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Synlett 1998; 1998(6): 655-657
DOI: 10.1055/s-1998-1747
DOI: 10.1055/s-1998-1747
letter
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An Enantio- and Diastereocontrolled Route to Mintlactone and Isomintlactone Using A Chiral Cyclohexadienone Equivalent
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)
![](https://www.thieme-connect.de/media/synlett/199806/lookinside/thumbnails/10.1055-s-1998-1747-1.jpg)
An enantio- and diastereocontrolled route to mintlactone and isomintlactone, aroma components of important commercial flavoring materials, has been established using a chiral cyclohexadienone synthetic equivalent.
chiral cyclohexadienone - chiral building block - monoterpene - radical reaction - retro-Diels-Alder reaction