Polyhalides as Efficient and Mild Oxidants for Oxidative Carbene Organocatalysis by Radical Processes. (Q47988100)

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9 April 2020

title

Polyhalides as Efficient and Mild Oxidants for Oxidative Carbene Organocatalysis by Radical Processes (English)

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9 April 2020

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1

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9 April 2020

Yuexia Zhang

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9 April 2020

author name string

Yuhuang Wang

3

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9 April 2020

Jie Ke

4

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9 April 2020

Martin Jeret

5

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9 April 2020

Rambabu N Reddi

6

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9 April 2020

Song Yang

7

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9 April 2020

Bao-An Song

8

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9 April 2020

Yonggui Robin Chi

9

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language of work or name

English

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publication date

2 February 2017

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Angewandte Chemie International Edition

9 April 2020

published in

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9 April 2020

volume

56

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9 April 2020

issue

11

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page(s)

2942-2946

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Crystal structure of the free radical intermediate of pyruvate:ferredoxin oxidoreductase

9 April 2020

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EPR spectroscopic and computational characterization of the hydroxyethylidene-thiamine pyrophosphate radical intermediate of pyruvate:ferredoxin oxidoreductase

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Catalysis with N-heterocyclic carbenes under oxidative conditions

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On the mechanism of N-heterocyclic carbene-catalyzed reactions involving acyl azoliums

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Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes

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Cooperative Catalysis and Activation with N-Heterocyclic Carbenes

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Direct β-activation of saturated aldehydes to formal Michael acceptors through oxidative NHC catalysis

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Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.

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N-Heterocyclic carbene-catalyzed oxidative [3 + 2] annulation of dioxindoles and enals: cross coupling of homoenolate and enolate

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Efficient catalytic, oxidative lactonization for the synthesis of benzodioxepinones using thiazolium-derived carbene catalysts

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N-Heterocyclic Carbene/Lewis Acid Catalyzed Enantioselective Aerobic Annulation of α,β-Unsaturated Aldehydes with 1,3-Dicarbonyl Compounds

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Carbene-catalysed reductive coupling of nitrobenzyl bromides and activated ketones or imines via single-electron-transfer process.

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

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Oxidatively Initiated NHC-Catalyzed Enantioselective Synthesis of 3,4-Disubstituted Cyclopentanones from Enals

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Photoredox Activation and Anion Binding Catalysis in the Dual Catalytic Enantioselective Synthesis of β-Amino Esters

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Decarboxylative trichloromethylation of aromatic aldehydes and its applications in continuous flow.

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Umpolung by N-Heterocyclic Carbenes: Generation and Reactivity of the Elusive 2,2-Diamino Enols (Breslow Intermediates)

21 January 2018

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NHC-catalysed benzoin condensation - is it all down to the Breslow intermediate?

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Organocatalytic enantioselective γ-aminoalkylation of unsaturated ester: access to pipecolic acid derivatives

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Oxidative γ-addition of enals to trifluoromethyl ketones: enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis

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Asymmetric access to the smallest enolate intermediate via organocatalytic activation of acetic ester

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Identifiers

DOI

10.1002/ANIE.201611692

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28151571%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

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