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Catalytic Synthesis of γ-Lactams via Direct Annulations of Enals and N-Sulfonylimines
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.198409481openalex-snapshot
The Dendralenes—a Neglected Group of Highly Unsaturated Hydrocarbons
inferredcites →https://doi.org/10.1002/anie.200460927openalex-snapshot
Butenyl‐Substituted Alkaline‐Earth Metallocenes: A First Step towards Olefin Complexes of the Alkaline‐Earth Metals
inferredcites →https://doi.org/10.1002/anie.200461572openalex-snapshot
Organocatalyzed Conjugate Umpolung of α,β‐Unsaturated Aldehydes for the Synthesis of γ‐Butyrolactones
inferredcites →https://doi.org/10.1016/0165-0173(94)90011-6openalex-snapshot
Piracetam and other structurally related nootropics
inferredcites →https://doi.org/10.1016/b978-0-08-052349-1.00036-6openalex-snapshot
Metal Homoenolates
inferredcites →https://doi.org/10.1016/s0040-4039(00)89172-8openalex-snapshot
Conjugate addition of organocopper reagents to n-tosylated α, β-unsaturated amides
inferredcites →https://doi.org/10.1016/s0040-4039(99)01653-6openalex-snapshot
Convenient synthesis of a reactive ester homoenolate
inferredcites →https://doi.org/10.1021/ja00996a056openalex-snapshot
Diazoalkanes from hydrazone anions. Novel oxidation reaction
inferredcites →https://doi.org/10.1021/jo982375xopenalex-snapshot
The [3 + 2] Annulation of Allylsilanes and Chlorosulfonyl Isocyanate: Stereoselective Synthesis of 2-Pyrrolidinones
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.4494474openalex-extracted
Catalytic Enantioselective Gilman-Speeter Synthesis of Β-Lactams by Nucleophilic Activation of Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/047084289x.rn01180openalex-snapshot
1,3-Bis(2,6-diisopropylphenyl)imidazolidinium Chloride
inferred← citeshttps://doi.org/10.1002/0471264229.os087.01openalex-snapshot
Metal‐Free One‐Pot Oxidative Amination of Aromatic Aldehydes: Conversion of Benzaldehyde to N ‐Benzoyl Pyrrolidine
inferred← citeshttps://doi.org/10.1002/9781118730379.ch9openalex-snapshot
Catalytic Reactions withN‐Mesityl‐SubstitutedN‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/9781119468769.hpcbm003openalex-snapshot
Synthesis of Pyrrolidones and Caprolactams by Ring Modification or Multi‐component Ring‐Forming Reaction
inferred← citeshttps://doi.org/10.1002/9781119736424.ch6openalex-snapshot
ASYMMETRIC CARBENE CATALYSIS
inferred← citeshttps://doi.org/10.1002/9783527652235.ch10openalex-snapshot
Enantioselective Annulations with Chiral N‐Mesityl N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/9783527675142.ch27openalex-snapshot
Catalysis with Stable Carbenes ( n ?→?π*)
inferred← citeshttps://doi.org/10.1002/adsc.200800051openalex-snapshot
Diastereoselective Synthesis of Trifluoromethylated γ‐Butyrolactones via N‐Heterocyclic Carbene‐Catalyzed Conjugated Umpolung of α,β‐Unsaturated Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.200800251openalex-snapshot
Stereoselective Synthesis of γ‐Butyrolactones via Organocatalytic Annulations of Enals and Keto Esters
inferred← citeshttps://doi.org/10.1002/adsc.200900538openalex-snapshot
N‐Heterocyclic Carbene‐Mediated Enantioselective Addition of Phenols to Unsymmetrical Alkylarylketenes
inferred← citeshttps://doi.org/10.1002/adsc.201000240openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Reaction of Alkynyl Aldehydes with 1,3‐Keto Esters or 1,3‐Diketones
inferred← citeshttps://doi.org/10.1002/adsc.201100622openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Enantioselective Annulation of Bromoenal and 1,3‐Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201200031openalex-snapshot
Exploiting Acyl and Enol Azolium Intermediates via N‐Hetero‐ cyclic Carbene‐Catalyzed Reactions of α‐Reducible Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.201200499openalex-snapshot
Construction of Contiguous Tetrasubstituted Carbon Stereocenters by Intramolecular Crossed Benzoin Reactions Catalyzed by N‐Heterocyclic Carbene (NHC) Organocatalyst
inferred← citeshttps://doi.org/10.1002/adsc.201300219openalex-snapshot
Enantioselective N‐Heterocyclic Carbene‐Catalyzed Annulations of 2‐Bromoenals with 1,3‐Dicarbonyl Compounds and Enamines via Chiral α,β‐Unsaturated Acylazoliums
inferred← citeshttps://doi.org/10.1002/adsc.201401070openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Umpolung Formal [3+3] Cycloaddition of Enals with Isatogens: Access to Fused Indolin‐3‐ones with a Tetrasubstituted Carbon Stereocenter
