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Asymmetric Conjugate Addition of Alkynylboronates to Enones

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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.199005461openalex-snapshot
Fast Heteronuclear 3D NMR Spectroscopy
inferredcites →https://doi.org/10.1002/anie.199712361openalex-snapshot
Asymmetric Catalysis with Heterobimetallic Compounds
inferredcites →https://doi.org/10.1016/s0022-328x(00)81551-xopenalex-snapshot
The chemistry of the carboncarbon triple bond
inferredcites →https://doi.org/10.1021/ja00086a066openalex-snapshot
Highly Enantioselective Alkynylation of Aldehydes Promoted by Chiral Oxazaborolidines
inferredcites →https://doi.org/10.1021/ja00272a059openalex-snapshot
Reactions of allylsilanes with simple iminium salts in water: A facile route to piperidines via a aminomethano desilylation-cyclization process
inferredcites →https://doi.org/10.1021/ja00445a054openalex-snapshot
Conjugate addition of B-1-alkynyl-9-borabicyclo[3.3.1]-nonanes to .alpha.,.beta.-unsaturated ketones. A convenient synthesis of .gamma.,.delta.-acetylenic ketones
inferredcites →https://doi.org/10.1021/ja960345aopenalex-snapshot
Asymmetric Synthesis of Stegobinone via Boronic Ester Chemistry
inferredcites →https://doi.org/10.1021/jo00010a004openalex-snapshot
Highly efficient synthesis of 13-dehydroprostaglandins by 1,4-addition reaction of alkynyl .omega. side-chain unit onto a cyclopentenone framework
inferredcites →https://doi.org/10.1021/jo00010a005openalex-snapshot
A novel method for the synthesis of spiroketal systems. Synthesis of the pheromones of the common wasp and the olive fruit fly
inferredcites →https://doi.org/10.1021/jo00038a003openalex-snapshot
Asymmetric aza-Diels-Alder reaction mediated by chiral boron reagent
inferredcites →https://doi.org/10.1021/jo01303a024openalex-snapshot
Nickel-catalyzed conjugate addition of alkynyl groups to .alpha.,.beta.-unsaturated ketones
inferredcites →https://doi.org/10.1139/v73-314openalex-snapshot
Stereospecific Conjugate Alkenyl Group Transfer to α,β-Enones Using Vinylalane Reagents

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

inferred← citeshttps://doi.org/10.2139/ssrn.4571982openalex-extracted
inferred← citeshttps://doi.org/10.1002/047084289x.rn01710openalex-snapshot
(R)-2,2′-Dihydroxy-3,3′diphenyl-1,1′-binaphthyl
inferred← citeshttps://doi.org/10.1002/1521-3757(20010817)113:16<3109::aid-ange3109>3.0.co;2-nopenalex-snapshot
Formale enantioselektive Michael-Addition mit Umpolung der Reaktivität
inferred← citeshttps://doi.org/10.1002/1521-3773(20010817)40:16<3022::aid-anie3022>3.0.co;2-wopenalex-snapshot
Formal Enantioselective Michael Addition with Umpolung of Reactivity
inferred← citeshttps://doi.org/10.1002/3527606548.ch1openalex-snapshot
Structure, Properties, and Preparation of Boronic Acid Derivatives. Overview of Their Reactions and Applications
inferred← citeshttps://doi.org/10.1002/9780471264194.fos00943openalex-snapshot
1,1′‐Binaphthalene‐2,2′‐diyl heteroesters
inferred← citeshttps://doi.org/10.1002/9780471264194.fos00943.pub2openalex-snapshot
1,1′‐Binaphthalene‐2,2′‐diyl heteroesters
inferred← citeshttps://doi.org/10.1002/9780471476665.ch16openalex-snapshot
