891491-89-7Relevant articles and documents
A highly enantioselective total synthesis of (+)-goniodiol
Tate, Edward W.,Dixon, Darren J.,Ley, Steven V.
, p. 1698 - 1706 (2008/02/11)
A high-yielding enantioselective total synthesis of the bioactive styryllactone (+)-goniodiol has been realised, starting from readily available (S)-glycidol. A key step is an oxygen-to-carbon rearrangement of a silyl enol ether linked via an anomeric cen
A total synthesis of (+)-Goniodiol using an anomeric oxygen-to-carbon rearrangement
Dixon, Darren J.,Ley, Steven V.,Tate, Edward W.
, p. 3125 - 3126 (2007/10/03)
A new route to (+)-Goniodiol 1, a potent and selective cytotoxin, is described, using a diastereoselective oxygen-to-carbon rearrangement of an anomerically linked silyl enol ether as the key step.