Issue 4, 2021

DDQ/FeCl3-mediated tandem oxidative carbon–carbon bond formation for the Synthesis of indole–fluorene hybrid molecules

Abstract

A series of diverse and complex hybrid structures of indole bearing fluorene were obtained in the presence of DDQ with high regioselectivity under mild conditions from biaryl tethered 3-(methylene)indoline in good to excellent yields. The strategy involves tandem allylic Csp3–H oxidation and subsequent intramolecular carbon–carbon bond formation. The yield of the product was dramatically improved in the presence of additives such as FeCl3 and molecular sieves (4 Å). A possible mechanism is proposed for this tandem process.

Graphical abstract: DDQ/FeCl3-mediated tandem oxidative carbon–carbon bond formation for the Synthesis of indole–fluorene hybrid molecules

Supplementary files

Article information

Article type
Paper
Submitted
25 Feb 2020
Accepted
17 Dec 2020
First published
17 Dec 2020

Org. Biomol. Chem., 2021,19, 906-910

DDQ/FeCl3-mediated tandem oxidative carbon–carbon bond formation for the Synthesis of indole–fluorene hybrid molecules

A. Kar, B. Chakraborty, S. Kundal, G. Rana and U. Jana, Org. Biomol. Chem., 2021, 19, 906 DOI: 10.1039/D0OB00413H

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