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Recent Developments in the Use of Catalytic Asymmetric Ammonium Enolates in Chemical Synthesis

https://doi.org/10.1021/cr0683764
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Catalytic, Asymmetric Baylis–Hillman Reaction of Imines with Methyl Vinyl Ketone and Methyl Acrylate
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Asymmetric Organocatalysis
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Asymmetric Catalysis by Alkaloids
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Organocatalysis: A Complementary Catalysis Strategy Advances Organic Synthesis
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Organic‐Catalyst‐Mediated Cyclopropanation Reaction
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In the Golden Age of Organocatalysis
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An Intramolecular Organocatalytic Cyclopropanation Reaction
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Enantioselective Organocatalytic Cyclopropanation via Ammonium Ylides
inferredcites →https://doi.org/10.1002/anie.200460698openalex-snapshot
Asymmetric Synthesis of Highly Substituted β‐Lactones by Nucleophile‐Catalyzed [2+2] Cycloadditions of Disubstituted Ketenes with Aldehydes
inferredcites →https://doi.org/10.1002/anie.200602129openalex-snapshot
Enantioselective Catalytic Intramolecular Cyclopropanation using Modified Cinchona Alkaloid Organocatalysts
inferredcites →https://doi.org/10.1002/anie.200602318openalex-snapshot
Cupreines and Cupreidines: An Emerging Class of Bifunctional Cinchona Organocatalysts
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Catalytic, Asymmetric Synthesis of 1,4‐Benzoxazinones: A Remarkably Enantioselective Route to α‐Amino Acid Derivatives from o‐Benzoquinone Imides
inferredcites →https://doi.org/10.1002/anie.200604366openalex-snapshot
The Enantioselective Morita–Baylis–Hillman Reaction and Its Aza Counterpart
inferredcites →https://doi.org/10.1002/chem.200400872openalex-snapshot
Catalytic, Asymmetric Aza‐Baylis–Hillman Reaction of N‐Sulfonated Imines with Activated Olefins by Quinidine‐Derived Chiral Amines
inferredcites →https://doi.org/10.1002/chin.200345028openalex-snapshot
Ni(II) Bis(oxazoline)‐Catalyzed Enantioselective Syn Aldol Reactions of N‐Propionylthiazolidinethiones in the Presence of Silyl Triflates.
inferredcites →https://doi.org/10.1002/ejoc.200600819openalex-snapshot
A Mechanistic Study on the Catalytic, Asymmetric α‐Bromination of Acid Chlorides
inferredcites →https://doi.org/10.1002/prac.19723140120openalex-snapshot
Kinetik und Mechanismus Katalytischer Additionsreaktionen an kumulierte Doppelbindungssysteme. V. Basenkatalysierte Addition von Alkoholen an Keten
inferredcites →https://doi.org/10.1002/recl.19861051009openalex-snapshot
A highly efficient synthesis of (R)‐ and (S)‐citramalic acid
inferredcites →https://doi.org/10.1016/0957-4166(95)00153-gopenalex-snapshot
Asymmetric Baylis-Hillman reactions using chiral 2,3-disubstituted 1,4-diazabicyclo[2.2.2]octanes catalysts under high pressure conditions
inferredcites →https://doi.org/10.1016/j.drudis.2006.11.004openalex-snapshot
Enantioselective organocatalysis
inferredcites →https://doi.org/10.1016/s0040-4020(02)00723-8openalex-snapshot
Synthesis of the C21–C34-segment of the aplyronines using the dimer of methylketene
inferredcites →https://doi.org/10.1016/s0040-4020(02)00987-0openalex-snapshot
Molecular mechanics calculations as predictors of enantioselectivity for chiral nucleophile catalyzed reactions
inferredcites →https://doi.org/10.1016/s0040-4020(03)00491-5openalex-snapshot
Asymmetric synthesis using ketenes
inferredcites →https://doi.org/10.1016/s0040-4020(99)00185-4openalex-snapshot
Methods for the synthesis of optically active β-lactones (2-oxetanones)
inferredcites →https://doi.org/10.1016/s0040-4039(00)92331-1openalex-snapshot
Synthesis of chiral 2,3-disubstituted 1,4-diazabicyclo [2.2.2] octane. New ligand for the osmium-catalyzed asymmetric dihydroxylation of olefins
inferredcites →https://doi.org/10.1016/s0040-4039(03)00289-2openalex-snapshot
Chiral quinuclidine-based amine catalysts for the asymmetric one-pot, three-component aza-Baylis–Hillman reaction
inferredcites →https://doi.org/10.1021/ar020137popenalex-snapshot
α-Imino Esters: Versatile Substrates for the Catalytic, Asymmetric Synthesis of α- and β-Amino Acids and β-Lactams
inferredcites →https://doi.org/10.1021/ar030045fopenalex-snapshot
Catalytic, Asymmetric Sulfur Ylide-Mediated Epoxidation of Carbonyl Compounds: Scope, Selectivity, and Applications in Synthesis
inferredcites →https://doi.org/10.1021/ar030048sopenalex-snapshot
Asymmetric Organic Catalysis with Modified Cinchona Alkaloids
inferredcites →https://doi.org/10.1021/ar030051bopenalex-snapshot
Asymmetric Catalysis with “Planar-Chiral” Derivatives of 4-(Dimethylamino)pyridine
inferredcites →https://doi.org/10.1021/ar030055gopenalex-snapshot
Advances in the Catalytic, Asymmetric Synthesis of β-Lactams
inferredcites →https://doi.org/10.1021/ar0300571openalex-snapshot
Enamine Catalysis Is a Powerful Strategy for the Catalytic Generation and Use of Carbanion Equivalents
inferredcites →https://doi.org/10.1021/ar030058topenalex-snapshot
Asymmetric Phase-Transfer Catalysis Utilizing Chiral Quaternary Ammonium Salts: Asymmetric Alkylation of Glycine Imines
inferredcites →https://doi.org/10.1021/ar0300625openalex-snapshot
The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters
inferredcites →https://doi.org/10.1021/ar068115gopenalex-snapshot
Applications of Planar-Chiral Heterocycles as Ligands in Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/cr00032a009openalex-snapshot
Catalytic Asymmetric Dihydroxylation
inferredcites →https://doi.org/10.1021/cr010043dopenalex-snapshot
Recent Advances in the Baylis−Hillman Reaction and Applications
inferredcites →https://doi.org/10.1021/cr020061aopenalex-snapshot
Nucleophilic Chiral Amines as Catalysts in Asymmetric Synthesis
inferredcites →https://doi.org/10.1021/cr960411ropenalex-snapshot
Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement
