Synthese de cetones aliphatiques encombrees : Action des organolithiens sur les dimethyl-4,4 oxazolines-2. Addition des organometalliques sur les sels de dimethyl-4,4 oxazolinium-2 |
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Authors: | C. Lion J.E. Dubois |
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Affiliation: | Laboratoire de Chimie Organique Physique de l''Université de Paris VII, associé au CNRS, 1, rue Guy de la Brosse, 75005 Paris, France |
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Abstract: | α,α-Disubstituted ketones result from the reaction of organolithium compounds with substituted 4,4-dimethyl-2-oxazolines, 4, after hydrolysis of the intermediate enamine. Alkylation of the latter also permits the synthesis of α,α,α-trisubstituted ketones. α,α-Disubstituted ketones have been prepared by addition of organometallic reagents to 4,4-dimethyl-2-oxazolinium salts, 6. The efficiency of this method has been compared to that of other currently used methods. |
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