inferred← citeshttps://doi.org/10.1002/adsc.201500295openalex-snapshot
Rhodium‐Catalyzed Addition of Alkyltrifluoroborate Salts to Imines
inferred← citeshttps://doi.org/10.1002/adsc.70087openalex-snapshot
Thiazolium Salts: From Thiamine to Cutting‐Edge Organocatalysts
inferred← citeshttps://doi.org/10.1002/adsc.70127openalex-snapshot
Chemodivergent Higher‐Order Annulation of Azaheptafulvenes with Enals Through N ‐Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/ajoc.201200153openalex-snapshot
Anomalous Effect of α,α,α‐Trifluoroacetophenone Derivatives on a Conjugated Umpolung Reaction: Enantioselective Direct Self‐Annulation of Enals Catalyzed by a Chiral Cyclophane‐type N‐Heterocyclic Carbene
inferred← citeshttps://doi.org/10.1002/ajoc.201400010openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed [3+3] Cyclocondensation of Bromoenals and Ketimines: Highly Enantioselective Synthesis of Dihydropyridinones
inferred← citeshttps://doi.org/10.1002/ajoc.201600074openalex-snapshot
Synthesis of Cyclopentachromans by N‐Heterocyclic Carbene‐Mediated Homoenolate Annulation of Chroman‐3‐ene‐4‐ones
inferred← citeshttps://doi.org/10.1002/ajoc.201600419openalex-snapshot
Sequential N‐Heterocyclic Carbene‐Catalyzed Reactions of Enals and Cyclic Aryldiene‐1,3‐Diones: Synthesis of Tricyclic Chromenones and Related Compounds
inferred← citeshttps://doi.org/10.1002/ajoc.201700520openalex-snapshot
N‐Heterocyclic‐Carbene‐Catalyzed Reactions of Nitroalkenes: Synthesizing Important Building Blocks
inferred← citeshttps://doi.org/10.1002/ange.200502617openalex-snapshot
Erweiterte Reaktionswege im Mechanismus der Heterazolium‐Katalyse – aussichtsreiche Konzepte für vielseitige Synthesemethoden
inferred← citeshttps://doi.org/10.1002/ange.200503885openalex-snapshot
Asymmetric Intramolecular Crossed‐Benzoin Reactions by N‐Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/ange.200603380openalex-snapshot
N‐heterocyclische Carbene als Organokatalysatoren
inferred← citeshttps://doi.org/10.1002/ange.200604943openalex-snapshot
Lewis‐Base‐Katalyse in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.200705229openalex-snapshot
Highly Stereoselective Synthesis of Substituted γ‐Lactams from Acylsilanes
inferred← citeshttps://doi.org/10.1002/ange.201005352openalex-snapshot
α,β‐Unsaturated Acyl Azoliums from N‐Heterocyclic Carbene Catalyzed Reactions: Observation and Mechanistic Investigation
inferred← citeshttps://doi.org/10.1002/ange.201005908openalex-snapshot
Lewis Acid Activated Synthesis of Highly Substituted Cyclopentanes by the N‐Heterocyclic Carbene Catalyzed Addition of Homoenolate Equivalents to Unsaturated Ketoesters
inferred← citeshttps://doi.org/10.1002/ange.201007144openalex-snapshot
A Highly Regio‐ and Stereoselective Cascade Annulation of Enals and Benzodi(enone)s Catalyzed by N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/ange.201008081openalex-snapshot
Hoch asymmetrische NHC‐katalysierte Hydroacylierung nichtaktivierter Alkene
inferred← citeshttps://doi.org/10.1002/ange.201103555openalex-snapshot
Durch ein N‐heterocyclisches Carben katalysierte Umpolung von Michael‐Akzeptoren für intermolekulare Reaktionen
inferred← citeshttps://doi.org/10.1002/ange.201105415openalex-snapshot
Durch N‐heterocyclische Carbene katalysierte Dominoreaktionen
inferred← citeshttps://doi.org/10.1002/ange.201107831openalex-snapshot
Katalytische Mehrkomponentenreaktionen zur stereoselektiven Synthese von cis‐4,5‐disubstituierten Pyrrolidinonen und Tetrahydro‐3H‐pyrrolo[3,2‐c]chinolinen
inferred← citeshttps://doi.org/10.1002/ange.201201643openalex-snapshot
An N‐Heterocyclic Carbene/Lewis Acid Strategy for the Stereoselective Synthesis of Spirooxindole Lactones
inferred← citeshttps://doi.org/10.1002/ange.201202442openalex-snapshot
Catalytic Asymmetric Cross‐Aza‐Benzoin Reactions of Aliphatic Aldehydes with N‐Boc‐Protected Imines
inferred← citeshttps://doi.org/10.1002/ange.201203449openalex-snapshot
N‐Heterocyclic Carbene Catalyzed Homoenolate‐Addition Reaction of Enals and Nitroalkenes: Asymmetric Synthesis of 5‐Carbon‐Synthon δ‐Nitroesters
inferred← citeshttps://doi.org/10.1002/ange.201301304openalex-snapshot
Enantioselective N‐Heterocyclic Carbene Catalyzed Aza‐Benzoin Reaction of Enals with Activated Ketimines
inferred← citeshttps://doi.org/10.1002/ange.201303903openalex-snapshot
N‐Heterocyclic Carbene Catalyzed [4+3] Annulation of Enals and o‐Quinone Methides: Highly Enantioselective Synthesis of Benzo‐ε‐Lactones
