Abstract
A synthesis of cyanolide A, a diolide natural product, has been achieved using a diastereoselective Barbier reaction, early-stage glycosylation, and intramolecular oxa-Michael addition to form the THP ring. © Georg Thieme Verlag Stuttgart New York.
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APA
Bates, R. W., & Lek, T. G. (2014). A synthesis of cyanolide a by intramolecular oxa-Michael addition. Synthesis (Germany), 46(13), 1731–1738. https://doi.org/10.1055/s-0033-1341153
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