A synthesis of Cyanolide A by intramolecular Oxa-Michael addition
Bates, Roderick W.
Lek, Tee Guan
Date of Issue2014
School of Physical and Mathematical Sciences
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.
DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
© 2014 Georg Thieme Verlag KG. This is the author created version of a work that has been peer reviewed and accepted for publication by Synthesis, Georg Thieme Verlag KG. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [Article DOI: http://dx.doi.org/10.1055/s-0033-1341153].