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Rhodium-Catalyzed Silylcarbocyclization (SiCaC) and Carbonylative Silylcarbocyclization (CO−SiCaC) Reactions of Enynes

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What this work says

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

inferredcites →https://doi.org/10.1002/0470025107.ch25openalex-snapshot
The Hydrosilylation Reaction
inferredcites →https://doi.org/10.1002/9780470132593.ch62openalex-snapshot
Tri‐μ‐Carbonyl‐Nonacarbonyltetra‐Rhodium, Rh 4 (Co) 9 (μ‐Co) 3
inferredcites →https://doi.org/10.1007/bf00702749openalex-snapshot
Organometallic chemistry and homogeneous catalysis of Rh and Rh-Co mixed metal carbonyl clusters
inferredcites →https://doi.org/10.1016/0022-328x(95)90101-jopenalex-snapshot
The organometallic chemistry of the transition metals
inferredcites →https://doi.org/10.1016/0022-328x(96)06359-0openalex-snapshot
New cascade silylcarbocyclization (SiCaC) of enediynes
inferredcites →https://doi.org/10.1016/0040-4020(96)00265-7openalex-snapshot
Palladium(II)-catalyzed carbocyclization: Vinylpalladium in 1,4-oxidation of conjugated dienes
inferredcites →https://doi.org/10.1016/0040-4039(91)80126-qopenalex-snapshot
A Novel Approach to α-Silylmethylene-β-lactams via Rh-catalyzed Silylcarbonylation of Propargylamine Derivatives
inferredcites →https://doi.org/10.1016/0040-4039(92)89035-bopenalex-snapshot
Rhodium catalyzed transformation of propargylamines to 2-silylmethyl-2-alkenals: Formal silylformylation of allenes
inferredcites →https://doi.org/10.1016/b978-0-08-052349-1.00245-6openalex-snapshot
Hydrosilylation of CC and CC
inferredcites →https://doi.org/10.1016/s0020-1693(97)05855-6openalex-snapshot
On the mechanism of silylformylation catalyzed by Rh-Co mixed metal complexes
inferredcites →https://doi.org/10.1016/s0020-1693(97)82717-xopenalex-snapshot
Silylcyclocarbonylation (SiCCa) of alkynylamines catalyzed by rhodium complexes
inferredcites →https://doi.org/10.1016/s0040-4020(01)87260-4openalex-snapshot
Silylformylation catalyzed by Rh and Rh-Co mixed metal complexes and its application to the synthesis of pyrrolizidine alkaloids
inferredcites →https://doi.org/10.1016/s0040-4039(00)01330-7openalex-snapshot
Yttrocene-catalyzed asymmetric cyclization–hydrosilylation of α,ω-dienes
inferredcites →https://doi.org/10.1016/s0040-4039(00)77286-8openalex-snapshot
Carbon-carbon bond formation in palladium(II)-catalyzed intramolecular 1,4-oxidation of conjugated dienes
inferredcites →https://doi.org/10.1016/s0040-4039(00)77453-3openalex-snapshot
Synthesis of pyrrolizidine alkaloids via rhodium-catalyzed silylformylation and amidocarbonylation
inferredcites →https://doi.org/10.1016/s0040-4039(99)00022-2openalex-snapshot
Cyclization/hydrosilylation of functionalized 1,7-dienes to form substituted six-membered carbocycles
inferredcites →https://doi.org/10.1016/s0040-4039(99)00849-7openalex-snapshot
Rhodium-catalyzed domino silylformylation of enynes involving carbocyclization
inferredcites →https://doi.org/10.1016/s0040-4039(99)01706-2openalex-snapshot
An improved catalyst for the cyclization/hydrosilylation of functionalized 1,6-dienes employing dimethylphenylsilane
inferredcites →https://doi.org/10.1021/cr00089a005openalex-snapshot
Chemistry of .eta.2-acyl, .eta.2-iminoacyl and related functional groups
inferredcites →https://doi.org/10.1021/ja00042a061openalex-snapshot
Silylcarbocyclization reactions catalyzed by rhodium and rhodium-cobalt complexes
