Issue 5, 2021

Facile access to benzofuran-fused tetrahydropyridines via catalytic asymmetric [4 + 2] cycloaddition of aurone-derived 1-azadienes with 3-vinylindoles

Abstract

A highly enantioselective [4 + 2] cycloaddition reaction of aurone-derived 1-azadienes with 3-vinylindoles has been developed. In the presence of chiral phosphoric acids, a wide range of benzofuran-fused tetrahydropyridines with three contiguous stereogenic centers were obtained in good yields, and with excellent diastereo- and enantio-selectivities.

Graphical abstract: Facile access to benzofuran-fused tetrahydropyridines via catalytic asymmetric [4 + 2] cycloaddition of aurone-derived 1-azadienes with 3-vinylindoles

Supplementary files

Article information

Article type
Research Article
Submitted
09 Oct 2020
Accepted
04 Jan 2021
First published
05 Jan 2021

Org. Chem. Front., 2021,8, 968-974

Facile access to benzofuran-fused tetrahydropyridines via catalytic asymmetric [4 + 2] cycloaddition of aurone-derived 1-azadienes with 3-vinylindoles

W. L. Koay, G. Mei and Y. Lu, Org. Chem. Front., 2021, 8, 968 DOI: 10.1039/D0QO01236J

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