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New frontiers of N-heterocyclic carbene catalysis

New frontiers of N-heterocyclic carbene catalysis

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New frontiers of N-heterocyclic carbene catalysis

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wetenschappelijk artikel

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наукова стаття, опублікована в листопаді 2015

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New frontiers of N-heterocyclic carbene catalysis

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New frontiers of N-heterocyclic carbene catalysis

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New frontiers of N-heterocyclic carbene catalysis

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New frontiers of N-heterocyclic carbene catalysis

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New frontiers of N-heterocyclic carbene catalysis

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New frontiers of N-heterocyclic carbene catalysis

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Q58867242-1996D260-363B-417C-8261-4ACB169F4378

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S11426-015-5514-7

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Science China. Chemistry

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New frontiers of N-heterocyclic carbene catalysis

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Jiean Chen

http://www.w3.org/2001/XMLSchema#string

Yong Huang

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Scope of the asymmetric intramolecular stetter reaction catalyzed by chiral nucleophilic triazolinylidene carbenes.

Asymmetric intramolecular crossed-benzoin reactions by N-heterocyclic carbene catalysis.

Acyl anion free N-heterocyclic carbene organocatalysis.

Enantioselective annulations for dihydroquinolones by in situ generation of azolium enolates

N-heterocyclic carbene-catalyzed conjugate additions of alcohols.

Enantioselective N-heterocyclic carbene-catalyzed β-hydroxylation of enals using nitroarenes: an atom transfer reaction that proceeds via single electron transfer.

N-heterocyclic carbene-catalyzed generation of alpha,beta-unsaturated acyl imidazoliums: synthesis of dihydropyranones by their reaction with enolates.

Proton transfer reactions of triazol-3-ylidenes: kinetic acidities and carbon acid pKa values for twenty triazolium salts in aqueous solution.

β-Carbon activation of saturated carboxylic esters through N-heterocyclic carbene organocatalysis.

Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a non-covalent organocatalyst.

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s11426-015-5514-7

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251-254

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scholarly article

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10.1007/S11426-015-5514-7

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3

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59

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2015-11-26T00:00:00Z

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