Issue 38, 2014

A simple and sustainable tetrabutylammonium fluoride (TBAF)-catalyzed synthesis of azaarene-substituted 3-hydroxy-2-oxindoles through sp3 C–H functionalization

Abstract

A green, practical, and metal-free protocol for direct addition of α-and γ-alkylazaarenes to isatins has been developed via sp3 C–H functionalization in water under controlled microwave radiation. This methodology provides a mild and fast route to biologically important azaarene-substituted 3-hydroxy-2-oxindoles in good to excellent yields.

Graphical abstract: A simple and sustainable tetrabutylammonium fluoride (TBAF)-catalyzed synthesis of azaarene-substituted 3-hydroxy-2-oxindoles through sp3 C–H functionalization

Supplementary files

Article information

Article type
Paper
Submitted
05 Dec 2013
Accepted
08 Apr 2014
First published
16 Apr 2014

RSC Adv., 2014,4, 19789-19793

Author version available

A simple and sustainable tetrabutylammonium fluoride (TBAF)-catalyzed synthesis of azaarene-substituted 3-hydroxy-2-oxindoles through sp3 C–H functionalization

K. Kumari, B. K. Allam and K. N. Singh, RSC Adv., 2014, 4, 19789 DOI: 10.1039/C3RA47332E

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