A Short Route to the Ester (±) HomoSarkomycin via Johnson-Claisen Rearrangement

نویسندگان

  • M Saied
  • Rafik Gatri
  • Abdullah Sulaiman Al-Ayed
  • Youssef Arfaoui
  • Mohamed Moncef El Gaied
چکیده

Background α-Methylene cycloalkanones are considered of interest because of their biological activity. Herein, in this paper the synthesis of (±) HomoSarkomycine Esters was described and characterized. Methods Using Bylis-Hillman adducts, triethlorthoacetate and propanoic acid, (±) HomoSarkomycine Esters could be synthesized by smoothly Johnson-Claisen rearrangement. Results A small library of target compounds was prepared under optimized reaction conditions in moderate yields. The reaction mechanism and the DFT study have been investigated. Conclusion This methodology provides ready access to 2-hydroxymethyl-2-cyclopentenone 1a which can be served as the raw materials of the synthesis of (±) HomoSarkomycine Ester.

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عنوان ژورنال:

دوره 14  شماره 

صفحات  -

تاریخ انتشار 2017