inferred← citeshttps://doi.org/10.1002/ange.201305023openalex-snapshot
Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N‐Heterocyclic‐Carbene/Thiourea/Tertiary‐Amine Multicatalysis
inferred← citeshttps://doi.org/10.1002/ange.201305571openalex-snapshot
Highly Enantioselective γ‐Amination by N‐Heterocyclic Carbene Catalyzed [4+2] Annulation of Oxidized Enals and Azodicarboxylates
inferred← citeshttps://doi.org/10.1002/ange.201405178openalex-snapshot
Konjugierte Umpolung von β,β‐disubstituierten Enalen durch duale Katalyse mit N‐heterocyclischen Carbenen und Brønsted‐Säuren: einfacher Aufbau benachbarter, quartärer Stereozentren
inferred← citeshttps://doi.org/10.1002/ange.201405381openalex-snapshot
Durch N‐heterocyclische Carbene katalysierte formale [3+2]‐Anellierungen von Enalen: enantioselektiver Zugang zu Spiroheterocyclen
inferred← citeshttps://doi.org/10.1002/ange.201708994openalex-snapshot
Control of N‐Heterocyclic Carbene Catalyzed Reactions of Enals: Asymmetric Synthesis of Oxindole‐γ‐Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/ange.201712785openalex-snapshot
Catalytic Enantioselective Aza‐Benzoin Reactions of Aldehydes with 2H‐Azirines
inferred← citeshttps://doi.org/10.1002/ange.201812585openalex-snapshot
Enantioselective N‐Heterocyclic Carbene Catalysis that Exploits Imine Umpolung
inferred← citeshttps://doi.org/10.1002/ange.202008631openalex-snapshot
Pendant Alkoxy Groups on N‐Aryl Substitutions Drive the Efficiency of Imidazolylidene Catalysts for Homoenolate Annulation from Enal and Aldehyde
inferred← citeshttps://doi.org/10.1002/ange.202307286openalex-snapshot
A Homo‐Mannich Reaction Strategy Enables Collective Access to Ibophyllidine, Aspidosperma, Kopsia, and Melodinus Alkaloids
inferred← citeshttps://doi.org/10.1002/ange.202513913openalex-snapshot
Umpolung Activation of Bicyclobutanes via N‐Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/anie.200502617openalex-snapshot
Extending Mechanistic Routes in Heterazolium Catalysis–Promising Concepts for Versatile Synthetic Methods
inferred← citeshttps://doi.org/10.1002/anie.200503885openalex-snapshot
Asymmetric Intramolecular Crossed‐Benzoin Reactions by N‐Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/anie.200603380openalex-snapshot
N‐Heterocyclic Carbenes as Organocatalysts
inferred← citeshttps://doi.org/10.1002/anie.200604943openalex-snapshot
Lewis Base Catalysis in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.200705229openalex-snapshot
Highly Stereoselective Synthesis of Substituted γ‐Lactams from Acylsilanes
inferred← citeshttps://doi.org/10.1002/anie.201005352openalex-snapshot
α,β‐Unsaturated Acyl Azoliums from N‐Heterocyclic Carbene Catalyzed Reactions: Observation and Mechanistic Investigation
inferred← citeshttps://doi.org/10.1002/anie.201005908openalex-snapshot
Lewis Acid Activated Synthesis of Highly Substituted Cyclopentanes by the N‐Heterocyclic Carbene Catalyzed Addition of Homoenolate Equivalents to Unsaturated Ketoesters
inferred← citeshttps://doi.org/10.1002/anie.201007144openalex-snapshot
A Highly Regio‐ and Stereoselective Cascade Annulation of Enals and Benzodi(enone)s Catalyzed by N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/anie.201008081openalex-snapshot
Highly Asymmetric NHC‐Catalyzed Hydroacylation of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201103555openalex-snapshot
N‐Heterocyclic Carbene Catalyzed Umpolung of Michael Acceptors for Intermolecular Reactions
inferred← citeshttps://doi.org/10.1002/anie.201105415openalex-snapshot
N‐Heterocyclic Carbene Catalyzed Domino Reactions
inferred← citeshttps://doi.org/10.1002/anie.201107831openalex-snapshot
A Catalytic Multicomponent Approach for the Stereoselective Synthesis of cis‐4,5‐Disubstituted Pyrrolidinones and Tetrahydro‐3H‐pyrrolo[3,2‐c]quinolines
inferred← citeshttps://doi.org/10.1002/anie.201201643openalex-snapshot
An N‐Heterocyclic Carbene/Lewis Acid Strategy for the Stereoselective Synthesis of Spirooxindole Lactones
inferred← citeshttps://doi.org/10.1002/anie.201202442openalex-snapshot
Catalytic Asymmetric Cross‐Aza‐Benzoin Reactions of Aliphatic Aldehydes with N‐Boc‐Protected Imines
inferred← citeshttps://doi.org/10.1002/anie.201203449openalex-snapshot
N‐Heterocyclic Carbene Catalyzed Homoenolate‐Addition Reaction of Enals and Nitroalkenes: Asymmetric Synthesis of 5‐Carbon‐Synthon δ‐Nitroesters
inferred← citeshttps://doi.org/10.1002/anie.201301304openalex-snapshot
Enantioselective N‐Heterocyclic Carbene Catalyzed Aza‐Benzoin Reaction of Enals with Activated Ketimines
