Formation of N-alkylpyrroles via intermolecular redox amination - Wikidata - awgldk - TriplyDB

Formation of N-alkylpyrroles via intermolecular redox amination

Formation of N-alkylpyrroles via intermolecular redox amination

http://www.wikidata.org/entity/Q33885988

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Merging rhodium-catalysed C-H activation and hydroamination in a highly selective [4+2] imine/alkyne annulation Redox-neutral α-sulfenylation of secondary amines: ring-fused N,S-acetals.Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolecular [1,5]-hydride shift/isomerization reaction Redox-neutral α-oxygenation of amines: reaction development and elucidation of the mechanism.The Rügheimer-Burrows reaction revisited: Facile preparation of 4-alkylisoquinolines and 3,5-dialkylpyridines from (partially) saturated amines Metal-free α-amination of secondary amines: computational and experimental evidence for azaquinone methide and azomethine ylide intermediates.Suzuki-Miyaura cross-coupling of potassium trifluoro(N-methylheteroaryl)borates with aryl and heteroaryl halides.Redox-neutral copper(II) carboxylate catalyzed α-alkynylation of amines.Facile Access to Ring-Fused Aminals via Direct α-Amination of Secondary Amines with ortho-Aminobenzaldehydes. Synthesis of Vasicine, Deoxyvasicine, Deoxyvasicinone, Mackinazolinone and Ruteacarpine.Organocatalytic C-H activation reactions.The azomethine ylide route to amine C-H functionalization: redox-versions of classic reactions and a pathway to new transformations.The redox-Mannich reaction.Redox-neutral α,β-difunctionalization of cyclic amines.C-H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds.Redox-neutral α-arylation of amines.Intramolecular [3 + 2]-cycloadditions of azomethine ylides derived from secondary amines via redox-neutral C-H functionalization.Redox-Neutral Aromatization of Cyclic Amines: Mechanistic Insights and Harnessing of Reactive Intermediates for Amine α- and β-C-H Functionalization.A tandem annulation with a [1,3]-hydride transfer as the key step leading to isochromans.Reductive amination catalyzed by iridium complexes using carbon monoxide as a reducing agent.Chiral Phosphoric Acid Catalyzed Kinetic Resolution of Indolines Based on a Self-Redox Reaction.Hf(OTf)4-Catalyzed highly diastereoselective synthesis of 1,3-disubstituted tetralin derivatives via benzylic C(sp3)-H bond functionalization.Synthesis of N-aryl-1-aminoindoles via intermolecular redox amination.Redox Amination Scope of Benzylic Ketones with Indoline: Synthetic and Mechanistic Insights Synthesis ofN-Alkylated Indolines and Indoles from Indoline and Aliphatic Ketones

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P2860

Formation of N-alkylpyrroles via intermolecular redox amination

http://www.wikidata.org/entity/Q33885988

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

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2009年論文

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2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

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name

Formation of N-alkylpyrroles via intermolecular redox amination

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Formation of N-alkylpyrroles via intermolecular redox amination

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Formation of N-alkylpyrroles via intermolecular redox amination

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Formation of N-alkylpyrroles via intermolecular redox amination

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Formation of N-alkylpyrroles via intermolecular redox amination

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Formation of N-alkylpyrroles via intermolecular redox amination

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P1433

Journal of the American Chemical Society

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Formation of N-alkylpyrroles via intermolecular redox amination

@en

P2093

Jon A Tunge

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Miranda Paley

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Nirmal K Pahadi

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Ranjan Jana

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Shelli R Waetzig

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P2860

C-H bond functionalization via hydride transfer: Lewis acid catalyzed alkylation reactions by direct intramolecular coupling of sp3 C-H bonds and reactive alkenyl oxocarbenium intermediates.

C-H bond functionalization via hydride transfer: synthesis of dihydrobenzopyrans from ortho-vinylaryl akyl ethers.

An atom-economic and selective ruthenium-catalyzed redox isomerization of propargylic alcohols. An efficient strategy for the synthesis of leukotrienes

Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donor

Remarkably stable tetrahedral intermediates: carbinols from nucleophilic additions to N-acylpyrroles.

3-pyrrolines are mechanism-based inactivators of the quinone-dependent amine oxidases but only substrates of the flavin-dependent amine oxidases.

Reduction of pyrrolyl- and indolylamides with BH3 x THF: cyclodeoxygenation versus deoxygenation.

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16626-16627

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scholarly article

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10.1021/JA907357G

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46

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131

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2009-11-01T00:00:00Z

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38064687

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19886656

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2878740

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