Synthesis of conjugated trienes and related oxidation products of α-farnesene

Article abstract of DOI:10.1071/CH9941979

The synthesis of conjugated trienes and related oxidation products of α-farnesene (1), principally from the epoxides of α-farnesene (1), is reported. Base-promoted ring opening of 6,7-epoxide (4) by KOBu^t/LiNPrⁱ₂ affords the conjugated triene (2), whilst the 3,4-epoxide (5) affords trienol (7). In contrast, 10,11-epoxide (6) fails to undergo epoxide ring opening; it rearranges to the conjugated triene epoxide (8). Base-promoted ring opening of bisepoxide (9) afforded trienol epoxide (11) at -30°C, whilst cyclization to tetrahydrofurans (10a,b) occurred at room temperature. Photosensitized oxidation of 10,11-epoxide (6) followed by in situ treatment with acid gave the cyclic peroxide (3) and on reduction triol (12). Bisallylic alcohol (13) was prepared by alkylation of 3-methylsulfolene with geranial. Trienes (2) and (3) have been isolated previously as autoxidation products of α-farnesene (1) and are implicated as the causal agents of superficial scald of stored apples.