2015
DOI: 10.1016/bs.adomc.2015.02.004
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Catalytic Oxidation of Alcohols

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Cited by 161 publications
(60 citation statements)
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“…As expected [7,9], the alicyclic cyclohexanol is less reactive than 1-phenylethanol: Table 3, entries 1-3). The linear aliphatic alcohols, 2-hexanol and 3-hexanol, lead to even lower yields in the 45-56 % range (Table 3, entries 4-9), under similar reaction conditions, as reported in other cases [2,3,6,7]. The activity of 1-3 in the oxidation of benzyl alcohol or 1-hexanol is quite modest since only rather moderated yields of benzaldehyde (30-34 % range) or hexanal (22-24 % range) are obtained under the same reaction conditions (Table 3, entries 10-12 and 13-15, respectively).…”
Section: Microwave-assisted Catalytic Peroxidativesupporting
confidence: 71%
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“…As expected [7,9], the alicyclic cyclohexanol is less reactive than 1-phenylethanol: Table 3, entries 1-3). The linear aliphatic alcohols, 2-hexanol and 3-hexanol, lead to even lower yields in the 45-56 % range (Table 3, entries 4-9), under similar reaction conditions, as reported in other cases [2,3,6,7]. The activity of 1-3 in the oxidation of benzyl alcohol or 1-hexanol is quite modest since only rather moderated yields of benzaldehyde (30-34 % range) or hexanal (22-24 % range) are obtained under the same reaction conditions (Table 3, entries 10-12 and 13-15, respectively).…”
Section: Microwave-assisted Catalytic Peroxidativesupporting
confidence: 71%
“…The catalytic systems of the present study seem to operate under heterogeneous conditions and, although yielding ketone products in the range reported for homogeneous ones [2,3,6,7], e.g., the tris{2,4-bis(trichloromethyl)-1,3,5-triazapentadienato}-Fe(III) complexes/MW/TBHP systems [11], they are advantageous due to the possibility of recycle and reuse of the catalysts up to three consecutive catalytic cycles without a marked loss of activity (see below).…”
Section: Microwave-assisted Catalytic Peroxidativementioning
confidence: 72%
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