| Ring-closing metathesis: novel routes to aromatic heterocycles. | |
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MedLine Citation:
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PMID: 18381742 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Olefin metathesis has been established as an important and general reaction in synthetic organic chemistry. Recently, it has attracted interest as a powerful tool for the construction of aromatic heterocycles. The importance of heteroaromatic motifs in medicinal chemistry and biology, as well as the efficiency and wealth of metathesis transformations, have resulted in significant success in this rapidly developing area. |
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Authors:
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Timothy J Donohoe; Lisa P Fishlock; Panayiotis A Procopiou |
Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Chemistry (Weinheim an der Bergstrasse, Germany) Volume: 14 ISSN: 0947-6539 ISO Abbreviation: Chemistry Publication Date: 2008 |
Date Detail:
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Created Date: 2008-06-26 Completed Date: 2008-09-26 Revised Date: 2009-08-04 |
Medline Journal Info:
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Nlm Unique ID: 9513783 Medline TA: Chemistry Country: Germany |
Other Details:
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Languages: eng Pagination: 5716-26 Citation Subset: IM |
Affiliation:
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Chemistry Research Laboratory, University of Oxford, Oxford, OX1 3TA UK. timothy.donohoe@chem.ox.ac.uk |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Alkenes
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chemistry* Chemistry, Organic / methods* Cyclization Furans / chemical synthesis Heterocyclic Compounds / chemical synthesis* Hydrocarbons, Aromatic / chemical synthesis* Indoles / chemical synthesis Models, Chemical Pyridines / chemical synthesis Pyrroles / chemical synthesis Stereoisomerism |
| Chemical | |
Reg. No./Substance:
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0/Alkenes; 0/Furans; 0/Heterocyclic Compounds; 0/Hydrocarbons, Aromatic; 0/Indoles; 0/Pyridines; 0/Pyrroles |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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