inferredcites →https://doi.org/10.1021/ja00083a053openalex-snapshot
Catalytic Asymmetric Michael Reactions Promoted by a Lithium-Free Lanthanum-BINOL Complex
inferredcites →https://doi.org/10.1021/ja001754gopenalex-snapshot
Catalytic, Asymmetric Synthesis of β-Lactams
inferredcites →https://doi.org/10.1021/ja003033nopenalex-snapshot
A Direct Catalytic Enantioselective Aldol Reaction via a Novel Catalyst Design
inferredcites →https://doi.org/10.1021/ja00365a030openalex-snapshot
Asymmetric synthesis of (S)- and (R)-malic acid from ketene and chloral
inferredcites →https://doi.org/10.1021/ja00392a029openalex-snapshot
Addition of aromatic thiols to conjugated cycloalkenones, catalyzed by chiral .beta.-hydroxy amines. A mechanistic study of homogeneous catalytic asymmetric synthesis
inferredcites →https://doi.org/10.1021/ja005791jopenalex-snapshot
Catalytic, Asymmetric α-Halogenation
inferredcites →https://doi.org/10.1021/ja01202a058openalex-snapshot
Ketene Dimers from Acid Halides
inferredcites →https://doi.org/10.1021/ja012427ropenalex-snapshot
Enantioselective Staudinger Synthesis of β-Lactams Catalyzed by a Planar-Chiral Nucleophile
inferredcites →https://doi.org/10.1021/ja016134+openalex-snapshot
Intramolecular, Nucleophile-Catalyzed Aldol-Lactonization (NCAL) Reactions: Catalytic, Asymmetric Synthesis of Bicyclic β-Lactones
inferredcites →https://doi.org/10.1021/ja0258226openalex-snapshot
The Development of the First Catalyzed Reaction of Ketenes and Imines: Catalytic, Asymmetric Synthesis of β-Lactams
inferredcites →https://doi.org/10.1021/ja0262378openalex-snapshot
The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes
inferredcites →https://doi.org/10.1021/ja027675hopenalex-snapshot
First Total Synthesis of a Natural Product Containing a Chiral, β-Diketone: Synthesis and Stereochemical Reassignment of Siphonarienedione and Siphonarienolone
inferredcites →https://doi.org/10.1021/ja035509jopenalex-snapshot
Ni(II) Bis(oxazoline)-Catalyzed Enantioselective Syn Aldol Reactions of N-Propionylthiazolidinethiones in the Presence of Silyl Triflates
inferredcites →https://doi.org/10.1021/ja039046topenalex-snapshot
Catalytic, Asymmetric α-Chlorination of Acid Halides
inferredcites →https://doi.org/10.1021/ja044179fopenalex-snapshot
Bifunctional Lewis Acid-Nucleophile-Based Asymmetric Catalysis: Mechanistic Evidence for Imine Activation Working in Tandem with Chiral Enolate Formation in the Synthesis of β-Lactams
inferredcites →https://doi.org/10.1021/ja0492900openalex-snapshot
Cinchona Alkaloid-Lewis Acid Catalyst Systems for Enantioselective Ketene−Aldehyde Cycloadditions
inferredcites →https://doi.org/10.1021/ja0500254openalex-snapshot
Bifunctional Organocatalysts for Enantioselective aza-Morita−Baylis−Hillman Reaction
inferredcites →https://doi.org/10.1021/ja051759jopenalex-snapshot
Catalytic Enantioselective Thioester Aldol Reactions That Are Compatible with Protic Functional Groups
inferredcites →https://doi.org/10.1021/ja052058popenalex-snapshot
Catalytic Asymmetric Staudinger Reactions to Form β-Lactams: An Unanticipated Dependence of Diastereoselectivity on the Choice of the Nitrogen Substituent
inferredcites →https://doi.org/10.1021/ja056751oopenalex-snapshot
Enantioselective Synthesis of Vinylcyclopropanes and Vinylepoxides Mediated by Camphor-Derived Sulfur Ylides: Rationale of Enantioselectivity, Scope, and Limitation
inferredcites →https://doi.org/10.1021/ja058077gopenalex-snapshot
Catalytic, Enantioselective [4 + 2]-Cycloadditions of Ketene Enolates and o-Quinones: Efficient Entry to Chiral, α-Oxygenated Carboxylic Acid Derivatives
inferredcites →https://doi.org/10.1021/ja061221topenalex-snapshot
Highly anti-Selective Catalytic Aldol Reactions of Amides with Aldehydes
inferredcites →https://doi.org/10.1021/ja061938gopenalex-snapshot
Catalytic Asymmetric Assembly of Stereodefined Propionate Units: An Enantioselective Total Synthesis of (−)-Pironetin
inferredcites →https://doi.org/10.1021/ja065754dopenalex-snapshot
Catalytic, Enantioselective Bifunctional Inverse Electron Demand Hetero-Diels−Alder Reactions of Ketene Enolates and o-Benzoquinone Diimides
inferredcites →https://doi.org/10.1021/ja990031yopenalex-snapshot
Direct Catalytic Asymmetric Aldol Reaction
inferredcites →https://doi.org/10.1021/ja992655+openalex-snapshot
Chiral Amine-Catalyzed Asymmetric Baylis−Hillman Reaction: A Reliable Route to Highly Enantiomerically Enriched (α-Methylene-β-hydroxy)esters
inferredcites →https://doi.org/10.1021/ja994280yopenalex-snapshot
Proline-Catalyzed Direct Asymmetric Aldol Reactions
inferredcites →https://doi.org/10.1021/jo00211a039openalex-snapshot
Catalytic asymmetric synthesis of chiral 4-substituted 2-oxetanones
inferredcites →https://doi.org/10.1021/jo0160367openalex-snapshot
Catalytic, Asymmetric Synthesis of Siphonarienal
inferredcites →https://doi.org/10.1021/jo034150eopenalex-snapshot
A Multistage, One-Pot Procedure Mediated by a Single Catalyst: A New Approach to the Catalytic Asymmetric Synthesis of β-Amino Acids
inferredcites →https://doi.org/10.1021/jo049804dopenalex-snapshot
Development of a New Dimeric Cyclophane Ligand: Application to Enhanced Diastereo- and Enantioselectivity in the Catalytic Synthesis of β-Lactams
inferredcites →https://doi.org/10.1021/jo050024uopenalex-snapshot
Asymmetric Synthesis of Bicyclic β-Lactones via the Intramolecular, Nucleophile-Catalyzed Aldol Lactonization: Improved Efficiency and Expanded Scope
inferredcites →https://doi.org/10.1021/jo060392dopenalex-snapshot
Practical, Catalytic, Asymmetric Synthesis of β-Lactones via a Sequential Ketene Dimerization/Hydrogenation Process: Inhibitors of the Thioesterase Domain of Fatty Acid Synthase
inferredcites →https://doi.org/10.1021/jo061522lopenalex-snapshot
Scalable Methodology for the Catalytic, Asymmetric α-Bromination of Acid Chlorides
inferredcites →https://doi.org/10.1021/jo961721copenalex-snapshot
Catalytic, Asymmetric Dimerization of Methylketene
inferredcites →https://doi.org/10.1021/jo9808977openalex-snapshot
One-Pot, Catalytic, Asymmetric Syntheses of All Four Stereoisomers of a Dipropionate Synthon
inferredcites →https://doi.org/10.1021/ol005714topenalex-snapshot
