Issue 18, 2018

Rh-Catalyzed regioselective C–H activation and C–C bond formation: synthesis and photophysical studies of indazolo[2,3-a]quinolines

Abstract

Rh(III)-Catalyzed regioselective C–H functionalization of 2-aryl-2H-indazoles with alkynes is reported to furnish indazoloquinolines utilizing Cu(OAc)2·H2O as an oxidant, which facilitates the reductive elimination step. Kinetic isotope studies suggest that C–H activation is presumably the product determining step. The products display a strong blue emission with high quantum yields.

Graphical abstract: Rh-Catalyzed regioselective C–H activation and C–C bond formation: synthesis and photophysical studies of indazolo[2,3-a]quinolines

Supplementary files

Article information

Article type
Research Article
Submitted
06 Jun 2018
Accepted
11 Jul 2018
First published
11 Jul 2018

Org. Chem. Front., 2018,5, 2630-2635

Rh-Catalyzed regioselective C–H activation and C–C bond formation: synthesis and photophysical studies of indazolo[2,3-a]quinolines

S. Vivek Kumar, S. Ellairaja, V. Satheesh, V. Sivasamy Vasantha and T. Punniyamurthy, Org. Chem. Front., 2018, 5, 2630 DOI: 10.1039/C8QO00557E

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