inferred← citeshttps://doi.org/10.1002/anie.201303903openalex-snapshot
N‐Heterocyclic Carbene Catalyzed [4+3] Annulation of Enals and o ‐Quinone Methides: Highly Enantioselective Synthesis of Benzo‐ε‐Lactones
inferred← citeshttps://doi.org/10.1002/anie.201305023openalex-snapshot
Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N‐Heterocyclic‐Carbene/Thiourea/Tertiary‐Amine Multicatalysis
inferred← citeshttps://doi.org/10.1002/anie.201305571openalex-snapshot
Highly Enantioselective γ‐Amination by N‐Heterocyclic Carbene Catalyzed [4+2] Annulation of Oxidized Enals and Azodicarboxylates
inferred← citeshttps://doi.org/10.1002/anie.201405178openalex-snapshot
Conjugate Umpolung of β,β‐Disubstituted Enals by Dual Catalysis with an N‐Heterocyclic Carbene and a Brønsted Acid: Facile Construction of Contiguous Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.201405381openalex-snapshot
N‐Heterocyclic Carbene Catalyzed Formal [3+2] Annulation Reaction of Enals: An Efficient Enantioselective Access to Spiro‐Heterocycles
inferred← citeshttps://doi.org/10.1002/anie.201708994openalex-snapshot
Control of N‐Heterocyclic Carbene Catalyzed Reactions of Enals: Asymmetric Synthesis of Oxindole‐γ‐Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/anie.201712785openalex-snapshot
Catalytic Enantioselective Aza‐Benzoin Reactions of Aldehydes with 2H‐Azirines
inferred← citeshttps://doi.org/10.1002/anie.201812585openalex-snapshot
Enantioselective N‐Heterocyclic Carbene Catalysis that Exploits Imine Umpolung
inferred← citeshttps://doi.org/10.1002/anie.202008631openalex-snapshot
Pendant Alkoxy Groups on N‐Aryl Substitutions Drive the Efficiency of Imidazolylidene Catalysts for Homoenolate Annulation from Enal and Aldehyde
inferred← citeshttps://doi.org/10.1002/anie.202307286openalex-snapshot
A Homo‐Mannich Reaction Strategy Enables Collective Access to Ibophyllidine, Aspidosperma, Kopsia, and Melodinus Alkaloids
inferred← citeshttps://doi.org/10.1002/anie.202513913openalex-snapshot
Umpolung Activation of Bicyclobutanes via N‐Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/asia.201000617openalex-snapshot
Late‐Stage Diversification of Chiral N‐Heterocyclic‐Carbene Precatalysts for Enantioselective Homoenolate Additions
inferred← citeshttps://doi.org/10.1002/asia.201601022openalex-snapshot
Insights into N‐Heterocyclic Carbene‐Catalyzed [4+2] Annulation Reaction of Enals with Nitroalkenes: Mechanisms, Origin of Chemo‐ and Stereoselectivity, and Role of Catalyst
inferred← citeshttps://doi.org/10.1002/cctc.202001513openalex-snapshot
Bifunctional N‐Heterocylic Carbene‐Catalyzed Highly Enantioselective Trans‐Cyclopentannulation of Enals and Enones via Homoenolate
inferred← citeshttps://doi.org/10.1002/chem.200800353openalex-snapshot
One‐Pot Oxidative Esterification and Amidation of Aldehydes
inferred← citeshttps://doi.org/10.1002/chem.200800942openalex-snapshot
Cyclophane‐Type Imidazolium Salts with Planar Chirality as a New Class of N‐Heterocyclic Carbene Precursors
inferred← citeshttps://doi.org/10.1002/chem.201201375openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Homoenolate Additions with N‐Aryl Ketimines as Electrophiles: Efficient Synthesis of Spirocyclic γ‐Lactam Oxindoles
inferred← citeshttps://doi.org/10.1002/chem.201204386openalex-snapshot
N‐Heterocyclic Carbene (NHC)‐Catalyzed/Lewis Acid Mediated Conjugate Umpolung of Alkynyl Aldehydes for the Synthesis of Butenolides: A Formal [3+2] Annulation
inferred← citeshttps://doi.org/10.1002/chem.201204428openalex-snapshot
Mechanistic Insight into the Staudinger Reaction Catalyzed by N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/chem.201304830openalex-snapshot
Nickel‐Catalyzed Synthesis of N‐Aryl‐1,2‐dihydropyridines by [2+2+2] Cycloaddition of Imines with Alkynes through T‐Shaped 14‐Electron Aza‐Nickelacycle Key Intermediates
inferred← citeshttps://doi.org/10.1002/chem.201500661openalex-snapshot
NHC‐Catalyzed Asymmetric Synthesis of Functionalized Succinimides from Enals and α‐Ketoamides
inferred← citeshttps://doi.org/10.1002/chem.201703263openalex-snapshot
Organocatalytic Asymmetric Synthesis of trans‐γ‐Lactams
inferred← citeshttps://doi.org/10.1002/chem.201901028openalex-snapshot
Catalytic Asymmetric γ‐Lactam Synthesis from Enolisable Anhydrides and Imines
inferred← citeshttps://doi.org/10.1002/chin.200545139openalex-snapshot
Catalytic Synthesis of γ‐Lactams via Direct Annulations of Enals and N‐Sulfonylimines.
