Abstract
(±)-Hongoquercin A (1), the racemate of an antibacterial fungal metabolite, has been synthesized starting from geranylacetone (2) and ethyl orsellinate (ethyl 2,4-dihydroxy-6-methylbenzoate, 5). The structure (±)-1 has been confirmed by X-ray analysis of its ethyl ester (±)-10. Synthesis of the naturally occurring (+)-hongoquercin A from (-)-sclareol (11) established its configuration as depicted in 1.
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Tsujimori, H., Bando, M., & Mori, K. (2000). Synthetic microbial chemistry, XXXII[≠] synthesis and absolute configuration of hongoquercin A, an antibacterial sesquiterpene-substituted orsellinic acid isolated as a fungal metabolite. European Journal of Organic Chemistry, (2), 297–302. https://doi.org/10.1002/(sici)1099-0690(200001)2000:2<297::aid-ejoc297>3.0.co;2-b
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