In previous work we have reported that Grignard reagents are readily prepared by magnesium bromide capture of the anion produced from the sodium naphthalene reduction of organic halides. 1 The resultant Grignard can be reacted by conventional reagents including organometallic halides to give other
Reactions of aromatic radical anions. X. Syntheses using a conveniently recoverable radical anion precursor
โ Scribed by Shelton Bank; Matthew Platz
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 183 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
In the past few years the high selectivity and yields of radical anion syntheses have found value for the cleavage of tosylates la and sulfonamideslb , preparation of alcoholslc, aminesld, anionsle, olefins'f'g, strained cyclic compoundslh, Grignard reagentsli, organo-
๐ SIMILAR VOLUMES
The reactions of oxide radical anions (O(-.)) with benzene and toluene under atmospheric pressure (APCI) and conventional chemical ionization (CI) conditions were compared. Hydrogen radical (H(-)) displacement by oxygen, yielding [M - H + O](-), was observed in both the APCI and the CI source. Howev