Preparation of Difunctional Compounds
inferred← citeshttps://doi.org/10.1002/9781118662083.cot08-015openalex-snapshot
Formation of Aldehydes and Ketones by 1,4‐Addition to α,β‐Unsaturated Carbonyl Compounds and Derivatives
inferred← citeshttps://doi.org/10.1002/9783527639328.ch1openalex-snapshot
Structure, Properties, and Preparation of Boronic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/9783527677894.ch7openalex-snapshot
Catalytic Conjugate Additions of Alkynes
inferred← citeshttps://doi.org/10.1002/adsc.200800117openalex-snapshot
Polystyryl‐BEMP as an Efficient Recyclable Catalyst for the Nucleophilic Addition of Nitroalkanes to α,β‐Unsaturated Carbonyl Compounds under Solvent‐Free Conditions
inferred← citeshttps://doi.org/10.1002/adsc.200800776openalex-snapshot
The Enantioselective Addition of Alkyne Nucleophiles to Carbonyl Groups
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.200461985openalex-snapshot
1‐Alkynyl(aryl)(tetrafluoroborato)‐λ3‐bromanes as Highly Efficient Michael Acceptors: Uncatalyzed Conjugate Addition of 1‐Alkynyl(trialkyl)stannanes To Yield Symmetrical and Unsymmetrical 1,3‐Butadiynes
inferred← citeshttps://doi.org/10.1002/ange.200904486openalex-snapshot
Asymmetric Synthesis of β‐Alkynyl Aldehydes by Rhodium‐Catalyzed Conjugate Alkynylation
inferred← citeshttps://doi.org/10.1002/anie.200461985openalex-snapshot
1‐Alkynyl(aryl)(tetrafluoroborato)‐λ3‐bromanes as Highly Efficient Michael Acceptors: Uncatalyzed Conjugate Addition of 1‐Alkynyl(trialkyl)stannanes To Yield Symmetrical and Unsymmetrical 1,3‐Butadiynes
inferred← citeshttps://doi.org/10.1002/anie.200904486openalex-snapshot
Asymmetric Synthesis of β‐Alkynyl Aldehydes by Rhodium‐Catalyzed Conjugate Alkynylation
inferred← citeshttps://doi.org/10.1002/asia.200600228openalex-snapshot
Enantioselective Synthesis of 3,4‐Dihydropyran‐2‐ones by Domino Michael Addition and Lactonization with New Asymmetric Organocatalysts: Cinchona‐Alkaloid‐Derived Chiral Quaternary Ammonium Phenoxides
inferred← citeshttps://doi.org/10.1002/asia.200800042openalex-snapshot
Rhodium‐Catalyzed Asymmetric Addition of Terminal Alkynes to Diarylphosphinylallenes
inferred← citeshttps://doi.org/10.1002/asia.201600167openalex-snapshot
Synthesis, Structure, and Optical Studies of Donor–Acceptor‐Type Near‐Infrared (NIR) Aza–Boron‐Dipyrromethene (BODIPY) Dyes
inferred← citeshttps://doi.org/10.1002/chem.200800034openalex-snapshot
Diastereo‐ and Enantiomerically Pure Allylboronates: Their Synthesis and Scope
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.201402353openalex-snapshot
Palladium‐Catalyzed Chemoselective Allylic Substitution, Suzuki–Miyaura Cross‐Coupling, and Allene Formation of Bifunctional 2‐B(pin)‐Substituted Allylic Acetate Derivatives
inferred← citeshttps://doi.org/10.1002/chem.202203331openalex-snapshot
The Chelate Effect Rationalizes Observed Rate Acceleration and Enantioselectivity in BINOL‐Catalyzed Petasis Reactions
inferred← citeshttps://doi.org/10.1002/chem.202302901openalex-snapshot
Iron‐Catalyzed Gamma‐Gamma Dimerization of Siloxydienes
inferred← citeshttps://doi.org/10.1002/chin.200021041openalex-snapshot
ChemInform Abstract: Asymmetric Conjugate Addition of Alkynylboronates to Enones.
