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Enantioselective Rhodium-Catalyzed Conjugate Alkynylation of 5-Benzylidene Meldrum’s Acids with TMS-acetylene

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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.200701098openalex-snapshot

CuI‐Catalyzed Conjugate Addition of Ethyl Propiolate

inferredcites →https://doi.org/10.1016/j.tetasy.2006.11.009openalex-snapshot

Asymmetric Cu-catalyzed 1,6-conjugate addition of dialkylzinc reagents to 5-(3-aryl-2-propenylidene) Meldrum’s acids

inferredcites →https://doi.org/10.1021/ja035311zopenalex-snapshot

The First Conjugate Addition Reaction of Terminal Alkynes Catalytic in Copper: Conjugate Addition of Alkynes in Water

inferredcites →https://doi.org/10.1021/ja043001qopenalex-snapshot

Ligand-Catalyzed Asymmetric Alkynylboration of Enones: A New Paradigm for Asymmetric Synthesis Using Organoboranes

inferredcites →https://doi.org/10.1021/ja052411ropenalex-snapshot

Catalytic, Enantioselective, Conjugate Alkyne Addition

inferredcites →https://doi.org/10.1021/ja056692eopenalex-snapshot

Asymmetric Synthesis of All-Carbon Benzylic Quaternary Stereocenters via Cu-Catalyzed Conjugate Addition of Dialkylzinc Reagents to 5-(1-Arylalkylidene) Meldrum's Acids

inferredcites →https://doi.org/10.1021/ja076346sopenalex-snapshot

Rhodium-Catalyzed Asymmetric Rearrangement of Alkynyl Alkenyl Carbinols: Synthetic Equivalent to Asymmetric Conjugate Alkynylation of Enones

inferredcites →https://doi.org/10.1021/ja710540sopenalex-snapshot

Steric Tuning of Silylacetylenes and Chiral Phosphine Ligands for Rhodium-Catalyzed Asymmetric Conjugate Alkynylation of Enones

inferredcites →https://doi.org/10.1021/ja903920jopenalex-snapshot

Asymmetric Organocatalytic Formal Alkynylation and Alkenylation of α,β-Unsaturated Aldehydes

inferredcites →https://doi.org/10.1021/ja992922bopenalex-snapshot

Asymmetric Conjugate Addition of Alkynylboronates to Enones

inferredcites →https://doi.org/10.1021/ol048623vopenalex-snapshot

Catalytic Enantioselective Conjugate Addition of Trimethylsilylacetylene to 2-Cyclohexen-1-one

inferredcites →https://doi.org/10.1021/ol0491585openalex-snapshot

Diastereoselective Zinc-Catalyzed Conjugate Addition of Alkynes

inferredcites →https://doi.org/10.1021/ol050643popenalex-snapshot

Chiral Amino Alcohol-Mediated Asymmetric Conjugate Addition of Arylalkynes to Nitroolefins

inferredcites →https://doi.org/10.1021/ol702613fopenalex-snapshot

Sequential Rh(I)/Pd-Catalyzed 1,4-Addition/Intramolecular Allylation: Stereocontrolled Construction of γ-Butyrolactones and Cyclopropanes

inferredcites →https://doi.org/10.1021/ol800923qopenalex-snapshot

Asymmetric Synthesis of Carboxylic Acid Derivatives Having an All-Carbon α-Quaternary Center through Cu-Catalyzed 1,4-Addition of Dialkylzinc Reagents to 2-Aryl Acetate Derivatives

inferredcites →https://doi.org/10.1021/ol9003959openalex-snapshot

Sc(OTf)3-Catalyzed Conjugate Allylation of Alkylidene Meldrum’s Acids

inferredcites →https://doi.org/10.1021/ol901119dopenalex-snapshot

Rhodium-Catalyzed Asymmetric Conjugate Alkynylation of Enones with Alkynylsilanols

inferredcites →https://doi.org/10.1246/bcsj.80.1635openalex-snapshot

Stereoselective Conjugate Addition Reactions Using In Situ Metallated Terminal Alkynes and the Development of Novel Chiral P,N-Ligands

inferredcites →https://doi.org/10.1517/13543770802665717openalex-snapshot

Progress in the discovery and development of small-molecule modulators of G-protein-coupled receptor 40 (GPR40/FFA1/FFAR1): an emerging target for type 2 diabetes

