Synthesis of beta-Methoxyacrylate Natural Products Based on Box-Pd-II-Catalyzed Intermolecular Methoxycarbonylation of Alkynoles

Bis(oxazoline)-palladium(II) catalyzed carbonylation of homopropargyl alcohols afforded acyclic methoxyacrylate 2 and 6-membered lactone 3a-k in good combined yield. In the case of propargyl alcohols, 5-membered lactones 3p, 3q, 16 were obtained in moderate yields. The one-pot synthesis of kawa lactones 3a, 3r, 3s and formal synthesis of dihydroxycystothiazole A and dihydroxycystothiazole C are presented. To elucidate the stereochemistry of (+)-annularin C and (-)-annularin H, the first asymmetric syntheses of these natural products were achieved.