1267588-45-3Relevant academic research and scientific papers
Rhodium catalyzed synthesis of isoindolinones via C-H activation of N-benzoylsulfonamides
Zhu, Chen,Falck, John R.
, p. 9192 - 9199 (2012/10/29)
An efficient approach to a wide range of isoindolinones, including 3-monosubstituted and 3,3-disubstituted isoindolinones, from the annulation of N-benzoylsulfonamides with olefins and diazoacetate has been developed. The transformation is broadly compatible with both terminal and internal olefins. Moreover, diazoacetate is for the first time incorporated into an amide-directed C-H functionalization reaction. Specifically, the rhodium complex [{RhCl 2Cp*}2] enables the in situ dimerization of diazoacetate in addition to its role in catalyzing C-H functionalization/cross- coupling.
N -acylsulfonamide assisted tandem C-H olefination/annulation: Synthesis of isoindolinones
Zhu, Chen,Falck
, p. 1214 - 1217 (2011/05/02)
A tandem C-H olefination/annulation sequence directed by N-acylsulfonamides affords a variety of isoindolinones. This transformation is compatible with aliphatic alkenes as well as conjugated alkenes. Notably, molecular oxygen can be used as the sole, eco-friendly oxidant.(Figure Presented)
