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Catalytic Enantioselective Cyanosilylation of Ketones
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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.199415551openalex-snapshot
Synthesis and Reactions of Optically Active Cyanohydrins
inferredcites →https://doi.org/10.1002/anie.199712361openalex-snapshot
Asymmetric Catalysis with Heterobimetallic Compounds
inferredcites →https://doi.org/10.1016/s0040-4039(99)02215-7openalex-snapshot
Asymmetric Strecker reactions of ketimines catalysed by titanium-based complexes
inferredcites →https://doi.org/10.1021/ol005636+openalex-snapshot
Enantioselective Catalytic Addition of HCN to Ketoimines. Catalytic Synthesis of Quaternary Amino Acids
inferredcites →https://doi.org/10.1055/s-1982-29804openalex-snapshot
An Improved Synthesis of Cyanotrimethylsilane
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.4647549openalex-extracted
B(C6f5)3-Catalyzed Regio- and Stereoselective Cyanation of Isatogens and Their Derivatives
inferred← citeshttps://doi.org/10.1002/0471227617.eoc024openalex-snapshot
Asymmetric Catalysis – Homogeneous
inferred← citeshttps://doi.org/10.1002/1099-0690(200103)2001:6<1045::aid-ejoc1045>3.0.co;2-iopenalex-snapshot
Synthesis of a Bifunctional Ligand for the Sequential Enantioselective Catalysis of Various Reactions
inferred← citeshttps://doi.org/10.1002/1521-3757(20020315)114:6<1051::aid-ange1051>3.0.co;2-zopenalex-snapshot
Aluminum-Catalyzed Asymmetric Addition of TMSCN to Aromatic and Aliphatic Ketones Promoted by an Easily Accessible and Recyclable Peptide Ligand
inferred← citeshttps://doi.org/10.1002/1521-3765(20011217)7:24<5246::aid-chem5246>3.0.co;2-oopenalex-snapshot
The Development of New Monometallic Bifunctional Catalysts with Lewis acidand Lewis Base Properties, and their Application in Asymmetric Cyanation Reactions
inferred← citeshttps://doi.org/10.1002/1521-3773(20020315)41:6<1009::aid-anie1009>3.0.co;2-fopenalex-snapshot
Aluminum-Catalyzed Asymmetric Addition of TMSCN to Aromatic and Aliphatic Ketones Promoted by an Easily Accessible and Recyclable Peptide Ligand
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0286openalex-snapshot
Synthetic Uses of Phenols
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0610openalex-snapshot
Catalysis of Organic Processes by Metal Phenolates
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343openalex-snapshot
Chiral auxiliaries and catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub2openalex-snapshot
Chiral auxiliaries and catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub3openalex-snapshot
Chiral auxiliaries and catalysts
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/10.1002/9780471476665.ch16openalex-snapshot
Preparation of Difunctional Compounds
inferred← citeshttps://doi.org/10.1002/9781118309872.ch4openalex-snapshot
Asymmetric Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9781118484722.ch3openalex-snapshot
Organosilicon and Relating Organotin Chemistry
inferred← citeshttps://doi.org/10.1002/9781118846919.ch3openalex-snapshot
Asymmetric Multifunctional Catalysis
inferred← citeshttps://doi.org/10.1002/9783527652235.ch43openalex-snapshot
Asymmetric Conia‐ene Carbocyclizations
inferred← citeshttps://doi.org/10.1002/9783527654543.ch13openalex-snapshot
1,2‐Addition of Nucleophiles to Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/9783527675142.ch10openalex-snapshot
Bifunctional Lewis Base Catalysis with Dual Activation of R – M and C = O (n → σ*)
inferred← citeshttps://doi.org/10.1002/9783527675142.ch25openalex-snapshot
Bifunctional and Synergistic Catalysis: Lewis Acid Catalysis and Lewis Base‐Assisted Bond Polarization ( n → σ*)
inferred← citeshttps://doi.org/10.1002/9783527675142.ch8openalex-snapshot
Mechanism of C – Si Bond Cleavage Using Lewis Bases ( n → σ*)
inferred← citeshttps://doi.org/10.1002/9783527681020.ch2openalex-snapshot
Lewis Acid–Lewis Base Catalysis
inferred← citeshttps://doi.org/10.1002/9783527834204.ch7openalex-snapshot
Carbohydrate‐Based Catalysts and Auxiliaries in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/adsc.200505415openalex-snapshot
