Ontology highlight
ABSTRACT:
SUBMITTER: Barton NA
PROVIDER: S-EPMC6005263 | biostudies-literature | 2016 May
REPOSITORIES: biostudies-literature
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]