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Journal ArticleDOI

Palladium-Catalyzed Intermolecular Aerobic Annulation of o-Alkenylanilines and Alkynes for Quinoline Synthesis.

TLDR
A new approach to construct 2,3-disubstituted quinolines is described via Pd-catalyzed oxidative cyclization of o-vinylanilines and alkynes with molecular oxygen.
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This article is published in Organic Letters.The article was published on 2016-07-15. It has received 57 citations till now. The article focuses on the topics: Alkyne & Annulation.

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Citations
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Synthesis of Heterocycles via Pd-Ligand Controlled Cyclization of 2-Chloro-N-(2-vinyl)aniline: Preparation of Carbazoles, Indoles, Dibenzazepines and Acridines

TL;DR: In this paper, the Pd-catalyzed condensation of 2-bromostyrene and 2-chloroaniline derivatives yields stable diphenylamine intermediates, which are selectively converted to five-, six-, or seven-membered heteroaromatics (indoles, carbazoles, acridines, and dibenzazepines).
Journal ArticleDOI

The Modern Face of Synthetic Heterocyclic Chemistry

TL;DR: Some recent advances in the construction of heterocycles are discussed, focusing on catalytic methodology, which has contributed in a major way to developments of green and sustainable chemistry.
Journal ArticleDOI

Visible-light-induced multicomponent cascade cycloaddition involving N-propargyl aromatic amines, diaryliodonium salts and sulfur dioxide: rapid access to 3-arylsulfonylquinolines

TL;DR: A visible-light-induced, Eosin Y catalyzed three-component synthesis of 3-arylsulfonylquinoline derivatives through N-propargyl aromatic amines, diaryliodonium salts and sulfur dioxide has been discovered.
Journal ArticleDOI

Advances in Palladium-Catalyzed Cascade Cyclizations

TL;DR: Palladium-catalyzed cross-coupling reactions, with their well understood multistep catalytic cycles, form a promising basis for the design of cascade reactions as mentioned in this paper.
Journal ArticleDOI

Cascade Reaction of Isatins with 1,1-Enediamines: Synthesis of Multisubstituted Quinoline-4-carboxamides

TL;DR: A one-step methodology for the synthesis of multisubstituted quinoline-4-carboxamides was developed by simply refluxing a mixture of isatins 1 and various kinds of 1,1-enediamines 2-4 in a reaction catalyzed by NH2SO3H.
References
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Journal ArticleDOI

A diarylquinoline drug active on the ATP synthase of Mycobacterium tuberculosis.

TL;DR: A diarylquinoline, R207910, is identified that potently inhibits both drug-sensitive and drug-resistant Mycobacterium tuberculosis in vitro and mutants selected in vitro suggest that the drug targets the proton pump of adenosine triphosphate (ATP) synthase.
Journal ArticleDOI

Quinoline, quinazoline and acridone alkaloids

TL;DR: This review covers the isolation, structure determination, synthesis and biological activity of quinoline, quinazoline and acridone alkaloids from plant, microbial and animal sources.
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Gold-catalyzed carbon-heteroatom bond-forming reactions.

TL;DR: Application to Total Synthesis 1699 6.1.
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Palladium(II)-Catalyzed Alkene Functionalization via Nucleopalladation: Stereochemical Pathways and Enantioselective Catalytic Applications

TL;DR: Enantioselective PdII-catalyzed functionalization of alkenes has experienced considerably less success than have many other classes of enantiOSElective transformations, despite the extensive history of the Wacker process and related oxidation reactions.
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