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.4846591openalex-extracted

Mesoporous Tio2 Supported Synthesis of Aryl Propionic Acid Derivatives, and Mild Peroxides, Organometallic Catalyst Free Oxidative Cleavage of C=C in Electron Deficient Olefins

inferred← citeshttps://doi.org/10.1002/047084289x.rn00832openalex-snapshot

(R)- and (S)-2,2′-Bis(diphenylphosphino)-6,6′-dimethoxy-1,1′-biphenyl

inferred← citeshttps://doi.org/10.1002/047084289x.rn00832.pub2openalex-snapshot

(R)- and (S)-2,2′-Bis(diphenylphosphino)-6,6′-dimethoxy-1,1′-biphenyl

inferred← citeshttps://doi.org/10.1002/047084289x.rn00832.pub3openalex-snapshot

(R)- and (S)-2,2′-Bis(diphenylphosphino)-6,6′-dimethoxy-1,1′-biphenyl

inferred← citeshttps://doi.org/10.1002/047084289x.rn02052openalex-snapshot

(R)- and (S)-2,2′-Bis(3,5-dimethylphenylphosphino)-6,6′-dimethoxy-1,1′-biphenyl

inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub4openalex-snapshot

Chiral Auxiliaries and Catalysts

inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub5openalex-snapshot

Chiral Auxiliaries and Catalysts

inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub6openalex-snapshot

Chiral Auxiliaries and Catalysts

inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub7openalex-snapshot

Chiral Auxiliaries and Catalysts

inferred← citeshttps://doi.org/10.1002/9781118662083.cot09-006openalex-snapshot

Conjugate Addition to α,β‐Unsaturated Nitriles, Carboxylic Acids, and Derivatives

inferred← citeshttps://doi.org/10.1002/9781118846919.ch2openalex-snapshot

Multicatalyst System

inferred← citeshttps://doi.org/10.1002/9783527677894.ch7openalex-snapshot

Catalytic Conjugate Additions of Alkynes

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Mutually Complementary Metal‐ and Organocatalysis with Collective Synthesis: Asymmetric Conjugate Addition of 1,3‐Carbonyl Compounds to Nitroenynes and Further Reactions of the Products

inferred← citeshttps://doi.org/10.1002/adsc.201201120openalex-snapshot

Enantioselective Synthesis of 4‐Substituted Dihydrocoumarins through a Zinc Bis(hydroxyamide)‐Catalyzed Conjugate Addition of Terminal Alkynes

inferred← citeshttps://doi.org/10.1002/ajoc.202300021openalex-snapshot

Copper‐Catalyzed Synthesis of β‐Alkynyl Ketones from Propargylic Alcohols and Enamides

inferred← citeshttps://doi.org/10.1002/ange.201204004openalex-snapshot

Enantioselective Rhodium‐Catalyzed Nucleophilic Allylation of Cyclic Imines with Allylboron Reagents

inferred← citeshttps://doi.org/10.1002/ange.201204646openalex-snapshot

Rhodium‐Catalyzed Three‐Component Cross‐Addition of Silylacetylenes, Alkynyl Esters, and Electron‐Deficient Alkenes or Isocyanates

inferred← citeshttps://doi.org/10.1002/ange.201303501openalex-snapshot

Combining NHC–Cu and Brønsted Base Catalysis: Enantioselective Allylic Substitution/Conjugate Additions with Alkynylaluminum Reagents and Stereospecific Isomerization of the Products to Trisubstituted Allenes

inferred← citeshttps://doi.org/10.1002/ange.201500983openalex-snapshot

Synthesis and Characterization of Tricarbastannatranes and Their Reactivity in B(C 6 F 5 ) 3 ‐Promoted Conjugate Additions

inferred← citeshttps://doi.org/10.1002/ange.201509778openalex-snapshot

Asymmetric Conjugate Alkynylation of Cyclic α,β‐Unsaturated Carbonyl Compounds with a Chiral Diene Rhodium Catalyst

inferred← citeshttps://doi.org/10.1002/ange.201601792openalex-snapshot

Iridium‐Catalyzed Enantioselective Hydroalkynylation of Enamides for the Synthesis of Homopropargyl Amides

inferred← citeshttps://doi.org/10.1002/ange.201703089openalex-snapshot

Palladium‐Catalyzed Enantioselective Redox‐Relay Heck Alkynylation of Alkenols To Access Propargylic Stereocenters

inferred← citeshttps://doi.org/10.1002/ange.202105562openalex-snapshot

Enantioselective Synthesis of Spiro‐oxiranes: An Asymmetric Addition/Aldol/Spirocyclization Domino Cascade