Nanocrystalline Titanium(IV) Oxide as an Efficient Heterogeneous Catalyst for Tandem Michael and Nucleophilic 1,2‐Addition to Enones
inferred← citeshttps://doi.org/10.1002/adsc.200505418openalex-snapshot
Enantioselective Cyanosilylation of Ketones Catalyzed by a Nitrogen‐Containing Bifunctional Catalyst
inferred← citeshttps://doi.org/10.1002/adsc.200700392openalex-snapshot
Highly Enantioselective Allylation of Aromatic α‐Keto Phosphonates Catalyzed by Chiral N,N′‐Dioxide‐Indium(III) Complexes
inferred← citeshttps://doi.org/10.1002/adsc.200700565openalex-snapshot
Discrete versus In Situ‐Generated Aluminum‐Salen Catalysts in Enantioselective Cyanosilylation of Ketones: Role of Achiral Ligands
inferred← citeshttps://doi.org/10.1002/adsc.200800314openalex-snapshot
Chiral Lithium Salts of Phosphoric Acids as Lewis Acid–Base Conjugate Catalysts for the Enantioselective Cyanosilylation of Ketones
inferred← citeshttps://doi.org/10.1002/adsc.200900207openalex-snapshot
Enantioselective Silylcyanation of Aldehydes and Ketones by a Titanium Catalyst Prepared from a Partially Hydrolyzed Titanium Alkoxide and a Schiff Base Ligand
inferred← citeshttps://doi.org/10.1002/adsc.201200027openalex-snapshot
Enantioselective Cyanosilylation of Ketones with Amino Acid/BINAP/Ruthenium(II)‐Lithium Phenoxide Catalyst Systems
inferred← citeshttps://doi.org/10.1002/adsc.201300913openalex-snapshot
Stereoselective Synthesis of Phosphoryl‐Substituted Phenols
inferred← citeshttps://doi.org/10.1002/adsc.201400939openalex-snapshot
Enantioselective Titanium‐Catalyzed Cyanation Reactions of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201900015openalex-snapshot
Catalytic Asymmetric Cyanation Reactions of Aldehydes and Ketones in Total Synthesis
inferred← citeshttps://doi.org/10.1002/ajoc.202100795openalex-snapshot
Kinetic Insights into Cyanosilylation of Aldehydes Catalyzed by a Covalently Bridged Dinuclear (Salen)titanium Complex
inferred← citeshttps://doi.org/10.1002/ange.200300604openalex-snapshot
Chemisch katalysierte asymmetrische Cyanhydrinsynthesen
inferred← citeshttps://doi.org/10.1002/ange.200300635openalex-snapshot
Hoch effiziente asymmetrische Katalyse durch doppelte Aktivierung von Nucleophil und Elektrophil
inferred← citeshttps://doi.org/10.1002/ange.200351230openalex-snapshot
Enantioselective Alkynylation of Ketones Catalyzed by Zn(Salen) Complexes
inferred← citeshttps://doi.org/10.1002/ange.200503791openalex-snapshot
Highly Diastereo‐ and Enantioselective Copper‐Catalyzed Domino Reduction/Aldol Reaction of Ketones with Methyl Acrylate
inferred← citeshttps://doi.org/10.1002/ange.200503995openalex-snapshot
Asymmetrische Synthese im Spiegel von Chemie und Biologie
inferred← citeshttps://doi.org/10.1002/ange.200600470openalex-snapshot
Construction of Enantiomerically Enriched Tertiary α‐Hydroxycarboxylic Acid Derivatives by Phase‐Transfer‐Catalyzed Asymmetric Alkylation of Diaryloxazolidin‐2,4‐diones
inferred← citeshttps://doi.org/10.1002/ange.200604943openalex-snapshot
Lewis‐Base‐Katalyse in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.200805805openalex-snapshot
Catalytic Asymmetric Cycloaddition of Ketenes and Nitroso Compounds: Enantioselective Synthesis of α‐Hydroxycarboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/ange.201000896openalex-snapshot
Improving the Atom Efficiency of the Wittig Reaction by a “Waste as Catalyst/Co‐catalyst” Strategy
inferred← citeshttps://doi.org/10.1002/ange.201510682openalex-snapshot
Enantioselective Cyanosilylation of Ketones with Lithium(I) Dicyanotrimethylsilicate(IV) Catalyzed by a Chiral Lithium(I) Phosphoryl Phenoxide
inferred← citeshttps://doi.org/10.1002/ange.201710310openalex-snapshot
Site‐Selective O‐Arylation of Glycosides
inferred← citeshttps://doi.org/10.1002/ange.202208443openalex-snapshot
Desymmetric Cyanosilylation of Acyclic 1,3‐Diketones
inferred← citeshttps://doi.org/10.1002/anie.200300604openalex-snapshot
Chemically Catalyzed Asymmetric Cyanohydrin Syntheses
inferred← citeshttps://doi.org/10.1002/anie.200300635openalex-snapshot
Towards Perfect Catalytic Asymmetric Synthesis: Dual Activation of the Electrophile and the Nucleophile
inferred← citeshttps://doi.org/10.1002/anie.200351230openalex-snapshot
Enantioselective Alkynylation of Ketones Catalyzed by Zn(Salen) Complexes
inferred← citeshttps://doi.org/10.1002/anie.200503791openalex-snapshot
Highly Diastereo‐ and Enantioselective Copper‐Catalyzed Domino Reduction/Aldol Reaction of Ketones with Methyl Acrylate
inferred← citeshttps://doi.org/10.1002/anie.200503995openalex-snapshot
Asymmetric Synthesis from a Chemical and Biological View
inferred← citeshttps://doi.org/10.1002/anie.200600470openalex-snapshot
Construction of Enantiomerically Enriched Tertiary α‐Hydroxycarboxylic Acid Derivatives by Phase‐Transfer‐Catalyzed Asymmetric Alkylation of Diaryloxazolidin‐2,4‐diones
inferred← citeshttps://doi.org/10.1002/anie.200604943openalex-snapshot
Lewis Base Catalysis in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.200805805openalex-snapshot
Catalytic Asymmetric Cycloaddition of Ketenes and Nitroso Compounds: Enantioselective Synthesis of α‐Hydroxycarboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/anie.201000896openalex-snapshot
Improving the Atom Efficiency of the Wittig Reaction by a “Waste as Catalyst/Co‐catalyst” Strategy
inferred← citeshttps://doi.org/10.1002/anie.201510682openalex-snapshot
Enantioselective Cyanosilylation of Ketones with Lithium(I) Dicyanotrimethylsilicate(IV) Catalyzed by a Chiral Lithium(I) Phosphoryl Phenoxide
inferred← citeshttps://doi.org/10.1002/anie.201710310openalex-snapshot
Site‐Selective O‐Arylation of Glycosides
inferred← citeshttps://doi.org/10.1002/anie.202208443openalex-snapshot
Desymmetric Cyanosilylation of Acyclic 1,3‐Diketones
inferred← citeshttps://doi.org/10.1002/aoc.1278openalex-snapshot
Cyanosilylation of carbonyl compounds catalyzed by sodium L ‐histidine
inferred← citeshttps://doi.org/10.1002/aoc.1284openalex-snapshot
Enantioselective cyanosilylation of aldehydes catalyzed by Mn(salen) complex/triphenyl phosphine oxide
inferred← citeshttps://doi.org/10.1002/aoc.1324openalex-snapshot
Solvent‐free cyanosilylation of aldehydes catalyzed by SmI2
inferred← citeshttps://doi.org/10.1002/aoc.1369openalex-snapshot
Studies on cyanosilylation reaction catalyzed by LnN complexes
inferred← citeshttps://doi.org/10.1002/aoc.1416openalex-snapshot
Copper perchlorate hexahydrate: a highly efficient catalyst for the cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1002/aoc.1600openalex-snapshot
Organocatalytic synthesis of cyanohydrin trimethylsilyl ethers by potassium 4‐benzylpiperidinedithiocarbamate under solvent‐free conditions
inferred← citeshttps://doi.org/10.1002/asia.201201021openalex-snapshot
Direct Catalytic Asymmetric Addition of Allylic Cyanides to Aldehydes for Expeditious Access to Enantioenriched Unsaturated δ‐Valerolactones
inferred← citeshttps://doi.org/10.1002/asia.201801600openalex-snapshot
Kinetic Resolution of Acylsilane Cyanohydrins via Organocatalytic Cycloetherification
inferred← citeshttps://doi.org/10.1002/chem.200400506openalex-snapshot
Enantioselective Cyanosilylation of Ketones by a Catalytic Double‐Activation Method with an Aluminium Complex and an N‐Oxide
inferred← citeshttps://doi.org/10.1002/chem.200801679openalex-snapshot
Mechanism‐Guided Development of VO(salen)X Complexes as Catalysts for the Asymmetric Synthesis of Cyanohydrin Trimethylsilyl Ethers
inferred← citeshttps://doi.org/10.1002/chem.200900936openalex-snapshot
Asymmetric Cyanation of Aldehydes, Ketones, Aldimines, and Ketimines Catalyzed by a Versatile Catalyst Generated from Cinchona Alkaloid, Achiral Substituted 2,2′‐Biphenol and Tetraisopropyl Titanate
inferred← citeshttps://doi.org/10.1002/chem.201202074openalex-snapshot
Highly Selective 1,4‐ and 1,6‐Addition of P(O)H Compounds to p‐Quinones: A Divergent Method for the Synthesis of C‐ and O‐Phosphoryl Hydroquinone Derivatives
inferred← citeshttps://doi.org/10.1002/chem.202104053openalex-snapshot
Direct Addition of Grignard Reagents to Aliphatic Carboxylic Acids Enabled by Bulky turbo‐Organomagnesium Anilides
inferred← citeshttps://doi.org/10.1002/chin.200047030openalex-snapshot
ChemInform Abstract: Catalytic Enantioselective Cyanosilylation of Ketones.
