Base-assisted regio- and diastereoselective conversion of functionalized furans to butenolides using singlet oxygen

Santoshkumar N. Patil; Fei Liu

doi:10.1021/ol062551l

Base-assisted regio- and diastereoselective conversion of functionalized furans to butenolides using singlet oxygen

Santoshkumar N. Patil, Fei Liu^*

^*Corresponding author for this work

Department of Molecular Sciences

Research output: Contribution to journal › Article

33 Citations (Scopus)

Abstract

(Chemical Equation Presented) A facile synthesis of β-functionalized γ-hydroxybutenolides was achieved using a Baylis-Hillman reaction followed by singlet oxygen oxidation. The conversion from 3-furfural was regio- and diastereoselective.

Original language	English
Pages (from-to)	195-198
Number of pages	4
Journal	Organic Letters
Volume	9
Issue number	2
DOIs	https://doi.org/10.1021/ol062551l
Publication status	Published - 18 Jan 2007

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title = "Base-assisted regio- and diastereoselective conversion of functionalized furans to butenolides using singlet oxygen",

abstract = "(Chemical Equation Presented) A facile synthesis of β-functionalized γ-hydroxybutenolides was achieved using a Baylis-Hillman reaction followed by singlet oxygen oxidation. The conversion from 3-furfural was regio- and diastereoselective.",

author = "Patil, {Santoshkumar N.} and Fei Liu",

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N2 - (Chemical Equation Presented) A facile synthesis of β-functionalized γ-hydroxybutenolides was achieved using a Baylis-Hillman reaction followed by singlet oxygen oxidation. The conversion from 3-furfural was regio- and diastereoselective.

AB - (Chemical Equation Presented) A facile synthesis of β-functionalized γ-hydroxybutenolides was achieved using a Baylis-Hillman reaction followed by singlet oxygen oxidation. The conversion from 3-furfural was regio- and diastereoselective.

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