Catalytic, Asymmetric Synthesis of the C1‘−C10‘ Segment of Pamamycin 621A
inferredcites →https://doi.org/10.1021/ol015814eopenalex-snapshot
One-Pot, Catalytic, Asymmetric Synthesis of Polypropionates
inferredcites →https://doi.org/10.1021/ol0160147openalex-snapshot
Reactive Ketenes through a Carbonate/Amine Shuttle Deprotonation Strategy: Catalytic, Enantioselective α-Bromination of Acid Chlorides
inferredcites →https://doi.org/10.1021/ol017087topenalex-snapshot
A Catalyst that Plays Multiple Roles: Asymmetric Synthesis of β-Substituted Aspartic Acid Derivatives through a Four-Stage, One-Pot Procedure
inferredcites →https://doi.org/10.1021/ol0172525openalex-snapshot
Generation of Ketenes from Acid Chlorides Using NaH/Crown Ether Shuttle-Deprotonation for Use in Asymmetric Catalysis
inferredcites →https://doi.org/10.1021/ol025805lopenalex-snapshot
Bifunctional Asymmetric Catalysis: A Tandem Nucleophile/Lewis Acid Promoted Synthesis of β-Lactams
inferredcites →https://doi.org/10.1021/ol035102jopenalex-snapshot
β-Isocupreidine-Catalyzed Asymmetric Baylis−Hillman Reaction of Imines
inferredcites →https://doi.org/10.1021/ol0359517openalex-snapshot
Catalytic, Asymmetric Preparation of Ketene Dimers from Acid Chlorides
inferredcites →https://doi.org/10.1021/ol050980yopenalex-snapshot
Performing the Synthesis of a Complex Molecule on Sequentially Linked Columns: Toward the Development of a “Synthesis Machine”
inferredcites →https://doi.org/10.1039/b514296mopenalex-snapshot
The ying and yang of asymmetric aminocatalysis
inferredcites →https://doi.org/10.1055/s-2001-16746openalex-snapshot
Bicyclic β-Lactones via Intramolecular NCAL Reactions with Cinchona Alkaloids: Effect of the C9-Substituent on Enantioselectivity and Catalyst Conformation
inferredcites →https://doi.org/10.1055/s-2002-33552openalex-snapshot
From α-Amino Acids to Peptides: All You Need for the Journey
inferredcites →https://doi.org/10.2174/0929867043364900openalex-snapshot
Asymmetric Synthesis of β-Lactams Through the Staudinger Reaction and Their Use as Building Blocks of Natural and Nonnatural Products

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Catalytic Enantioselective Gilman-Speeter Synthesis of Β-Lactams by Nucleophilic Activation of Carboxylic Acids
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Acid–Base Properties of Enols and Enolates
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NMR of Organoselenium and Organotellurium Compounds
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Recent Advances on Stereoselective Organocatalytic Reactions. Organocatalytic Synthesis of Natural Products and Drugs
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Organocatalytic Conjugate Addition in Stereoselective Synthesis
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Metal–Organo Multicatalysis: An Emerging Concept
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Monoterpenes and Iridoids
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Multicatalyst System
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L ewis Base– L ewis Acid Cooperative Catalysis
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L ewis Base‐Transition Metal Cooperative Catalysis
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Cinchona‐Catalyzed Cycloaddition Reactions
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Organocatalysis
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Ylides
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Formation of 3‐, 4‐ and 5‐Membered Cycles by Intermolecular Reactions
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The Proline‐Catalyzed Mannich Reaction and the Advent of Enamine Catalysis
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Catalytic Generation of Ammonium Enolates and Related Tertiary Amine‐Derived Intermediates: Applications, Mechanism, and Stereochemical Models ( n ?→?π * )
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Organoamines‐catalyzed Cycloadditions
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Multifunctional “Click” Prolinamides: A New Platform for Asymmetric Aldol Reactions in the Presence of Water with Catalyst Recycling
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Using Conveniently Designed α‐Amino Ketones in Michael Reactions under Iminium Catalysis: Enantioselective Synthesis of γ‐Lactams and γ‐Amino‐δ‐keto Esters
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A Magnetoclick Imidazolidinone Nanocatalyst for Asymmetric 1,3‐Dipolar Cycloadditions
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Asymmetric Synthesis of Spirooxindole β ‐lactams via Isothiourea‐catalyzed Mannich/lactamization Reaction of Aryl Acetic Acids with Isatin‐derived Ketimines
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C−H Reactivity of the α‐Position in Nitrones and Nitronates
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Enantioselective Ammonium Ylide Mediated One‐Pot Synthesis of Highly Substituted γ‐Butyrolactones
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Recent Developments in Enantioselective Multicatalyzed Tandem Reactions
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Enantioselective Syntheses of 3,4‐Dihydropyrans Employing Isochalcogenourea‐Catalyzed Formal (4+2)‐Cycloadditions of Allenoates
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Ammonium Ylide Mediated Cyclization Reactions
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Catalyst‐free Synthesis of Benzothiazolopyrimidines via Visible‐Light‐Induced Wolff Rearrangement/[4+2] Cycloaddition Process
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Organocatalyst Mediated Pot‐Economical Total Synthesis of (−)‐Quinine and its Derivatives
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C 3 ‐Symmetric Chiral Cage‐Shaped Phosphates: Synthesis and Application as Organocatalysts in Asymmetric Iodolactonizations
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Asymmetrische Organokatalyse: Eintritt in die Reifezeit
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Wie werden Iminium‐katalysierte Cyclopropanierungen durch elektrostatische Aktivierung gesteuert?
