Issue 10, 2022

Facile synthesis of the spiro-pyridoindolone scaffold via a gold-catalysed intramolecular alkynol cyclisation/hydroindolylation

Abstract

A simple approach for the synthesis of pyridoindolone scaffolds with a spiroannulated tetrahydrofuran ring is described. The overall process comprises intramolecular sequential gold-catalysed 5-endo-dig alkynol cycloisomerization and subsequent addition of indole C2 to the in situ generated oxocarbenium cation.

Graphical abstract: Facile synthesis of the spiro-pyridoindolone scaffold via a gold-catalysed intramolecular alkynol cyclisation/hydroindolylation

Supplementary files

Article information

Article type
Paper
Submitted
25 Dec 2021
Accepted
15 Feb 2022
First published
15 Feb 2022

Org. Biomol. Chem., 2022,20, 2086-2095

Facile synthesis of the spiro-pyridoindolone scaffold via a gold-catalysed intramolecular alkynol cyclisation/hydroindolylation

M. H. Shinde and C. V. Ramana, Org. Biomol. Chem., 2022, 20, 2086 DOI: 10.1039/D1OB02483C

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