99794-41-9Relevant academic research and scientific papers
One-step Synthesis of Tricyclo3,8>undecan-4,11-diones by Three Consecutive Michael Reactions. A Formal Synthesis of (+/-)-Seychellene
Hagiwara, Hisahiro,Okano, Akihiro,Uda, Hisashi
, p. 1047 (1985)
Divinylketone and the trimethylsilyl enol ethers of cyclohex-2-en-1-ones undergo Lewis acid assisted triple Michael reactions yielding tricyclo3,8>undecan-4,11-diones; the application of this reaction enabled a formal synthesis of (+/-)
One-pot Annulation to Tricyclo3,8>undecane-2,6-diones by Sequential Three-fold Michael Reactions. A Formal Synthesis of (+/-)-Seychellene
Hagiwara, Hisahiro,Okano, Akihiro,Uda, Hisashi
, p. 2109 - 2113 (2007/10/02)
Lewis acid-assisted triple Michael reactions yield tricyclo3,8>undecane-2,6-dione derivatives from the trimethylsilyl enol ethers of cyclohex-2-enones and divinyl ketone.The application of this reaction allowed a formal synthesis of (+/-)-seychellene.
