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Iron‐Catalyzed Asymmetric Hydrosilylation of 1,1‐Disubstituted Alkenes
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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/adsc.200390027openalex-snapshot
Iridium‐Catalyzed Enantioselective Hydrogenation of Olefins
inferredcites →https://doi.org/10.1002/adsc.200600458openalex-snapshot
The Role of Secondary Interactions in the Asymmetric Palladium‐Catalysed Hydrosilylation of Olefins with Monophosphane Ligands
inferredcites →https://doi.org/10.1002/adsc.201300827openalex-snapshot
Iron‐Catalysed Chemo‐, Regio‐, and Stereoselective Hydrosilylation of Alkenes and Alkynes using a Bench‐Stable Iron(II) Pre‐Catalyst
inferredcites →https://doi.org/10.1002/ange.200805604openalex-snapshot
Asymmetrische Hydroborierung von 1,1‐disubstituierten Alkenen
inferredcites →https://doi.org/10.1002/ange.201102398openalex-snapshot
NHC‐Cu‐Catalyzed Enantioselective Hydroboration of Acyclic and Exocyclic 1,1‐Disubstituted Aryl Alkenes
inferredcites →https://doi.org/10.1002/ange.201305496openalex-snapshot
Chiral Silanediols in Anion‐Binding Catalysis
inferredcites →https://doi.org/10.1002/anie.200805604openalex-snapshot
Asymmetric Hydroboration of 1,1‐Disubstituted Alkenes
inferredcites →https://doi.org/10.1002/anie.201102398openalex-snapshot
NHC‐Cu‐Catalyzed Enantioselective Hydroboration of Acyclic and Exocyclic 1,1‐Disubstituted Aryl Alkenes
inferredcites →https://doi.org/10.1002/anie.201305496openalex-snapshot
Chiral Silanediols in Anion‐Binding Catalysis
inferredcites →https://doi.org/10.1002/cctc.200900263openalex-snapshot
Palladium‐Catalyzed Enantioselective Hydrosilylation of Aromatic Olefins
inferredcites →https://doi.org/10.1002/ddr.20177openalex-snapshot
Novel therapeutics with enhanced biological activity generated by the strategic introduction of silicon isosteres into known drug scaffolds
inferredcites →https://doi.org/10.1002/ejoc.200800107openalex-snapshot
Enantio‐ and Diastereotopos Differentiation in the Palladium(II)‐Catalyzed Hydrosilylation of Bicyclo[2.2.1]alkene Scaffolds with Silicon‐Stereogenic Silanes
inferredcites →https://doi.org/10.1007/3418_2011_5openalex-snapshot
Bifunctional Phebox Complexes for Asymmetric Catalysis
inferredcites →https://doi.org/10.1016/0022-328x(93)83315-mopenalex-snapshot
Completely selective synthesis of (E)-β-(triethylsilyl) styrenes by Fe3(CO)12-catalyzed reaction of styrenes with triethylsilane
inferredcites →https://doi.org/10.1016/j.tetasy.2004.05.038openalex-snapshot
Asymmetric palladium-catalyzed hydrosilylation of styrenes using efficient chiral spiro phosphoramidite ligands
inferredcites →https://doi.org/10.1016/s0022-328x(00)86640-1openalex-snapshot
Catalytic asymmetric hydrosilylation of olefins
inferredcites →https://doi.org/10.1016/s0022-328x(00)92151-xopenalex-snapshot
Catalytic asymmetric hydrosilylation of olefins
inferredcites →https://doi.org/10.1016/s0022-328x(00)93214-5openalex-snapshot
Catalytic asymmetric hydrosilylation of olefins.
inferredcites →https://doi.org/10.1016/s0040-4039(00)00741-3openalex-snapshot
Highly asymmetric dihydroxylation of 1-aryl-1′-pyridyl alkenes
inferredcites →https://doi.org/10.1016/s0040-4039(00)88558-5openalex-snapshot
Catalytic asymmetric intramolecular hydrosilation
inferredcites →https://doi.org/10.1016/s0040-4039(01)01471-xopenalex-snapshot
Bidentate planar chiral η6-arene tricarbonyl chromium(0) complexes: ligands for catalytic asymmetric alkene hydrosilylation
inferredcites →https://doi.org/10.1016/s0957-4166(98)00234-1openalex-snapshot
A new stereocontrolled route to (+)-curcuphenol, a phenolic sesquiterpene from the marine sponge Didiscus flavus
inferredcites →https://doi.org/10.1021/ar200149wopenalex-snapshot
The Diarylprolinol Silyl Ether System: A General Organocatalyst
inferredcites →https://doi.org/10.1021/ar300200hopenalex-snapshot
Efficient Routes to Carbon–Silicon Bond Formation for the Synthesis of Silicon-Containing Peptides and Azasilaheterocycles
inferredcites →https://doi.org/10.1021/ar7001107openalex-snapshot
Asymmetric Hydrogenation Using Monodentate Phosphoramidite Ligands
inferredcites →https://doi.org/10.1021/ar700113gopenalex-snapshot
Iridium-Catalyzed Asymmetric Hydrogenation of Olefins
inferredcites →https://doi.org/10.1021/ar700114kopenalex-snapshot
Industrial-Scale Synthesis and Applications of Asymmetric Hydrogenation Catalysts
inferredcites →https://doi.org/10.1021/ar700141vopenalex-snapshot
Unlocking the Potential of Asymmetric Hydrogenation at Merck
inferredcites →https://doi.org/10.1021/ar800039xopenalex-snapshot
The Promise and Challenge of Iron-Catalyzed Cross Coupling
inferredcites →https://doi.org/10.1021/cr00037a008openalex-snapshot
Diastereoselective Reactions of Chiral Allyl and Allenyl Silanes with Activated C:X .pi.-Bonds
inferredcites →https://doi.org/10.1021/cr020004hopenalex-snapshot
Pyridine-2,6-bis(oxazolines), Helpful Ligands for Asymmetric Catalysts
inferredcites →https://doi.org/10.1021/cr0306135openalex-snapshot