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Tertiary Amine Mediated Tandem Cross‐Rauhut–Currier/Acetalization Reactions: Access to Functionalized Spiro‐3,4‐Dihydropyrans
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Asymmetric Organocatalytic Electrophilic Phosphination
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Enantioselective Amine‐Catalyzed [4+2] Annulations of Allenoates and Oxo‐dienes: An Asymmetric Synthesis of Dihydropyrans
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Organocatalytic Synthesis of Highly Functionalized Pyridines at Room Temperature
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Direct Catalytic Asymmetric Synthesis of N‐Heterocycles from Commodity Acid Chlorides by Employing α,β‐Unsaturated Acylammonium Salts
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Isothiourea‐Mediated One‐Pot Synthesis of Functionalized Pyridines
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One‐Pot Tandem Approach to Spirocyclic Oxindoles Featuring Adjacent Spiro‐Stereocenters
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Metal‐Free Catalyst for the Chemoselective Methylation of Amines Using Carbon Dioxide as a Carbon Source
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Michael Addition Catalyzed by Chiral Secondary Amine Phosphoramide Using Fluorinated Silyl Enol Ethers: Formation of Quaternary Carbon Stereocenters
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Asymmetrische Organokatalyse: α,β‐ungesättigte Acylammoniumsalze erweisen sich als immer nützlicher
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Exploiting the Imidazolium Effect in Base‐free Ammonium Enolate Generation: Synthetic and Mechanistic Studies
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Stereospecific Construction of Contiguous Quaternary All‐Carbon Centers by Oxidative Ring Contraction
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Asymmetric [4+2] Annulation of C1 Ammonium Enolates with Copper‐Allenylidenes
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Aryloxide‐Facilitated Catalyst Turnover in Enantioselective α,β‐Unsaturated Acyl Ammonium Catalysis
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Catalytic Asymmetric [8+2] Annulation Reactions Promoted by a Recyclable Immobilized Isothiourea
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C‐H‐Aktivierung ermöglicht eine kurze Totalsynthese von Chinin und Analoga mit erhöhter Anti‐Malaria‐Aktivität
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Direct Catalytic Asymmetric Aldol Reaction of α‐Alkoxyamides to α‐Fluorinated Ketones
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Catalytic Generation of C1 Ammonium Enolates from Halides and CO for Asymmetric Cascade Reactions
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A Regio‐ and Stereodivergent Synthesis of Homoallylic Amines by a One‐Pot Cooperative‐Catalysis‐Based Allylic Alkylation/Hofmann Rearrangement Strategy
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Base‐free Enantioselective C(1)‐Ammonium Enolate Catalysis Exploiting Aryloxides: A Synthetic and Mechanistic Study
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Acyl Donor Intermediates in N‐Heterocyclic Carbene Catalysis: Acyl Azolium or Azolium Enolate?
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Copper(I)‐Catalyzed Asymmetric Interrupted Kinugasa Reaction: Synthesis of α‐Thiofunctional Chiral β‐Lactams
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Enantioselective Synthesis of α‐Aryl‐β2‐Amino‐Esters by Cooperative Isothiourea and Brønsted Acid Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202100601openalex-snapshot
Modular Synthesis of α‐Quaternary Chiral β‐Lactams by a Synergistic Copper/Palladium‐Catalyzed Multicomponent Reaction
inferred← citeshttps://doi.org/10.1002/ange.202202621openalex-snapshot
Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β‐Unsaturated Esters
inferred← citeshttps://doi.org/10.1002/ange.202204378openalex-snapshot
Sigmatrope [1,5]‐Kohlenstoffverschiebung transienter C3‐Ammoniumenolate
inferred← citeshttps://doi.org/10.1002/ange.202206647openalex-snapshot
Lewis Base Catalyzed Synthesis of Sulfur Heterocycles via the C1‐Pyridinium Enolate
inferred← citeshttps://doi.org/10.1002/ange.202208800openalex-snapshot
A Desilylative Approach to Alkyl Substituted C(1)‐Ammonium Enolates: Application in Enantioselective [2+2] Cycloadditions
inferred← citeshttps://doi.org/10.1002/ange.202315345openalex-snapshot
Chiral Isochalcogenourea‐Catalysed Enantioselective (4+2) Cycloadditions of Allenoates
inferred← citeshttps://doi.org/10.1002/anie.200704684openalex-snapshot
Asymmetric Organocatalysis: From Infancy to Adolescence
inferred← citeshttps://doi.org/10.1002/anie.200900933openalex-snapshot
How Does Electrostatic Activation Control Iminium‐Catalyzed Cyclopropanations?
