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Acyl chlorides organocadmium compounds

The most common application of organocadmium compounds has been in the preparation of ketones by reaction with acyl chlorides. A major disadvantage of the use of organocadmium reagents is the toxicity and environmental problems associated with use of cadmium, and this has limited the recent use of organocadmium reagents. [Pg.662]

The successful conversion of polystyrene-bound acyl chlorides into ketones by treatment with organocadmium compounds has also been reported (Entry 4, Table... [Pg.319]

Lithium bromide [1, 604, before references]. This halide markedly promotes the reaction of an organocadmium compound with acyl chlorides (but not with ketones). The effect was used to advantage in the synthesis of a-oxo esters.8... [Pg.399]


See other pages where Acyl chlorides organocadmium compounds is mentioned: [Pg.566]    [Pg.130]    [Pg.1443]    [Pg.253]    [Pg.389]    [Pg.759]    [Pg.759]    [Pg.915]    [Pg.915]   
See also in sourсe #XX -- [ Pg.661 ]




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Acyl chlorides

Acyl compounds

Acylation acyl chlorides

Chloride compounds

Organocadmium

Organocadmium compound

Organocadmiums

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