Recent Developments in the Synthesis and Structure of Organosilanols
inferredcites →https://doi.org/10.1021/cr040664hopenalex-snapshot
Iron-Catalyzed Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1021/cr100198wopenalex-snapshot
Direct C−H Transformation via Iron Catalysis
inferredcites →https://doi.org/10.1021/cr300236ropenalex-snapshot
Chiral Iron Catalysts for Asymmetric Synthesis
inferredcites →https://doi.org/10.1021/cs400515wopenalex-snapshot
Organocatalytic Oxidation of Organosilanes to Silanols
inferredcites →https://doi.org/10.1021/ja00026a044openalex-snapshot
Catalytic asymmetric synthesis of optically active 2-alkanols via hydrosilylation of 1-alkenes with a chiral monophosphine-palladium catalyst
inferredcites →https://doi.org/10.1021/ja00032a028openalex-snapshot
Asymmetric catalysis. Production of chiral diols by enantioselective catalytic intramolecular hydrosilation of olefins
inferredcites →https://doi.org/10.1021/ja00132a015openalex-snapshot
Regioselection and Enantioselection in Organolanthanide-Catalyzed Olefin Hydrosilylation. A Kinetic and Mechanistic Study
inferredcites →https://doi.org/10.1021/ja00394a060openalex-snapshot
Photogeneration of very active homogeneous catalysts using laser light excitation of iron carbonyl precursors
inferredcites →https://doi.org/10.1021/ja025617qopenalex-snapshot
Highly Enantioselective Hydrosilylation of Aromatic Alkenes
inferredcites →https://doi.org/10.1021/ja026158wopenalex-snapshot
Silicon-Based Metalloprotease Inhibitors: Synthesis and Evaluation of Silanol and Silanediol Peptide Analogues as Inhibitors of Angiotensin-Converting Enzyme1
inferredcites →https://doi.org/10.1021/ja046753topenalex-snapshot
Preparation and Molecular and Electronic Structures of Iron(0) Dinitrogen and Silane Complexes and Their Application to Catalytic Hydrogenation and Hydrosilation
inferredcites →https://doi.org/10.1021/ja065721yopenalex-snapshot
Control of Absolute Helicity in Single-Stranded Abiotic Metallofoldamers
inferredcites →https://doi.org/10.1021/ja073900popenalex-snapshot
trans-Cyclohexane-1,2-diamine Is a Weak Director of Absolute Helicity in Chiral Nickel−Salen Complexes
inferredcites →https://doi.org/10.1021/ja106853yopenalex-snapshot
A Strategy for the Synthesis of Well-Defined Iron Catalysts and Application to Regioselective Diene Hydrosilylation
inferredcites →https://doi.org/10.1021/ja300503kopenalex-snapshot
Enantiopure C 1 -Symmetric Bis(imino)pyridine Cobalt Complexes for Asymmetric Alkene Hydrogenation
inferredcites →https://doi.org/10.1021/ja3046684openalex-snapshot
Iron Catalyzed Asymmetric Oxyamination of Olefins
inferredcites →https://doi.org/10.1021/ja311923zopenalex-snapshot
Iron(II)-Catalyzed Intramolecular Aminohydroxylation of Olefins with Functionalized Hydroxylamines
inferredcites →https://doi.org/10.1021/ja402082popenalex-snapshot
Enantioselective Iron-Catalyzed Azidation of β-Keto Esters and Oxindoles
inferredcites →https://doi.org/10.1021/ja404963fopenalex-snapshot
Phosphinite-Iminopyridine Iron Catalysts for Chemoselective Alkene Hydrosilylation
inferredcites →https://doi.org/10.1021/ja5003636openalex-snapshot
Iron Catalyzed Asymmetric Hydrogenation of Ketones
inferredcites →https://doi.org/10.1021/ja507853fopenalex-snapshot
A New Iron(III)–Salen Catalyst for Enantioselective Conia-ene Carbocyclization
inferredcites →https://doi.org/10.1021/ja508057uopenalex-snapshot
Iron(II)-Catalyzed Intermolecular Amino-Oxygenation of Olefins through the N–O Bond Cleavage of Functionalized Hydroxylamines
inferredcites →https://doi.org/10.1021/ja5093908openalex-snapshot
Cobalt-Catalyzed Enantioselective Hydroboration of 1,1-Disubstituted Aryl Alkenes
inferredcites →https://doi.org/10.1021/ja509786vopenalex-snapshot
Enantioselective CuH-Catalyzed Anti-Markovnikov Hydroamination of 1,1-Disubstituted Alkenes
inferredcites →https://doi.org/10.1021/jm3010114openalex-snapshot
Organosilicon Molecules with Medicinal Applications
inferredcites →https://doi.org/10.1021/jo00118a005openalex-snapshot
New Ligands and Improved Enantioselectivities for the Asymmetric Dihydroxylation of Olefins
inferredcites →https://doi.org/10.1021/jo1012493openalex-snapshot
Total Synthesis and Anticancer Activities of (−)- and (+)-Thespesone
inferredcites →https://doi.org/10.1021/np0101191openalex-snapshot
Thymol Derivatives from Eupatorium fortunei
inferredcites →https://doi.org/10.1021/ol050242+openalex-snapshot
Organosilanols as Catalysts in Asymmetric Aryl Transfer Reactions
inferredcites →https://doi.org/10.1021/ol203428copenalex-snapshot
General and Practical One-Pot Synthesis of Dihydrobenzosiloles from Styrenes
inferredcites →https://doi.org/10.1021/ol503282ropenalex-snapshot
Iminopyridine Oxazoline Iron Catalyst for Asymmetric Hydroboration of 1,1-Disubtituted Aryl Alkenes
inferredcites →https://doi.org/10.1021/om990690jopenalex-snapshot
Hydrosilylation Catalysis by C2-Symmetric Bis(silylamido) Complexes of Yttrium
inferredcites →https://doi.org/10.1023/a:1021235922742openalex-snapshot
Catalysis of hydrosilylation of carbon-carbon multiple bonds: Recent progress
