Results 261 to 270 of about 29,655,632 (304)
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Understanding and Exploiting C—H Bond Activation
ChemInform, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Labinger, Jay A., Bercaw, John E.
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2014
The C–H activation reaction is a reaction that cleaves a carbon–hydrogen bond. Here the carbon–hydrogen bond is mostly referred to unactivated carbon–hydrogen bonds.
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The C–H activation reaction is a reaction that cleaves a carbon–hydrogen bond. Here the carbon–hydrogen bond is mostly referred to unactivated carbon–hydrogen bonds.
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Electrophilic C−H Activation at {Cp*Ir}: Ancillary-Ligand Control of the Mechanism of C−H Activation
Journal of the American Chemical Society, 2006Density functional calculations on the low-temperature cyclometalation of dimethylbenzylamine with [IrCl2Cp*]2/NaOAc have characterized a novel electrophilic activation pathway for C-H bond activation. C-H activation occurs from [Ir(DMBA-H)(kappa2-OAc)Cp*]+, and OAc plays a central role in determining the barrier for reaction.
Davies, David L. +4 more
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Angewandte Chemie, 2018
AbstractDisclosed herein is the merging of C−H activation and radical chemistry, enabling rapid access to a structurally diverse family of fused carbohelicenes through the fusion of α‐acetylnaphthalenes with alkynes under oxidative conditions. This cascade process exhibits exquisite chemoselectivity and regioselectivity.
Jiangliang Yin, Jingsong You
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AbstractDisclosed herein is the merging of C−H activation and radical chemistry, enabling rapid access to a structurally diverse family of fused carbohelicenes through the fusion of α‐acetylnaphthalenes with alkynes under oxidative conditions. This cascade process exhibits exquisite chemoselectivity and regioselectivity.
Jiangliang Yin, Jingsong You
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Chemical Communications, 2009
An organocatalytic stereoselective alpha-alkylation reaction of aldehydes based on C-H activation is presented.
F. Benfatti +4 more
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An organocatalytic stereoselective alpha-alkylation reaction of aldehydes based on C-H activation is presented.
F. Benfatti +4 more
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C–H bond activation of ethylene by a zirconacycle
Chemical Communications, 2013The reaction of C2H4 and β-SiH containing azasilazirconacycle Cp2Zr{κ(2)-N(SiHMe2)SiHMeCH2} (3), formed via a γ-abstraction reaction of Cp2Zr{N(SiHMe2)2}H (1), follows an unusual pathway in which a rare σ-bond metathesis reaction of ethylene generates a vinyl intermediate. That species undergoes a β-hydrogen abstraction under the reaction conditions to
KaKing, Yan, Aaron D, Sadow
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A Minimalist Approach to CH Activation by Copper
Helvetica Chimica Acta, 2006AbstractThe complex [Cu2(1)2]2+ (1 = 1,3‐bis(1‐methyl‐1H‐benzimidazol‐2‐yl)benzene) undergoes slow oxidation by dioxygen in DMF solution to give the hydroxylated product [Cu2(2‐H)2]2+ (2 = 2,6‐bis(1‐methyl‐1H‐benzimidazol‐2‐yl)phenol) characterized by an X‐ray crystal‐structure analysis. The oxidation occurs much faster when CuII is mixed with 1 in the
Kuebel Pollak, Anita +5 more
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Diastereoselective Remote CH Activation by Hydroboration
Chemistry – A European Journal, 2004AbstractHydroboration of tetrasubstituted or trisubstituted alkenes with BH3 and subsequent thermolysis allows remote diastereoselective CH activation of neighboring aryl rings. Tetrasubstituted and trisubstituted 1,1‐diphenylethylene derivatives undergo a highly stereoselective 1,2‐rearrangement followed by remote CH activation to lead, after ...
Jesús A, Varela +6 more
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2013
Transition metal-catalyzed carbonylation reactions represent an enormous toolbox for CO–X bond formation (X = C, N, O, etc.). While most coupling reactions take place with heteronucleophiles nowadays, carbonylations including C–H activation are attracting more and more attention because the use of stoichiometric amounts of organometallic reagents can ...
Matthias Beller, Xiao-Feng Wu
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Transition metal-catalyzed carbonylation reactions represent an enormous toolbox for CO–X bond formation (X = C, N, O, etc.). While most coupling reactions take place with heteronucleophiles nowadays, carbonylations including C–H activation are attracting more and more attention because the use of stoichiometric amounts of organometallic reagents can ...
Matthias Beller, Xiao-Feng Wu
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