The reaction of triphenylphosphinemethylenes with lithium aluminum hydride
โ Scribed by Martin Saunders; Grace Burchman
- Publisher
- Elsevier Science
- Year
- 1959
- Tongue
- French
- Weight
- 96 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
ALTHOUGH triphenylphoaphineacylmethylenea have been known for some time,' Wittig'e recent preparation of the simpler analoge has been of interest because of their eynthetio utility.2 We wish to report a new reaction which these compounds undergo on treatment with lithium aluminum hydride, When the triphenylphosphinemethylenee, (C6H5)3P-CHR: (I) R=H, (II) R= COCH3, (III) R-COC6H5, (IV) R=COC(CH3)2COCH(CH3)2 3
๐ SIMILAR VOLUMES
THE reduction of ketoximas and aldoximes with lithium aluminum hydride (LAH) has been reported in numerous instances to give the corresponding primary amine. 1 However, in the reduction of cyclodecanone oxime 2 and in the reduction of certain aryl ketoximes 3 the primary amine was accompanied by an
Although the rearrangement which occurs on reduction of aranat~c ketoximes with lithium aluminum hydride (equation la) Is well known, 192 the reductive rearrangement of aromatic aldoximes under similar conditions (equation lb) has not been reported, despite the fact that a mznber of aldoximes have b