inferredcites →https://doi.org/10.1039/a803280gopenalex-snapshot
Enantioselective radical-chain hydrosilylation of alkenes using homochiral thiols as polarity-reversal catalysts
inferredcites →https://doi.org/10.1039/b909334fopenalex-snapshot
Synthesis and application of bulky phosphoramidites: highly effective monophosphorus ligands for asymmetric hydrosilylation of styrenes
inferredcites →https://doi.org/10.1039/c0cc01547dopenalex-snapshot
Highly regio- and enantioselective catalytic asymmetric hydroboration of α-substituted styrenyl derivatives
inferredcites →https://doi.org/10.1039/c39950001533openalex-snapshot
Palladium-catalysed asymmetric hydrosilylation of styrenes with a new chiral monodentate phosphine ligand
inferredcites →https://doi.org/10.1039/c3cs60185dopenalex-snapshot
Acylsilanes: valuable organosilicon reagents in organic synthesis
inferredcites →https://doi.org/10.1039/c4qo00295dopenalex-snapshot
Asymmetric cobalt catalysts for hydroboration of 1,1-disubstituted alkenes
inferredcites →https://doi.org/10.1055/s-0034-1380843openalex-snapshot
Iron-Catalyzed Asymmetric Hydrogenation of Ketones
inferredcites →https://doi.org/10.1080/00304940903240836openalex-snapshot
Recent Progress in the Synthesis of 2,3-Dihydrobenzofurans
inferredcites →https://doi.org/10.1126/science.1214451openalex-snapshot
Iron Catalysts for Selective Anti-Markovnikov Alkene Hydrosilylation Using Tertiary Silanes
inferredcites →https://doi.org/10.1126/science.1244466openalex-snapshot
Amine(imine)diphosphine Iron Catalysts for Asymmetric Transfer Hydrogenation of Ketones and Imines
inferredcites →https://doi.org/10.1246/bcsj.64.2855openalex-snapshot
Conversion of (+)-8,11,13-Abietatriene into (15R)-16-Hydroxyferruginol and Its (15S)-Epimer
inferredcites →https://doi.org/10.2174/138955706778560120openalex-snapshot
Silicon Switches of Marketed Drugs
inferredcites →https://doi.org/10.3390/12081606openalex-snapshot
Antibacterial Thymol Derivatives Isolated from Centipeda minima
inferredcites →https://doi.org/10.5860/choice.38-4470openalex-snapshot
Silicon in organic, organometallic, and polymer chemistry
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.4581369openalex-extracted
Anti-Markovnikov Hydrosilylation and Markovnikov Hydroboration of Alkenes by a Phenanthroline-Based Tridentate Manganese(Ii) Catalyst
inferred← citeshttps://doi.org/10.1002/9781119125082.ch10openalex-snapshot
Addition Reactions: Polar Additions
inferred← citeshttps://doi.org/10.1002/9783527802142.ch3openalex-snapshot
Iron‐based Chiral Lewis Acids
inferred← citeshttps://doi.org/10.1002/9783527804801.ch4openalex-snapshot
Hydrofunctionalization of Carbon–Carbon Double Bonds
inferred← citeshttps://doi.org/10.1002/9783527814787.ch11openalex-snapshot
Hydrosilylation Catalyzed by Base Metals
inferred← citeshttps://doi.org/10.1002/adsc.201600570openalex-snapshot
Amine‐Activated Iron Catalysis: Air‐ and Moisture‐Stable Alkene and Alkyne Hydrofunctionalization
inferred← citeshttps://doi.org/10.1002/adsc.201700162openalex-snapshot
Iridium‐Catalyzed Enantioselective Hydrogenation of Vinylsilanes
inferred← citeshttps://doi.org/10.1002/ajoc.201700446openalex-snapshot
Nickel‐Catalyzed C−H Heteroarylation of Chiral Oxazolines
inferred← citeshttps://doi.org/10.1002/ajoc.202000334openalex-snapshot
Iron‐Catalyzed Cross‐Coupling Reactions for the Construction of Carbon‐Heteroatom Bonds
inferred← citeshttps://doi.org/10.1002/ange.201606832openalex-snapshot
An Easily Accessed Nickel Nanoparticle Catalyst for Alkene Hydrosilylation with Tertiary Silanes
inferred← citeshttps://doi.org/10.1002/ange.201610121openalex-snapshot
Regio‐ and Enantioselective Cobalt‐Catalyzed Sequential Hydrosilylation/Hydrogenation of Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/ange.201612460openalex-snapshot
(Aminomethyl)pyridine Complexes for the Cobalt‐Catalyzed Anti‐Markovnikov Hydrosilylation of Alkoxy‐ or Siloxy(vinyl)silanes with Alkoxy‐ or Siloxyhydrosilanes
inferred← citeshttps://doi.org/10.1002/ange.201702349openalex-snapshot
Iron‐Catalyzed Intermolecular 1,2‐Difunctionalization of Styrenes and Conjugated Alkenes with Silanes and Nucleophiles
inferred← citeshttps://doi.org/10.1002/ange.201814340openalex-snapshot
Enantioselektiver Aufbau von α‐chiralen Silanen durch nickelkatalysierte C(sp3)‐C(sp3)‐Kreuzkupplung
inferred← citeshttps://doi.org/10.1002/ange.202007930openalex-snapshot
Ligand‐Regulated Regiodivergent Hydrosilylation of Isoprene under Iron Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202100775openalex-snapshot
Asymmetric Cobalt‐Catalyzed Regioselective Hydrosilylation/Cyclization of 1,6‐Enynes
inferred← citeshttps://doi.org/10.1002/ange.202114918openalex-snapshot
Highly Regio‐ and Enantioselective Hydrosilylation of gem‐Difluoroalkenes by Nickel Catalysis
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/ange.202205624openalex-snapshot
Cobalt‐Catalyzed Regio‐, Diastereo‐ and Enantioselective Intermolecular Hydrosilylation of 1,3‐Dienes with Prochiral Silanes
inferred← citeshttps://doi.org/10.1002/ange.202214534openalex-snapshot
