Answers are grounded in this paper and cite their sources.
[structure: see text] An efficient total synthesis of the annonaceous acetogenin jimenezin was achieved. The key steps used were a highly stereoselective intramolecular allylboration to establish the tetrahydropyran ring and an intramolecular Williamson reaction to close the tetrahydrofuran ring.
No takes yet. Share an insight, caveat, or question.
Bandur et al. (2006) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: