Universal access to megastigmanes through controlled cyclisation towards highly substituted cyclohexenes

作者:Gonzalez Delgado Jose A; Romero Miguel A; Pischel Uwe; Arteaga Jesus F*
来源:Organic and Biomolecular Chemistry, 2017, 15(2): 408-415.
DOI:10.1039/c6ob02587k

摘要

We report the selective formation of cyclohexenes with a tetrasubstituted double bond, the structural key element of megastigmanes. For this purpose the ZrCl4-mediated epoxide ring opening of epoxy-geranylacetone was employed. This approach provides a universal entry to the preparation of the members of the megastigmane family, which was exemplified in the asymmetric synthesis of tectoionol B.

  • 出版日期2017-1-14

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