inferred← citeshttps://doi.org/10.1002/anie.200905091openalex-snapshot
Tertiary Amine Mediated Tandem Cross‐Rauhut–Currier/Acetalization Reactions: Access to Functionalized Spiro‐3,4‐Dihydropyrans
inferred← citeshttps://doi.org/10.1002/anie.201007188openalex-snapshot
Asymmetric Organocatalytic Electrophilic Phosphination
inferred← citeshttps://doi.org/10.1002/anie.201100945openalex-snapshot
Enantioselective Amine‐Catalyzed [4+2] Annulations of Allenoates and Oxo‐dienes: An Asymmetric Synthesis of Dihydropyrans
inferred← citeshttps://doi.org/10.1002/anie.201301519openalex-snapshot
Organocatalytic Synthesis of Highly Functionalized Pyridines at Room Temperature
inferred← citeshttps://doi.org/10.1002/anie.201306050openalex-snapshot
Direct Catalytic Asymmetric Synthesis of N‐Heterocycles from Commodity Acid Chlorides by Employing α,β‐Unsaturated Acylammonium Salts
inferred← citeshttps://doi.org/10.1002/anie.201306786openalex-snapshot
Isothiourea‐Mediated One‐Pot Synthesis of Functionalized Pyridines
inferred← citeshttps://doi.org/10.1002/anie.201307250openalex-snapshot
One‐Pot Tandem Approach to Spirocyclic Oxindoles Featuring Adjacent Spiro‐Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.201407689openalex-snapshot
Metal‐Free Catalyst for the Chemoselective Methylation of Amines Using Carbon Dioxide as a Carbon Source
inferred← citeshttps://doi.org/10.1002/anie.201501747openalex-snapshot
Michael Addition Catalyzed by Chiral Secondary Amine Phosphoramide Using Fluorinated Silyl Enol Ethers: Formation of Quaternary Carbon Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.201602217openalex-snapshot
Asymmetric Organocatalysis: The Emerging Utility of α,β‐Unsaturated Acylammonium Salts
inferred← citeshttps://doi.org/10.1002/anie.201608046openalex-snapshot
Exploiting the Imidazolium Effect in Base‐free Ammonium Enolate Generation: Synthetic and Mechanistic Studies
inferred← citeshttps://doi.org/10.1002/anie.201609975openalex-snapshot
Stereospecific Construction of Contiguous Quaternary All‐Carbon Centers by Oxidative Ring Contraction
inferred← citeshttps://doi.org/10.1002/anie.201700105openalex-snapshot
Asymmetric [4+2] Annulation of C1 Ammonium Enolates with Copper‐Allenylidenes
inferred← citeshttps://doi.org/10.1002/anie.201706402openalex-snapshot
Aryloxide‐Facilitated Catalyst Turnover in Enantioselective α,β‐Unsaturated Acyl Ammonium Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201707341openalex-snapshot
Catalytic Asymmetric [8+2] Annulation Reactions Promoted by a Recyclable Immobilized Isothiourea
inferred← citeshttps://doi.org/10.1002/anie.201804551openalex-snapshot
C−H Activation Enables a Concise Total Synthesis of Quinine and Analogues with Enhanced Antimalarial Activity
inferred← citeshttps://doi.org/10.1002/anie.201814607openalex-snapshot
Direct Catalytic Asymmetric Aldol Reaction of α‐Alkoxyamides to α‐Fluorinated Ketones
inferred← citeshttps://doi.org/10.1002/anie.201901501openalex-snapshot
Catalytic Generation of C1 Ammonium Enolates from Halides and CO for Asymmetric Cascade Reactions
inferred← citeshttps://doi.org/10.1002/anie.201905426openalex-snapshot
A Regio‐ and Stereodivergent Synthesis of Homoallylic Amines by a One‐Pot Cooperative‐Catalysis‐Based Allylic Alkylation/Hofmann Rearrangement Strategy
inferred← citeshttps://doi.org/10.1002/anie.201908627openalex-snapshot
Base‐free Enantioselective C(1)‐Ammonium Enolate Catalysis Exploiting Aryloxides: A Synthetic and Mechanistic Study
inferred← citeshttps://doi.org/10.1002/anie.202010348openalex-snapshot
Acyl Donor Intermediates in N‐Heterocyclic Carbene Catalysis: Acyl Azolium or Azolium Enolate?
inferred← citeshttps://doi.org/10.1002/anie.202013450openalex-snapshot
Copper(I)‐Catalyzed Asymmetric Interrupted Kinugasa Reaction: Synthesis of α‐Thiofunctional Chiral β‐Lactams
inferred← citeshttps://doi.org/10.1002/anie.202016220openalex-snapshot
Enantioselective Synthesis of α‐Aryl‐β2‐Amino‐Esters by Cooperative Isothiourea and Brønsted Acid Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202100601openalex-snapshot
Modular Synthesis of α‐Quaternary Chiral β‐Lactams by a Synergistic Copper/Palladium‐Catalyzed Multicomponent Reaction
inferred← citeshttps://doi.org/10.1002/anie.202202621openalex-snapshot
Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β‐Unsaturated Esters
inferred← citeshttps://doi.org/10.1002/anie.202204378openalex-snapshot
Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates
inferred← citeshttps://doi.org/10.1002/anie.202206647openalex-snapshot
Lewis Base Catalyzed Synthesis of Sulfur Heterocycles via the C1‐Pyridinium Enolate
inferred← citeshttps://doi.org/10.1002/anie.202208800openalex-snapshot
A Desilylative Approach to Alkyl Substituted C(1)‐Ammonium Enolates: Application in Enantioselective [2+2] Cycloadditions
inferred← citeshttps://doi.org/10.1002/anie.202315345openalex-snapshot
Chiral Isochalcogenourea‐Catalysed Enantioselective (4+2) Cycloadditions of Allenoates
inferred← citeshttps://doi.org/10.1002/cctc.202000882openalex-snapshot
Isothiourea‐Catalyzed Synthesis of Pyrrole‐ and Indole‐Functionalized Tetrasubstituted Pyridines
inferred← citeshttps://doi.org/10.1002/cctc.202001371openalex-snapshot
Recent Advances in Applying Carbonyl‐stabilized Phosphorus Ylides for Catalysis
inferred← citeshttps://doi.org/10.1002/cctc.202200126openalex-snapshot
Catalytic Asymmetric Isomerization of (Homo)Allylic Alcohols: Recent Advances and Challenges
inferred← citeshttps://doi.org/10.1002/ceur.202300015openalex-snapshot
Isothiourea‐Catalyzed Enantioselective Functionalisation of Glycine Schiff Base Aryl Esters via 1,6‐ and 1,4‐Additions
inferred← citeshttps://doi.org/10.1002/chem.200800145openalex-snapshot
Organocatalytic Multicomponent α‐Methylenation/Diels–Alder Reactions: A Versatile Route to Substituted Cyclohexenecarbaldehyde Derivatives
