jacobsro
Faglige interesser
- Legemiddelkjemi
- Organisk syntese
- Naturproduktsyntese
Undervisning
Bakgrunn
- Avdelingsingeniør, Farmasøytisk institutt, seksjon for legemiddelkjemi, Universitetet i Oslo, 2025 -
- Siv.ing. i kjemi (syntetisk organisk kjemi), Norges Teknisk-Naturvitenskapelig Universitet, 2019 - 2025
Emneord:
Legemiddelkjemi,
Organisk kjemi,
Syntetisk organisk kjemi,
Naturproduktsyntese,
Kjemikaliehåndtering,
Laboratoriesikkerhet
Publikasjoner
-
Rolfsen, Jacob Strand; Cherukupalli, Srinivasulu; Sundby, Eirik & Hoff, Bård Helge
(2026).
Triazole-Functionalized 7-Azaindoles: A synthetic Study Using Sonogashira Cross-Coupling and Copper-Catalyzed Azide-Alkyne Cycloaddition.
Fulltekst i vitenarkiv
Vis sammendrag
The majority of recently approved small-molecule drugs contain at least one nitrogen heterocycle.1 Among these, the 7-azaindole scaffold is recognized as a
kinase-privileged fragment and is featured in several commercial inhibitors, including the colony-stimulating factor 1 receptor inhibitor Pexidartinib.2 Likewise,
1,2,3-triazoles have emerged as significant motifs in drug discovery due to their ease of synthesis and broad pharmacological activity.3,4 Combining structural
features of Pexidartinib and 1,2,3-triazoles, herein we outline our latest work on triazole functionalized 7-azaindoles.
Se alle arbeider i NVA
Publisert
30. jan. 2026 06:58
- Sist endret
5. mai 2026 10:48