Construction of a Pentacyclic Framework Enabled by Nickel Catalysis.
Naeem IqbalMuhammad Awais AshrafAnam Rana GulJaehan BaeNaila IqbalTae Jung ParkEun Jin ChoPublished in: Organic letters (2023)
We present a novel nickel-catalyzed reaction of indole-tethered 2-alkynylphenol esters with various (hetero)aryl boronic acids, resulting in the synthesis of diversely functionalized pentacyclic benzofurocyclohepta[ b ]indole derivatives. This unprecedented cascade reaction involves the arylative cyclization of alkynes, nucleophilic attack of the indole moiety on the oxonium ion intermediate, 1,2-alkyl group migration, and aromatization. The synthesized molecules exhibit exceptional cytotoxicity against multiple cancer cell lines while maintaining biocompatibility toward healthy cells.
Keyphrases
- oxide nanoparticles
- induced apoptosis
- papillary thyroid
- cell cycle arrest
- reduced graphene oxide
- squamous cell
- carbon nanotubes
- room temperature
- quantum dots
- metal organic framework
- cell death
- endoplasmic reticulum stress
- lymph node metastasis
- oxidative stress
- electron transfer
- mass spectrometry
- young adults
- high resolution
- cell proliferation
- childhood cancer
- simultaneous determination
- high density