Synthetic microbial chemistry, XXXII[≠] synthesis and absolute configuration of hongoquercin A, an antibacterial sesquiterpene-substituted orsellinic acid isolated as a fungal metabolite

40Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free