inferred← citeshttps://doi.org/10.1002/chin.200639246openalex-snapshot
In the Arena of Enantioselective Synthesis, Titanium Complexes Wear the Laurel Wreath
inferred← citeshttps://doi.org/10.1002/chir.20534openalex-snapshot
Enantioselective cyanosilylation of ketones catalyzed by recyclable polymeric and dimeric MN(III) salen complexes at room temperature
inferred← citeshttps://doi.org/10.1002/chir.20661openalex-snapshot
Asymmetric Henry reaction catalyzed by bifunctional copper‐based catalysts
inferred← citeshttps://doi.org/10.1002/ejic.201402375openalex-snapshot
Two‐Dimensional {Co3+–Co2+} and {Fe3+–Co2+} Networks and Their Heterogeneous Catalytic Activities
inferred← citeshttps://doi.org/10.1002/ejic.201403072openalex-snapshot
A Metalloligand Appended with Thiazole Rings: Heterometallic {Co3+–Zn2+} and {Co3+–Cd2+} Complexes and Their Heterogeneous Catalytic Applications
inferred← citeshttps://doi.org/10.1002/ejoc.200300415openalex-snapshot
Asymmetric Cyanosilylation of Ketones Catalyzed by Bifunctional Chiral N‐Oxide Titanium Complex Catalysts
inferred← citeshttps://doi.org/10.1002/ejoc.200400246openalex-snapshot
Acetylenes in Catalysis: Enantioselective Additions to Carbonyl Groups and Imines and Applications Beyond
inferred← citeshttps://doi.org/10.1002/ejoc.200400411openalex-snapshot
Effective Activation of the Chiral Salen/Ti(OiPr)4 Catalyst with Achiral Phenolic N‐Oxides as Additives in the Enantioselective Cyanosilylation of Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.200400721openalex-snapshot
Asymmetric Cyanohydrin Synthesis Catalyzed by Al(salen)/Triphenylphosphane Oxide
inferred← citeshttps://doi.org/10.1002/ejoc.200700318openalex-snapshot
Enantioselective Catalytic Formation of Quaternary Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/ejoc.200701161openalex-snapshot
A Novel Chiral (salen)AlIII Complex Catalyzed Asymmetric Cyanosilylation of Aldehydes
inferred← citeshttps://doi.org/10.1002/ejoc.200900055openalex-snapshot
Chiral Lewis Base Catalyzed Enantioselective Acetylcyanation of α‐Oxo Esters
inferred← citeshttps://doi.org/10.1002/ejoc.200900678openalex-snapshot
Enamine–Metal Lewis Acid Bifunctional Catalysis: Application to Direct Asymmetric Aldol Reaction of Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.200901501openalex-snapshot
Asymmetric Cyanosilylation of α‐Keto Esters Catalyzed by the [Ru(phgly)2(binap)]–C6H5OLi System
inferred← citeshttps://doi.org/10.1002/ejoc.201000462openalex-snapshot
Recent Progress in the Chemically Catalyzed Enantioselective Synthesis of Cyanohydrins
inferred← citeshttps://doi.org/10.1002/ejoc.201200333openalex-snapshot
Silylcyanation of Aldehydes, Ketones, and Imines Catalyzed by a 6,6′‐Bis‐sulfonamide Derivative of 7,7′‐Dihydroxy‐8,8′‐biquinolyl (azaBINOL)
inferred← citeshttps://doi.org/10.1002/ejoc.201201637openalex-snapshot
Solvent‐Assisted Diastereoselective Trimethylsilyl Cyanide Additions to Cyclic α‐Fluoro Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.201900419openalex-snapshot
Base‐Catalyzed Stereoselective 1,6‐Conjugated Addition/Aromatization of P(O)–H Compounds with para‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/hc.20652openalex-snapshot
A novel bifunctional Ti(IV) complex catalyzed asymmetric silylcyanation of aldehydes
inferred← citeshttps://doi.org/10.1002/jccs.200600058openalex-snapshot
Diastereoselective Cyanation of α-Keto Amides Derived fromN-Phenyl Camphorpyrazolidinone and Camphorsultam
inferred← citeshttps://doi.org/10.1007/3-540-45731-3_4openalex-snapshot
New Chiral Organophosphorus Catalysts in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1007/3418_2015_143openalex-snapshot
Brønsted Acid/Lewis Base Hybrid Complexes
inferred← citeshttps://doi.org/10.1007/3418_2015_161openalex-snapshot
“Early–Late” Heterobimetallic Catalysis and Beyond
inferred← citeshttps://doi.org/10.1007/978-3-540-30429-6_23openalex-snapshot
Monosaccharides as Chiral Auxiliaries and Ligands for Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1007/s10562-022-04116-xopenalex-snapshot
Enhanced Catalytic Activity of a Cd(II) Complex Containing an Unsymmetrical Primary Amide Functionalized Ligand for the Solvent-Free Cyanosilylation Reaction
