This is the authors' abstract. We don't add key points for this paper.
The first total synthesis of (−)-euxanmodin B is described. An axially chiral, enantiomerically pure biphenyl, available by enzymatic desymmetrization of σ-symmetric biaryl diacetate, was used as the key chiral biaryl building block. Two annulation reactions allowed the construction of the xanthone–anthraquinone composite structure with full stereochemical control.
No takes yet. Share an insight, caveat, or question.
Takahashi et al. (2011) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: