Preparation and spectra of mercuribis (α-diazo ketones)
✍ Scribed by P. Yates; F.X. Garneau; J.P. Lokensgard
- Book ID
- 103402125
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 546 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4020
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📜 SIMILAR VOLUMES
Oxidation of the monohydrazones of a-diketones with yellow mercuric oxide in the presence of base is a weil-known method for the preparation of a-diazo ketones (1). Some years ago, the interestinq observation was made (2) that when this reaction was applied to I, the hydrazone of an a-ketoaldehyde,
The rational synthesis of diazocyclopentadiene by the reaction of cyclopentadienyllithium with tosyl aside designed by Doering and De Puy(1) more than a decade ago has only recently been extended to the preparation of other diazo compounds (2,3,4,5). Regitz(&,j) has reported its application
The Wolff rearrangement of a-diazo ketones to prepare homologous acids or their derivatives has not been generally applied to the preparation of B-acetoxy acids. We have attempted to use this reaction to accomplish such a transformation but find that the major products are those resulting from g-eli