Enantioselective Synthesis of (−)-Acetylapoaranotin

نویسندگان

  • Haoxuan Wang
  • Clinton J Regan
  • Julian A Codelli
  • Paola Romanato
  • Angela L A Puchlopek-Dermenci
  • Sarah E Reisman
چکیده

The first enantioselective total synthesis of the epipolythiodiketopiperazine (ETP) natural product (-)-acetylapoaranotin (3) is reported. The concise synthesis was enabled by an eight-step synthesis of a key cyclohexadienol-containing amino ester building block. The absolute stereochemistry of both amino ester building blocks used in the synthesis is set through catalytic asymmetric (1,3)-dipolar cycloaddition reactions. The formal syntheses of (-)-emethallicin E and (-)-haemotocin are also achieved through the preparation of a symmetric cyclohexadienol-containing diketopiperazine.

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عنوان ژورنال:

دوره 19  شماره 

صفحات  -

تاریخ انتشار 2017