posted on 2015-03-18, 00:00authored byArtem Shvartsbart, Amos B. Smith
Presented
here is a full account on the development of a strategy
culminating in the first total synthesis of the architecturally complex
daphniphyllum alkaloid, (−)-calyciphylline N. Highlights
of the approach include a highly diastereoselective, intramolecular
Diels–Alder reaction of a silicon-tethered acrylate; an efficient
Stille carbonylation of a sterically encumbered vinyl triflate;
a one-pot Nazarov cyclization/proto-desilylation sequence;
and the chemoselective hydrogenation of a fully substituted
diene ester.