Lizenz: Creative Commons Namensnennung 4.0 International PDF - Veröffentlichte Version early view (7MB) |
- URN zum Zitieren dieses Dokuments:
- urn:nbn:de:bvb:355-epub-532618
- DOI zum Zitieren dieses Dokuments:
- 10.5283/epub.53261
Es ist eine neuere Version dieses Eintrags verfügbar. |
Zusammenfassung
A two-step protocol allowing the C−H amination of cyclic ethers with iminoiodinanes, followed by the reduction of the resulting intermediate has been developed for the preparation of amino alcohols. The initial C−H functionalization is accelerated by visible light, improving the reactivity compared to the thermal process performed in the dark. The effect of different substituents on the ...