Issue 25, 2019, Issue in Progress

Synthesis of tetracyclic indolin-3-ones through Pd-catalyzed intramolecular deacetylative dearomatization of 3-acetoxy-indoles

Abstract

An efficient palladium-catalyzed intramolecular deacetylative dearomatization reaction of 3-acetoxyindoles has been developed. A range of tetracyclic indolin-3-ones bearing C2-quaternary stereocenters are achieved in good yields, showing a wide substrate scope for this reaction. A preliminary enantioselective reaction is established to furnish the product in 63% ee by using (R,R,R)-phosphoramide-PE as a chiral ligand.

Graphical abstract: Synthesis of tetracyclic indolin-3-ones through Pd-catalyzed intramolecular deacetylative dearomatization of 3-acetoxy-indoles

Supplementary files

Article information

Article type
Paper
Submitted
05 Apr 2019
Accepted
29 Apr 2019
First published
07 May 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 13959-13967

Synthesis of tetracyclic indolin-3-ones through Pd-catalyzed intramolecular deacetylative dearomatization of 3-acetoxy-indoles

R. Liang, K. Wang, L. Song, W. Sheng and Y. Jia, RSC Adv., 2019, 9, 13959 DOI: 10.1039/C9RA02569C

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