Enantioselective Hydrosilylation of β,β‐Disubstituted Enamides to Construct α‐Aminosilanes with Vicinal Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.202215029openalex-snapshot
Cobalt‐Catalyzed Regiodivergent Double Hydrosilylation of Arylacetylenes
inferred← citeshttps://doi.org/10.1002/ange.202216878openalex-snapshot
Enantioselective Nickel‐Catalyzed Hydrosilylation of 1,1‐Disubstituted Allenes
inferred← citeshttps://doi.org/10.1002/ange.202303470openalex-snapshot
Thioethers as Dichotomous Electrophiles for Site‐Selective Silylation via C−S Bond Cleavage
inferred← citeshttps://doi.org/10.1002/ange.202307602openalex-snapshot
Chemoenzymatic Synthesis of Cylindrocyclophanes A and F and Merocyclophanes A and D
inferred← citeshttps://doi.org/10.1002/ange.202410334openalex-snapshot
Triphasic Hydroxysilylation of Alkenes by Mechanically Piezoelectric Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202506157openalex-snapshot
Regio‐, Diastereo‐, and Enantioselective Hydrosilylation of Alkyl gem‐Difluoroalkenes to Construct Carbon and Silicon Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/anie.201606832openalex-snapshot
An Easily Accessed Nickel Nanoparticle Catalyst for Alkene Hydrosilylation with Tertiary Silanes
inferred← citeshttps://doi.org/10.1002/anie.201610121openalex-snapshot
Regio‐ and Enantioselective Cobalt‐Catalyzed Sequential Hydrosilylation/Hydrogenation of Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/anie.201612460openalex-snapshot
(Aminomethyl)pyridine Complexes for the Cobalt‐Catalyzed Anti‐Markovnikov Hydrosilylation of Alkoxy‐ or Siloxy(vinyl)silanes with Alkoxy‐ or Siloxyhydrosilanes
inferred← citeshttps://doi.org/10.1002/anie.201702349openalex-snapshot
Iron‐Catalyzed Intermolecular 1,2‐Difunctionalization of Styrenes and Conjugated Alkenes with Silanes and Nucleophiles
inferred← citeshttps://doi.org/10.1002/anie.201814340openalex-snapshot
Enantioselective Construction of α‐Chiral Silanes by Nickel‐Catalyzed C(sp3)−C(sp3) Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/anie.202007930openalex-snapshot
Ligand‐Regulated Regiodivergent Hydrosilylation of Isoprene under Iron Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202100775openalex-snapshot
Asymmetric Cobalt‐Catalyzed Regioselective Hydrosilylation/Cyclization of 1,6‐Enynes
inferred← citeshttps://doi.org/10.1002/anie.202114918openalex-snapshot
Highly Regio‐ and Enantioselective Hydrosilylation of gem‐Difluoroalkenes by Nickel Catalysis
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/anie.202205624openalex-snapshot
Cobalt‐Catalyzed Regio‐, Diastereo‐ and Enantioselective Intermolecular Hydrosilylation of 1,3‐Dienes with Prochiral Silanes
inferred← citeshttps://doi.org/10.1002/anie.202214534openalex-snapshot
Enantioselective Hydrosilylation of β,β‐Disubstituted Enamides to Construct α‐Aminosilanes with Vicinal Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.202215029openalex-snapshot
Cobalt‐Catalyzed Regiodivergent Double Hydrosilylation of Arylacetylenes
inferred← citeshttps://doi.org/10.1002/anie.202216878openalex-snapshot
Enantioselective Nickel‐Catalyzed Hydrosilylation of 1,1‐Disubstituted Allenes
inferred← citeshttps://doi.org/10.1002/anie.202303470openalex-snapshot
Thioethers as Dichotomous Electrophiles for Site‐Selective Silylation via C−S Bond Cleavage
inferred← citeshttps://doi.org/10.1002/anie.202307602openalex-snapshot
Chemoenzymatic Synthesis of Cylindrocyclophanes A and F and Merocyclophanes A and D
inferred← citeshttps://doi.org/10.1002/anie.202410334openalex-snapshot
Triphasic Hydroxysilylation of Alkenes by Mechanically Piezoelectric Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202506157openalex-snapshot
Regio‐, Diastereo‐, and Enantioselective Hydrosilylation of Alkyl gem ‐Difluoroalkenes to Construct Carbon and Silicon Stereogenic Centers
inferred← citeshttps://doi.org/10.1002/anie.202517311openalex-snapshot
Iron‐Catalyzed Enantioselective Deoxygenative Addition of Propargyl, Allyl, and Benzyl Alcohols to Cyclic N ‐Sulfonyl α‐Ketiminoesters Mediated by Visible Light
inferred← citeshttps://doi.org/10.1002/aoc.7493openalex-snapshot
Synthesis of organosilicon‐containing phosphinyl ligands and application in the iron catalyzed hydrosilylation of olefins
inferred← citeshttps://doi.org/10.1002/asia.202100804openalex-snapshot
Base Metal‐terpyridine Complex Immobilized on Stationary Phase Aimed as Reusable Hydrosilylation Catalyst
inferred← citeshttps://doi.org/10.1002/cctc.201500348openalex-snapshot
An Iron Catalyst for Asymmetric Alkene Hydrosilylation
inferred← citeshttps://doi.org/10.1002/cctc.201800161openalex-snapshot
Solution Synthesis of N,N‐Dimethylformamide‐Stabilized Iron‐Oxide Nanoparticles as an Efficient and Recyclable Catalyst for Alkene Hydrosilylation
inferred← citeshttps://doi.org/10.1002/chem.202401440openalex-snapshot
Hydrosilylation of Arynes with Silanes and Silicon‐Based Polymer
inferred← citeshttps://doi.org/10.1002/chin.201532204openalex-snapshot
ChemInform Abstract: Iron‐Catalyzed Asymmetric Hydrosilylation of 1,1‐Disubstituted Alkenes.
