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Synthesis of (.+-.)-illudol

MF Semmelhack, S Tomoda…

文献索引:Semmelhack, M.F.; Tomoda, Shuji; Hurst, K.M. Journal of the American Chemical Society, 1980 , vol. 102, # 25 p. 7567 - 7568

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被引用次数: 28

摘要

Sir: Among natural sesquiterpene alcohols, those possessing the A6-protoilludane skeleton (1) have attracted attention as synthesis targets because of the unique methylene- cyclobutane structural feature.'Illudol (2), a member of this class, has recently been obtained by total synthesis2 Fomannosin (3) has been shown to arise through protoilludane precursors in nature3 and has not yet been successfully~ ynthesized.~ The relation ...