Ruthenium-catalysed conversion of 1,4-alkynediols into pyrroles

S J Pridmore; P A Slatford; A Daniel; M K Whittlesey; J M J Williams

doi:10.1016/j.tetlet.2007.05.070

Ruthenium-catalysed conversion of 1,4-alkynediols into pyrroles

S J Pridmore, P A Slatford, A Daniel, M K Whittlesey, J M J Williams

Department of Chemistry

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76 Citations (SciVal)

Abstract

Various 1,2,5-substituted pyrroles have been synthesised from 1,4-alkynediols using a ruthenium catalysed isomerisation to give the corresponding 1,4-dicarbonyl compounds, which undergo in situ cyclisation to pyrroles in the presence of amine. (C) 2007 Published by Elsevier Ltd.

Original language	English
Pages (from-to)	5115-5120
Number of pages	6
Journal	Tetrahedron Letters
Volume	48
Issue number	29
DOIs	https://doi.org/10.1016/j.tetlet.2007.05.070
Publication status	Published - 2007

Bibliographical note

ID number: ISI:000247995900036

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10.1016/j.tetlet.2007.05.070

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title = "Ruthenium-catalysed conversion of 1,4-alkynediols into pyrroles",

abstract = "Various 1,2,5-substituted pyrroles have been synthesised from 1,4-alkynediols using a ruthenium catalysed isomerisation to give the corresponding 1,4-dicarbonyl compounds, which undergo in situ cyclisation to pyrroles in the presence of amine. (C) 2007 Published by Elsevier Ltd.",

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language = "English",

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journal = "Tetrahedron Letters",

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T1 - Ruthenium-catalysed conversion of 1,4-alkynediols into pyrroles

AU - Pridmore, S J

AU - Slatford, P A

AU - Daniel, A

AU - Whittlesey, M K

AU - Williams, J M J

N1 - ID number: ISI:000247995900036

PY - 2007

Y1 - 2007

N2 - Various 1,2,5-substituted pyrroles have been synthesised from 1,4-alkynediols using a ruthenium catalysed isomerisation to give the corresponding 1,4-dicarbonyl compounds, which undergo in situ cyclisation to pyrroles in the presence of amine. (C) 2007 Published by Elsevier Ltd.

AB - Various 1,2,5-substituted pyrroles have been synthesised from 1,4-alkynediols using a ruthenium catalysed isomerisation to give the corresponding 1,4-dicarbonyl compounds, which undergo in situ cyclisation to pyrroles in the presence of amine. (C) 2007 Published by Elsevier Ltd.

UR - https://www.scopus.com/pages/publications/34250375713

U2 - 10.1016/j.tetlet.2007.05.070

DO - 10.1016/j.tetlet.2007.05.070

M3 - Article

SN - 0040-4039

VL - 48

SP - 5115

EP - 5120

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 29

ER -

Ruthenium-catalysed conversion of 1,4-alkynediols into pyrroles

Abstract

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