| Literature DB >> 24385001 |
Marco Buccini1, Kathryn A Punch, Belinda Kaskow, Gavin R Flematti, Brian W Skelton, Lawrence J Abraham, Matthew J Piggott.
Abstract
An improved synthesis of the anti-inflammatory natural product antrocamphin A (2), involving a key Castro-Stephens reaction, is presented, along with the first total synthesis of its congener antrocamphin B (3). Approaches towards the more complex co-metabolite antrodioxolanone (4) were unsuccessful, but a samarium diiodide-mediated pinacol coupling of antrocamphin B did provide the chiral epimers (51). Antrocamphin A (2) inhibits Tumour Necrosis Factor (TNF) reporter gene expression, but its development as an anti-inflammatory agent may be limited by cytotoxicity.Entities:
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Year: 2014 PMID: 24385001 DOI: 10.1039/c3ob42333f
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876