Selective oxidation of optically active sec,sec-1,2-diols by dioxiranes. A practical method for the synthesis of homochiral alpha-hydroxy ketones in high optical purity
Academic Article
Publication Date:
1993
abstract:
By employing either dimethyldioxirane or its trifluoromethyl analog, the direct, high-yield conversion of one cyclic and three open chain optically sec,sec-1,2-diols to the corresponding alpha-hydroxy ketones in high optical yield has been achieved
Iris type:
01.01 Articolo in rivista
Keywords:
Catalyzed asymmetric dihydroxylation; enantioselective synthesis; methyl(trifluoromethyl)dioxirane; alcohols
List of contributors:
Fusco, Caterina
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