Rapid construction of the ABD tricyclic skeleton in meliacarpinin B from carvone enabled by an INOC strategy

Literature Information

Publication Date 2020-06-17
DOI 10.1039/D0QO00576B
Impact Factor 5.281
Authors

Changming Dong, Tianjiao Qiao, Yi Xie, Xiao Zhang, Junli Ao, Guangxin Liang


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Abstract

A highly diastereoselective synthesis of the ABD skeleton of meliacarpinin B is presented. The construction of the key trans-decalin unit features an intramolecular nitrile oxide-alkene cycloaddtion (INOC) reaction on a readily available carvone derivative. This strategy enabled prepration of the tricyclic core bearing 6 contiguous stereogenic centres in 14 straightforward linear steps from R-carvone.

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