inferred← citeshttps://doi.org/10.1002/cjoc.201800314openalex-snapshot
Recent Advances in Hydrometallation of Alkenes and Alkynes via the First Row Transition Metal Catalysis
inferred← citeshttps://doi.org/10.1002/cjoc.201800367openalex-snapshot
Diverse Fates of β‐Silyl Radical under Manganese Catalysis: Hydrosilylation and Dehydrogenative Silylation of Alkenes
inferred← citeshttps://doi.org/10.1002/cjoc.201900079openalex-snapshot
Highly Regioselective Sequential 1,1‐Dihydrosilylation of Terminal Aliphatic Alkynes with Primary Silanes
inferred← citeshttps://doi.org/10.1002/cjoc.70268openalex-snapshot
Iron‐Catalyzed Enantioselective Hydrosilylation of α ‐Substituted Vinylsilanes †
inferred← citeshttps://doi.org/10.1002/cplu.201900366openalex-snapshot
Hydrosilylation of Ketones Catalyzed by Iron Iminobipyridine Complexes and Accelerated by Lewis Bases
inferred← citeshttps://doi.org/10.1002/cssc.201500930openalex-snapshot
Fighting Fenton Chemistry: A Highly Active Iron(III) Tetracarbene Complex in Epoxidation Catalysis
inferred← citeshttps://doi.org/10.1002/cssc.202200367openalex-snapshot
Visible Light‐Induced Hydrosilylation of Electron‐Deficient Alkenes by Iron Catalysis
inferred← citeshttps://doi.org/10.1002/ejic.201801068openalex-snapshot
Cobalt Catalysts for Alkene Hydrosilylation under Aerobic Conditions without Dry Solvents or Additives
inferred← citeshttps://doi.org/10.1002/ejic.202300148openalex-snapshot
Design of Stereogenic‐at‐Iron Catalysts with a (3+2+1)‐Ligand Sphere
inferred← citeshttps://doi.org/10.1002/ejoc.201800330openalex-snapshot
Branched‐Selective Decarboxylative Heck Reaction with Electronically Unbiased Olefins
inferred← citeshttps://doi.org/10.1002/ejoc.201901513openalex-snapshot
Thioether‐Facilitated Iridium‐Catalyzed Hydrosilylation of Steric 1,1‐Disubstituted Olefins
inferred← citeshttps://doi.org/10.1002/ejoc.202500578openalex-snapshot
Efficient Hydrosilylation Reaction of Olefins Catalyzed by a Dinuclear Ruthenium Complex
inferred← citeshttps://doi.org/10.1002/ijch.201900072openalex-snapshot
Tackling Remote sp 3 C−H Functionalization via Ni‐Catalyzed “chain‐walking” Reactions
inferred← citeshttps://doi.org/10.1007/3418_2023_102openalex-snapshot
Iron and Manganese Catalyzed Hydrosilylation Reactions
inferred← citeshttps://doi.org/10.1007/3418_2023_105openalex-snapshot
Hydrosilylation of Carbon–Carbon Multiple Bonds in Organic Synthesis
inferred← citeshttps://doi.org/10.1007/s11426-022-1480-yopenalex-snapshot
Catalytic asymmetric silicon-carbon bond-forming transformations based on Si-H functionalization
inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00121-9openalex-snapshot
Hydrometallation of Organometallic Complexes
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00015-9openalex-snapshot
Olefins Hydrofunctionalization; Hydrofunctionalization of Olefins With B, Si, Ge, Sn (Metalloids) Heteroatoms
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00015-6openalex-snapshot
Hydrosilylation of C–C π-Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00045-4openalex-snapshot
Synthesis of Organosilanes, Silyl Ethers, and Silanols
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00110-1openalex-snapshot
Addition of Organosilicon Reagents to Unsaturated Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00125-3openalex-snapshot
Update Hydrometallation Group 4 (Si, Ge and Sn)
inferred← citeshttps://doi.org/10.1016/b978-0-443-15712-7.00003-3openalex-snapshot
Hydrosilylation reactions with homogeneous catalysts
inferred← citeshttps://doi.org/10.1016/bs.acat.2024.06.001openalex-snapshot
Chiral iron complexes for asymmetric catalysis
inferred← citeshttps://doi.org/10.1016/j.catcom.2016.02.009openalex-snapshot
The cobalt(II) complex of a new tridentate Schiff-base ligand as a catalyst for hydrosilylation of olefins
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.01.011openalex-snapshot
Recent developments in enantioselective iron-catalyzed transformations
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.01.024openalex-snapshot
Recent advances in tridentate iron and cobalt complexes for alkene and alkyne hydrofunctionalizations
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.213110openalex-snapshot
Earth-abundant metal catalyzed hydrosilylative reduction of various functional groups
inferred← citeshttps://doi.org/10.1016/j.chempr.2019.02.001openalex-snapshot
Cobalt-Catalyzed Asymmetric Synthesis of gem-Bis(silyl)alkanes by Double Hydrosilylation of Aliphatic Terminal Alkynes
inferred← citeshttps://doi.org/10.1016/j.ica.2021.120403openalex-snapshot
Catalytic hydrosilylation of olefins and ketones by base metal complexes bearing a 2,2′:6′,2″-terpyridine ancillary ligand
inferred← citeshttps://doi.org/10.1016/j.isci.2020.100985openalex-snapshot
Iron-Catalyzed Asymmetric Hydrosilylation of Vinylcyclopropanes via Stereospecific C-C Bond Cleavage
inferred← citeshttps://doi.org/10.1016/j.jcat.2023.115197openalex-snapshot
Anti-Markovnikov hydrosilylation and Markovnikov hydroboration of alkenes by a phenanthroline-based tridentate manganese catalyst
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134835openalex-snapshot
Fe-catalyzed sp3-sp3 coupling enabled by hydrofunctionalizations of alkenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154798openalex-snapshot
Recent developments in alkene hydrosilylation utilizing manganese catalysts
inferred← citeshttps://doi.org/10.1021/acs.accounts.1c00212openalex-snapshot
Iron- and Cobalt-Catalyzed Asymmetric Hydrofunctionalization of Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00372openalex-snapshot
Iron Catalysis in Reduction and Hydrometalation Reactions
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00555openalex-snapshot
First-Row Transition Metal (De)Hydrogenation Catalysis Based On Functional Pincer Ligands
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02020openalex-snapshot
Iron Catalyzed Hydroboration of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1021/acs.organomet.0c00551openalex-snapshot
Cationic Nickel(II)-Catalyzed Hydrosilylation of Alkenes: Role of P, N-Type Ligand Scaffold on Selectivity and Reactivity
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00046openalex-snapshot
Synthesis and Asymmetric Alkene Hydrogenation Activity of C2-Symmetric Enantioenriched Pyridine Dicarbene Iron Dialkyl Complexes
inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00201openalex-snapshot
Combinatorial Approach to the Catalytic Hydrosilylation of Styrene Derivatives: Catalyst Systems Composed of Organoiron(0) or (II) Precursors and Isocyanides
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00087openalex-snapshot
Hydrosilylation of Olefins Catalyzed by Iron Complexes Bearing Ketimine-Type Iminobipyridine Ligands
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00389openalex-snapshot
Cobalt(0) and Iron(0) Isocyanides as Catalysts for Alkene Hydrosilylation with Hydrosiloxanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01170openalex-snapshot
Copper-Catalyzed Enantioselective and Exo-Selective Addition of Silicon Nucleophiles to 7-Oxa- and 7-Azabenzonorbornadiene Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01937openalex-snapshot
Development and Mechanistic Studies of Iron-Catalyzed Construction of Csp 2 –B Bonds via C–O Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01967openalex-snapshot
Iron-Catalyzed Diborylation of Unactivated Aliphatic gem -Dihalogenoalkenes: Synthesis of 1,2-Bis(boryl)alkanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03170openalex-snapshot
Formal Hydrotrimethylsilylation of Styrenes with Anti-Markovnikov Selectivity Using Hexamethyldisilane
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00289openalex-snapshot
Amide-Directed, Rhodium-Catalyzed Enantioselective Hydrosilylation of Unactivated Internal Alkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03491openalex-snapshot
Rhodium-Catalyzed Enantioselective Hydrosilylation of 1,1-Disubstituted Enamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03041openalex-snapshot
Palladium-Catalyzed C-2 C–H Heteroarylation of Chiral Oxazolines: Diverse Synthesis of Chiral Oxazoline Ligands
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00453openalex-snapshot
Cobalt-Catalyzed Asymmetric Hydrogenation of 1,1-Diarylethenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02260openalex-snapshot
Iminophenyl Oxazolinylphenylamine for Enantioselective Cobalt-Catalyzed Hydrosilylation of Aryl Ketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00227openalex-snapshot
Iron-Catalyzed, Markovnikov-Selective Hydroboration of Styrenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01135openalex-snapshot
Copper-Catalyzed Asymmetric Hydroboration of 1,1-Disubstituted Alkenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02691openalex-snapshot
Iron-Catalyzed Hydroboration of Vinylcyclopropanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04305openalex-snapshot
Cobalt-Catalyzed Migrational Isomerization of Styrenes
inferred← citeshttps://doi.org/10.1021/acscatal.2c03580openalex-snapshot
(NHC)Ni(0)-Catalyzed Branched-Selective Alkene Hydrosilylation with Secondary and Tertiary Silanes
inferred← citeshttps://doi.org/10.1021/acscatal.4c00788openalex-snapshot
Light-Promoted Efficient Generation of Fe(I) to Initiate Amination
inferred← citeshttps://doi.org/10.1021/acscatal.5c05846openalex-snapshot
Highly Enantioselective Synthesis of Chiral (Hetero)aryl-Fused Cyclopentanes Enabled by Malonate-Directed Sequential Olefin Isomerization and Asymmetric Hydrogenation
inferred← citeshttps://doi.org/10.1021/acscatal.6b00304openalex-snapshot
Bench-Stable, Substrate-Activated Cobalt Carboxylate Pre-Catalysts for Alkene Hydrosilylation with Tertiary Silanes
inferred← citeshttps://doi.org/10.1021/acscatal.6b01134openalex-snapshot
Alkene Hydrosilylation Using Tertiary Silanes with α-Diimine Nickel Catalysts. Redox-Active Ligands Promote a Distinct Mechanistic Pathway from Platinum Catalysts
inferred← citeshttps://doi.org/10.1021/acscatal.6b02272openalex-snapshot
Selective Cobalt-Catalyzed Reduction of Terminal Alkenes and Alkynes Using (EtO)2Si(Me)H as a Stoichiometric Reductant
inferred← citeshttps://doi.org/10.1021/acscatal.6b02278openalex-snapshot
Dual-Stereocontrol Asymmetric Cobalt-Catalyzed Hydroboration of Sterically Hindered Styrenes
inferred← citeshttps://doi.org/10.1021/acscatal.6b02990openalex-snapshot
Advances in Base-Metal-Catalyzed Alkene Hydrosilylation
inferred← citeshttps://doi.org/10.1021/acscatal.6b03373openalex-snapshot
Control of Selectivity through Synergy between Catalysts, Silanes, and Reaction Conditions in Cobalt-Catalyzed Hydrosilylation of Dienes and Terminal Alkenes
inferred← citeshttps://doi.org/10.1021/acscatal.8b02624openalex-snapshot
One-Pot Pyrolysis to N-Doped Graphene with High-Density Pt Single Atomic Sites as Heterogeneous Catalyst for Alkene Hydrosilylation
inferred← citeshttps://doi.org/10.1021/acscatal.8b04481openalex-snapshot
Cobalt-Catalyzed Regio- and Enantioselective Markovnikov 1,2-Hydrosilylation of Conjugated Dienes
inferred← citeshttps://doi.org/10.1021/acscatal.8b05135openalex-snapshot
