Late-stage C–H amination of abietane diterpenoids

This study aims at highlighting the synthetic versatility of the rhodium-catalyzed C–H amination reactions using iodine(III) oxidants for the late-stage functionalization of natural products. Inter- and intramolecular nitrene insertions have been performed from various abietane diterpenoids, leading to the amination of the C-3, C-6, C-7, C-11 and C-15 positions. Ca. 20 aminated compounds have been isolated with yields of up to 86% and high levels of regio-, chemo- and stereoselectivities.

Références

Titre
Late-stage C–H amination of abietane diterpenoids
Type de publication
Article de revue
Année de publication
2019
Revue
Org. Biomol. Chem.
Volume
17
Ticket
19
Start Page
4736
Pagination
4736-4746
Date de publication
03/2019
Soumis le 28 mars 2019