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Michael Heidelberger, 1933
Dr. Michael Heidelberger. Contributions of Chemistry of the Knowledge of Immune Processes Lecture delivered March 17th, 1933 Posted with permission
JEFFREY RAVETCH AND MICHAEL YOUNG
Congratulations to Jeffrey Ravetch and Michael Young, recipients of the 2012 Canada Gairdner International Award
Rigid analytic quantum groups and quantum Arens-Michael envelopes
Nicolas Dupré
Aug 19, 2019
We introduce a rigid analytification of the quantized coordinate algebra of a semisimple algebraic group and a quantized Arens-Michael envelope of the enveloping algebra of the corresponding Lie algebra, working over a...
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Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones

Enantioselective sulfa-Michael additions to α,β unsaturated diazocarbonyl compounds have been developed. Quinine-derived squaramide was found to be the best catalyst to promote C-S bond formation in a highly stereoselective...

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Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones

Enantioselective sulfa-Michael additions to α,β unsaturated diazocarbonyl compounds have been developed. Quinine-derived squaramide was found to be the best catalyst to promote C-S bond formation in a highly stereoselective...

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Stoichiometric and catalytic reactivity of Ni(6-Mes)(PPh<sub>3</sub>)<sub>2</sub>
The three-coordinate Ni(0) N-heterocyclic carbene complex Ni(6-Mes)(PPh3)2 (1; 6-Mes = 1,3-bis(2,4,6-trimethylphenyl)-3,4,5,6-tetrahydropyrimidin-2-ylidene) is formed in the reaction of Ni(cod)2 with a 1:2 mixture of 6-Mes and...
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Stoichiometric and catalytic reactivity of Ni(6-Mes)(PPh<sub>3</sub>)<sub>2</sub>
The three-coordinate Ni(0) N-heterocyclic carbene complex Ni(6-Mes)(PPh3)2 (1; 6-Mes = 1,3-bis(2,4,6-trimethylphenyl)-3,4,5,6-tetrahydropyrimidin-2-ylidene) is formed in the reaction of Ni(cod)2 with a 1:2 mixture of 6-Mes and...
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(carbene)CuF Complexes Featuring Bulky Arduengo-Type, Ring-Expanded, and Cyclic (Alkyl)(amino)carbenes
Five examples of two-coordinate copper(I) fluoride complexes stabilized by five-, six-, and seven-membered-ring N-heterocyclic carbenes or a cyclic (alkyl)(amino)carbene have been prepared, structurally characterized, and...
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Room Temperature Regioselective Catalytic Hydrodefluorination of Fluoroarenes with <i>trans</i>-[Ru(NHC)<sub>4</sub>H<sub>2</sub>] Via a Converted Nucleophlic Ru-H Attack Pathway
The efficient and highly selective room temperature hydrodefluorination (HDF) of fluoroarenes by the trans-[Ru(IMe4)4H2] catalyst, 3, is reported. Mechanistic studies show 3 acts directly in catalysis without any ligand...
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(carbene)CuF Complexes Featuring Bulky Arduengo-Type, Ring-Expanded, and Cyclic (Alkyl)(amino)carbenes
Five examples of two-coordinate copper(I) fluoride complexes stabilized by five-, six-, and seven-membered-ring N-heterocyclic carbenes or a cyclic (alkyl)(amino)carbene have been prepared, structurally characterized, and...
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Transforming PPh3 into Bidentate Phosphine Ligands at Ru-Zn Heterobimetallic Complexes

The reaction of [Ru(PPh 3) 3Cl 2] with excess ZnMe 2 led to P-C/C-H bond activation and P-C/C-C bond formation to generate a chelating diphenylphosphinobenzene ligand as well as a...

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Transforming PPh3 into Bidentate Phosphine Ligands at Ru-Zn Heterobimetallic Complexes

The reaction of [Ru(PPh 3) 3Cl 2] with excess ZnMe 2 led to P-C/C-H bond activation and P-C/C-C bond formation to generate a chelating diphenylphosphinobenzene ligand as well as a...

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Unexpected Migratory Insertion Reactions of M(alkyl)<sub>2</sub> (M = Zn, Cd) and Diamidocarbenes
The electrophilic character of free diamidocarbenes (DACs) allows them to activate inert bonds in small molecules, such as NH3 and P4. Herein, we report that metal coordinated DACs also exhibit...
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Unexpected Migratory Insertion Reactions of M(alkyl)<sub>2</sub> (M = Zn, Cd) and Diamidocarbenes
The electrophilic character of free diamidocarbenes (DACs) allows them to activate inert bonds in small molecules, such as NH3 and P4. Herein, we report that metal coordinated DACs also exhibit...
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Use of ring-expanded diamino- and diamidocarbene ligands in copper catalyzed azide-alkyne "click" reactions

The two-coordinate ring-expanded N-heterocyclic carbene copper(I) complexes [Cu(RE-NHC)2]+ (RE-NHC = 6-Mes, 7-o-Tol, 7-Mes) have been prepared and shown to be effective catalysts under neat conditions...

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