New 1, 4-diketone synthesis using nitroolefins and trimethylsilyl enol ethers. A convenient regiospecific route to cyclopentenones
M Miyashita, T Yanami…
Index: Miyashita,M. et al. Journal of the American Chemical Society, 1976 , vol. 98, p. 4679 - 4681
Full Text: HTML
Citation Number: 99
Abstract
88 a All new compounds showed the expected spectra and gave satisfactory elemental analyses. b Only optimum Lewis acids are listed. C Isolated yield. d Diastereomer mixture. e Hydrochloric acid (10%) was used for hydrolytic treatment. fDouble bond isomerization product. g Mixture of double bond isomers and diastereomers. h This compound was prepared in 50% yield from 2-octanone by treatment with lithium diisopropylamide ...
Related Articles:
Domino Asymmetric Conjugate Addition–Conjugate Addition
[Miyashita, Masaaki; Awen, Bahlul Z. E.; Yoshikoshi, Akira Synthesis, 1990 , # 7 p. 563 - 564]