inferred← citeshttps://doi.org/10.1002/chir.22134openalex-snapshot
Biomimetic Synthesis and Studies Toward Enantioselective Synthesis of Flindersial Alkaloids
inferred← citeshttps://doi.org/10.1002/ejoc.200390127openalex-snapshot
Synthesis and Pyrolytic and Kinetic Behaviour of β,δ′‐Dioxo‐Stabilised Phosphorus Ylides: Convenient Preparation of γ,δ‐Alkynyl Ketones and 2,3‐Functionalised Butadienes
inferred← citeshttps://doi.org/10.1002/ejoc.200800681openalex-snapshot
Synthetic and Theoretical Investigations on the Construction of Oxanorbornenes by a Michael Addition and Intramolecular Diels–Alder Furan Reaction
inferred← citeshttps://doi.org/10.1002/hc.10028openalex-snapshot
Asymmetric synthesis of epoxides from aromatic aldehydes and benzyl halides catalyzed by C2 symmetric optically active sulfides having a binaphthyl skeleton
inferred← citeshttps://doi.org/10.1007/bf02903687openalex-snapshot
Preparation of (R)- and (S)-2-Allyl-1, 3, 2-dinaphtho (α, β) [d.f] dioxaborepin and their reactions with aldehydes
inferred← citeshttps://doi.org/10.1007/s10562-010-0451-8openalex-snapshot
1, 4-Addition of Terminal Alkynes to Conjugated Enones in Water Using Green Catalyst Bis[(l)prolinato-N,O]Zn—An Environmentally Benign Protocol
inferred← citeshttps://doi.org/10.1007/s11426-010-0137-5openalex-snapshot
New observation on a class of old reactions: Chemoselectivity for the solvent-free reaction of aromatic aldehydes with alkylketones catalyzed by a double-component inorganic base system
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00007-6openalex-snapshot
One or More CC Bonds Formed by Addition: Addition of Carbon Electrophiles and Nucleophiles to CC Multiple Bonds
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00045-3openalex-snapshot
Alkynylarsenic, -antimony, -bismuth, -boron, -silicon, -germanium, and Metal Compounds
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00112-6openalex-snapshot
Boron
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00130-8openalex-snapshot
C–C Bond Formation through Conjugate Addition of C–M to CC–CO and CC–NO2
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00315-3openalex-snapshot
3.15 Non-Chiral Pool Derived Synthetic Auxiliaries: Use of C2-Symmetric Chiral Diols
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00322-0openalex-snapshot
3.22 Chiral Ligation for Boron and Aluminum in Stoichiometric Asymmetric Synthesis
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/b978-0-443-31482-7.00112-0openalex-snapshot
Alkynylarsenic, -Antimony, -Bismuth, -Boron, -Silicon, -Germanium, and Metal Compounds
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.07.103openalex-snapshot
Discovery of potent and novel S-nitrosoglutathione reductase inhibitors devoid of cytochrome P450 activities
inferred← citeshttps://doi.org/10.1016/j.bmcl.2023.129497openalex-snapshot
5-HT6 receptor antagonists. Design, synthesis, and structure–activity relationship of substituted 2-(1-methyl-4-piperazinyl)pyridines
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.09.046openalex-snapshot
Indium(I) bromide-promoted stereoselective preparation of (E)-α,β-unsaturated ketones via sequential intermolecular aldol-type coupling/elimination reactions of α,α-dichloroketones with aldehydes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.05.027openalex-snapshot
Alkynylboron compounds in organic synthesis
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.2013.09.017openalex-snapshot
Imidazolium-based chiral ionic liquids: synthesis and application
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.05.033openalex-snapshot
A mild and efficient palladium-catalyzed homocoupling of lithium alkynyltriisopropoxyborates: a new route to synthesis of 1,3-diynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.07.036openalex-snapshot
Rhodium-catalyzed 1,4-addition of terminal alkynes to vinyl ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.09.114openalex-snapshot