inferred← citeshttps://doi.org/10.1002/ange.202201099openalex-snapshot

Iridium‐Catalyzed Regiodivergent and Enantioselective Hydroalkynylation of Unactivated 1,1‐Disubstituted Alkenes

inferred← citeshttps://doi.org/10.1002/anie.201204004openalex-snapshot

Enantioselective Rhodium‐Catalyzed Nucleophilic Allylation of Cyclic Imines with Allylboron Reagents

inferred← citeshttps://doi.org/10.1002/anie.201204646openalex-snapshot

Rhodium‐Catalyzed Three‐Component Cross‐Addition of Silylacetylenes, Alkynyl Esters, and Electron‐Deficient Alkenes or Isocyanates

inferred← citeshttps://doi.org/10.1002/anie.201303501openalex-snapshot

inferred← citeshttps://doi.org/10.1002/anie.201500983openalex-snapshot

Synthesis and Characterization of Tricarbastannatranes and Their Reactivity in B(C6F5)3‐Promoted Conjugate Additions

inferred← citeshttps://doi.org/10.1002/anie.201509778openalex-snapshot

Asymmetric Conjugate Alkynylation of Cyclic α,β‐Unsaturated Carbonyl Compounds with a Chiral Diene Rhodium Catalyst

inferred← citeshttps://doi.org/10.1002/anie.201601792openalex-snapshot

Iridium‐Catalyzed Enantioselective Hydroalkynylation of Enamides for the Synthesis of Homopropargyl Amides

inferred← citeshttps://doi.org/10.1002/anie.201703089openalex-snapshot

Palladium‐Catalyzed Enantioselective Redox‐Relay Heck Alkynylation of Alkenols To Access Propargylic Stereocenters

inferred← citeshttps://doi.org/10.1002/anie.202105562openalex-snapshot

Enantioselective Synthesis of Spiro‐oxiranes: An Asymmetric Addition/Aldol/Spirocyclization Domino Cascade

inferred← citeshttps://doi.org/10.1002/anie.202201099openalex-snapshot

Iridium‐Catalyzed Regiodivergent and Enantioselective Hydroalkynylation of Unactivated 1,1‐Disubstituted Alkenes

inferred← citeshttps://doi.org/10.1002/asia.201000561openalex-snapshot

Enantioselective and Regioselective Organocatalytic Conjugate Addition of Malonates to Nitroenynes

inferred← citeshttps://doi.org/10.1002/asia.201100050openalex-snapshot

Cooperative Activation of Alkyne and Thioamide Functionalities; Direct Catalytic Asymmetric Conjugate Addition of Terminal Alkynes to α,β‐Unsaturated Thioamides

inferred← citeshttps://doi.org/10.1002/chem.201201607openalex-snapshot

Highly Stereoselective Synthesis of Tertiary Propargylic Centers and Their Isomerization to Enantiomerically Enriched Allenes

inferred← citeshttps://doi.org/10.1002/chem.201201765openalex-snapshot

Enantioselective Zinc‐Mediated Conjugate Addition of Terminal Alkynes to Enones

inferred← citeshttps://doi.org/10.1002/chem.201303920openalex-snapshot

Highly Enantioselective Copper(I)‐Catalyzed Conjugate Addition of Terminal Alkynes to 1,1‐Difluoro‐1‐(phenylsulfonyl)‐3‐en‐2‐ones: New Ester/Amide Surrogates in Asymmetric Catalysis

inferred← citeshttps://doi.org/10.1002/chem.201601303openalex-snapshot

Catalytic Enantioselective Conjugate Alkynylation of α,β‐Unsaturated 1,1,1‐Trifluoromethyl Ketones with Terminal Alkynes

inferred← citeshttps://doi.org/10.1002/chin.201008168openalex-snapshot

ChemInform Abstract: Enantioselective Rhodium‐Catalyzed Conjugate Alkynylation of 5‐Benzylidene Meldrum′s Acids with TMS‐Acetylene.

