Our??paper entitled “Enantioselective Biomimetic Total Syntheses of Kuwanons I and J and?Brosimones A and B” has been published on Angew. Chem. Int. Ed. 2014, DOI:anie.201404499 Abstract: The first enantioselective total syntheses of prenylflavonoid Diels-Alder natural products (-)-kuwanon I, (+)-kuwanon J, (-)-brosimone A and (-)-brosimone B have been accomplished based on a concise synthetic strategy. Key […]
Abstract: The first enantioselective total syntheses of prenylflavonoid Diels-Alder natural products (-)-kuwanon I, (+)-kuwanon J, (-)-brosimone A and (-)-brosimone B have been accomplished based on a concise synthetic strategy. Key elements of the synthesis include a biosynthesis-inspired asymmetric Diels-Alder cycloaddition mediated by a chiral VANOL-boron Lewis acid, as well as a process involving regioselective Schenck ene reaction, reduction and dehydration to realize a biomimetic dehydrogenation for generation of the required diene precursor. Furthermore, a remarkable tandem inter-/intramolecular asymmetric Diels-Alder cycloaddition process was applied for the synthesis of brosimone A.