This project designs an innovative approach towards the synthesis of Amaryllidaceae alkaloids (AAs), and other biologically active isoquinoline derivatives with the isocarbostyril scaffold. The strategy for accessing this exceptional class of secondary metabolites hinges on the development of a unique Pd-catalyzed cross-coupling / allylic isomerization sequence leading to the precursor of a highly reactive isoquinoline radialene. Subsequent Diels-Alder reaction will then provide facile access to the projected analogs. Biological evaluation of prepared alkaloids and their unnatural derivatives will also be carried out.
Číslo: GAUK362421
Období: 01.01.2021 - 31.12.2023
Poskytovatel: Univerzita Karlova - Grantová agentura UK
Hlavní řešitel: Perdomo Stefanie Magela, M.Sc., Ph.D. - Farmaceutická fakulta v Hradci Králové
Celkový objem financí: 800 000,00 Kč