inferred← citeshttps://doi.org/10.1002/chem.200902896openalex-snapshot
Catalytic Asymmetric Formation of δ‐Lactones from Unsaturated Acyl Halides
inferred← citeshttps://doi.org/10.1002/chem.200903484openalex-snapshot
Boronic Acid Catalysis for Mild and Selective [3+2] Dipolar Cycloadditions to Unsaturated Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/chem.201100534openalex-snapshot
Lewis Base Assisted Brønsted Base Catalysis: Direct Regioselective Asymmetric Vinylogous Alkylation of Allylic Sulfones
inferred← citeshttps://doi.org/10.1002/chem.201101755openalex-snapshot
Increasing the Reactivity of Nitrogen Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201102522openalex-snapshot
Organocatalytic Enantioselective Amination of Morita–Baylis–Hillman Carbonates with Masked Ammonia: A Facile Method for the Synthesis of Unprotected α‐Methylene‐β‐Amino Esters
inferred← citeshttps://doi.org/10.1002/chem.201200655openalex-snapshot
Diastereodivergent Synthesis of 3‐Spirocyclopropyl‐2‐oxindoles through Direct Enantioselective Cyclopropanation of Oxindoles
inferred← citeshttps://doi.org/10.1002/chem.201500481openalex-snapshot
Chiral Iminophosphoranes—An Emerging Class of Superbase Organocatalysts
inferred← citeshttps://doi.org/10.1002/chem.201501481openalex-snapshot
Nucleophilic β‐Carbon Activation of Propionic Acid as a 3‐Carbon Synthon by Carbene Organocatalysis
inferred← citeshttps://doi.org/10.1002/chem.202002059openalex-snapshot
Generation and Reactivity of C(1)‐Ammonium Enolates by Using Isothiourea Catalysis
inferred← citeshttps://doi.org/10.1002/chin.200816242openalex-snapshot
ChemInform Abstract: Recent Developments in the Use of Catalytic Asymmetric Ammonium Enolates in Chemical Synthesis
inferred← citeshttps://doi.org/10.1002/chin.201016262openalex-snapshot
ChemInform Abstract: Acid—Base Properties of Enols and Enolates
inferred← citeshttps://doi.org/10.1002/chir.20942openalex-snapshot
Asymmetric Diels–Alder reaction involving chiral benzimidazoles as organocatalysts
inferred← citeshttps://doi.org/10.1002/chir.22678openalex-snapshot
Synthesis of l ‐threitol‐based crown ethers and their application as enantioselective phase transfer catalyst in Michael additions
inferred← citeshttps://doi.org/10.1002/cjoc.202100476openalex-snapshot
Synergistic Copper and Chiral Lewis Base Catalysis for the Asymmetric Synthesis of Pyrrolo[1,2‐a]indoles
inferred← citeshttps://doi.org/10.1002/cjoc.70740openalex-snapshot
Facile Access to Polysubstituted Seven‐Membered Lactones via Relay Visible‐Light/Pd‐Catalyzed [3+2+2] Cycloaddition
inferred← citeshttps://doi.org/10.1002/cssc.202102157openalex-snapshot
Mechanochemical Organocatalysis: Do High Enantioselectivities Contradict What We Might Expect?
inferred← citeshttps://doi.org/10.1002/ejic.201900572openalex-snapshot
Transfer Hydrogenation of Azo Compounds with Ammonia Borane Using a Simple Acyclic Phosphite Precatalyst
inferred← citeshttps://doi.org/10.1002/ejoc.200900020openalex-snapshot
Synthesis and Solid‐State Structure of Tetrabutylammonium Imidazolate–Dipyrrole Formed by Self Assembly
inferred← citeshttps://doi.org/10.1002/ejoc.200900932openalex-snapshot
Enantioselective Michael Addition of Aromatic Ketones to Nitroolefins Catalyzed by Bifunctional Thioureas and Mechanistic Insight
inferred← citeshttps://doi.org/10.1002/ejoc.201101255openalex-snapshot
Lewis Base Assisted Brønsted Base Catalysis: Direct Asymmetric Allylic Alkylation of Indenes
inferred← citeshttps://doi.org/10.1002/ejoc.201201701openalex-snapshot
Chiral α‐Arylethanamines: An Organocatalyst for the Enantioselective α‐Amination of Branched Aldehydes
inferred← citeshttps://doi.org/10.1002/ejoc.201300136openalex-snapshot
Unusual Skeletal Rearrangement of Unsaturated Seven‐Membered Lactams into Fused Pyrrolidinolactones
inferred← citeshttps://doi.org/10.1002/ejoc.201300738openalex-snapshot
Organocatalytic Asymmetric Allylic Alkylation of Morita–Baylis–Hillman Carbonates with Phosphorus Ylides: Synthesis of Chiral 3‐Substituted 2,4‐Functionalized 1,4‐Pentadienes
inferred← citeshttps://doi.org/10.1002/ejoc.201900326openalex-snapshot
Synthesis of Fused Indoline‐Cyclobutanone Derivatives via an Intramolecular [2+2] Cycloaddition
inferred← citeshttps://doi.org/10.1002/ejoc.202200112openalex-snapshot
Enantioselective Cyclopropanation of 2‐Cyano‐3‐arylacrylates Using Carbohydrate‐Based Crown Ethers
inferred← citeshttps://doi.org/10.1002/ejoc.202201238openalex-snapshot
Organophosphites: An Addition to the Arsenal of Organocatalysts
inferred← citeshttps://doi.org/10.1002/ejoc.202300704openalex-snapshot
Chiral Lewis Base‐Catalysed Asymmetric Syntheses of Benzo‐fused ϵ‐Lactones
inferred← citeshttps://doi.org/10.1002/ejoc.202300982openalex-snapshot
Cooperative Chiral Lewis Base/Palladium‐Catalyzed Asymmetric Syntheses of Methylene‐Containing δ‐Lactams
inferred← citeshttps://doi.org/10.1002/ejoc.202401443openalex-snapshot
Synthesis and Reactivity of 1,4‐Ethano‐1,5‐Naphthyridine Derivatives Using Microwave Activation or Flow Chemistry
inferred← citeshttps://doi.org/10.1002/ejoc.202500434openalex-snapshot
Catalytic Asymmetric Transformations of Ketenes
inferred← citeshttps://doi.org/10.1002/ejoc.70673openalex-snapshot
Isotelluroureas for Asymmetric C1 Ammonium Enolate Reactions
inferred← citeshttps://doi.org/10.1002/hlca.201000384openalex-snapshot
Copper‐Catalyzed Bis(methoxycarbonyl)carbene Reactions of α,β‐Unsaturated Carboxamides
inferred← citeshttps://doi.org/10.1002/hlca.201100020openalex-snapshot
An Efficient Synthesis of a (−)‐Physostigmine's Library for Identifying Potential Anti‐Alzheimer's Agents
inferred← citeshttps://doi.org/10.1002/hlca.201200004openalex-snapshot
The Reactions of α‐Ylidene (Vinylidene, Benzylidene, Styrylmethylidene) Bis[carbonyls] with Copper Mono/Bis[carbonylcarbenoids]
