A rapid construction of the ABC tricyclic skeleton of malabanone A†
Xingang
Xie 
*a
and
Xuegong
She
a
*a
and
Xuegong
She
a
Abstract
The construction of the ABC tricyclic skeleton of malabanone A with the required 4 stereocenters was accomplished in a concise route starting from R-carvone. The synthesis featured an intramolecular [3 + 2] cycloaddition reaction to assemble its A ring and an intramolecular Diels–Alder reaction to construct its C ring.
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