Construction of “normal”- and “iso-type” oxazolidine rings in C<sub>20</sub>-diterpenoid alkaloids: Oxidative cyclization with potassium ferricyanide期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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Construction of “normal”- and “iso-type” oxazolidine rings in C₂₀-diterpenoid alkaloids: Oxidative cyclization with potassium ferricyanide

Authors:	SWilliam Pelletier Abdel-Monem M Ateya Naresh V Mody Haridutt K Desai Lee C Schramm

Institution:	Institute for Natural Products Research, the Department of Chemistry, and the School of Pharmacy The University of Georgia, Athens, Georgia 30602, U.S.A.

Abstract:	An efficient and simple method using alkaline ferricyanide for converting the NCH₂CH₂OH group-containing alkaloid derivatives into their “normal”- and “iso-type”-oxazolidine ring-containing alkaloids has been developed. This is the first one-step oxidation method which affords both types of oxazolidine rings simultaneously.

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