Efficient synthetic access to a new family of highly potent bryostatin analogues via a Prins-driven macrocyclization strategy.


The step-economical synthesis of a new class of bryostatin analogues that contain the complete oxycarbocyclic core ring system of the bryostatin natural products is reported. These agents are convergently assembled via a highly efficient, functional-group-tolerant, and stereoselective Prins-driven macrocyclization. These tetrahydropyranyl B-ring analogues… (More)
DOI: 10.1021/ja8015632


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