Lewis Acid-Mediated Displacements of Alkoxydioxolanes: Synthesis of a 1,2-Dioxolane Natural Product
摘要:
[GRAPHICS]Addition of electron-rich alkenes to the peroxycarbenium ions derived from Lewis acid-mediated ionization of 8-alkoxy-1,2-dioxolanes provides an efficient route for the synthesis of substituted 1,2-dioxolanes. The methodology is illustrated with a rapid synthesis of a 1,2-dioxolane natural product related to the plakinic acids.
Lewis Acid-Mediated Displacements of Alkoxydioxolanes: Synthesis of a 1,2-Dioxolane Natural Product
作者:Patrick H. Dussault、Xuejun Liu
DOI:10.1021/ol990954y
日期:1999.11.1
[GRAPHICS]Addition of electron-rich alkenes to the peroxycarbenium ions derived from Lewis acid-mediated ionization of 8-alkoxy-1,2-dioxolanes provides an efficient route for the synthesis of substituted 1,2-dioxolanes. The methodology is illustrated with a rapid synthesis of a 1,2-dioxolane natural product related to the plakinic acids.
Dai, Peng; Dussault, Patrick H.; Trullinger, Tony K., Journal of Organic Chemistry, 2004, vol. 69, # 8, p. 2851 - 2852
作者:Dai, Peng、Dussault, Patrick H.、Trullinger, Tony K.