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Controllable <i>Z</i>/<i>E</i>-selective synthesis of α-amino-ketoximes from <i>N</i>-nitrososulfonamides and aryl alkenes under neutral conditions

Pan‐Feng Yuan, Tao Huang, Jian He, Xie‐Tian Huang, Xiaoling Jin, Chun‐Lin Sun, Li‐Zhu Wu, Qiang Liu

2021Organic Chemistry Frontiers30 citationsDOI

Abstract

An amidoximation of alkenes with N -nitrososulfonamides enabled by triplet energy transfer under neutral conditions is presented. Both ( Z )- and ( E )-α-amino-ketoximes are selectively accessible depending on the triplet energy of the photosensitizer.

Topics & Concepts

ChemistryArylPhotosensitizerEnergy transferPhotochemistryMedicinal chemistryCombinatorial chemistryOrganic chemistryChemical physicsAlkylSynthesis and Catalytic ReactionsSulfur-Based Synthesis TechniquesCatalytic C–H Functionalization Methods
Controllable <i>Z</i>/<i>E</i>-selective synthesis of α-amino-ketoximes from <i>N</i>-nitrososulfonamides and aryl alkenes under neutral conditions | Litcius