inferred← citeshttps://doi.org/10.1002/ejoc.202300449openalex-snapshot

Quantifying the Electronic Effect of C4 and C4′ Positions of Bipyridine Ligand on Pd(II)/Rh(I)‐Catalyzed Conjugate Addition Reaction: A DFT Study

inferred← citeshttps://doi.org/10.1002/ijch.201100164openalex-snapshot

Cooperative Asymmetric Catalysis Using Thioamides toward Truly Practical Organic Syntheses

inferred← citeshttps://doi.org/10.1002/slct.202404128openalex-snapshot

Mesoporous TiO 2 /Celite‐Supported Hydrolysis/Decarboxylation of Benzyl Meldrum's Acid Derivatives: Application to the Synthesis of Hydrocinnamic Acid Derivatives

inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00413-4openalex-snapshot

4.14 Reactions using Thioamide and Allylic Cyanide

inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00056-1openalex-snapshot

Olefins Hydrofunctionnalization; Hydroarylation (Vinylation, Alkynylation) of Electron Deficient Olefins

inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00027-8openalex-snapshot

Alkynes

inferred← citeshttps://doi.org/10.1016/j.tet.2010.04.019openalex-snapshot

Asymmetric syntheses of a GPR40 receptor agonist via diastereoselective and enantioselective conjugate alkynylation

inferred← citeshttps://doi.org/10.1016/j.tet.2015.05.087openalex-snapshot

Palladium-catalyzed 1,4-addition of terminal alkynes to acrolein

inferred← citeshttps://doi.org/10.1016/j.tet.2020.130967openalex-snapshot

Boron/zinc exchange for the conjugate arylation of unsaturated Meldrum’s acid derivatives

inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.04.039openalex-snapshot

Rhodium-catalyzed enantioselective alkynylative cyclization of allenyl aldehydes with terminal alkynes

inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.124openalex-snapshot

Zinc-mediated synthesis of 3-alkynyl-3-hydroxyindolin-2-ones by addition of iodoalkynes to isatins

inferred← citeshttps://doi.org/10.1021/acs.chemrev.5c00177openalex-snapshot

Recent Advances on Catalytic Asymmetric Synthesis of Molecules Bearing a Fluorine-Containing Stereogenic Carbon Center (2015–2024)

inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00692openalex-snapshot

Recent Advances in Metal-Catalyzed Asymmetric 1,4-Conjugate Addition (ACA) of Nonorganometallic Nucleophiles

inferred← citeshttps://doi.org/10.1021/acs.joc.5b00281openalex-snapshot

FeCl3-Mediated Synthesis of β-Alkynyl Ketones via Domino Nucleophilic-Substitution/Intramolecular-Cyclization/Reverse Claisen Condensation of N-Cyclohexyl Propargylamines and 1,3-Diketones

inferred← citeshttps://doi.org/10.1021/acs.joc.5c00945openalex-snapshot

Chiral Binaphthol-Catalyzed Enantioselective Conjugate Addition of Alkynyl Trifluoroborates to α,β-Unsaturated Cyclic N-Sulfonyl Ketimines

inferred← citeshttps://doi.org/10.1021/acs.joc.5c02755openalex-snapshot

Iridium-Catalyzed Desymmetric Hydroalkynylation of Cyclopentenes to Construct 1,3-Stereocenters

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01325openalex-snapshot

Enantioselective Copper-Catalyzed Remote C(sp3)–H Alkynylation of Linear Primary Sulfonamides

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03707openalex-snapshot

Iridium-Catalyzed Regioselective Hydroalkynylation of Internal Alkenes Directed by an Oxime

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01101openalex-snapshot

Switchable Enantioselectivity in Conjugate Alkyne Addition of β,γ-Unsaturated α-Keto Esters by Asymmetric Binary Acid Catalysis

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00984openalex-snapshot

Formation of Carbocycles via a 1,4-Rh Shift Triggered by a Rhodium-Catalyzed Addition of Terminal Alkynes to 3,3-Diarylcyclopropenes

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01004openalex-snapshot

Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: A Divergent Entry to β-Branched Carbonyl Compounds

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c05211openalex-snapshot

Nickel-Catalyzed Regioselective Hydroalkynylation of Nitrogen Heterocycle-Tethered Unactivated Alkenes

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00971openalex-snapshot

Enantioselective Synthesis of 3-Alkynyl-3-hydroxyindolin-2-ones by Copper-Catalyzed Asymmetric Addition of Terminal Alkynes to Isatins

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01494openalex-snapshot

Catalytic Enantioselective Conjugate Alkynylation of β-Aryl-β-trifluoromethyl Enones Constructing Propargylic All-Carbon Quaternary Stereogenic Centers

inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03193openalex-snapshot

Native Amine-Directed NiH-Catalyzed Markovnikov Hydroalkynylation of Unactivated Alkenes

