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A metathesis approach to aromatic heterocycles

Authors :
Matilda Bingham
Allan J. Orr
Katherine Gosby
Timothy J. Donohoe
Source :
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. 2005(10)
Publication Year :
2005

Abstract

The ring closing metathesis (RCM) reaction can be used to prepare substituted furans and pyrroles. By utilising a Pd-catalysed coupling reaction with methoxyallene, allylic alcohols and sulfonamides can be converted into substrates that are ideal precursors to ring closing metathesis. After the RCM reaction is complete, the addition of acid promotes an elimination of methanol to form the fully aromatised system. A range of different substitution patterns and functional groups are compatible with this sequence. Double allene coupling, RCM and elimination reactions are also possible and allow the formation of biaryl systems. © Wiley-VCH Verlag GmbH and Co. KGaA, 69451 Weinheim, Germany, 2005.

Details

ISSN :
10990690 and 1434193X
Volume :
2005
Issue :
10
Database :
OpenAIRE
Journal :
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Accession number :
edsair.doi.dedup.....5d87899d3cdd54682d3de9d98ac7049f