Journal
CHEMICAL COMMUNICATIONS
Volume 48, Issue 6, Pages 901-903Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cc16468f
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Total synthesis of antimalarial diterpenoid (+)-kalihinol A, isolated from marine sponge Acanthella sp., is achieved. This total synthesis involves regioselective alkylation of an epoxide, construction of a tetrahydropyran ring by iodo-etherification, construction of a cis-decalin ring by intramolecular Diels-Alder reaction, isomerization of cis-decalin to trans-decalin, and subsequent functionalization of the trans-decalin ring.
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