inferredcites →https://doi.org/10.1021/ja00058a074openalex-snapshot
Rhodium-catalyzed silylformylation of aldehydes: a mild and efficient catalytic route to .alpha.-silyloxyaldehydes
inferredcites →https://doi.org/10.1021/ja00120a033openalex-snapshot
Rhodium-Catalyzed Intramolecular Silylformylation of Acetylenes: A Vehicle for Complete Regio- and Stereoselectivity in the Formylation of Acetylenic Bonds
inferredcites →https://doi.org/10.1021/ja00130a027openalex-snapshot
Extremely Regioselective Intramolecular Silylformylation of Alkynes
inferredcites →https://doi.org/10.1021/ja00172a033openalex-snapshot
Ready access of .alpha.-(triorganosilyl)methylene .beta.-lactones by means of rhodium-catalyzed cyclocarbonylation of substituted propargyl alcohols
inferredcites →https://doi.org/10.1021/ja00178a021openalex-snapshot
Unusual activity and selectivity in alkyne hydrosilylation with an iridium catalyst stabilized by an oxygen-donor ligand
inferredcites →https://doi.org/10.1021/ja00178a022openalex-snapshot
The ladder structure of [(tert-BuCH2)2TaN]5.cntdot.NH3.cntdot.2C7H8 and its relationship to cubic tantalum nitride
inferredcites →https://doi.org/10.1021/ja973095mopenalex-snapshot
Rhodium-Catalyzed Intramolecular Silylformylation of Alkenes
inferredcites →https://doi.org/10.1021/ja980242nopenalex-snapshot
Tandem Cyclization/Hydrosilylation of Functionalized 1,6-Dienes Catalyzed by a Cationic Palladium Complex
inferredcites →https://doi.org/10.1021/ja980907lopenalex-snapshot
Silylcarbocyclizations of 1,6-Diynes
inferredcites →https://doi.org/10.1021/ja9815529openalex-snapshot
Rhodium-Catalyzed Intramolecular Silylcarbotricyclization (SiCaT) of Triynes
inferredcites →https://doi.org/10.1021/ja990461oopenalex-snapshot
Asymmetric Cyclization/Hydrosilylation of Functionalized 1,6-Dienes Catalyzed by Enantiomerically Pure Palladium Pyridine−Oxazoline Complexes
inferredcites →https://doi.org/10.1021/ja993977gopenalex-snapshot
Rhodium-Catalyzed Novel Carbonylative Carbotricyclization of Enediynes
inferredcites →https://doi.org/10.1021/jo0003192openalex-snapshot
Enantioselective Diene Cyclization/Hydrosilylation Catalyzed by Optically Active Palladium Bisoxazoline and Pyridine−Oxazoline Complexes
inferredcites →https://doi.org/10.1021/jo00104a012openalex-snapshot
Silylcarbobicyclization of 1,6-Diynes: A Novel Catalytic Route to Bicyclo[3.3.0]octenones
inferredcites →https://doi.org/10.1021/jo00122a038openalex-snapshot
Phenyldimethylsilyl as an Alcohol Surrogate in Intramolecular Diels-Alder Cycloaddition: Synthesis of .alpha.-Dictyopterol
inferredcites →https://doi.org/10.1021/jo00250a023openalex-snapshot
Palladium- and nickel-catalyzed reaction of trimethylsilyl cyanide with acetylenes. Addition of trimethylsilyl cyanide to the carbon-carbon triple bonds
inferredcites →https://doi.org/10.1021/jo971788fopenalex-snapshot
Palladium-Catalyzed Hydrostannation−Cyclization of 1,6-Diynes. Generation of 1,2-Dialkylidenecyclopentanes with a Tributylstannane Moiety
inferredcites →https://doi.org/10.1021/jo980100bopenalex-snapshot
Cyclization of o-Allylstyrene via Hydrosilylation: Mechanistic Aspects of Hydrosilylation of Styrenes Catalyzed by Palladium−Phosphine Complexes
inferredcites →https://doi.org/10.1021/jo9913006openalex-snapshot
Cyclization/Hydrosilylation of Functionalized Dienes Catalyzed by a Cationic Palladium Phenanthroline Complex
inferredcites →https://doi.org/10.1021/jo9913311openalex-snapshot
