The title acid was prepd. from cyclohexanone. Cyclohexanone was treated with H2O2 in HClO4, water was added, and the org. phase was sepd. and added to TiCl3, CH2:CHCOMe, and Me2CO at room temp. to give 9-oxodecanoic acid. Similarly, 10-oxoundecanoic acid was prepd. from cycloheptanone

One-step synthesis of 9-oxodecanoic acid and its methyl ester; a useful starting material for prostaglandin synthesis

CITTERIO, ATTILIO;VISMARA, ELENA
1980-01-01

Abstract

The title acid was prepd. from cyclohexanone. Cyclohexanone was treated with H2O2 in HClO4, water was added, and the org. phase was sepd. and added to TiCl3, CH2:CHCOMe, and Me2CO at room temp. to give 9-oxodecanoic acid. Similarly, 10-oxoundecanoic acid was prepd. from cycloheptanone
1980
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/662924
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