Research graph
References from Intramolecular Activation of C–O Bond by an o -Boryl Group in o -(Alkoxysilyl)(diarylboryl)benzenes. Local targets link to admitted publications; unresolved targets remain external evidence.
10.1093/oso/9780198500995.001.0001
10.1093/oso/9780198500995.001.0001 · 1999 · External reference
Arylboron Compounds as Acid Catalysts in Organic Synthetic Transformations
10.1002/(sici)1099-0690(199903)1999:3<527::aid-ejoc527>3.0.co;2-r · 1999 · External reference
Cocatalysts for Metal-Catalyzed Olefin Polymerization: Activators, Activation Processes, and Structure–Activity Relationships
10.1021/cr980462j · 2000 · External reference
Tris(pentafluorophenyl)boron-Catalyzed Hydrosilation of Aromatic Aldehydes, Ketones, and Esters
10.1021/ja961536g · 1996 · External reference
Studies on the Mechanism of B(C6F5)3-Catalyzed Hydrosilation of Carbonyl Functions
10.1021/jo991828a · 2000 · External reference
B(C6F5)3 catalyzed hydrosilation of enones and silyl enol ethers
10.1016/s0040-4020(02)00974-2 · 2002 · External reference
Conclusive Evidence for an SN2-Si Mechanism in the B(C6F5)3-Catalyzed Hydrosilylation of Carbonyl Compounds: Implications for the Related Hydrogenation
10.1002/anie.200801675 · 2008 · External reference
B(C6F5)3-Catalyzed Reduction of Ketones and Imines Using Silicon-Stereogenic Silanes: Stereoinduction by Single-Point Binding
10.1002/ejoc.200900796 · 2009 · External reference
Illuminating the Mechanism of the Borane-Catalyzed Hydrosilylation of Imines with Both an Axially Chiral Borane and Silane
10.1002/chem.201202693 · 2012 · External reference
Organosubstituierte 2,5-Dihydro-1,2,5-oxoniasilaboratole Charakterisierung und Reaktivität
10.1002/cber.19911240506 · 1991 · External reference
2,5-Dihydro-1,2,5-azoniasilaboratole Derivatives – Useful Starting Materials in Heterocyclic Synthesis
10.1002/cber.19961290207 · 1996 · External reference
Reaction of Alkyn-1-yl(diorganyl)silanes with 1-Boraadamantane: Si-H-B Bridges Confirmed by the Molecular Structure in the Solid State and in Solution
10.1002/chem.200304961 · 2003 · External reference
Dehydrogenative Condensation of (o-Borylphenyl)hydrosilane with Alcohols and Amines
10.1246/cl.2007.362 · 2007 · External reference
Reaction of o-(HSiR2)(BMes2)C6H4 with a fluoride ion: Fluoride attack at silicon and hydride transfer from silicon to boron to form F-Si···H-B interaction
10.1002/hc.20709 · 2011 · External reference
Intramolecular H-Ar Ligand Exchange between Silicon and Boron: Functionality Transfer of Si-H to B-H
10.1002/asia.201100678 · 2012 · External reference
Intramolecular Reaction of Silanol and Triarylborane: Boron-Aryl Bond Cleavage and Formation of a Si-O-B Heterocyle
10.1021/om8004405 · 2008 · External reference
Anion complexation and migration in (8-silyl-1-naphthyl)boranes. Participation of hypervalent silicon
10.1021/ja00284a031 · 1986 · External reference
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10.1107/s0021889898007717
10.1107/s0021889898007717 · 1999 · External reference
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1991 · External reference
Trisilyloxonium Ions: Preparation, NMR Spectroscopy, Ab Initio/IGLO Studies, and Their Role in Cationic Polymerization of Cyclosiloxanes
10.1021/ja00140a010 · 1995 · External reference
Chemistry of organosilicon compounds. 292. An NMR Study of the Formation of Silyloxonium Ions by Using Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate as Counteranion
10.1021/ja00043a013 · 1992 · External reference
Siloxycarbenium Tetrakis[3,5-bis(trifluoromethyl)phenyl]borates and Their Role in Reactions of Ketones with Nucleophiles
10.1246/cl.1992.555 · 1992 · External reference
E(SiMe3)4+ Ions (E=P, As): Persilylated Phosphonium and Arsonium Ions
10.1002/1521-3773(20010618)40:12<2308::aid-anie2308>3.0.co;2-q · 2001 · External reference
Silyl Chalconium Ions: Synthesis, Structure and Application in Hydrodefluorination Reactions
10.1002/chem.201700995 · 2017 · External reference
On Silylated Oxonium and Sulfonium Ions and Their Interaction with Weakly Coordinating Borate Anions
10.1002/chem.201904403 · 2019 · External reference
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Benzosiloxaboroles: Silicon Benzoxaborole Congeners with Improved Lewis Acidity, High Diol Affinity, and Potent Bioactivity
10.1021/acs.organomet.5b00265 · 2015 · External reference