Organolanthanide-Catalyzed Cyclization/Silylation of Nitrogen-Containing Enynes
inferredcites →https://doi.org/10.1021/ol005810uopenalex-snapshot
Use of Pentamethyldisiloxane in the Palladium-Catalyzed Cyclization/Hydrosilylation of Functionalized Dienes
inferredcites →https://doi.org/10.1021/om00016a012openalex-snapshot
Highly Regioselective and Stereoselective Silylformylation of Alkynes Under Mild Conditions Promoted by Dirhodium(II) Perfluorobutyrate
inferredcites →https://doi.org/10.1021/om00017a015openalex-snapshot
Zwitterionic Rhodium(I) Complex Catalyzed Net Silylhydroformylation of Terminal Alkynes
inferredcites →https://doi.org/10.1021/om00025a005openalex-snapshot
Highly efficient regioselective silylcarbonylation of alkynes catalyzed by dirhodium(II) perfluorobutyrate
inferredcites →https://doi.org/10.1021/om00047a021openalex-snapshot
Silylformylation of 1-hexyne catalyzed by rhodium-cobalt mixed-metal carbonyl clusters
inferredcites →https://doi.org/10.1021/om00055a044openalex-snapshot
Reactions of Co2Rh2(CO)12 with isocyanides and 1-alkynes. Characterization of new isocyanide and 1-alkyne complexes of Co-Rh mixed-metal systems and the structures of [Rh(C.tplbond.N-C6H3Me2-2,6)4][Co(CO)4] and Co2Rh2(CO)7(.mu.-CO)2(.mu.4,.eta.2-HC.tplbond.CBun)(PPh3)
inferredcites →https://doi.org/10.1021/om00138a024openalex-snapshot
Cobalt-rhodium heptacarbonyl: a coordinatively unsaturated dinuclear metal carbonyl
inferredcites →https://doi.org/10.1021/om00162a026openalex-snapshot
Hydrosilylation of 1-hexyne catalyzed by rhodium and cobalt-rhodium mixed-metal complexes. Mechanism of apparent trans addition
inferredcites →https://doi.org/10.1021/om970704qopenalex-snapshot
Palladium-Catalyzed Borylstannylative Carbocyclization of Diynes and an Enyne Compound
inferredcites →https://doi.org/10.1021/om9807250openalex-snapshot
Nickel-Catalyzed Silaborative Dimerization of Alkynes
inferredcites →https://doi.org/10.1039/p19950000599openalex-snapshot
Palladium complex-catalysed carbocyclization–distannylation, –disilylation and –silastannylation of bis-dienes using distannanes, disilanes and silylstannanes

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.4636655openalex-extracted
Probing the MAO Enzymes with a Novel Family of Quaternary Propargylamine Derivatives
inferred← citeshttps://doi.org/10.1002/047084289x.rd477.pub2openalex-snapshot
Dodecacarbonyltetrarhodium
inferred← citeshttps://doi.org/10.1002/047084289x.rn01369openalex-snapshot
Diethoxymethylsilane
inferred← citeshttps://doi.org/10.1002/047084289x.rt215.pub2openalex-snapshot
Triethoxysilane
inferred← citeshttps://doi.org/10.1002/047084289x.rt215.pub3openalex-snapshot
Triethoxysilane
inferred← citeshttps://doi.org/10.1002/047084289x.rt385.pub2openalex-snapshot
Triphenylsilane
inferred← citeshttps://doi.org/10.1002/0471227617.eoc065.pub2openalex-snapshot
Cyclization—Homogeneous
inferred← citeshttps://doi.org/10.1002/9780470842898.rt385.pub2openalex-snapshot
Triphenylsilane
inferred← citeshttps://doi.org/10.1002/9780471264194.fos05707openalex-snapshot
Hydrosilanes
inferred← citeshttps://doi.org/10.1002/9780471264194.fos05707.pub2openalex-snapshot
Hydrosilanes
inferred← citeshttps://doi.org/10.1002/9780471264194.fos05707.pub3openalex-snapshot
Hydrosilanes
inferred← citeshttps://doi.org/10.1002/9780471264194.fos05707.pub4openalex-snapshot
Hydrosilanes
inferred← citeshttps://doi.org/10.1002/9780471264194.fos05707.pub5openalex-snapshot
Hydrosilanes