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00909openalex-snapshot

Rhodium-Catalyzed Asymmetric Conjugate Alkynylation of β,γ-Unsaturated α-Ketoesters

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03663openalex-snapshot

Rhodium-Catalyzed Homocoupling of γ-Alkylatedtert-Propargylic Alcohols

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00153openalex-snapshot

Rhodium-Catalyzed Asymmetric Conjugate Alkynylation/Aldol Cyclization Cascade for the Formation of α-Propargyl-β-hydroxyketones

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01567openalex-snapshot

Multicomponent Domino Synthesis of Cyclopenta[b]furan-2-ones

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00249openalex-snapshot

Highly Enantioselective Rhodium-Catalyzed Cross-Addition of Silylacetylenes to Cyclohexadienone-Tethered Internal Alkynes

inferred← citeshttps://doi.org/10.1021/acscatal.9b04285openalex-snapshot

Palladium-Catalyzed Amide-Directed Hydrocarbofunctionalization of 3-Alkenamides with Alkynes

inferred← citeshttps://doi.org/10.1021/ar900229zopenalex-snapshot

Meldrum’s Acids and 5-Alkylidene Meldrum’s Acids in Catalytic Carbon−Carbon Bond-Forming Processes

inferred← citeshttps://doi.org/10.1021/ja105141xopenalex-snapshot

Direct Catalytic Asymmetric Conjugate Addition of Terminal Alkynes to α,β-Unsaturated Thioamides

inferred← citeshttps://doi.org/10.1021/ja2010829openalex-snapshot

Enantioselective Synthesis of Alkyne-Substituted Quaternary Carbon Stereogenic Centers through NHC−Cu-Catalyzed Allylic Substitution Reactions with ( i -Bu) 2 (Alkynyl)aluminum Reagents

inferred← citeshttps://doi.org/10.1021/ja203171xopenalex-snapshot

A New Strategy for the Synthesis of Chiral β-Alkynyl Esters via Sequential Palladium and Copper Catalysis

inferred← citeshttps://doi.org/10.1021/ja309756kopenalex-snapshot

Cobalt-Catalyzed Asymmetric 1,6-Addition of (Triisopropylsilyl)-acetylene to α,β,γ,δ-Unsaturated Carbonyl Compounds

inferred← citeshttps://doi.org/10.1021/ja909105sopenalex-snapshot

Practical Asymmetric Conjugate Alkynylation of Meldrum’s Acid-Derived Acceptors: Access to Chiral β-Alkynyl Acids

inferred← citeshttps://doi.org/10.1021/jacs.1c04493openalex-snapshot

Ir-Catalyzed Regio- and Enantioselective Hydroalkynylation of Trisubstituted Alkene to Access All-Carbon Quaternary Stereocenters

inferred← citeshttps://doi.org/10.1021/jacs.6b10415openalex-snapshot

Synthesis of Amides with Remote Stereocenters by Catalytic Asymmetric γ-Alkynylation of α,β-Unsaturated Amides

inferred← citeshttps://doi.org/10.1021/jacs.7b00363openalex-snapshot

Enantioselective Alkyne Conjugate Addition Enabled by Readily Tuned Atropisomeric P , N -Ligands

inferred← citeshttps://doi.org/10.1021/jacs.7b12054openalex-snapshot

Highly Enantioselective Synthesis of Propargyl Amides through Rh-Catalyzed Asymmetric Hydroalkynylation of Enamides: Scope, Mechanism, and Origin of Selectivity

inferred← citeshttps://doi.org/10.1021/jacs.8b07436openalex-snapshot

Enantioselective Trifluoromethylalkynylation of Alkenes via Copper-Catalyzed Radical Relay

inferred← citeshttps://doi.org/10.1021/jacs.9b03027openalex-snapshot

Construction of Acyclic Quaternary Carbon Stereocenters by Catalytic Asymmetric Hydroalkynylation of Unactivated Alkenes

inferred← citeshttps://doi.org/10.1021/jo401604nopenalex-snapshot

Cobalt-Catalyzed Asymmetric Addition of Silylacetylenes to 1,1-Disubstituted Allenes

inferred← citeshttps://doi.org/10.1021/jo4017524openalex-snapshot

Scandium Triflate-Catalyzed Nucleophilic Additions to Indolylmethyl Meldrum’s Acid Derivatives via a Gramine-Type Fragmentation: Synthesis of Substituted Indolemethanes

