Lewis acid-mediated displacements of alkoxydioxolanes: Synthesis of a 1,2-dioxolane natural product

Patrick H. Dussault; Xuejun Liu

doi:10.1021/ol990954y

Lewis acid-mediated displacements of alkoxydioxolanes: Synthesis of a 1,2-dioxolane natural product

Patrick H. Dussault, Xuejun Liu

Chemistry

Research output: Contribution to journal › Article › peer-review

33 Scopus citations

Abstract

(formula presented) Addition of electron-rich alkenes to the peroxycarbenium ions derived from Lewis acid-mediated ionization of 3-alkoxy-1,2-dioxolanes provides natural product related to the plakinic acids.

Original language	English (US)
Pages (from-to)	1391-1393
Number of pages	3
Journal	Organic Letters
Volume	1
Issue number	9
DOIs	https://doi.org/10.1021/ol990954y
State	Published - Nov 4 1999

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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title = "Lewis acid-mediated displacements of alkoxydioxolanes: Synthesis of a 1,2-dioxolane natural product",

abstract = "(formula presented) Addition of electron-rich alkenes to the peroxycarbenium ions derived from Lewis acid-mediated ionization of 3-alkoxy-1,2-dioxolanes provides natural product related to the plakinic acids.",

author = "Dussault, {Patrick H.} and Xuejun Liu",

year = "1999",

month = nov,

day = "4",

doi = "10.1021/ol990954y",

language = "English (US)",

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journal = "Organic Letters",

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AB - (formula presented) Addition of electron-rich alkenes to the peroxycarbenium ions derived from Lewis acid-mediated ionization of 3-alkoxy-1,2-dioxolanes provides natural product related to the plakinic acids.

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