inferred← citeshttps://doi.org/10.1007/s10563-009-9071-yopenalex-snapshot
Dimeric & Polymeric Chiral Schiff Base Complexes and Supported BINOL Complexes as Potential Recyclable Catalysts in Asymmetric Kinetic Resolution and C–C Bond Formation Reactions
inferred← citeshttps://doi.org/10.1007/s10876-019-01589-6openalex-snapshot
RETRACTED ARTICLE: Three-Dimensional Ni(II)-MOF Containing an Asymmetric Pyridyl-Carboxylate Ligand: Catalytic Cyanosilylation of Aldehydes and Inhibits Human Promyelocytic Leukemia Cancer Cells
inferred← citeshttps://doi.org/10.1007/s11164-010-0132-7openalex-snapshot
Synthesis of chiral α-ethylphenylamine salts of tartaric acid and novel application to cyanosilylation of prochiral ketones
inferred← citeshttps://doi.org/10.1007/s11164-012-0792-6openalex-snapshot
The catalytic activity of Zn(II) and Mn(II) organometallic complexes
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00063-5openalex-snapshot
Nitriles: General Methods and Aliphatic Nitriles
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00415-8openalex-snapshot
4.16 Enantioselective Cyanation of Carbonyls and Imines
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00124-5openalex-snapshot
1.18 CN Addition to CO and CN Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00616-1openalex-snapshot
Asymmetric Cyanation Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-444-53202-2.50127-5openalex-snapshot
Novel Catalyst for Enantioselective Cyanosilylation of Aldehydes and Ketones Using Partially Hydrolyzed Titanium Alkoxide as a Lewis Acidic Metal
inferred← citeshttps://doi.org/10.1016/j.carres.2025.109447openalex-snapshot
Regioselective O-arylation of 6-hydroxy groups in carbohydrates
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.09.010openalex-snapshot
Metal catalyzed asymmetric cyanation reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.10.009openalex-snapshot
Stereoselective reactions involving hypervalent silicate complexes
inferred← citeshttps://doi.org/10.1016/j.ccr.2010.03.005openalex-snapshot
Use of sugar-based ligands in selective catalysis: Recent developments
inferred← citeshttps://doi.org/10.1016/j.ccr.2016.07.011openalex-snapshot
Enantioselective Main Group Catalysis: Modern Catalysts for Organic Transformations
inferred← citeshttps://doi.org/10.1016/j.ica.2014.11.018openalex-snapshot
Catalytic activity of copper(II) benzenetricarboxylate (HKUST-1) in reactions of aromatic aldehydes condensation with nitromethane: Kinetic and diffusion study
inferred← citeshttps://doi.org/10.1016/j.ica.2017.07.004openalex-snapshot
Trinuclear and polymeric cobalt(II or II/III) complexes with an arylhydrazone of acetoacetanilide and their application in cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1016/j.ica.2017.10.042openalex-snapshot
Cyanosilylation of aldehydes catalyzed by mixed ligand copper(II) complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2003.09.014openalex-snapshot
An improved synthesis of cyanohydrins in the presence of solid LiClO4 under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.01.025openalex-snapshot
Mild and efficient silylcyanation of ketones catalyzed by cesium fluoride
inferred← citeshttps://doi.org/10.1016/j.molcata.2016.11.036openalex-snapshot
Effective cyanosilylation of aldehydes with copper(II)-based polymeric catalysts
inferred← citeshttps://doi.org/10.1016/j.molcatb.2009.12.014openalex-snapshot
Microbial-catalysed resolution of sterically demanding cyanohydrins
inferred← citeshttps://doi.org/10.1016/j.steroids.2004.10.011openalex-snapshot
Cyanosilylation at pregnane side-chainsSelective synthesis and crystal structure of 20(R)-silylated cyanohydrins
inferred← citeshttps://doi.org/10.1016/j.tet.2004.02.008openalex-snapshot
Silylative N-hydroxyalkylation of amide compounds: application to the synthesis of acyclic alditol-based nucleoside analogues
inferred← citeshttps://doi.org/10.1016/j.tet.2004.06.133openalex-snapshot
Enantioselective cyanosilylation of ketones catalyzed by double-activation catalysts with N-oxides
inferred← citeshttps://doi.org/10.1016/j.tet.2004.08.080openalex-snapshot
Asymmetric catalysis in a micro reactor—Ce, Yb and Lu catalysed enantioselective addition of trimethylsilyl cyanide to benzaldehyde
