Catalyzed Desymmetrization of meso‐1,3‐Diones: Asymmetric Synthesis of Chiral Cyclohexenones
inferred← citeshttps://doi.org/10.1002/ange.200905332openalex-snapshot
Asymmetrische Gegenanion‐vermittelte Übergangsmetallkatalyse: enantioselektive Epoxidierung von Alkenen mit Mangan(III)‐Salen‐Phosphatkomplexen
inferred← citeshttps://doi.org/10.1002/ange.200906407openalex-snapshot
Metalltriflimidate sind bessere Katalysatoren für die organische Synthese als Metalltriflate – der Effekt eines stark delokalisierten Gegenions
inferred← citeshttps://doi.org/10.1002/ange.200906629openalex-snapshot
Das schwer fassbare Enamin‐Intermediat in prolinkatalysierten Aldolreaktionen: NMR‐Detektion, Entstehungsweg und Stabilisierungstrends
inferred← citeshttps://doi.org/10.1002/ange.201000637openalex-snapshot
Ein neues Strukturmotiv für difunktionelle Brønsted‐Säure/Base‐ Organokatalyse
inferred← citeshttps://doi.org/10.1002/ange.201000824openalex-snapshot
Which Is the Actual Catalyst: Chiral Phosphoric Acid or Chiral Calcium Phosphate?
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