A short synthesis of aphanamol I in both racemic and enantiopure forms

A short synthesis of aphanamol I in both racemic and enantiopure forms

A short synthesis of the biologically active sesquiterpene natural product (+)-aphanamol I in both racemic and enantiopure forms is reported. Key steps include: a catalytic enantioselective conjugate addition, an oxidative radical cyclisation, and a ringexpanding Claisen rearrangement.

Opis bibliograficzny
Główni autorzy:	Burton, J, Ferrara, S
Format:	Journal article
Wydane:	Wiley 2016

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