An efficient palladium-catalyzed coupling reaction of lithium alkynyltriisopropoxyborates with acid chlorides: a new access to synthesis of conjugated ynones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.02.046openalex-snapshot
Catalyzation of 1,4-additions of arylboronic acids to α,β-unsaturated substrates using nickel(I) complexes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.166openalex-snapshot
Experimental mechanistic insight into the BINOL-catalyzed enantioselective conjugate addition of boronates to enones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.02.061openalex-snapshot
Enantioselective organocatalytic conjugate addition of organoboron nucleophiles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153412openalex-snapshot
Reaction rate differences between organotrifluoroborates and boronic acids in BINOL-catalyzed conjugate addition to enones
inferred← citeshttps://doi.org/10.1016/s0010-8545(03)00026-2openalex-snapshot
1,1′-Binaphthyl-2,2′-diol and 2,2′-diamino-1,1′-binaphthyl: versatile frameworks for chiral ligands in coordination and metallosupramolecular chemistry
inferred← citeshttps://doi.org/10.1016/s0022-328x(03)00237-7openalex-snapshot
Synthesis and reaction of secondary and primary diorganozinc reagents using a boron–zinc exchange reaction
inferred← citeshttps://doi.org/10.1016/s0040-4020(00)00618-9openalex-snapshot
Enantioselective Conjugate Additions
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00967-5openalex-snapshot
Asymmetric catalysis by 1,1′-binaphthyl compounds with conformation-defined 3,3′-aryl substituents
inferred← citeshttps://doi.org/10.1016/s1381-1169(01)00425-3openalex-snapshot
Further studies on hydration of alkynes by the PtCl4–CO catalyst
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02106openalex-snapshot
Chiral-Boron-Complex-Catalyzed Asymmetric [3 + 2] Cycloaddition of β-Trifluoromethyl α,β-Unsaturated Ketones with N,N′-Cyclic Azomethine Imines
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01511openalex-snapshot
BF3·OEt2-Promoted Synthesis of 2,3-Metallocenocyclohexanones: A 1,2-Hydride Shift and Cationic Cyclization Strategy
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02124openalex-snapshot
Enantioselective Phase-Transfer-Catalyzed Synthesis of Chiral N-Substituted 3,3-Dinitroazetidines by Aza-Michael Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02394openalex-snapshot
Organocatalytic Enantioselective Conjugate Alkynylation of β-Aminoenones: Access to Chiral β-Alkynyl-β-Amino Carbonyl Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01395openalex-snapshot
Enantioselective Conjugate Addition of Alkenyl Trifluoroborates to Alkenyl-Substituted Benzimidazoles Catalyzed by Chiral Binaphthols
inferred← citeshttps://doi.org/10.1021/cr020025bopenalex-snapshot
Modified BINOL Ligands in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1021/ja043001qopenalex-snapshot
Ligand-Catalyzed Asymmetric Alkynylboration of Enones: A New Paradigm for Asymmetric Synthesis Using Organoboranes
inferred← citeshttps://doi.org/10.1021/ja0713734openalex-snapshot
Asymmetric Conjugate Alkenylation of Enones Catalyzed by Chiral Diols
inferred← citeshttps://doi.org/10.1021/ja077664uopenalex-snapshot
Generation and Tandem Reactions of 1-Alkenyl-1,1-Heterobimetallics: Practical and Versatile Reagents for Organic Synthesis
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/ja309076gopenalex-snapshot
Enantioselective Addition of Boronates to o-Quinone Methides Catalyzed by Chiral Biphenols
inferred← citeshttps://doi.org/10.1021/ja905336popenalex-snapshot
Enantioselective Rhodium-Catalyzed Conjugate Alkynylation of 5-Benzylidene Meldrum’s Acids with TMS-acetylene
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.7b02317openalex-snapshot
Pyro-Borates, Spiro-Borates, and Boroxinates of BINOL—Assembly, Structures, and Reactivity