inferred← citeshttps://doi.org/10.1002/chin.200645087openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Reaction of Chalcones and Enals via Homoenolate: An Efficient Synthesis of 1,3,4‐Trisubstituted Cyclopentenes.
inferred← citeshttps://doi.org/10.1002/chir.22157openalex-snapshot
Theoretical Study of N‐Heterocyclic Carbenes‐Catalyzed Cascade Annulation of Benzodienones and Enals
inferred← citeshttps://doi.org/10.1002/cjoc.201400411openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed All Carbon‐[4+2] Cyclocondensation of α,β‐Unsaturated Acyl Chlorides with 3‐Alkylenyloxindoles
inferred← citeshttps://doi.org/10.1002/cjoc.202000107openalex-snapshot
N‐Heterocyclic Carbene Organocatalysis: Activation Modes and Typical Reactive Intermediates
inferred← citeshttps://doi.org/10.1002/ejoc.200600718openalex-snapshot
Synthesis of 3‐Alkylcoumarins from Salicylaldehydes and α,β‐Unsaturated Aldehydes Utilizing Nucleophilic Carbenes: A New Umpoled Domino Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201000774openalex-snapshot
Theoretical Investigations towards the Staudinger Reaction Catalyzed by N‐Heterocyclic Carbene: Mechanism and Stereoselectivity
inferred← citeshttps://doi.org/10.1002/ejoc.201200525openalex-snapshot
One‐Step Formation both of C–N and of C–O Bonds of N‐Alkoxyamides through NHC‐Catalyzed Three‐Component Reactions of Enals, Nitrosoarenes, and Enones
inferred← citeshttps://doi.org/10.1002/ejoc.201301366openalex-snapshot
Design, Synthesis, and Organocatalytic Activity of N‐Heterocyclic Carbenes Functionalized with Hydrogen‐Bond Donors in Enantioselective Reactions of Homoenolates
inferred← citeshttps://doi.org/10.1002/hlca.202400206openalex-snapshot
Recent Progress in Visible Light‐Mediated Synthesis of γ‐lactams
inferred← citeshttps://doi.org/10.1002/jhet.70089openalex-snapshot
A “One‐Pot” Metal‐Free Synthesis and Evaluation of Antiproliferative Activity of Diversely Functionalized Pyrrolidine‐2‐Ones
inferred← citeshttps://doi.org/10.1002/mrc.1965openalex-snapshot
Determination of the stereochemistry of γ‐Butyrolactones by DPFGSE‐NOE experiments
inferred← citeshttps://doi.org/10.1002/slct.202502484openalex-snapshot
Inverse Electron Demand Formal Dihetero Diels–Alder Reactions: Synthesis of C‐Substituted Piperazines and Morpholines
inferred← citeshttps://doi.org/10.1002/slct.73608openalex-snapshot
Asymmetric Construction of Lactam Scaffolds Catalyzed by N‐heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1007/2789_2008_079openalex-snapshot
N-Heterocyclic Carbenes: Organocatalysts Displaying Diverse Modes of Action
inferred← citeshttps://doi.org/10.1007/2789_2008_081openalex-snapshot
Nucleophilic Carbenes as Organocatalysts
inferred← citeshttps://doi.org/10.1007/3418_2012_47openalex-snapshot
Carbene Catalysis: Beyond the Benzoin and Stetter Reactions
inferred← citeshttps://doi.org/10.1007/978-981-97-8205-5_2openalex-snapshot
Photo-Redox Catalyst-Mediated Green Synthesis of Various Compounds
inferred← citeshttps://doi.org/10.1007/s11426-023-1578-yopenalex-snapshot
Biomimetic asymmetric catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-08-096807-0.00008-7openalex-snapshot
Five-Membered Ring Systems: With More than One N Atom
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00216-0openalex-snapshot
2.15 Metal Homoenolates
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00037-8openalex-snapshot
(3 + 2) Cycloadditions by Nucleophilic Organocatalysis
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00043-0openalex-snapshot
Metal Homoenolates and Homoallyl Anions
inferred← citeshttps://doi.org/10.1016/j.carres.2011.06.010openalex-snapshot
Highly diastereoselective conjugate addition of nitroalkanes to α,β-unsaturated sugar lactones for the efficient synthesis of chiral 2-pyrrolidones
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.08.112openalex-snapshot
Transition metal-catalyzed conversion of aldehydes to ketones
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109061openalex-snapshot
POV-based molecular catalysts for highly efficient esterification of alcohols with aldehydes as acylating agents
inferred← citeshttps://doi.org/10.1016/j.ccr.2017.03.005openalex-snapshot
Carbohydrate– N -heterocyclic carbene metal complexes: Synthesis, catalysis and biological studies
inferred← citeshttps://doi.org/10.1016/j.comptc.2022.114007openalex-snapshot
NHC-catalyzed N H functionalization/cycloaddition reaction of indole aldehyde and ketone: A DFT perspective
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.05.007openalex-snapshot
Carbohydrate-containing N-heterocyclic carbene complexes
inferred← citeshttps://doi.org/10.1016/j.mcat.2020.110952openalex-snapshot
