| Literature DB >> 31233670 |
Daniel Hernández-Guerra1, Anna Hlavačková1, Chiranan Pramthaisong1, Ilaria Vespoli1, Radek Pohl1, Tomáš Slanina1, Ullrich Jahn1.
Abstract
A mild, atom-economic, and metal-free α-C-H amination of ethers using relatively stable nonafluorobutanesulfonyl (nonaflyl, Nf) azide as the aminating reagent to give N-sulfonyl hemiaminals is reported. This enables unprecedented C(sp3 ) difunctionalization reactions, leading to diverse functionalized amino group containing compounds starting from simple ethers in one pot.Entities:
Keywords: C−H activation; amination; photoreactions; radicals; sulfonyl azides
Year: 2019 PMID: 31233670 DOI: 10.1002/anie.201905209
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336