A stereospecific total synthesis of DL-hexahydroapoerysopine.
Da-Shu FangJun DengJianfeng ZhengWei-Dong Z LiPublished in: Chemical communications (Cambridge, England) (2022)
A stereospecific total synthesis of DL-hexahydroapoerysopine, an intriguing and historically important Apo rearrangement product of the aromatic Erythrina alkaloids bearing the all- cis ring fusion stereochemistry, was achieved via an efficient acid-mediated stereospecific skeletal rearrangement.
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