Abstract
Aucubin, a natural iridoid widely extracted from Aucuba japonica presents a strong interest as semisynthetic raw substantial, thanks to its numerous features. In this study, we describe an unprecedented reaction between trimethylsilyldiazomethane and the aldehyde-derived aucubin (3a) leading to different original non-natural skeletons exemplified by the tricyclic compounds 6 and 9 (Figure 1). The influence of catalysts, solvents and temperature on the formation of the products together with the hydrolysis of enoxysilane 4 will be presented. © ARKAT-USA, Inc.
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Lemus, C., Koch, M., Michel, S., & Deguin, B. (2014). Influence of solvents and catalysts on the formation and hydrolysis of polyfunctional enoxysilanes derived from aucubin. Arkivoc, 2014(3), 184–196. https://doi.org/10.3998/ark.5550190.p008.499
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