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Synthesis of oximes, conversion to nitrile oxides and their subsequent 1,3-dipolar cycloaddition reactions under microwave irradiation and solvent-free reaction conditions

✍ Scribed by Béatrice Touaux; Françoise Texier-Boullet; Jack Hamelin


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
147 KB
Volume
9
Category
Article
ISSN
1042-7163

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✦ Synopsis


Aldoximes and ketoximes were readily synthesized from aldehydes and hydroxylamine hydrochloride on Al 2 O 3 without solvent under microwave irradiation. At higher irradiation power, aldoximes dehydrated to nitriles and ketoximes rearranged to amides. Aldoximes reacted in a one-pot reaction with Nchlorosuccinimide and alkenes or alkynes over alumina under microwave irradiation to give isoxazolines or isoxazoles.


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