Mild gold-catalyzed three-component dehydrogenative coupling of terminal alkynes to amines and indole-2-carboxaldehyde. - Wikidata - wikimedia - TriplyDB

Mild gold-catalyzed three-component dehydrogenative coupling of terminal alkynes to amines and indole-2-carboxaldehyde.

Mild gold-catalyzed three-component dehydrogenative coupling of terminal alkynes to amines and indole-2-carboxaldehyde.

http://www.wikidata.org/entity/Q51749025

about

Redox-neutral α-sulfenylation of secondary amines: ring-fused N,S-acetals.The Rügheimer-Burrows reaction revisited: Facile preparation of 4-alkylisoquinolines and 3,5-dialkylpyridines from (partially) saturated amines Asymmetric Redox-Annulation of Cyclic Amines.Redox-Annulation of Cyclic Amines and β-Ketoaldehydes.Intramolecular Redox-Mannich Reactions: Facile Access to the Tetrahydroprotoberberine Core.The redox-Mannich reaction.C-H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds.An Ugi Reaction Incorporating a Redox-Neutral Amine C-H Functionalization Step Acetic Acid Promoted Redox Annulations with Dual C-H Functionalization.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.Direct N-H/α,α,β,β-C(sp3)-H functionalization of piperidine via an azomethine ylide route: synthesis of spirooxindoles bearing 3-substituted oxindoles.

P2860

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P2860

Mild gold-catalyzed three-component dehydrogenative coupling of terminal alkynes to amines and indole-2-carboxaldehyde.

http://www.wikidata.org/entity/Q51749025

description

2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

@zh-my

2014年学术文章

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2014年學術文章

@yue

2014年學術文章

@zh-hant

name

Mild gold-catalyzed three-comp ...... s and indole-2-carboxaldehyde.

@en

Mild gold-catalyzed three-comp ...... s and indole-2-carboxaldehyde.

@nl

type

label

Mild gold-catalyzed three-comp ...... s and indole-2-carboxaldehyde.

@en

Mild gold-catalyzed three-comp ...... s and indole-2-carboxaldehyde.

@nl

prefLabel

Mild gold-catalyzed three-comp ...... s and indole-2-carboxaldehyde.

@en

Mild gold-catalyzed three-comp ...... s and indole-2-carboxaldehyde.

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P1433

Organic and Biomolecular Chemistry

P1476

Mild gold-catalyzed three-comp ...... s and indole-2-carboxaldehyde.

@en

P2093

Hongni Wang

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Jian Li

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

Jiangtao Sun

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

Li Liu

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

Yang Yang

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

P2860

Maximizing synthetic efficiency: multi-component transformations lead the way

Synthesis and functionalization of indoles through palladium-catalyzed reactions.

Water Soluble Phosphane-Gold(I) Complexes. Applications as Recyclable Catalysts in a Three-component Coupling Reaction and as Antimicrobial and Anticancer Agents.

Efficient and General Synthesis of 3-Aminoindolines and 3-Aminoindoles via Copper-Catalyzed Three Component Coupling Reaction

Redox-neutral copper(II) carboxylate catalyzed α-alkynylation of amines.

Catalytic functionalization of indoles in a new dimension.

Marine indole alkaloids: potential new drug leads for the control of depression and anxiety.

Organocatalytic strategies for the asymmetric functionalization of indoles.

Indoles in multicomponent processes (MCPs).

Mechanistic insights into the gold-catalyzed cycloisomerization of bromoallenyl ketones: ligand-controlled regioselectivity.

P304

2523-2527

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scholarly article

P356

10.1039/C3OB42431F

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16

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12

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P577

2014-04-01T00:00:00Z

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P698

24619486

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