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Flexible metathesis-based approaches to highly functionalised furans and pyrroles

Abstract:
A range of differentially functionalised furans and pyrroles have been synthesised in short order by the judicious use of a ring-closing metathesis/aromatisation strategy. Two contrasting approaches are described exploiting a palladium-catalysed union of allylic alcohols and sulfonamides in one case, and a titanium mediated methylenation of homoallylic esters in another. A number of groups that are difficult to install via traditional methods were incorporated successfully. © 2007 Elsevier Ltd. All rights reserved.
Publication status:
Published

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Publisher copy:
10.1016/j.tet.2007.09.087

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Journal:
TETRAHEDRON More from this journal
Volume:
64
Issue:
5
Pages:
809-820
Publication date:
2008-01-28
DOI:
ISSN:
0040-4020


Language:
English
Keywords:
Pubs id:
pubs:40610
UUID:
uuid:efecbc58-8b59-4266-8c61-71d25fc5d22f
Local pid:
pubs:40610
Source identifiers:
40610
Deposit date:
2012-12-19
ARK identifier:

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