Oxidation of Primary Alcohols over Hydrous Zirconium(IV) Oxide
نویسندگان
چکیده
منابع مشابه
Chemoselective, iron(II)-catalyzed oxidation of a variety of secondary alcohols over primary alcohols utilizing H2O2 as the oxidant.
A mild, iron-based catalyst system is presented that selectively oxidizes secondary alcohols to the corresponding hydroxy ketones in the presence of primary alcohols within 15 minutes at room temperature, utilizing H2O2 as the oxidant.
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A main obstacle in the rational development of heterogeneous catalysts is the difficulty in identifying active sites. Here we show metal/oxide interfacial sites are highly active for the oxidation of benzyl alcohol and other industrially important primary alcohols on a range of metals and oxides combinations. Scanning tunnelling microscopy together with density functional theory calculations on...
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A series of transition metal complexes with two thiosemicarbazide Schiff bases, 1-(4-dimethylaminobenzyl- idene)thiosemicarbazide (ABTSC) and 1-(2-pyridincarboxyl-idene) thiosemicarbazide (TCTS) were synthesized with Co(II), Ni(II), Zn(II), Cd(II) and Ag(I) salts (chloride and acetate). These complexes were characterized by different methods including proton nuclear magnetic resonance (1HNMR),...
متن کاملOxidation of primary alcohols to methyl esters by hydrogen transfer.
The oxidation of alcohols in the presence of methanol has been achieved using a ruthenium catalyst with crotononitrile as the hydrogen acceptor.
متن کاملShape-selective oxidation of primary alcohols using perruthenate-containing zeolites.
Potassium perruthenate (KRuO4), a known, effective oxidant for the conversion of primary and secondary alcohols into carbonyl compounds is impregnated into zeolite X and shown to be a shape-selective oxidant using benzyl alcohol (reacted) and pyrenemethanol (not reacted).
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ژورنال
عنوان ژورنال: Bulletin of the Chemical Society of Japan
سال: 1991
ISSN: 0009-2673,1348-0634
DOI: 10.1246/bcsj.64.312