| The Neber route to substituted indoles. | |
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MedLine Citation:
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PMID: 16433505 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Two complementary procedures have been developed for the conversion of the oximes of alpha-aryl ketones to azirines. On heating, the azirines rearrange smoothly to the corresponding indoles. The overall transformation offers a versatile route to indoles, complementary to the Fischer indole synthesis. |
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Authors:
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Douglass F Taber; Weiwei Tian |
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Publication Detail:
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Type: Journal Article; Research Support, N.I.H., Extramural |
Journal Detail:
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Title: Journal of the American Chemical Society Volume: 128 ISSN: 0002-7863 ISO Abbreviation: J. Am. Chem. Soc. Publication Date: 2006 Feb |
Date Detail:
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Created Date: 2006-01-25 Completed Date: 2006-04-13 Revised Date: 2012-01-17 |
Medline Journal Info:
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Nlm Unique ID: 7503056 Medline TA: J Am Chem Soc Country: United States |
Other Details:
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Languages: eng Pagination: 1058-9 Citation Subset: IM |
Affiliation:
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Department of Chemistry and Biochemistry, University of Delaware, Newark, 19716, USA. taberdf@udel.edu |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Indoles
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chemical synthesis* Ketones / chemistry Oximes / chemistry |
| Grant Support | |
ID/Acronym/Agency:
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GM 60287/GM/NIGMS NIH HHS; R01 GM060287-08/GM/NIGMS NIH HHS |
| Chemical | |
Reg. No./Substance:
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0/Indoles; 0/Ketones; 0/Oximes |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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