inferred← citeshttps://doi.org/10.1002/hlca.201200459openalex-snapshot
Synthesis and Reactions of 2‐[1‐Methyl‐1‐(pyrrolidin‐2‐yl)ethyl]‐1H‐pyrrole and Some Derivatives with Aldehydes: Chiral Structures Combining a Secondary‐Amine Group with an 1H‐Pyrrole Moiety as Excellent H‐Bond Donor
inferred← citeshttps://doi.org/10.1002/pola.23439openalex-snapshot
Synthesis and chiral micellization behavior of optically active amphiphilic diblock copolymer bearing quinine pendants
inferred← citeshttps://doi.org/10.1002/slct.201600995openalex-snapshot
Synthesis of Magnetic Nanoparticles and Polymer Supported Imidazolidinone Catalysts for Enantioselective Friedel‐Crafts Alkylation of Indoles
inferred← citeshttps://doi.org/10.1002/slct.201701221openalex-snapshot
Formal [2+1] Annulation (Spiro‐Cyclopropanation) Reaction between Sulfur Ylides Derived from Baylis‐Hillman Bromides and Arylidene Indane‐1,3‐Dione
inferred← citeshttps://doi.org/10.1002/smtd.202301363openalex-snapshot
Preparation and Application of Single‐Atom Cobalt Catalysts in Organic Synthesis and Environmental Remediation
inferred← citeshttps://doi.org/10.1002/tcr.202200054openalex-snapshot
N‐Heterocyclic Carbene (NHC)‐Catalyzed Transformations Involving Azolium Enolates
inferred← citeshttps://doi.org/10.1002/tcr.202300042openalex-snapshot
Asymmetric Organocatalyzed Intermolecular Functionalization of Cyclohexanone‐Derived Dienones
inferred← citeshttps://doi.org/10.1007/7081_2025_93openalex-snapshot
Photoinduced Wolff Rearrangement for Synthesizing Chiral Heterocycles
inferred← citeshttps://doi.org/10.1007/978-3-642-28118-1_2openalex-snapshot
Background
inferred← citeshttps://doi.org/10.1007/978-94-007-1454-0_2openalex-snapshot
“Green” Asymmetric Synthesis: The Catalysts
inferred← citeshttps://doi.org/10.1007/s00706-016-1866-8openalex-snapshot
On the origin of the stereoselectivity in chiral amide-based ammonium ylide-mediated epoxidations
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00121-9openalex-snapshot
Formation of Four-membered Heterocycles
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00309-8openalex-snapshot
3.9 Alkaloid Derived Auxiliaries: Cinchona Alkaloids and Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00125-7openalex-snapshot
1.19 Carbonyl and Imine Activation
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00405-5openalex-snapshot
4.03 Organocatalytic Asymmetric Nucleophilic Addition to Electron-Deficient Alkenes
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00426-2openalex-snapshot
4.20 Addition of Ketocarbenes to Alkenes, Alkynes, and Aromatic Systems
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00503-6openalex-snapshot
5.03 Formation of Four-Membered Heterocycles
inferred← citeshttps://doi.org/10.1016/b978-0-12-385464-3.00001-7openalex-snapshot
The Literature of Heterocyclic Chemistry, Part X, 2005–2007
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14634-7openalex-snapshot
Rings of Power: Enzymatic Routes to β-Lactones
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00045-7openalex-snapshot
[4 + 2] Cycloadditions Catalyzed by Nucleophilic Catalysts
inferred← citeshttps://doi.org/10.1016/b978-0-323-91729-2.00021-5openalex-snapshot
Carbohydrate-based chiral organocatalysts
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00074-0openalex-snapshot
Formation of Four-Membered Heterocycles
inferred← citeshttps://doi.org/10.1016/b978-0-615-39515-9.50006-0openalex-snapshot
Cyclization
inferred← citeshttps://doi.org/10.1016/j.arabjc.2024.106027openalex-snapshot
Organocatalyst as a synthetic gadget for pharmaceutically potent molecules
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.03.018openalex-snapshot
Metal-free synthesis of substituted phenols from arylboronic acids in water at room temperature
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.110923openalex-snapshot
Highly stereo- and enantio‑selective synthesis of spiro cyclopropyl oxindoles via organic catalyst-mediated cyclopropanation
inferred← citeshttps://doi.org/10.1016/j.ccr.2014.12.017openalex-snapshot
Magnetically retrievable catalysts for asymmetric synthesis
inferred← citeshttps://doi.org/10.1016/j.ccr.2025.216636openalex-snapshot
Advances in catalysis using Xantphos-like ligands; simplicity goes a long way
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2025.110434openalex-snapshot
Enantioselective isothiourea-catalysed α-fluorination of C1-ammonium enolates generated from arylesters
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114445openalex-snapshot
Mechanistic studies on an isothiourea-catalyzed reaction of an aromatic ester with an imine
inferred← citeshttps://doi.org/10.1016/j.rechem.2023.101067openalex-snapshot
Catalytic enantioselective Gilman-Speeter synthesis of β-lactams by nucleophilic activation of carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100063openalex-snapshot
Enantioselective α-heterofunctionalization reactions of catalytically generated C1-Lewis base enolates
inferred← citeshttps://doi.org/10.1016/j.tet.2008.03.075openalex-snapshot
Synthesis of isoxazoline N-oxides and its application in the formal synthesis of dehydroclausenamide
inferred← citeshttps://doi.org/10.1016/j.tet.2011.05.088openalex-snapshot
Tandem intramolecular oxa-Michael addition/decarboxylation reaction catalyzed by bifunctional cinchona alkaloids: facile synthesis of chiral flavanone derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.103openalex-snapshot
Asymmetric organocatalytic cycloadditions
inferred← citeshttps://doi.org/10.1016/j.tet.2012.10.028openalex-snapshot
Facile and controllable synthesis of multiply substituted benzenes via a formal [3+3] cycloaddition approach
inferred← citeshttps://doi.org/10.1016/j.tet.2013.06.020openalex-snapshot
