Enantioselective Synthesis of Both the Enantiomers of Jasmine Ketolactone and Its Epimer

Biosci Biotechnol Biochem. 1999;63(6):1122-4. doi: 10.1271/bbb.63.1122.

Abstract

The enantioselective synthesis of jasmine ketolactone 1, which was isolated as a component of Italian jasmine oil, and its epimer 2 is described. Lactones 1 and 2 were synthesized in 5 and 4 steps, respectively, by Yamaguchi's macrolactonization method from alcohol 4.

Keywords: Jasminum grandiflorum L.; jasmine ketolactone; macrolactonization; potato tuberization.