Oxidation of alcohols by transfer hydrogenation: driving the equilibrium with an intramolecular trap

N J Wise; J M J Williams

doi:10.1016/j.tetlet.2007.03.135

Oxidation of alcohols by transfer hydrogenation: driving the equilibrium with an intramolecular trap

N J Wise, J M J Williams

Department of Chemistry

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34 Citations (SciVal)

Abstract

Levulinic acid and its esters participate in transfer hydrogenation with a range of secondary alcohols. Reduction of the levulinate leads to cyclisation into a gamma-lactone, thereby acting as an oxidant for alcohols without the need for a large excess of reagents. (c) 2007 Elsevier Ltd. All rights reserved.

Original language	English
Pages (from-to)	3639-3641
Number of pages	3
Journal	Tetrahedron Letters
Volume	48
Issue number	21
DOIs	https://doi.org/10.1016/j.tetlet.2007.03.135
Publication status	Published - 2007

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ID number: ISI:000246708600002

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10.1016/j.tetlet.2007.03.135

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title = "Oxidation of alcohols by transfer hydrogenation: driving the equilibrium with an intramolecular trap",

abstract = "Levulinic acid and its esters participate in transfer hydrogenation with a range of secondary alcohols. Reduction of the levulinate leads to cyclisation into a gamma-lactone, thereby acting as an oxidant for alcohols without the need for a large excess of reagents. (c) 2007 Elsevier Ltd. All rights reserved.",

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T1 - Oxidation of alcohols by transfer hydrogenation: driving the equilibrium with an intramolecular trap

AU - Wise, N J

AU - Williams, J M J

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Y1 - 2007

N2 - Levulinic acid and its esters participate in transfer hydrogenation with a range of secondary alcohols. Reduction of the levulinate leads to cyclisation into a gamma-lactone, thereby acting as an oxidant for alcohols without the need for a large excess of reagents. (c) 2007 Elsevier Ltd. All rights reserved.

AB - Levulinic acid and its esters participate in transfer hydrogenation with a range of secondary alcohols. Reduction of the levulinate leads to cyclisation into a gamma-lactone, thereby acting as an oxidant for alcohols without the need for a large excess of reagents. (c) 2007 Elsevier Ltd. All rights reserved.

UR - https://www.scopus.com/pages/publications/34247263716

U2 - 10.1016/j.tetlet.2007.03.135

DO - 10.1016/j.tetlet.2007.03.135

M3 - Article

SN - 0040-4039

VL - 48

SP - 3639

EP - 3641

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 21

ER -

Oxidation of alcohols by transfer hydrogenation: driving the equilibrium with an intramolecular trap

Abstract

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