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Reactions of C-silyl-substituted P-chloro ylides with carbonyl compounds

Journal Article · · J. Gen. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:5286442

C-(Trimethylsilyl)-substituted P-chloro ylides react with aldehydes and ketones with the elimination of chlorotrimethylsilane and the formation of phosphorus-containing olefins. The reactions of P-chloro ylides with aldehydes go stereoselectively and give E olefins. In the case of 2,2,2-trifluoroacetophenone a mixture of E and Z olefins is formed. Phosphorus 31 chemical shifts, coupling constants, and NMR line structure are given.

Research Organization:
Institute of Organic Chemistry, Kiev (USSR)
OSTI ID:
5286442
Journal Information:
J. Gen. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Gen. Chem. USSR (Engl. Transl.); (United States) Vol. 56:5; ISSN JGCHA
Country of Publication:
United States
Language:
English

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