Organocatalytic stereoselective synthesis of passifloricin A.
نویسندگان
چکیده
The enantioselective synthesis of passifloricin A has been achieved in high diastereomeric excess. The 1,3-polyol moiety was constructed by iterative proline-catalyzed sequential α-aminoxylation and Horner-Wadsworth-Emmons (HWE) olefination of aldehydes while the synthesis of lactone moiety was achieved by ring-closing metathesis (RCM).
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عنوان ژورنال:
- Organic & biomolecular chemistry
دوره 10 9 شماره
صفحات -
تاریخ انتشار 2012