Recent developments in enantioselective multicatalysed tandem reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2019.06.020openalex-snapshot
Synthesis of chiral crown ethers derived from d-galactose and their application in enantioselective reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131648openalex-snapshot
Isosterically designed chiral catalysts: Rationale, optimization and their application in enantioselective nucleophilic addition to aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2008.11.007openalex-snapshot
An unexpected tandem enantioselective Michael addition/oxa-nucleophilic rearrangement reaction of β,γ-unsaturated α-keto esters catalyzed by cinchona alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.01.009openalex-snapshot
Synthesis and asymmetric catalytic activity of (1S,1′S)-4,4′-biquinazoline-based primary amines
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.01.011openalex-snapshot
A highly chemo- and enantioselective nitroaldol reaction of haloenals: preparation of chiral functionalized allylic alcohols
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.01.011openalex-snapshot
Novel efficient bifunctional calixarene thiourea organocatalysts: synthesis and application in the direct enantioselective aldol reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.10.085openalex-snapshot
Facile preparation of optically pure diamines and their applications in asymmetric aldol reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.021openalex-snapshot
Nitrogen ylide-mediated cyclopropanation of lactams and lactones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.132openalex-snapshot
Mild and efficient boronic acid catalysis of Diels–Alder cycloadditions to 2-alkynoic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.02.095openalex-snapshot
Asymmetric cyclopropanation of chalcones using chiral phase-transfer catalysts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.02.036openalex-snapshot
Organocatalytic reactions involving nitrogen-ylides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.08.082openalex-snapshot
Highly efficient organocatalytic asymmetric Michael addition of homoserine lactone derived cyclic imino esters to nitroolefins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151183openalex-snapshot
Enantioselective synthesis of chiral carbocyclic pyrimidine nucleosides via asymmetric cyclopropanation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152552openalex-snapshot
Stereoselective cyclopropanations of amino-acid derived enones
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00564openalex-snapshot
Catalytic Enantioselective Alkylation of Prochiral Enolates
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00203openalex-snapshot
The Golden Age of Transfer Hydrogenation
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01717openalex-snapshot
Carboxylative Cyclization of 2-Butenoates with Carbon Dioxide: Access to Glutaconic Anhydrides
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02208openalex-snapshot
Asymmetric Cascade Carbonylation/Annulation of Benzyl Bromides, CO, and Vinyl Benzoxazinanones Enabled by Pd/Chiral Lewis-Base Relay Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00367openalex-snapshot
Asymmetric Synthesis of cis-3,4-Dihydrocoumarins via [4 + 2] Cycloadditions Catalyzed by Amidine Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.7b03278openalex-snapshot
Domino Reaction of Pyrrolidinium Ylides: Michael Addition/[1,2]-Stevens Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00531openalex-snapshot
Mechanism-Based Design and Optimization of a Catalytic Electrophilic Cyclopropanation without Diazomethane
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00361openalex-snapshot
Three-Component [1 + 1 + 1] Cyclopropanation with Ruthenium(II)
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00461openalex-snapshot
Isothiourea and Brønsted Acid Cooperative Catalysis: Enantioselective Construction of Dihydropyridinones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01447openalex-snapshot
Sequential Visible-Light and N -Heterocyclic Carbene Catalysis: Stereoselective Synthesis of Tetrahydropyrano[2,3- b ]indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02256openalex-snapshot
Enantioselective α-Chlorination Reactions of in Situ Generated C1 Ammonium Enolates under Base-Free Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00986openalex-snapshot
Photochemical Wolff Rearrangement Initiated Generation and Subsequent α-Chlorination of C1 Ammonium Enolates
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01659openalex-snapshot
Total Syntheses of Cinchona Alkaloids via Photoredox-Catalyzed Deoxygenative Arylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01442openalex-snapshot
Relay Annulation of Ammonium Ylides with Oxindole-Derived α,β-Unsaturated Ketimines: Catalytic Construction of Spiro-polycyclic Oxindoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01639openalex-snapshot
Asymmetric Catalytic Synthesis of Thiochromenes via an Acyl Transfer-Initiated Cascade
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03110openalex-snapshot
Highly Enantioselective Synthesis of Chiral Cyclopropyl Nucleosides via Catalytic Asymmetric Intermolecular Cyclopropanation
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02423openalex-snapshot
Isothiourea-Catalyzed Enantioselective Functionalization of 2-Pyrrolyl Acetic Acid: Two-Step Synthesis of Stereodefined Dihydroindolizinones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02521openalex-snapshot
Asymmetric Synthesis of Allenyl α-Amino Amides by an Isothiourea Catalyzed Enantioselective [2,3]-Sigmatropic Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03777openalex-snapshot
Selective Synthesis of (+)-Dysoline
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