Cobalt-Catalyzed Asymmetric Markovnikov Hydroboration of Styrenes
inferred← citeshttps://doi.org/10.1021/acsomega.7b00713openalex-snapshot
Manganese-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones
inferred← citeshttps://doi.org/10.1021/jacs.0c08746openalex-snapshot
Application of Trimethylgermanyl-Substituted Bisphosphine Ligands with Enhanced Dispersion Interactions to Copper-Catalyzed Hydroboration of Disubstituted Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.1c04773openalex-snapshot
Iron-Catalyzed Highly Enantioselective Hydrogenation of Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.1c09263openalex-snapshot
Metal-Free Hydrosilylation Polymerization by Merging Photoredox and Hydrogen Atom Transfer Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.2c09356openalex-snapshot
Breaking Conventional Site Selectivity in C–H Bond Activation: Selective sp3 versus sp2 Silylation by a Pincer-Based Pocket
inferred← citeshttps://doi.org/10.1021/jacs.5b10148openalex-snapshot
Cobalt-Catalyzed Enantioselective Hydrogenation of Minimally Functionalized Alkenes: Isotopic Labeling Provides Insight into the Origin of Stereoselectivity and Alkene Insertion Preferences
inferred← citeshttps://doi.org/10.1021/jacs.5c21898openalex-snapshot
Synthesis of Acyclic α-Quaternary Chiral Nitriles via Ni-Catalyzed Asymmetric Markovnikov Hydrocyanation of 1,1-Disubstituted and Trisubstituted Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.6b13029openalex-snapshot
Asymmetric Copper Hydride-Catalyzed Markovnikov Hydrosilylation of Vinylarenes and Vinyl Heterocycles
inferred← citeshttps://doi.org/10.1021/jacs.7b00879openalex-snapshot
Mechanistic Investigation of Bis(imino)pyridine Manganese Catalyzed Carbonyl and Carboxylate Hydrosilylation
inferred← citeshttps://doi.org/10.1021/jacs.7b04137openalex-snapshot
Highly Enantioselective Cobalt-Catalyzed Hydrosilylation of Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.7b06679openalex-snapshot
Ir-Catalyzed Enantioselective, Intramolecular Silylation of Methyl C–H Bonds
inferred← citeshttps://doi.org/10.1021/jacs.7b08379openalex-snapshot
Copper-Catalyzed Enantioselective Hydroboration of Unactivated 1,1-Disubstituted Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.8b01638openalex-snapshot
Iron-Catalyzed Highly Enantioselective Hydrosilylation of Unactivated Terminal Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.9b12214openalex-snapshot
A Boron Activating Effect Enables Cobalt-Catalyzed Asymmetric Hydrogenation of Sterically Hindered Alkenes
inferred← citeshttps://doi.org/10.1038/s41467-017-02472-6openalex-snapshot
Ligands with 1,10-phenanthroline scaffold for highly regioselective iron-catalyzed alkene hydrosilylation
inferred← citeshttps://doi.org/10.1038/s41467-018-06240-yopenalex-snapshot
Asymmetric remote C-H borylation of internal alkenes via alkene isomerization
inferred← citeshttps://doi.org/10.1038/s41467-019-11392-6openalex-snapshot
Enantioselective benzylic C–H arylation via photoredox and nickel dual catalysis
inferred← citeshttps://doi.org/10.1038/s41467-020-14459-xopenalex-snapshot
Ligand-promoted cobalt-catalyzed radical hydroamination of alkenes
inferred← citeshttps://doi.org/10.1038/s41467-022-32291-3openalex-snapshot
Cobalt-catalyzed branched selective hydroallylation of terminal alkynes
inferred← citeshttps://doi.org/10.1038/s41467-024-48175-7openalex-snapshot
Enantioselective synthesis of chiral α,α-dialkyl indoles and related azoles by cobalt-catalyzed hydroalkylation and regioselectivity switch
inferred← citeshttps://doi.org/10.1038/s41467-024-50743-wopenalex-snapshot
Nickel-catalyzed regiodivergent hydrosilylation of α-(fluoroalkyl)styrenes without defluorination
inferred← citeshttps://doi.org/10.1038/s41467-024-55592-1openalex-snapshot
Copper-catalyzed intermolecular Regio- and Enantioselective Hydrosilylation of Alkenes with Prochiral Silanes
inferred← citeshttps://doi.org/10.1038/s41467-025-59364-3openalex-snapshot
Iron-catalyzed sequential hydrosilylation
inferred← citeshttps://doi.org/10.1038/s44160-025-00860-1openalex-snapshot
Iron-catalysed radical difunctionalization of alkenes
inferred← citeshttps://doi.org/10.1039/9781788012775-00246openalex-snapshot
Accessing Low Oxidation-state Iron Catalysts; Iron-catalysed Reductive Functionalisation
inferred← citeshttps://doi.org/10.1039/c5cc05312aopenalex-snapshot
Regioselective aerobic oxidative Heck reactions with electronically unbiased alkenes: efficient access to α-alkyl vinylarenes
inferred← citeshttps://doi.org/10.1039/c5qo00426hopenalex-snapshot
Synthesis of 1,1-diboronate esters by cobalt-catalyzed sequential hydroboration of terminal alkynes
inferred← citeshttps://doi.org/10.1039/c6ob02817aopenalex-snapshot
Recent advances in chiral imino-containing ligands for metal-catalyzed asymmetric transformations
inferred← citeshttps://doi.org/10.1039/c7cc01531copenalex-snapshot
Unexpected catalytic activity of simple triethylborohydrides in the hydrosilylation of alkenes
inferred← citeshttps://doi.org/10.1039/c7cc08210jopenalex-snapshot
Rhodium-catalyzed carbonylative synthesis of silyl-substituted indenones
inferred← citeshttps://doi.org/10.1039/c7qo00613fopenalex-snapshot
Asymmetric hydrofunctionalization of minimally functionalized alkenes via earth abundant transition metal catalysis
inferred← citeshttps://doi.org/10.1039/c7qo00816copenalex-snapshot
10 gram-scale synthesis of a chiral oxazoline iminopyridine ligand and its applications
inferred← citeshttps://doi.org/10.1039/c8dt01998copenalex-snapshot