inferred← citeshttps://doi.org/10.1002/9780471264194.fos05707.pub6openalex-snapshot
Hydrosilanes
inferred← citeshttps://doi.org/10.1002/9780471264194.fos05707.pub7openalex-snapshot
Hydrosilanes
inferred← citeshttps://doi.org/10.1002/9781118651421.ch2openalex-snapshot
Organorhodium Chemistry
inferred← citeshttps://doi.org/10.1002/9781118662083.cot08-007openalex-snapshot
Formation of Aldehydes and Ketones by Carbonylation and Related Reactions
inferred← citeshttps://doi.org/10.1002/9783527811908.ch7openalex-snapshot
Rhodium(I)‐Catalyzed Reductive Carbon–Carbon Bond Formation
inferred← citeshttps://doi.org/10.1002/adsc.201000434openalex-snapshot
Regioselective Preparation of Functionalized exo‐Methylene‐ cyclopentanes and exo‐Methylenepyrrolidines via Silaborative Carbocyclization of 1,6‐Enynes
inferred← citeshttps://doi.org/10.1002/ange.200603533openalex-snapshot
Highly Enantioselective Hydrosilylation/Cyclization of 1,6‐Enynes Catalyzed by Rhodium(I) Complexes of Spiro Diphosphines
inferred← citeshttps://doi.org/10.1002/ange.200701589openalex-snapshot
Cycloisomerisierungen von 1,n‐Eninen: faszinierende metallkatalysierte Umlagerungen und mechanistische Einblicke
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.202508702openalex-snapshot
Enantioselective Divergent Cyclization of Amide‐Type 1,6‐Enynes Enabled by H–[Pd]–CN Catalysis
inferred← citeshttps://doi.org/10.1002/anie.200603533openalex-snapshot
Highly Enantioselective Hydrosilylation/Cyclization of 1,6‐Enynes Catalyzed by Rhodium(I) Complexes of Spiro Diphosphines
inferred← citeshttps://doi.org/10.1002/anie.200701589openalex-snapshot
Cycloisomerization of 1,n‐Enynes: Challenging Metal‐Catalyzed Rearrangements and Mechanistic Insights
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.202508702openalex-snapshot
Enantioselective Divergent Cyclization of Amide‐Type 1,6‐Enynes Enabled by H–[Pd]–CN Catalysis
inferred← citeshttps://doi.org/10.1002/asia.202201241openalex-snapshot
Cationic Rhodium(I)‐Catalyzed Asymmetric Cyclohydroformylation of 1,6‐Enynes with Formaldehyde
inferred← citeshttps://doi.org/10.1002/cctc.200900003openalex-snapshot
The Role of Water in Platinum‐Catalyzed Cycloisomerization of 1,6‐Enynes: A Combined Experimental and Theoretical Gas Phase Study
inferred← citeshttps://doi.org/10.1002/chem.200700256openalex-snapshot
N‐Heterocyclic Carbene and Phosphine Ruthenium Indenylidene Precatalysts: A Comparative Study in Olefin Metathesis
inferred← citeshttps://doi.org/10.1002/chem.200901614openalex-snapshot
Gold‐Catalyzed Intermolecular Addition of Carbonyl Compounds to 1,6‐Enynes: Reactivity, Scope, and Mechanistic Aspects
inferred← citeshttps://doi.org/10.1002/chem.201204039openalex-snapshot
Rhodium‐Catalyzed Carbocyclization and Chlorosulfonylation of 1,6‐Enynes with Sulfonyl Chlorides
inferred← citeshttps://doi.org/10.1002/chem.201504753openalex-snapshot
Alkoxyallene‐ynes: Selective Preparation of Bicyclo[5.3.0] Ring Systems Including a δ‐Alkoxy Cyclopentadienone
inferred← citeshttps://doi.org/10.1002/cjoc.202000651openalex-snapshot
Diastereodivergent Hydrosilylative Enyne Cyclization Catalyzed by N‐Heterocyclic Carbene‐Ni (0)†
inferred← citeshttps://doi.org/10.1002/ejic.201701160openalex-snapshot
Cluster [Co3(CO)3(µ2‐CO)3(µ3‐C8H8)]– as a Ligand: Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1002/ejoc.200300487openalex-snapshot
Use of Rhodium N‐Heterocyclic Carbene Complexes in Catalytic Cyclization and Hydrosilylation of 1,6‐Enynes to 2‐Methyl‐1‐silylmethylidene‐2‐cyclopentane
