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B(C 6 F 5 ) 3 -catalyzed divergent cyanosilylations of chromones dependent on temperature

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What this work says

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

inferredcites →https://doi.org/10.1002/9780470186886openalex-snapshot
Chemistry of Heterocyclic Compounds
inferredcites →https://doi.org/10.1002/anie.199508091openalex-snapshot
Bis(pentafluorophenyl)borane: Synthesis, Properties, and Hydroboration Chemistry of a Highly Electrophilic Borane Reagent
inferredcites →https://doi.org/10.1002/anie.200300604openalex-snapshot
Chemically Catalyzed Asymmetric Cyanohydrin Syntheses
inferredcites →https://doi.org/10.1002/anie.200903708openalex-snapshot
Frustrated Lewis Pairs: Metal‐free Hydrogen Activation and More
inferredcites →https://doi.org/10.1002/anie.201309253openalex-snapshot
Metal‐Free Hydrogenation of Unsaturated Hydrocarbons Employing Molecular Hydrogen
inferredcites →https://doi.org/10.1002/anie.201409800openalex-snapshot
Frustrated Lewis Pair Chemistry: Development and Perspectives
inferredcites →https://doi.org/10.1002/aoc.1479openalex-snapshot
Metal and solvent‐free cyanosilylation of carbonyl compounds with tris(pentafluorophenyl)borane
inferredcites →https://doi.org/10.1002/asia.201701796openalex-snapshot
Boron‐Based Catalysts for C−C Bond‐Formation Reactions
inferredcites →https://doi.org/10.1002/cctc.201402838openalex-snapshot
Enantioselective Metal‐Free Hydrogenation Catalyzed by Chiral Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1002/jcc.22885openalex-snapshot
Multiwfn: A multifunctional wavefunction analyzer
inferredcites →https://doi.org/10.1002/jlcr.629openalex-snapshot
Synthesis of [14C]‐labelled repinotan hydrochloride and its major metabolite M‐6
inferredcites →https://doi.org/10.1016/j.tet.2009.03.073openalex-snapshot
Synthesis of α-aryl nitriles through B(C6F5)3-catalyzed direct cyanation of α-aryl alcohols and thiols
inferredcites →https://doi.org/10.1016/j.tet.2009.06.020openalex-snapshot
One-pot three components synthesis of O-acetylcyanohydrins with TMSCN, acetic anhydride and carbonyl compounds under solvent-free condition
inferredcites →https://doi.org/10.1016/s0022-328x(00)80518-5openalex-snapshot
Perfluorophenyl derivatives of the elements
inferredcites →https://doi.org/10.1016/s0065-3055(04)52001-4openalex-snapshot
The Chemistry of Perfluoroaryl Boranes
inferredcites →https://doi.org/10.1021/acs.accounts.7b00530openalex-snapshot
Frustrated Lewis Pairs Catalyzed Asymmetric Metal-Free Hydrogenations and Hydrosilylations
inferredcites →https://doi.org/10.1021/acs.chemrev.8b00352openalex-snapshot
Polymerization of Polar Monomers Mediated by Main-Group Lewis Acid–Base Pairs
inferredcites →https://doi.org/10.1021/acs.inorgchem.6b02911openalex-snapshot
Tris(pentafluorophenyl)borane and Beyond: Modern Advances in Borylation Chemistry
inferredcites →https://doi.org/10.1021/acs.orglett.7b02313openalex-snapshot
Catalytic Activation of 1-Cyano-3,3-dimethyl-3-(1 H )-1,2-benziodoxole with B(C 6 F 5 ) 3 Enabling the Electrophilic Cyanation of Silyl Enol Ethers
inferredcites →https://doi.org/10.1021/acscatal.8b00955openalex-snapshot
Boron-Catalyzed Double Hydrofunctionalization Reactions of Unactivated Alkynes
inferredcites →https://doi.org/10.1021/ar500375jopenalex-snapshot
Frustrated Lewis Pairs: From Concept to Catalysis
inferredcites →https://doi.org/10.1021/cr020038popenalex-snapshot
Catalytic Enantioselective Strecker Reactions and Analogous Syntheses
inferredcites →https://doi.org/10.1021/cr200057topenalex-snapshot
Asymmetric Strecker Reactions
inferredcites →https://doi.org/10.1021/ja961536gopenalex-snapshot
Tris(pentafluorophenyl)boron-Catalyzed Hydrosilation of Aromatic Aldehydes, Ketones, and Esters
inferredcites →https://doi.org/10.1021/jacs.5b06794openalex-snapshot
Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1021/jm100762ropenalex-snapshot
Nitrile-Containing Pharmaceuticals: Efficacious Roles of the Nitrile Pharmacophore
inferredcites →https://doi.org/10.1021/om980673eopenalex-snapshot
Synthesis, Properties, and Hydroboration Activity of the Highly Electrophilic Borane Bis(pentafluorophenyl)borane, HB(C6F5)21
inferredcites →https://doi.org/10.1039/b503688gopenalex-snapshot
Tris(pentafluorophenyl)borane: a special boron Lewis acid for special reactions
inferredcites →https://doi.org/10.1039/c1cs15004aopenalex-snapshot
Recent developments and perspectives in palladium-catalyzed cyanation of aryl halides: synthesis of benzonitriles
inferredcites →https://doi.org/10.1039/c4cs00451eopenalex-snapshot
A unified survey of Si–H and H–H bond activation catalysed by electron-deficient boranes
inferredcites →https://doi.org/10.1039/c7qo00214aopenalex-snapshot
Intramolecular aminocyanation of alkenes promoted by hypervalent iodine
inferredcites →https://doi.org/10.1039/cs9972600345openalex-snapshot
Pentafluorophenylboranes: from obscurity to applications
inferredcites →https://doi.org/10.1042/bst0061096openalex-snapshot
The Chemistry of Heterocyclic Compounds: Chromenes, Chromanones and Chromones
inferredcites →https://doi.org/10.1124/dmd.108.020479openalex-snapshot
Trend Analysis of a Database of Intravenous Pharmacokinetic Parameters in Humans for 670 Drug Compounds
inferredcites →https://doi.org/10.1126/science.1134230openalex-snapshot
Reversible, Metal-Free Hydrogen Activation
inferredcites →https://doi.org/10.1126/science.aaf7229openalex-snapshot
The broadening reach of frustrated Lewis pair chemistry
inferredcites →https://doi.org/10.1142/s0219633612500113openalex-snapshot
ATOMIC DIPOLE MOMENT CORRECTED HIRSHFELD POPULATION METHOD
inferredcites →https://doi.org/10.1345/aph.1g708openalex-snapshot
Nebivolol: A Third-Generation β-Adrenergic Blocker
inferredcites →https://doi.org/10.1351/pac-con-11-01-02openalex-snapshot
Design of frustrated Lewis pair catalysts for metal-free and selective hydrogenation
inferredcites →https://doi.org/10.6023/a14040344openalex-snapshot
Frustrated Lewis Pair Catalyzed Asymmetric Hydrogenation
inferredcites →https://doi.org/10.6023/cjoc1202132openalex-snapshot
Application of Nitrile in Drug Design

