A tandem Baylis-Hillman-singlet oxygen oxidation reaction for facile synthesis of γ-substituted γ-hydroxybutenolides

Santoshkumar N. Patil; Benjamin E. Stephens; Fei Liu

doi:10.1016/j.tet.2008.09.019

A tandem Baylis-Hillman-singlet oxygen oxidation reaction for facile synthesis of γ-substituted γ-hydroxybutenolides

Santoshkumar N. Patil, Benjamin E. Stephens, Fei Liu^*

^*Corresponding author for this work

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

10 Citations (Scopus)

Abstract

A series of highly functionalised γ-hydroxyacryl γ-hydroxybutenolides, 2, were synthesised in 25-50% overall yields in two or three steps from 2-furfural using a tandem Baylis-Hillman-singlet oxygen oxidation reaction. Crown

Original language	English
Pages (from-to)	10831-10836
Number of pages	6
Journal	Tetrahedron
Volume	64
Issue number	48
DOIs	https://doi.org/10.1016/j.tet.2008.09.019
Publication status	Published - 24 Nov 2008

Access to Document

10.1016/j.tet.2008.09.019

Cite this

@article{a1dcd58a28fd4439a7283f651e2560f1,

title = "A tandem Baylis-Hillman-singlet oxygen oxidation reaction for facile synthesis of γ-substituted γ-hydroxybutenolides",

abstract = "A series of highly functionalised γ-hydroxyacryl γ-hydroxybutenolides, 2, were synthesised in 25-50% overall yields in two or three steps from 2-furfural using a tandem Baylis-Hillman-singlet oxygen oxidation reaction. Crown",

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

year = "2008",

month = nov,

day = "24",

doi = "10.1016/j.tet.2008.09.019",

language = "English",

volume = "64",

pages = "10831--10836",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier",

number = "48",

}

TY - JOUR

T1 - A tandem Baylis-Hillman-singlet oxygen oxidation reaction for facile synthesis of γ-substituted γ-hydroxybutenolides

AU - Patil, Santoshkumar N.

AU - Stephens, Benjamin E.

AU - Liu, Fei

PY - 2008/11/24

Y1 - 2008/11/24

N2 - A series of highly functionalised γ-hydroxyacryl γ-hydroxybutenolides, 2, were synthesised in 25-50% overall yields in two or three steps from 2-furfural using a tandem Baylis-Hillman-singlet oxygen oxidation reaction. Crown

AB - A series of highly functionalised γ-hydroxyacryl γ-hydroxybutenolides, 2, were synthesised in 25-50% overall yields in two or three steps from 2-furfural using a tandem Baylis-Hillman-singlet oxygen oxidation reaction. Crown

UR - http://www.scopus.com/inward/record.url?scp=53449099984&partnerID=8YFLogxK

U2 - 10.1016/j.tet.2008.09.019

DO - 10.1016/j.tet.2008.09.019

M3 - Article

AN - SCOPUS:53449099984

VL - 64

SP - 10831

EP - 10836

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 48

ER -

A tandem Baylis-Hillman-singlet oxygen oxidation reaction for facile synthesis of γ-substituted γ-hydroxybutenolides

Abstract

Access to Document

Other files and links

Fingerprint

Cite this