Tandem Oxidation Processes: The Direct Conversion of Activated Alcohols into Oximes; Synthesis of Citaldoxime
Abstract The direct conversion of primary alcohols into oximes is reported using manganese dioxide and alkoxylamines/hydroxylamine as their hydrochloride salts or supported on Amberlyst 15. This transformation has been applied to a range of benzylic, allylic and propargylic alcohols and utilised to...
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Veröffentlicht in: | Synlett 2002, Vol.2002 (8), p.1287-1290 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Abstract
The direct conversion of primary alcohols into oximes is reported
using manganese dioxide and alkoxylamines/hydroxylamine
as their hydrochloride salts or supported on Amberlyst 15. This
transformation has been applied to a range of benzylic, allylic and
propargylic alcohols and utilised to prepare the natural product citaldoxime. |
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ISSN: | 0936-5214 1437-2096 |
DOI: | 10.1055/s-2002-32949 |