inferred← citeshttps://doi.org/10.1002/ejoc.200700402openalex-snapshot
On the Mechanism of the Puzzling “Endocyclic” Skeletal Rearrangement of 1,6‐Enynes
inferred← citeshttps://doi.org/10.1002/ejoc.200701219openalex-snapshot
Synthesis and Reactivity of Silylformylation Products Derived from Alkynes
inferred← citeshttps://doi.org/10.1002/ejoc.201700455openalex-snapshot
Synthesis of Functionalised 3‐Isochromanones by Silylcarbocyclisation/Desilylation Reactions
inferred← citeshttps://doi.org/10.1002/ijch.201000036openalex-snapshot
Sequential Processes in Palladium‐Catalyzed Silicon‐Based Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/slct.201900524openalex-snapshot
Synthesis of Functionalised Indoline and Isoquinoline Derivatives through a Silylcarbocyclisation/Desilylation Sequence
inferred← citeshttps://doi.org/10.1007/128_2007_123openalex-snapshot
Reductive Coupling of Unactivated Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1007/978-1-4020-6793-8_3openalex-snapshot
New Cyclization and Cycloaddition Reactions in Organic Synthesis
inferred← citeshttps://doi.org/10.1007/978-1-4020-8172-9_2openalex-snapshot
Hydrosilylation of Alkynes and Their Derivatives
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00040-4openalex-snapshot
Vinyl- and Arylsilicon, germanium, and boron Compounds
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00129-1openalex-snapshot
C–C Bond Formation (Part 1) by Addition Reactions: through Carbometallation Catalyzed by Group 8–11 Metals
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00132-1openalex-snapshot
Metal-catalyzed Reductive Carbocyclization (CC, CC, CO Bonds)
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00155-2openalex-snapshot
Silane-initiated Carbocyclization Catalyzed by Transition Metal Complexes
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00159-xopenalex-snapshot
Silylformylation
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00171-xopenalex-snapshot
Transition Metal-Catalyzed Cyclization of 1,n-Enynes, 1,n-Dienes, 1,n-Enallenes, and 1,n-Yne-Allenes
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00106-5openalex-snapshot
Vinyl- and Arylsilicon, Germanium, and Boron Compounds
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.109520openalex-snapshot
Rhodium(III)-catalyzed diastereo- and enantioselective hydrosilylation/cyclization reaction of cyclohexadienone-tethered α,β-unsaturated aldehydes
inferred← citeshttps://doi.org/10.1016/j.ccr.2004.05.002openalex-snapshot
Transition metals in organic synthesis: highlights for the year 2002
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121432openalex-snapshot
Two different faces of the triangular cluster Rh3Cp3(μ2-CO)3 towards metalloelectrophiles: Structural and theoretical study
inferred← citeshttps://doi.org/10.1016/j.tet.2003.09.056openalex-snapshot
Ring expansion of 5- to 6-member zirconacycles by carbenoid insertion
inferred← citeshttps://doi.org/10.1016/j.tet.2004.04.046openalex-snapshot
Synthesis of heterocycles by carbonylation of acetylenic compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2006.04.065openalex-snapshot
Sequential addition reaction of lithium acetylides and Grignard reagents to thioiminium salts from thiolactams leading to 2,2-disubstituted cyclic amines
inferred← citeshttps://doi.org/10.1016/j.tet.2009.07.007openalex-snapshot
Cyclisation of bisphosphonate substituted enynes
