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?-Phenylation of ketones via tin enolates catalysed by a palladium complex

✍ Scribed by Kosugi, Masanori; Hagiwara, Isao; Sumiya, Takashi; Migita, Toshihiko

Book ID
120986439
Publisher
The Royal Society of Chemistry
Year
1983
Tongue
English
Weight
129 KB
Volume
7
Category
Article
ISSN
0022-4936

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πŸ“œ SIMILAR VOLUMES

Regiospecifically controlled formation o
Regiospecifically controlled formation of tetrasubstituted tributyltin ketone enolates catalyzed by a palladium complex
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The paZZadium-catalyzed hydrostannolysis of a-disubstituted ally1 B-keto esters yields the corresponding tributyltin B-keto carboxylates which loose carbon dioxide at very moderate temperature, thus leading to the regiospeeifie formation of tributyltin tetrambstituted enolates.

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