inferred← citeshttps://doi.org/10.1016/j.tet.2004.08.081openalex-snapshot
Catalytic asymmetric synthesis of (S)-oxybutynin and a versatile intermediate for antimuscarinic agents
inferred← citeshttps://doi.org/10.1016/j.tet.2005.09.131openalex-snapshot
Asymmetric addition of trimethylsilyl cyanide to ketones catalyzed by Al(salen)/triphenylphosphine oxide
inferred← citeshttps://doi.org/10.1016/j.tet.2006.06.077openalex-snapshot
Enantioselective cyanocarbonation of ketones with chiral base
inferred← citeshttps://doi.org/10.1016/j.tet.2007.02.104openalex-snapshot
Enantioselective allylation of aldehydes catalyzed by new bifunctional bisoxazoline–metal complexes
inferred← citeshttps://doi.org/10.1016/j.tet.2007.07.016openalex-snapshot
Enantioselective and diastereoselective syntheses of cyanohydrin carbonates
inferred← citeshttps://doi.org/10.1016/j.tet.2007.10.093openalex-snapshot
Highly enantioselective cyanosilylation of ketones catalyzed by a bifunctional Ti(IV) complex
inferred← citeshttps://doi.org/10.1016/j.tet.2013.03.090openalex-snapshot
Enantioselective alkylation of aldehydes using dialkylzincs catalyzed by simple chiral diols derived from naturally occurring monosaccharides
inferred← citeshttps://doi.org/10.1016/j.tet.2013.09.001openalex-snapshot
Systematic study for the stereochemistry of the Atherton–Todd reaction
inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.01.030openalex-snapshot
A study of substituent effects on the enantioselective trimethylsilylcyanation of benzaldehyde catalyzed by chiral Schiff base–titanium(IV) complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2006.03.016openalex-snapshot
Salicylaldehyde Schiff bases derived from 2-ferrocenyl-2-amino alcohols. Part 1: New chiral ligands for the titanium-catalyzed enantioselective cyanation of aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2006.04.011openalex-snapshot
Enantioselective cyanosilylation of ketones catalyzed by Mn(salen)/Ph3PO
inferred← citeshttps://doi.org/10.1016/j.tetasy.2006.12.026openalex-snapshot
Synthesis of optically active cyanohydrins from aromatic ketones: evidence of an increased substrate range and inverted stereoselectivity for the hydroxynitrile lyase from Linum usitatissimum
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.12.016openalex-snapshot
A practical synthesis of syn- and anti-α,β-dihydroxyphosphinates via diastereoselective reduction of α-phosphinoyl ketones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.01.009openalex-snapshot
Asymmetric cyanohydrin formation from aldehydes catalyzed by manganese Schiff base complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.07.029openalex-snapshot
Asymmetric cyanosilylation of ketones catalyzed by recyclable polymer-supported copper(II) salen complexes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.07.005openalex-snapshot
Curtin–Hammett versus non-Curtin–Hammett frameworks in optimizing the enantioselective binolam/titanium(IV)-catalyzed cyanobenzoylation of aldehydes: Part 2
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.07.006openalex-snapshot
Mechanistic studies on the enantioselective BINOLAM/titanium(IV)-catalyzed cyanobenzoylation of aldehydes: Part 1
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.05.069openalex-snapshot
Achiral phenolic N-oxides as additives: an alternative strategy for asymmetric cyanosilylation of ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.01.177openalex-snapshot
Ionic liquid [omim][PF6] as an efficient and recyclable reaction media for the cyanosilylation of aldehydes without Lewis acid or any special activation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.04.084openalex-snapshot
New chiral bis(diphenylphospholane) ligands: design, synthesis, and application to catalytic enantioselective aldol reaction to ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.12.097openalex-snapshot
Catalytic enantioselective intermolecular reductive aldol reaction to ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.12.135openalex-snapshot
