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    Synergistic effect between Pt0 and Bi2O3−x for efficient room-temperature alcohol oxidation under base-free aqueous conditions
    Catalysis Science & Technology (2017)
    Juanjuan LiuShihui ZouHui WangLiping XiaoHongting ZhaoJie Fan
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    Abstract:
    The synergistic effect between Pt0 and nearby partially reduced Bi2O3−x species was found to be efficient (conversion of 94.1 ± 2.7%, selectivity to aldehyde >99%) for benzyl alcohol oxidation at room temperature (26 °C) under base-free aqueous conditions.
    Keywords:
    Base (topology)
    Alcohol Oxidation
    Topics:
    Oxidative Organic Chemistry Reactions
    Catalytic Processes in Materials Science
    Electrocatalysts for Energy Conversion
    EFFICIENT, ECOLOGICALLY BENIGN, AEROBIC OXIDATION OF ALCOHOLS
    Advances in inorganic chemistry (2004)
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    Allylic alcohol
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    Derivative (finance)
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    Catalytic oxidation of alcohols to esters with Ru3(CO)12
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    Yigal D. BlumYouval Shvo
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    Difference in the mechanism of oxidation of alcohols and sulfides with oxygen in the presence of aldehydes
    Petroleum Chemistry (2008)
    А. Д. Малиевский
    Alcohol Oxidation
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    Journal of the Chemical Society (Resumed) (1952)
    C. L. ArcusHermann Strauß
    C. L. Arcus and H. E. Strauss, J. Chem. Soc., 1952, 2669 DOI: 10.1039/JR9520002669
    Alcohol Oxidation
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    Dry and wet prolines for asymmetric organic solvent-free aldehyde–aldehyde and aldehyde–ketone aldol reactions
    Chemical Communications (2006)
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    Dry and wet prolines were found to catalyze the direct aldol reactions of aldehyde-aldehyde and aldehyde-ketone, respectively, to afford aldols with excellent diastereo- and enantioselectivities, and an organic solvent-free reaction was realized in some cases.
    Aldol reaction
    Aldol condensation
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    The oxidation of alcohols and ethers using calcium hypochlorite [Ca(OCl)2]
    Tetrahedron Letters (1982)
    Stephen O. NwaukwaPhilip M. Keehn
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    Alcohol Oxidation
    Primary (astronomy)
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    Phenylpropargyl Aldehyde
    Organic Syntheses (2003)
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    Abstract Phenylpropargyl aldehyde intermediate: α‐Bromocinnamic aldehyde intermediate: α‐ Bromocinnamic aldehyde acetal intermediate: phenylpropargyl aldehyde acetal product: phenylpropargyl aldehyde
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    [Studies on the reaction of alcohol dehydrogenases with tritium-labelled substrates. 3. Primary aliphatic alcohols and aldehydes as substrates of liver alcohol dehydrogenase].
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    the reductivity of aldehyde and ketone was compared,the reaction of aldehyde and weak oxidizer was discussed,and it was pointed out that Fehling Reagent can't appreciate aldihyde and ketone,fatty aldehyde and aromatic aldehyde.
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    Oxidations involving silver. II. The oxidation of alcohols and aldehydes with silver(II) picolinate
    Canadian Journal of Chemistry (1969)
    Thomas ClarkeN.A. HampsonJ. B. LeeJ. R. MorleyB. Scanlon
    The oxidation of alcohols by argentic picolinate has been studied and has been shown to give high yields of aldehyde and ketone. Examination of the oxidation of aldehydes shows that smooth conversion to the acid occurs in most cases, but in some cases, an anomalous reaction occurs, which probably involves attack upon the aromatic ring of substituted benzaldehydes. The oxidation of aldehydes occurs much more slowly than alcohol-oxidation under similar conditions.
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    Citations (51)