{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Yang X"],"funding":["Ministry of Education - Singapore"],"pagination":["6424"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9614196"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13(1)"],"pubmed_abstract":["Catalyzed oxidative C-C bond coupling reactions play an important role in the chemical synthesis of complex natural products of medicinal importance. However, the poor functional group tolerance renders them unfit for the synthesis of naturally occurring polyphenolic flavones. We find that molecular oxygen in alkaline water acts as a hydrogen atom acceptor and oxidant in catalyst-free (without added catalyst) oxidative coupling of luteolin and other flavones. By this facile method, we achieve the synthesis of a small collection of flavone dimers and trimers including naturally occurring dicranolomin, philonotisflavone, dehydrohegoflavone, distichumtriluteolin, and cyclodistichumtriluteolin. Mechanistic studies using both experimental and computational chemistry uncover the underlying reaso"],"journal":["Nature communications"],"pubmed_title":["Oxygen mediated oxidative couplings of flavones in alkaline water."],"pmcid":["PMC9614196"],"funding_grant_id":["R160-000-B04-114"],"pubmed_authors":["Wu J","Huang D","Sun C","Houk KN","Kuang Y","Shi X","Tang H","Yang X","Sun M","Zhang Y","Wang T","Zhao F","Toy JYH","Lin J","Wang X","Du K","Lim SHM","Liu F","Song Z"],"additional_accession":[]},"is_claimable":false,"name":"Oxygen mediated oxidative couplings of flavones in alkaline water.","description":"Catalyzed oxidative C-C bond coupling reactions play an important role in the chemical synthesis of complex natural products of medicinal importance. However, the poor functional group tolerance renders them unfit for the synthesis of naturally occurring polyphenolic flavones. We find that molecular oxygen in alkaline water acts as a hydrogen atom acceptor and oxidant in catalyst-free (without added catalyst) oxidative coupling of luteolin and other flavones. By this facile method, we achieve the synthesis of a small collection of flavone dimers and trimers including naturally occurring dicranolomin, philonotisflavone, dehydrohegoflavone, distichumtriluteolin, and cyclodistichumtriluteolin. Mechanistic studies using both experimental and computational chemistry uncover the underlying reaso","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Oct","modification":"2026-05-28T00:36:51.506Z","creation":"2025-04-05T21:24:36.871Z"},"accession":"S-EPMC9614196","cross_references":{"pubmed":["36307433"],"doi":["10.1038/s41467-022-34123-w"]}}