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

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

37 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",

year = "2007",

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doi = "10.1021/ol062551l",

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journal = "Organic Letters",

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T1 - Base-assisted regio- and diastereoselective conversion of functionalized furans to butenolides using singlet oxygen

AU - Patil, Santoshkumar N.

AU - Liu, Fei

PY - 2007/1/18

Y1 - 2007/1/18

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.

UR - https://www.scopus.com/pages/publications/33846569452

U2 - 10.1021/ol062551l

DO - 10.1021/ol062551l

M3 - Article

C2 - 17217263

AN - SCOPUS:33846569452

SN - 1523-7060

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SP - 195

EP - 198

JO - Organic Letters

JF - Organic Letters

IS - 2

ER -

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

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