Efficient hydroboration of carbonyls by an iron( ii ) amide catalyst
inferred← citeshttps://doi.org/10.1039/c8dt04608eopenalex-snapshot
Anti-Markovnikov terminal and gem -olefin hydrosilylation using a κ 4 -diimine nickel catalyst: selectivity for alkene hydrosilylation over ether C–O bond cleavage
inferred← citeshttps://doi.org/10.1039/c8gc02369gopenalex-snapshot
Thiyl radical promoted chemo- and regioselective oxidation of CC bonds using molecular oxygen via iron catalysis
inferred← citeshttps://doi.org/10.1039/c8ob03065kopenalex-snapshot
Iron-catalyzed asymmetric intramolecular cyclopropanation reactions using chiral tetramethyl-1,1′-spirobiindane-based bisoxazoline (TMSI-BOX) ligands
inferred← citeshttps://doi.org/10.1039/c8qo00279gopenalex-snapshot
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
inferred← citeshttps://doi.org/10.1039/c8sc01427bopenalex-snapshot
Silylation reactions on nanoporous gold via homolytic Si–H activation of silanes
inferred← citeshttps://doi.org/10.1039/c8sc02768dopenalex-snapshot
A β-diketiminate manganese catalyst for alkene hydrosilylation: substrate scope, silicone preparation, and mechanistic insight
inferred← citeshttps://doi.org/10.1039/c9cs00508kopenalex-snapshot
Iron N-heterocyclic carbene complexes in homogeneous catalysis
inferred← citeshttps://doi.org/10.1039/d0cs00688bopenalex-snapshot
Organic synthesis with the most abundant transition metal–iron: from rust to multitasking catalysts
inferred← citeshttps://doi.org/10.1039/d1nj02982gopenalex-snapshot
Synthesis and properties of [PCP] pincer silylene cobalt( i ) complexes
inferred← citeshttps://doi.org/10.1039/d1ob02318gopenalex-snapshot
Copper-promoted difunctionalization of unactivated alkenes with silanes
inferred← citeshttps://doi.org/10.1039/d1qo00018gopenalex-snapshot
Cobalt- and iron-catalyzed regiodivergent alkene hydrosilylations
inferred← citeshttps://doi.org/10.1039/d1qo00839kopenalex-snapshot
Iron-catalyzed C–F bond silylation and borylation of fluoroarenes
inferred← citeshttps://doi.org/10.1039/d1sc06727copenalex-snapshot
Phenanthroline-imine ligands for iron-catalyzed alkene hydrosilylation
inferred← citeshttps://doi.org/10.1039/d2qo01266aopenalex-snapshot
Regiodivergent hydrosilylation in the nickel(0)-catalyzed cyclization of 1,6-enynes
inferred← citeshttps://doi.org/10.1039/d2ra04239hopenalex-snapshot
Applications of iron pincer complexes in hydrosilylation reactions
inferred← citeshttps://doi.org/10.1039/d2sc01581aopenalex-snapshot
Modular allylation of C(sp 3 )–H bonds by combining decatungstate photocatalysis and HWE olefination in flow
inferred← citeshttps://doi.org/10.1039/d4cc00288aopenalex-snapshot
Advances in disilylation reactions to access cis / trans -1,2-disilylated and gem -disilylated alkenes
inferred← citeshttps://doi.org/10.1039/d4md00169aopenalex-snapshot
The role of silicon in drug discovery: a review
inferred← citeshttps://doi.org/10.1039/d5cc02919hopenalex-snapshot
Advances in dicarbofunctionalization of alkenes, alkynes and allenes via iron catalysis
inferred← citeshttps://doi.org/10.1039/d5dt02099aopenalex-snapshot
Catalytic olefin hydrosilylation with an original bis(iminophosphorane)phosphine NPN Co II complex
inferred← citeshttps://doi.org/10.1055/s-0039-1690820openalex-snapshot
Recent Advances in Synthetic Strategies to 2,3-Dihydrobenzofurans
inferred← citeshttps://doi.org/10.1055/sos-sd-239-00077openalex-snapshot
2.2 Cobalt- and Iron-Catalyzed Hydrosilylation
inferred← citeshttps://doi.org/10.1126/sciadv.abo6586openalex-snapshot
Selective dehydrogenation of small and large molecules by a chloroiridium catalyst
inferred← citeshttps://doi.org/10.1246/bcsj.20150359openalex-snapshot
Highly Efficient Olefin Hydrosilylation Catalyzed by Iron Complexes with Iminobipyridine Ligand
inferred← citeshttps://doi.org/10.1246/bcsj.20180197openalex-snapshot
Hydrosilylation of Diene Derivatives Catalyzed by Fe-Iminobipyridine Complexes Aiming at Syntheses of Organosilane Compounds Containing a Terminal Olefin Portion
inferred← citeshttps://doi.org/10.1246/bcsj.20200043openalex-snapshot
Regioselective Hydrosilylation of Olefins Catalyzed by Co-Iminobipyridine Complexes: The Role of Cyclohexyl Substituent on the Imino Nitrogen
inferred← citeshttps://doi.org/10.3390/polym9100534openalex-snapshot
Fifty Years of Hydrosilylation in Polymer Science: A Review of Current Trends of Low-Cost Transition-Metal and Metal-Free Catalysts, Non-Thermally Triggered Hydrosilylation Reactions, and Industrial Applications
inferred← citeshttps://doi.org/10.33915/etd.7432openalex-snapshot
In Situ Infrared Spectroscopic Study of Iron-Catalyzed Hydromagnesiation of Vinyl Arenes
inferred← citeshttps://doi.org/10.6023/cjoc202108045openalex-snapshot
Cross-Coupling of C—Si Bond by Using of Silyl Electrophiles
inferred← citeshttps://doi.org/10.6023/cjoc202305016openalex-snapshot
Hydrosilylation Reactions of Alkene with Tertiary Silanes Catalyzed by Iron-Series Metals
inferred← citeshttps://doi.org/10.70675/0242aae4z2aaez4248z9fa3zfdb7e2cfe0c2openalex-snapshot
Synthèse asymétrique de nοuveaux cοmpοsés fluοrés et silylés et de sila-hétérοcycles
inferred← citeshttps://doi.org/10.70675/8b66a4abz9625z4b59z9bafze696008052b0openalex-snapshot
Synthèse et applications de complexes de nickel(II) pour l’optimisation et la compréhension des réactions d’hydrofonctionnalisation et d’activation C–H.
inferred← citeshttps://doi.org/10.70675/c9654db2zc7c3z4206zb79bz0148c603fd3copenalex-snapshot
Nouveaux catalyseurs d’hydrosilylation pour la synthèse de silicones
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