inferred← citeshttps://doi.org/10.1021/jo201476hopenalex-snapshot
A Homogeneous, Recyclable Polymer Support for Rh(I)-Catalyzed C–C Bond Formation
inferred← citeshttps://doi.org/10.1021/jo500599hopenalex-snapshot
Boron Carboxylate Catalysis of Homoallylboration
inferred← citeshttps://doi.org/10.1021/jo502004ropenalex-snapshot
Covalent Dimers of 1,3-Diphenylisobenzofuran for Singlet Fission: Synthesis and Electrochemistry
inferred← citeshttps://doi.org/10.1021/jo8007463openalex-snapshot
Theoretical Study of the Asymmetric Conjugate Alkenylation of Enones Catalyzed by Binaphthols
inferred← citeshttps://doi.org/10.1021/ml200045sopenalex-snapshot
Discovery of S-Nitrosoglutathione Reductase Inhibitors: Potential Agents for the Treatment of Asthma and Other Inflammatory Diseases
inferred← citeshttps://doi.org/10.1021/ol048623vopenalex-snapshot
Catalytic Enantioselective Conjugate Addition of Trimethylsilylacetylene to 2-Cyclohexen-1-one
inferred← citeshttps://doi.org/10.1021/ol0490882openalex-snapshot
Asymmetric Allylboration of Aldehydes and Ketones Using 3,3‘-Disubstitutedbinaphthol-Modified Boronates
inferred← citeshttps://doi.org/10.1021/ol0523087openalex-snapshot
Asymmetric Synthesis of Propargylamides via 3,3‘-Disubstituted Binaphthol-Modified Alkynylboronates
inferred← citeshttps://doi.org/10.1021/ol0611595openalex-snapshot
N-Propargylamides via the Asymmetric Michael Addition of B-Alkynyl-10-TMS-9- borabicyclo[3.3.2]decanes to N-Acylimines
inferred← citeshttps://doi.org/10.1021/ol2020847openalex-snapshot
Enantioselective Conjugate Addition of Alkenylboronic Acids to Indole-Appended Enones
inferred← citeshttps://doi.org/10.1021/ol3030605openalex-snapshot
A General Method for the Enantioselective Synthesis of α-Chiral Heterocycles
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/ol801247vopenalex-snapshot
Highly Regioselective Isomerization−Hydroformylation of Internal Olefins to Linear Aldehyde Using Rh Complexes with Tetraphosphorus Ligands
inferred← citeshttps://doi.org/10.1021/ol901119dopenalex-snapshot
Rhodium-Catalyzed Asymmetric Conjugate Alkynylation of Enones with Alkynylsilanols
inferred← citeshttps://doi.org/10.1038/ncomms11806openalex-snapshot
Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism
inferred← citeshttps://doi.org/10.1039/b009236nopenalex-snapshot
Stoichiometric asymmetric processes
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/c5ra11760gopenalex-snapshot
Chiral octahedral complexes of Co( iii ) as catalysts for asymmetric epoxidation of chalcones under phase transfer conditions
inferred← citeshttps://doi.org/10.1039/c8cc07908kopenalex-snapshot
Catalytic asymmetric propargyl- and allylboration of hydrazonoesters: a metal-free approach to sterically encumbered chiral α-amino acid derivatives
inferred← citeshttps://doi.org/10.1039/d1dt00842kopenalex-snapshot
Synthesis, structures and catalytic activity of some BINOL based boronates and boronium salts
inferred← citeshttps://doi.org/10.1055/s-0037-1610182openalex-snapshot
Conjugate Alkynylation of Electrophilic Double Bonds. From Regioselectivity to Enantioselectivity
inferred← citeshttps://doi.org/10.1246/bcsj.80.1635openalex-snapshot
Stereoselective Conjugate Addition Reactions Using In Situ Metallated Terminal Alkynes and the Development of Novel Chiral P,N-Ligands
inferred← citeshttps://doi.org/10.3390/molecules26061615openalex-snapshot
Rate Dependence on Inductive and Resonance Effects for the Organocatalyzed Enantioselective Conjugate Addition of Alkenyl and Alkynyl Boronic Acids to β-Indolyl Enones and β-Pyrrolyl Enones
inferred← citeshttps://doi.org/10.3987/com-06-s(k)48openalex-snapshot
Efficient Synthesis of Substituted 3-Amino-3,4-dihydropyran-2-ones Diastereo and Enantioselective Tandem Michael Addition and Lactonization between α,β-Unsaturated Ketones and Glycine-Derived Silyl Enolates Using a Chiral Quaternary Ammonium Phenoxide
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