Catalytic cyanosilylation of ketones using organic catalyst 1,1,3,3-tetramethylguanidine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.04.003openalex-snapshot
Asymmetric cyanosilylation of ketones catalyzed by novel chiral N,N′-dioxide titanium complexes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.04.090openalex-snapshot
An expeditious synthesis of cyanohydrin trimethylsilyl ethers using tetraethylammonium 2-(carbamoyl)benzoate as a bifunctional organocatalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.123openalex-snapshot
DMAP-catalyzed cyanation of aldehydes and ketones with ethyl cyanoformate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.070openalex-snapshot
Polystyrene-supported TBD as an efficient and reusable organocatalyst for cyanosilylation of aldehydes, ketones, and imines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.06.031openalex-snapshot
Chiral zinc amidate catalyzed additions of diethylzinc to aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154909openalex-snapshot
B(C6F5)3-catalyzed regio- and stereoselective cyanation of isatogens and their derivatives
inferred← citeshttps://doi.org/10.1016/j.theochem.2008.05.016openalex-snapshot
Computational study on 1,1,3,3-tetramethylguanidine-catalyzed cyanosilylation mechanism of hypnone
inferred← citeshttps://doi.org/10.1016/j.theochem.2008.12.007openalex-snapshot
Understanding the role of the bifunctional titanium catalyst in cyanosilylation of ketones: A computational study
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)01200-5openalex-snapshot
HSAB matching and mismatching in selective catalysis and synthesis
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00908-6openalex-snapshot
A mild and efficient cyanosilylation of ketones catalyzed by a Lewis acid–Lewis base bifunctional catalyst
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)02039-6openalex-snapshot
Catalytic enantioselective cyanosilylation of ketones: improvement of enantioselectivity and catalyst turn-over by ligand tuning
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)02004-4openalex-snapshot
New soluble bifunctional polymeric chiral ligands for enantioselectively catalytic reactions
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)00450-1openalex-snapshot
Practical synthesis of chiral ligands for catalytic enantioselective cyanosilylation of ketones
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02135-4openalex-snapshot
A practical synthesis of (S)-oxybutynin
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)02321-3openalex-snapshot
Iodine as novel reagent for the 1,2-addition of trimethylsilyl cyanide to ketones including α,β-unsaturated ketones
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00825-xopenalex-snapshot
Synthesis and applications of non-racemic cyanohydrins
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00838-8openalex-snapshot
Stereoselective conjugate addition of diethylzinc to enones and nitroalkenes
inferred← citeshttps://doi.org/10.1016/s1874-6004(04)80017-0openalex-snapshot
Catalytic Asymmetric Total Synthesis of (−)-Strychnine and Fostriecin
inferred← citeshttps://doi.org/10.1021/acs.cgd.5b00697openalex-snapshot
Three-Dimensional Heterometallic Coordination Networks: Syntheses, Crystal Structures, Topologies, and Heterogeneous Catalysis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00488openalex-snapshot
Synthetic Strategies Employed for the Construction of Fostriecin and Related Natural Products
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00561openalex-snapshot
Stereodivergent Catalysis
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c03916openalex-snapshot
Asymmetric Cyanosilylation of Aldehydes by a Lewis Acid/Base Synergistic Catalyst of Chiral Metal Clusters
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02402openalex-snapshot
Site-Selective O-Arylation of Carbohydrate Derivatives through Nickel–Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02413openalex-snapshot
Nucleophilic Aromatic Substitution (SNAr) as an Approach to Challenging Carbohydrate–Aryl Ethers
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03076openalex-snapshot
Highly Enantioselective Hydrosilylation of Ketones Catalyzed by a Chiral Oxazaborolidinium Ion
inferred← citeshttps://doi.org/10.1021/acscatal.0c01918openalex-snapshot
Catalytic Enantioselective Cyanation: Recent Advances and Perspectives
inferred← citeshttps://doi.org/10.1021/acscatal.5b02184openalex-snapshot
Catalytic Asymmetric Cyanation Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.6b01227openalex-snapshot
A Career in Catalysis: Masakatsu Shibasaki
inferred← citeshttps://doi.org/10.1021/ar700261aopenalex-snapshot
Bifunctional Asymmetric Catalysis: Cooperative Lewis Acid/Base Systems
inferred← citeshttps://doi.org/10.1021/cr010297zopenalex-snapshot
Lanthanide Complexes in Multifunctional Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1021/cr040698popenalex-snapshot
In the Arena of Enantioselective Synthesis, Titanium Complexes Wear the Laurel Wreath
inferred← citeshttps://doi.org/10.1021/cr078340ropenalex-snapshot
Asymmetric Synthesis of Tertiary Alcohols and α-Tertiary Amines via Cu-Catalyzed C−C Bond Formation to Ketones and Ketimines
inferred← citeshttps://doi.org/10.1021/cr800255kopenalex-snapshot
Lewis Acid Catalyzed Asymmetric Cyanohydrin Synthesis
inferred← citeshttps://doi.org/10.1021/ic400536eopenalex-snapshot
Three-Dimensional {Co3+–Zn2+} and {Co3+–Cd2+} Networks Originated from Carboxylate-rich Building Blocks: Syntheses, Structures, and Heterogeneous Catalysis
inferred← citeshttps://doi.org/10.1021/ja010690mopenalex-snapshot
A Highly Enantioselective Chiral Lewis Base-Catalyzed Asymmetric Cyanation of Ketones
inferred← citeshttps://doi.org/10.1021/ja016682nopenalex-snapshot
Switching Enantiofacial Selectivities Using One Chiral Source: Catalytic Enantioselective Synthesis of the Key Intermediate for (20S)-Camptothecin Family by (S)-Selective Cyanosilylation of Ketones
inferred← citeshttps://doi.org/10.1021/ja036222popenalex-snapshot
Catalytic Asymmetric Cyanosilylation of Ketones with Chiral Lewis Base
inferred← citeshttps://doi.org/10.1021/ja043770+openalex-snapshot
Dynamic Ligand Exchange of the Lanthanide Complex Leading to Structural and Functional Transformation: One-Pot Sequential Catalytic Asymmetric Epoxidation-Regioselective Epoxide-Opening Process
inferred← citeshttps://doi.org/10.1021/ja0475959openalex-snapshot
Highly Enantioselective Cyanosilylation of Aldehydes Catalyzed by a Chiral Oxazaborolidinium Ion
inferred← citeshttps://doi.org/10.1021/ja050543eopenalex-snapshot
Enantioselective Cyanosilylation of Ketones Catalyzed by a Chiral Oxazaborolidinium Ion
inferred← citeshttps://doi.org/10.1021/ja052511xopenalex-snapshot
Thiourea-Catalyzed Enantioselective Cyanosilylation of Ketones
inferred← citeshttps://doi.org/10.1021/ja052629dopenalex-snapshot
Catalytic Asymmetric Cyanosilylation of Ketones by a Chiral Amino Acid Salt
inferred← citeshttps://doi.org/10.1021/ja0562043openalex-snapshot
Catalyst-Controlled Asymmetric Synthesis of Fostriecin and 8-epi-Fostriecin
inferred← citeshttps://doi.org/10.1021/ja101687popenalex-snapshot
Direct Catalytic Asymmetric Addition of Allyl Cyanide to Ketones via Soft Lewis Acid/Hard Brønsted Base/Hard Lewis Base Catalysis
inferred← citeshttps://doi.org/10.1021/ja3047816openalex-snapshot
Palladium-Catalyzed C(sp3)–H Arylation of Diarylmethanes at Room Temperature: Synthesis of Triarylmethanes via Deprotonative-Cross-Coupling Processes
inferred← citeshttps://doi.org/10.1021/ja900001uopenalex-snapshot
Direct Catalytic Asymmetric Addition of Allyl Cyanide to Ketones
inferred← citeshttps://doi.org/10.1021/jacs.5b11476openalex-snapshot
Activation of Chiral (Salen)AlCl Complex by Phosphorane for Highly Enantioselective Cyanosilylation of Ketones and Enones
inferred← citeshttps://doi.org/10.1021/jacs.6b05601openalex-snapshot
Me2(CH2Cl)SiCN: Bifunctional Cyanating Reagent for the Synthesis of Tertiary Alcohols with a Chloromethyl Ketone Moiety via Ketone Cyanosilylation
inferred← citeshttps://doi.org/10.1021/jo049258oopenalex-snapshot
Practical Synthesis of Chiral Ligands for Catalytic Enantioselective Cyanosilylation of Ketones and Ketoimines
inferred← citeshttps://doi.org/10.1021/jo060772zopenalex-snapshot
Highly Enantioselective Cyanation of Aldehydes Catalyzed by a Multicomponent Titanium Complex
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