Journal of Organic Chemistry 2005-04-29

A tandem Heck-carbocyclization/Suzuki-coupling approach to the stereoselective syntheses of asymmetric 3,3-(diarylmethylene)indolinones.

Wing S Cheung, Raymond J Patch, Mark R Player

Index: J. Org. Chem. 70(9) , 3741-4, (2005)

Full Text: HTML

Abstract

[reaction: see text] An efficient and versatile method for stereoselective synthesis of (E)-3,3-(diarylmethylene)indolinones by a palladium-catalyzed tandem Heck-carbocyclization/Suzuki-coupling sequence is presented. Factors influencing yield and selectivity, namely catalyst, coordinating ligand, and solvent, are detailed.

Related Compounds

Structure Name/CAS No. Articles
4-Chloro-2-iodoaniline Structure 4-Chloro-2-iodoaniline
CAS:63069-48-7