Novel enzymatic reduction of α-amido- and α-cyanoalkyl-β-keto esters catalyzed by ketoreductases
inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112122openalex-snapshot
Unraveling the mechanism and substituent effects on the N-heterocyclic carbene-catalyzed transformation reaction of enals and imines
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.tet.2006.05.024openalex-snapshot
Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions
inferred← citeshttps://doi.org/10.1016/j.tet.2007.03.006openalex-snapshot
Stereoselective synthesis of β-carboethoxy-γ-lactams via imino Mukaiyama aldol-type reaction of 1,4-bis(trimethylsilyloxy)-1,4-diethoxy-1,3-butadiene
inferred← citeshttps://doi.org/10.1016/j.tet.2008.03.072openalex-snapshot
A modular synthesis of chiral aminoindanol-derived imidazolium salts
inferred← citeshttps://doi.org/10.1016/j.tet.2008.06.082openalex-snapshot
N-Heterocyclic carbene catalyzed intramolecular nucleophilic addition of carbonyl anion equivalents to enol ethers
inferred← citeshttps://doi.org/10.1016/j.tet.2009.03.103openalex-snapshot
Formal synthesis of salinosporamide A via NHC-catalyzed intramolecular lactonization
inferred← citeshttps://doi.org/10.1016/j.tet.2011.09.113openalex-snapshot
NHC-catalyzed annulation of enals and chalcones: further explorations on the novel synthesis of 1,3,4-trisubstituted cyclopentenes
inferred← citeshttps://doi.org/10.1016/j.tet.2015.08.062openalex-snapshot
Expedient synthesis of tricyclic benzopyran-2-ones via N-Heterocyclic carbene catalyzed annulation of enals to α-methylene cycloalkanones
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132191openalex-snapshot
β,γ-trans-selective γ-butyrolactone formation via homoenolate cross-annulation of enals and aldehydes catalyzed by sterically hindered N-heterocyclic carbene
inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.12.020openalex-snapshot
Intramolecular asymmetric C–H insertion of N-arylalkyl, N-bis(trimethylsilyl)methyldiazoamides mediated by chiral rhodium(II) catalysts. Synthesis of (R)-β-benzyl-γ-aminobutyric acid
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.03.001openalex-snapshot
Chiral relay in NHC-mediated asymmetric β-lactam synthesis I; substituent effects in NHCs derived from (1R,2R)-cyclohexane-1,2-diamine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.04.001openalex-snapshot
Catalytic enantioselective Steglich rearrangements using chiral N-heterocyclic carbenes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.09.004openalex-snapshot
Asymmetric induction afforded by chiral azolylidene N-heterocyclic carbenes (NHC) catalysts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.02.175openalex-snapshot
Chiral bicyclic imidazolium salts as a new class of N-heterocyclic carbene precursors
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.097openalex-snapshot
Nucleophilic carbene-catalysed oxidative esterification reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.11.032openalex-snapshot
Assembly of functionalized α-hydroxy carbonyl compounds via combination of N-heterocyclic carbene and Pd catalysts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.01.058openalex-snapshot
NHC-catalyzed efficient synthesis of β′-amino enones via carbonyl umpolung reaction of enals with aziridines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.12.022openalex-snapshot
1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride in combination with triethylamine: an improved catalytic system for hydroacylation/reduction of activated ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.08.157openalex-snapshot
N-Heterocyclic carbene (NHC) catalyzed annulation of enals and vinyl ketones: a novel synthesis of [2H]-pyranones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.01.100openalex-snapshot
NHC-catalysed annulation of enals to ene-1,4-diones: stereoselective synthesis of 1,3-diaryl-4-acyl cyclopentenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.03.101openalex-snapshot
The first NHC-induced regioselective introduction of C- and N-nucleophiles in to Baylis–Hillman enals
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.10.044openalex-snapshot
Synthesis of 4-acylcoumarins by NHC-catalyzed nucleophilic substitution
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151419openalex-snapshot
Synthesis of pentafluorobenzene-based NHC adducts and their catalytic activity in the microwave-assisted reactions of aldehydes
inferred← citeshttps://doi.org/10.1016/s0959-6380(07)80012-2openalex-snapshot
Five membered ring systems: with more than one N atom
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00060openalex-snapshot
Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1021/acs.chemrev.9b00481openalex-snapshot
New Developments of the Principle of Vinylogy as Applied to π-Extended Enolate-Type Donor Systems
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00360openalex-snapshot
N-Heterocyclic Carbene Catalysis Exploiting Oxidative Imine Umpolung for the Generation of Imidoyl Azoliums
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00457openalex-snapshot
Organocatalytic Direct N-Acylation of Amides with Aldehydes under Oxidative Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00481openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Asymmetric Benzoin Reaction in Water
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02520openalex-snapshot
Participation of β-Ketothioamides in N-Heterocyclic Carbene-Catalyzed [3 + 3] Spiroannulation: Asymmetric Synthesis of Functionalized Spiro-piperidinone Derivatives
inferred← citeshttps://doi.org/10.1021/acs.jpca.2c00900openalex-snapshot
Theoretical Insights into Enantioselective [3 + 2] Cycloaddition between Cinnamaldehyde and Cyclic N-Sulfonyl Trifluoromethylated Ketimine Catalyzed by N-Heterocyclic Carbene
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00699openalex-snapshot
Highly Chemoselective and Enantioselective Synthesis of 3,4-2H-Pyrindin-2-ones by an NHC-Catalyzed [3 + 3] Cyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00226openalex-snapshot
Metal-Free α-C(sp 3 )–H Aroylation of Amines via a Photoredox Catalytic Radical–Radical Cross-Coupling Process
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03059openalex-snapshot
Synthesis of Functionalized Dihydrocoumarins by NHC-Catalyzed [3 + 3] Annulation of Enals with 2-Substituted Naphthoquinones
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00426openalex-snapshot
Access to Chiral β-Boryl δ-Lactones via NHC-Catalyzed [4 + 2] Annulation
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00316openalex-snapshot
Amide and Amine Nucleophiles in Polar Radical Crossover Cycloadditions: Synthesis of γ-Lactams and Pyrrolidines
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00726openalex-snapshot
Rapid Access to Spirocylic Oxindoles: Application of Asymmetric N-Heterocyclic Carbene-Catalyzed [3 + 3] Cycloaddition of Imines to Oxindole-Derived Enals
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01692openalex-snapshot
Chemoselective N-Heterocyclic Carbene-Catalyzed Cascade of Enals with Nitroalkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01604openalex-snapshot
Reductive N-Heterocyclic Carbene Catalysis via Hydride Transfer: Generating Homoenolates from Unsaturated Esters
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c05230openalex-snapshot
Carbene-Catalyzed C–H Arylation of Aldehyde-Hydrazone via Radical Cross-Coupling with Iodobenzene
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01105openalex-snapshot
Tuning the Catalyst Reactivity of Imidazolylidene Catalysts through Substituent Effects on the N-Aryl Groups
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01195openalex-snapshot
Access to Amide from Aldimine via Aerobic Oxidative Carbene Catalysis and LiCl as Cooperative Lewis Acid
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01860openalex-snapshot
Enantioselective [3 + 2] Annulation of Enals with 2-Aminoacrylates Catalyzed by N -Heterocyclic Carbene
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02707openalex-snapshot
Carbene-Catalyzed [4 + 2] Cycloadditions of Vinyl Enolate and (in Situ Generated) Imines for Enantioselective Synthesis of Quaternary α-Amino Phosphonates
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02927openalex-snapshot
NHC-Catalyzed Asymmetric Formal [4 + 2] Annulation To Construct Spirocyclohexane Pyrazolone Skeletons
inferred← citeshttps://doi.org/10.1021/ar400239vopenalex-snapshot
On the Mechanism of N-Heterocyclic Carbene-Catalyzed Reactions Involving Acyl Azoliums
inferred← citeshttps://doi.org/10.1021/cr068372zopenalex-snapshot
Organocatalysis by N-Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1021/cs400602vopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed Formal [3+2] Annulation of Alkynyl Aldehydes with Nitrosobenzenes: A Highly Regioselective Umpolung Strategy
inferred← citeshttps://doi.org/10.1021/ja0625677openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Reaction of Chalcones and Enals via Homoenolate: an Efficient Synthesis of 1,3,4-Trisubstituted Cyclopentenes
inferred← citeshttps://doi.org/10.1021/ja102130sopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed Cascade Reaction Involving the Hydroacylation of Unactivated Alkynes
