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Accessing low-oxidation state taxanes: is taxadiene-4(5)-epoxide on the taxol biosynthetic pathway?


ABSTRACT: We have shown for the first time that taxadiene (3) can be epoxidised in a regio- and diastereoselective manner to provide taxadiene-4(5)-epoxide (12) as a single diastereoisomer, and that this epoxide can be rearranged to give taxa-4(20),11(12)-dien-5?-ol (4). Furthermore, the epoxide 12 rearranges under acidic conditions to give taxa-4(20),11(12)-dien-5?-ol (4), the known bridged ether OCT (5) and the new oxacyclotaxane (OCT2) 15. Contrary to previous speculation, taxadiene-4(5)-epoxide (12) is susceptible to rearrangement when exposed to an ironIII porphyrin, and these observations justify consideration of epoxide 12 as a chemically competent intermediate on the taxol biosynthetic pathway.

SUBMITTER: Barton NA 

PROVIDER: S-EPMC6005263 | biostudies-literature | 2016 May

REPOSITORIES: biostudies-literature

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Accessing low-oxidation state taxanes: is taxadiene-4(5)-epoxide on the taxol biosynthetic pathway?

Barton Naomi A NA   Marsh Benjamin J BJ   Lewis William W   Narraidoo Nathalie N   Seymour Graham B GB   Fray Rupert R   Hayes Christopher J CJ  

Chemical science 20160126 5


We have shown for the first time that taxadiene (<b>3</b>) can be epoxidised in a regio- and diastereoselective manner to provide taxadiene-4(5)-epoxide (<b>12</b>) as a single diastereoisomer, and that this epoxide can be rearranged to give taxa-4(20),11(12)-dien-5α-ol (<b>4</b>). Furthermore, the epoxide <b>12</b> rearranges under acidic conditions to give taxa-4(20),11(12)-dien-5α-ol (<b>4</b>), the known bridged ether OCT (<b>5</b>) and the new oxacyclotaxane (OCT2) <b>15</b>. Contrary to pr  ...[more]

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