Answers are grounded in this paper and cite their sources.
A convergent synthesis of (+)-SCH 351448 (1), a monosodium salt of a C(2)-symmetric macrodiolide, is described. Our approach is based on a [4 + 2] annulation with a chiral allyl silane (anti-5c) to assemble the pyran subunits. Homodimerization was carried out in a stepwise fashion; initial esterification at C29' followed by macrocyclization at C29 afforded the desired macrodiolide.
No takes yet. Share an insight, caveat, or question.
Zhu et al. (2011) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: