Abstract
AbstractEnantiomerically pure (S)‐2,4,4‐trimethyl‐2‐cyclohexen‐1‐ol (1) was efficiently converted into four degraded lactonic carotenoids: (S)‐dihydroactinidiolide (5), (S)‐actinidiolide (9), (6S,7aR)‐loliolide (11) and (6S,7aS)‐epiloliolide (12). (R)‐Actinidiolide (9), (6R,7aS)‐loliolide (11) and (6R,7aR)‐epiloliolide (12) were also prepared from (R)‐1.
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