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.089openalex-snapshot
Facile access to cyclooctanoid ring systems via microwave-assisted tandem 6-exo dig cyclization–rearrangement sequence
inferred← citeshttps://doi.org/10.1016/j.tet.2018.12.002openalex-snapshot
Copper-catalyzed asymmetric silylative cyclization of cyclohexadienone-containing 1,6-enynes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2004.08.019openalex-snapshot
Catalytic asymmetric carbonylative silylcarbocyclization of enynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.04.017openalex-snapshot
Grubbs catalyst-mediated cycloisomerization of allenenes
inferred← citeshttps://doi.org/10.1016/s0010-8545(03)00035-3openalex-snapshot
Application of transition metals in hydroformylation annual survey covering the year 2002
inferred← citeshttps://doi.org/10.1016/s0065-3055(07)55001-xopenalex-snapshot
A Review of Recent Progress in Catalyzed Homogeneous Hydrosilation (Hydrosilylation)
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00343openalex-snapshot
Synthesis and Reactivity of Propargylamines in Organic Chemistry
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01555openalex-snapshot
Cobalt-Catalyzed Hydrosilylation/Cyclization of 1,6-Enynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02979openalex-snapshot
Rhodium-Catalyzed Asymmetric Hydroboration/Cyclization of 1,6-Enynes Enabled by Spirosiladiphosphine Ligands: Constructing Chiral Five-Membered Rings with a Boron Handle
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03479openalex-snapshot
Silaborative Carbocyclizations of 1,7-Enynes. Diastereoselective Preparation of Chromane Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00930openalex-snapshot
Rhodium-Catalyzed Carbonylative Synthesis of Benzosilinones
inferred← citeshttps://doi.org/10.1021/cr020095iopenalex-snapshot
Transition-Metal-Catalyzed Reactions in Heterocyclic Synthesis
inferred← citeshttps://doi.org/10.1021/cr500208kopenalex-snapshot
Multimetallic Catalysis Based on Heterometallic Complexes and Clusters
inferred← citeshttps://doi.org/10.1021/ja048627vopenalex-snapshot
Synthesis of Tertiary Propargylamines by Sequential Reactions of in Situ Generated Thioiminium Salts with Organolithium and -magnesium Reagents
inferred← citeshttps://doi.org/10.1021/ja049806fopenalex-snapshot
Mechanism of Palladium-Catalyzed Diene Cyclization/Hydrosilylation: Direct Observation of Intramolecular Carbometalation
inferred← citeshttps://doi.org/10.1021/ja054221mopenalex-snapshot
Silicon-Initiated Carbonylative Carbotricyclization and [2+2+2+1] Cycloaddition of Enediynes Catalyzed by Rhodium Complexes
inferred← citeshttps://doi.org/10.1021/ja0558342openalex-snapshot
Cationic Palladium-Catalyzed Hydrosilylative Cross-Coupling of Alkynes with Alkenes
inferred← citeshttps://doi.org/10.1021/ja067854popenalex-snapshot
Sequential Silylcarbocyclization/Silicon-Based Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/ja9063475openalex-snapshot
Total Syntheses of Isodomoic Acids G and H
inferred← citeshttps://doi.org/10.1021/jacs.2c00288openalex-snapshot
Cobalt-Catalyzed Sequential Site- and Stereoselective Hydrosilylation of 1,3- and 1,4-Enynes
inferred← citeshttps://doi.org/10.1021/jacs.7b00482openalex-snapshot
Palladium-Catalyzed Hydrohalogenation of 1,6-Enynes: Hydrogen Halide Salts and Alkyl Halides as Convenient HX Surrogates
inferred← citeshttps://doi.org/10.1021/jo049072popenalex-snapshot
