Figure 1: Representative natural products containing benzoxa[3.2.1]octane skeleton and approaches to it. | Nature Communications

Figure 1: Representative natural products containing benzoxa[3.2.1]octane skeleton and approaches to it.

From: Tandem C–H oxidation/cyclization/rearrangement and its application to asymmetric syntheses of (−)-brussonol and (−)-przewalskine E

Figure 1

(a) Selected bioactive natural products having benzoxa[3.2.1]octane skeleton. (b) Previous methods for construction of benzoxa[3.2.1]octane skeleton. (c) Our synthetic proposal via a tandem C–H oxidation/cyclization/rearrangement reaction.

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