Backbone Rearrangement of 3β,4β-Epoxyfriedelane. A Formation of Germanicol and Solvent Effects
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/50/12/50_12_3381/_pdf
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1. Approaches to the synthesis of triterpenoids. I. Methyl group migration to the 9β-position in steroids as a route to the cucurbitacins. A possible structural feature directing epoxide cleavage rearrangements
2. The Backbone Rearrangement of 3β,4β-Epoxyfriedelane and the Synthesis of Dendropanoxide
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