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/10.1016/b978-0-12-822127-3.00005-3openalex-snapshot
Applications of boron compounds in catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01471openalex-snapshot
α-Olefination of Nitriles: Base-Promoted Ring-Opening Coupling of Nitriles and Chromone
inferred← citeshttps://doi.org/10.1021/acscatal.2c05509openalex-snapshot
Asymmetric Catalytic Conjugate Addition of Cyanide to Chromones and β-Substituted Cyclohexenones
inferred← citeshttps://doi.org/10.1039/d0ob02478copenalex-snapshot
Tris(pentafluorophenyl)borane catalyzed C–C and C–heteroatom bond formation
inferred← citeshttps://doi.org/10.1039/d1cc03292eopenalex-snapshot
Metal-free enaminone C–N bond cyanation for the stereoselective synthesis of ( E )- and ( Z )-β-cyano enones
inferred← citeshttps://doi.org/10.1039/d1nj04233eopenalex-snapshot
A four-component domino reaction for the synthesis of novel bridgehead nitrogen-containing pyrido[1,2- d ][1,4]diazepines
inferred← citeshttps://doi.org/10.1039/d2cc02194copenalex-snapshot
Cp*Ir( iii ) and Cp*Rh( iii )-catalyzed annulation of salicylaldehydes with fluorinated vinyl tosylates
inferred← citeshttps://doi.org/10.6023/cjoc202403025openalex-snapshot
Progresses in the Preparation of Chromone Compounds and Their Applications in Organic Synthesis
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