Halogenation of thiocarboxylic acid 0-silyl esters gave acylsulfenyl halides in high yields, involving a thiophilic attack of halogen ion on the sulfur atom of thiocarbonyl group. Aliphatic acylsulfenyl bromide was isolated for the first time. In spite of the easy availability of thiocarboxylic aci
โฆ LIBER โฆ
Surface-Mediated Hydrohalogenation of Isoprene: A Facile Preparation of Prenyl Halides.
โ Scribed by Marcio C. S. de Mattos; Antonio Manzolillo Sanseverino
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 69 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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