Cyclodecane and cyclohexane were converted to the corresponding cycloalkanones and cycloalkanols upon ozonation at acidic pH. Also some ring cleavage to dicarboxylic acids or aldehydoacids was observed

Barletta, B., Bolzacchini, E., Fossati, L., Meinardi, S., Orlandi, M., Rindone, B. (1998). Metal-free functionalization of the unactivated carbon-hydrogen bond: the oxidation of cycloalkanes to cycloalkanones with ozone. OZONE: SCIENCE & ENGINEERING, 20(2), 91-98 [10.1080/01919519808547278].

Metal-free functionalization of the unactivated carbon-hydrogen bond: the oxidation of cycloalkanes to cycloalkanones with ozone

BOLZACCHINI, EZIO;ORLANDI, MARCO EMILIO;RINDONE, BRUNO
1998

Abstract

Cyclodecane and cyclohexane were converted to the corresponding cycloalkanones and cycloalkanols upon ozonation at acidic pH. Also some ring cleavage to dicarboxylic acids or aldehydoacids was observed
Articolo in rivista - Articolo scientifico
ozone; cyclodecane; cyclodecanone; cyclodecanol; cyclohexane; 10-oxodecanoic acid; decandioic acid; cyclohexanone; cyclohexanol
English
1998
20
2
91
98
none
Barletta, B., Bolzacchini, E., Fossati, L., Meinardi, S., Orlandi, M., Rindone, B. (1998). Metal-free functionalization of the unactivated carbon-hydrogen bond: the oxidation of cycloalkanes to cycloalkanones with ozone. OZONE: SCIENCE & ENGINEERING, 20(2), 91-98 [10.1080/01919519808547278].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/33670
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