Palladium(0)-Catalyzed Cyclization of Electron-Deficient Enynes and Enediynes
inferred← citeshttps://doi.org/10.1021/jo101790zopenalex-snapshot
Stereocontrolled Total Syntheses of Isodomoic Acids G and H via a Unified Strategy
inferred← citeshttps://doi.org/10.1021/ol027196nopenalex-snapshot
Enantioselective Cyclization/Hydrosilylation of 1,6-Enynes Catalyzed by a Cationic Rhodium Bis(phosphine) Complex
inferred← citeshttps://doi.org/10.1021/ol035895+openalex-snapshot
Immobilized Cobalt/Rhodium Heterobimetallic Nanoparticle-Catalyzed Silylcarbocylization and Carbonylative Silylcarbocyclization of 1,6-Enynes
inferred← citeshttps://doi.org/10.1021/ol102019wopenalex-snapshot
Nickel-Catalyzed Hydrosilylation/Cyclization of Difluoro-Substituted 1,6-Enynes
inferred← citeshttps://doi.org/10.1021/om050478hopenalex-snapshot
Silylcarbonylation of Vinylsilanes Catalyzed by Iridium(I) Siloxide Complexes
inferred← citeshttps://doi.org/10.1021/om7012277openalex-snapshot
Carbonylative and Hydrosilylative Carbocyclization of 1,5-Diynes for the Synthesis of Cyclic Dienones
inferred← citeshttps://doi.org/10.1021/om9009697openalex-snapshot
Ruthenium Olefin Metathesis Catalysts with N-Heterocyclic Carbene Ligands Bearing N-Naphthyl Side Chains
inferred← citeshttps://doi.org/10.1039/9781788016131-00343openalex-snapshot
Transition Metal-catalysed Nucleophilic Additions of Terminal Alkynes in Water: Development and Synthetic Utility
inferred← citeshttps://doi.org/10.1039/b718609fopenalex-snapshot
Cobalt–rhodium heterobimetallic nanoparticle-catalyzed reactions
inferred← citeshttps://doi.org/10.1039/c2cc34468hopenalex-snapshot
Pd-catalyzed borylative cyclisation of 1,7-enynes
inferred← citeshttps://doi.org/10.1039/c7qo00321hopenalex-snapshot
Nickel-catalyzed highly chemo- and stereoselective borylative cyclization of 1,6-enynes with bis(pinacolato)diboron
inferred← citeshttps://doi.org/10.1039/c8cc00097bopenalex-snapshot
Palladium-catalyzed silaborative carbocyclizations of 1,6-diynes
inferred← citeshttps://doi.org/10.1039/d2ob01771gopenalex-snapshot
Nickel-catalyzed cascade hydrosilylation/cyclization of 1,7-enynes leading to silyl-containing quinolinones
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/d2sc06349bopenalex-snapshot
Chiral spirosiladiphosphines: ligand development and applications in Rh-catalyzed asymmetric hydrosilylation/cyclization of 1,6-enynes with enhanced reactivity
inferred← citeshttps://doi.org/10.1055/s-0040-1707247openalex-snapshot
Silylboranes as Powerful Tools in Organic Synthesis: Stereo- and Regioselective Reactions with 1,n-Enynes
inferred← citeshttps://doi.org/10.1055/sos-sd-104-00274openalex-snapshot
4.4.4.8 Silyl Hydrides (Update 2015)
inferred← citeshttps://doi.org/10.1246/bcsj.80.1814openalex-snapshot
Cationic Palladium Complex-Catalyzed Hydrosilylative Cross-Coupling of Alkynes with Alkenes. 1,4-Addition of Trichlorosilane to Form 4-Silyl-1-butene Framework
inferred← citeshttps://doi.org/10.1246/cl.2012.2openalex-snapshot
Thioamides and Thioformamides for Sequential Reactions with Organolithium and Grignard Reagents
inferred← citeshttps://doi.org/10.3390/catal10091012openalex-snapshot
From Alkynes to Heterocycles through Metal-Promoted Silylformylation and Silylcarbocyclization Reactions
inferred← citeshttps://doi.org/10.3390/molecules29112486openalex-snapshot
Are Terminal Alkynes Necessary for MAO-A/MAO-B Inhibition? A New Scaffold Is Revealed
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