Silver-catalyzed tandem 5- and 6-endo-cyclizations via concomitant yne-ol-imine activation: selective entry to 2-aryldihydrofuroquinolines

Author:

Karmakar Swastik1ORCID,Das Prasanta1,Kundu Sandip2

Affiliation:

1. Department of Chemistry, Basirhat College, A/w West Bengal State University, Basirhat-743412, West Bengal, India

2. CIF Division, Indian Institute of Chemical Biology (IICB), Jadavpur-700032, West Bengal, India

Abstract

Ag(i)-catalyzed domino imination-intramolecular bi-heterocyclization-aromatization cascade has been developed to construct 2-aryldihydrofuroquinolines from aldehyde and unprotected 4-(2-aminophenyl)but-3-yn-1-ol via tandem 5-endo-dig and 6-endo-trig cyclization.

Funder

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Reference49 articles.

1. G. W.Gribble , Indole Ring Synthesis: From Natural Products to Drug Discovery , Wiley , 2016

2. Synthesis of Heterocycles via Palladium-Catalyzed Oxidative Addition

3. Coinage Metal-Assisted Synthesis of Heterocycles

4. Amination of Aromatic Olefins with Anilines: A New Domino Synthesis of Quinolines

5. G.Collin and H.Höke , Quinoline and Isoquinoline, ‘Ullmann's Encyclopedia of Industrial Chemistry’ , Weinheim , Wiley-VCH , 2000

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