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• W2031439447 abstract "Abstract Electrochemical oxidation of 2,4‐dimethylphenol directly provides pentacyclic systems being generated by an oxidative trimerization. The major pentacyclic scaffold is exclusively formed as a single diastereoisomer and is easily isolated. Three further pentacyclic compounds which occur in minor quantities were also fully characterized including their solid‐state structures. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)" @default.
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• W2031439447 date "2005-12-14" @default.
• W2031439447 modified "2023-10-18" @default.
• W2031439447 title "Facile and Highly Diastereoselective Formation of a Novel Pentacyclic Scaffold by Direct Anodic Oxidation of 2,4‐Dimethylphenol" @default.
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• W2031439447 doi "https://doi.org/10.1002/ejoc.200500517" @default.
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