| Literature DB >> 20684519 |
Amie M Stewart1, Kathrin Meier, Barbara Schulz, Michael Steinert, Barry B Snider.
Abstract
Dinemasone C was prepared in three steps (8% overall yield) from cis-tetrahydro-4-hydroxy-6-methyl-2-pyrone by aldol reaction with 2,4-hexadienal, epoxidation followed by cyclization, and epimerization of the ring fusion. Dinemasone C, epi-dinemasone C, anhydrodinemasone BC, and nor-dinemasone B are active against bacteria, including Legionella pneumophila Corby, algae, and fungi.Entities:
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Year: 2010 PMID: 20684519 PMCID: PMC2975019 DOI: 10.1021/jo101408s
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354