inferred← citeshttps://doi.org/10.1021/ol102998wopenalex-snapshot

Enantioselective Synthesis of a GPR40 Agonist AMG 837 via Catalytic Asymmetric Conjugate Addition of Terminal Alkyne to α,β-Unsaturated Thioamide

inferred← citeshttps://doi.org/10.1021/ol300988nopenalex-snapshot

Palladium-Catalyzed Conjugate Addition of Terminal Alkynes to Enones

inferred← citeshttps://doi.org/10.1021/ol501158bopenalex-snapshot

Asymmetric Catalytic Conjugate Addition of Acetaldehyde to Nitrodienynes/Nitroenynes: Applications to the Syntheses of (+)-α-Lycorane and Chiral β-Alkynyl Acids

inferred← citeshttps://doi.org/10.1021/ol502811jopenalex-snapshot

Expedient Synthesis of Complex γ-Butyrolactones from 5-(1-Arylalkylidene) Meldrum’s Acids via Sequential Conjugate Alkynylation/Ag(I)-Catalyzed Lactonization

inferred← citeshttps://doi.org/10.1021/ol902216yopenalex-snapshot

Asymmetric Addition of Alkenylstannanes to Alkylidene Meldrum’s Acids

inferred← citeshttps://doi.org/10.1021/op1003055openalex-snapshot

Development of a Scalable Synthesis of a GPR40 Receptor Agonist

inferred← citeshttps://doi.org/10.1039/b919762copenalex-snapshot

Synthetic applications of rhodium catalysed conjugate addition

inferred← citeshttps://doi.org/10.1039/c0cc02181dopenalex-snapshot

Rhodium-catalyzed asymmetric conjugate alkynylation of nitroalkenes

inferred← citeshttps://doi.org/10.1039/c1cc14098aopenalex-snapshot

Cobalt-catalyzed conjugate addition of silylacetylenes to α,β-unsaturated ketones

inferred← citeshttps://doi.org/10.1039/c1ob06586fopenalex-snapshot

Rhodium-catalysed enantioselective synthesis of 4-arylchroman-2-ones

inferred← citeshttps://doi.org/10.1039/c3cc48508kopenalex-snapshot

Catalytic asymmetric conjugate addition of terminal alkynes to β-trifluoromethyl α,β-enones

inferred← citeshttps://doi.org/10.1039/c5cc01676bopenalex-snapshot

Highly enantioselective copper( i )-catalyzed conjugate addition of 1,3-diynes to α,β-unsaturated trifluoromethyl ketones

inferred← citeshttps://doi.org/10.1039/c5ob00380fopenalex-snapshot

A copper-catalyzed one-pot, three-component tandem conjugative alkynylation/6-endo cyclization sequence: access to pyrano[2,3-d]pyrimidines

inferred← citeshttps://doi.org/10.1039/c6sc01724jopenalex-snapshot

Asymmetric synthesis of chiral β-alkynyl carbonyl and sulfonyl derivatives via sequential palladium and copper catalysis

inferred← citeshttps://doi.org/10.1039/c8qo00136gopenalex-snapshot

Iridium-catalysed conjugated alkynylation of α,β-unsaturated amide through alkene isomerization

inferred← citeshttps://doi.org/10.1039/d0cc04221hopenalex-snapshot

Enantioselective zinc-mediated conjugate alkynylation of saccharin-derived 1- aza -butadienes

inferred← citeshttps://doi.org/10.1039/d1cc07092dopenalex-snapshot

Palladium-catalyzed intermolecular alkynylcarbonylation of unactivated alkenes: easy access to β-alkynylcarboxylic esters

inferred← citeshttps://doi.org/10.1039/d5cc01032bopenalex-snapshot

Recent advances of asymmetric catalytic transformations of alkylidene Meldrum's acid derivatives

inferred← citeshttps://doi.org/10.1055/a-2873-1433openalex-snapshot

Rhodium-Catalyzed Double Alkynylation of Isatins

inferred← citeshttps://doi.org/10.1055/s-0037-1610182openalex-snapshot

Conjugate Alkynylation of Electrophilic Double Bonds. From Regioselectivity to Enantioselectivity

inferred← citeshttps://doi.org/10.1126/sciadv.ady4028openalex-snapshot

Noncovalent interaction–driven regio- and enantioselective hydroalkynylation of unactivated alkenes to access remote chiral nitriles

inferred← citeshttps://doi.org/10.3762/bjoc.11.60openalex-snapshot

Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams

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