Chen Zhu1, J R Falck. 1. Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA. chen.zhu@utsouthwestern.edu
Abstract
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.
A tandem C-H olefination/annulation sequence directed by n class="Chemical">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.
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