inferred← citeshttps://doi.org/10.1021/ja106925fopenalex-snapshot
Synthesis of Water-Tolerant Indium Homoenolate in Aqueous Media and Its Application in the Synthesis of 1,4-Dicarbonyl Compounds via Palladium-Catalyzed Coupling with Acid Chloride
inferred← citeshttps://doi.org/10.1021/ja205714gopenalex-snapshot
N-Heterocyclic Carbene and Brønsted Acid Cooperative Catalysis: Asymmetric Synthesis of trans-γ-Lactams
inferred← citeshttps://doi.org/10.1021/ja3030164openalex-snapshot
Catalytic Asymmetric α-Acylation of Tertiary Amines Mediated by a Dual Catalysis Mode: N-Heterocyclic Carbene and Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/ja306766nopenalex-snapshot
Catalytic, Enantioselective N-Acylation of Lactams and Thiolactams Using Amidine-Based Catalysts
inferred← citeshttps://doi.org/10.1021/ja308420copenalex-snapshot
Proton Transfer Reactions of Triazol-3-ylidenes: Kinetic Acidities and Carbon Acid p K a Values for Twenty Triazolium Salts in Aqueous Solution
inferred← citeshttps://doi.org/10.1021/ja403847eopenalex-snapshot
Asymmetric N-Heterocyclic Carbene Catalyzed Addition of Enals to Nitroalkenes: Controlling Stereochemistry via the Homoenolate Reactivity Pathway To Access δ-Lactams
inferred← citeshttps://doi.org/10.1021/ja410932topenalex-snapshot
Asymmetric Homoenolate Additions to Acyl Phosphonates through Rational Design of a TailoredN-Heterocyclic Carbene Catalyst
inferred← citeshttps://doi.org/10.1021/ja5080739openalex-snapshot
Enantioselective N-Heterocyclic Carbene-Catalyzed β-Hydroxylation of Enals Using Nitroarenes: An Atom Transfer Reaction That Proceeds via Single Electron Transfer
inferred← citeshttps://doi.org/10.1021/ja510737nopenalex-snapshot
N-Heterocyclic Carbene Catalyzed Switchable Reactions of Enals with Azoalkenes: Formal [4 + 3] and [4 + 1] Annulations for the Synthesis of 1,2-Diazepines and Pyrazoles
inferred← citeshttps://doi.org/10.1021/ja808811uopenalex-snapshot
Amide Enolate Additions to Acylsilanes: In Situ Generation of Unusual and Stereoselective Homoenolate Equivalents
inferred← citeshttps://doi.org/10.1021/ja902143wopenalex-snapshot
α′-Hydroxyenones as Mechanistic Probes and Scope-Expanding Surrogates for α,β-Unsaturated Aldehydes in N-Heterocyclic Carbene-Catalyzed Reactions
inferred← citeshttps://doi.org/10.1021/ja906361gopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed Hydroacylation of Unactivated Double Bonds
inferred← citeshttps://doi.org/10.1021/jacs.5b06390openalex-snapshot
Oxidatively Initiated NHC-Catalyzed Enantioselective Synthesis of 3,4-Disubstituted Cyclopentanones from Enals
inferred← citeshttps://doi.org/10.1021/jacs.7b02889openalex-snapshot
Enantioselective β-Protonation of Enals via a Shuttling Strategy
inferred← citeshttps://doi.org/10.1021/jacsau.4c01166openalex-snapshot
N-Heterocyclic-Carbene-Catalyzed Imine Umpolung for the Cross-Coupling of Quinoxalin-2-ones with Isatins
inferred← citeshttps://doi.org/10.1021/jo0615706openalex-snapshot
An N-Heterocyclic Carbene-Catalyzed [8 + 3] Annulation of Tropone and Enals via Homoenolate
inferred← citeshttps://doi.org/10.1021/jo071247iopenalex-snapshot
N-Heterocyclic Carbene Catalyzed Aza-Morita−Baylis−Hillman Reaction of Cyclic Enones with N-Tosylarylimines
inferred← citeshttps://doi.org/10.1021/jo800569gopenalex-snapshot
Unexpected Transfer of Tosyl Group of ArCH═NTs-Catalyzed by N-Heterocyclic Carbene
inferred← citeshttps://doi.org/10.1021/jo802515gopenalex-snapshot
An Unexpected N-Heterocyclic Carbene-Catalyzed Annulation of Enals and Nitroso Compounds
inferred← citeshttps://doi.org/10.1021/ol052926nopenalex-snapshot
N-Heterocyclic Carbene Catalyzed Reaction of Enals and 1,2-Dicarbonyl Compounds: Stereoselective Synthesis of Spiro γ-Butyrolactones
inferred← citeshttps://doi.org/10.1021/ol0630494openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Mukaiyama Aldol Reactions
inferred← citeshttps://doi.org/10.1021/ol1008697openalex-snapshot
NHC Catalyzed Transformation of Aromatic Aldehydes to Acids by Carbon Dioxide: An Unexpected Reaction
inferred← citeshttps://doi.org/10.1021/ol102148bopenalex-snapshot
One-Pot Synthesis of Chiral α-Methylene-γ-lactams with Excellent Diastereoselectivities and Enantioselectivities
inferred← citeshttps://doi.org/10.1021/ol1021564openalex-snapshot
Di- and Trisubstituted γ-Lactams via Rh(II)-carbenoid Reaction of N-Cα-Branched, N-Bis(trimethylsilyl)methyl α-Diazoamides. Synthesis of (±)-α-Allokainic Acid
inferred← citeshttps://doi.org/10.1021/ol102536sopenalex-snapshot
NHC-Catalyzed Intramolecular Redox Amidation for the Synthesis of Functionalized Lactams
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