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  2. Babler oxidation - Wikipedia

    en.wikipedia.org/wiki/Babler_oxidation

    The oxidiser is added in stoichiometric amounts, usually 1.5 eq of alcohol. A different approach to minimise toxic chromium(VI) use involves performing the reaction with only a catalytic amount of PCC and an excess of another oxidant, to re-oxidise the chromium species as part of the catalytic cycle.

  3. Pyridinium chlorochromate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chlorochromate

    PCC is used as an oxidant.In particular, it has proven to be highly effective in oxidizing primary and secondary alcohols to aldehydes and ketones, respectively.The reagent is more selective than the related Jones' Reagent, so there is little chance of over-oxidation to form carboxylic acids if acidified potassium permanganate is used as long as water is not present in the reaction mixture.

  4. Oxidation with chromium(VI) complexes - Wikipedia

    en.wikipedia.org/wiki/Oxidation_with_chromium(VI...

    Enones can be synthesized from tertiary allylic alcohols through the action of a variety of chromium(VI)-amine reagents, in a reaction known as the Babler oxidation. The reaction is driven by the formation of a more substituted double bond. (E)-Enones form in greater amounts than (Z) isomers because of chromium-mediated geometric isomerization ...

  5. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  6. Sarett oxidation - Wikipedia

    en.wikipedia.org/wiki/Sarett_oxidation

    The Sarett oxidation is an organic reaction that oxidizes primary and secondary alcohols to aldehydes and ketones, respectively, using chromium trioxide and pyridine.Unlike the similar Jones oxidation, the Sarett oxidation will not further oxidize primary alcohols to their carboxylic acid form, neither will it affect carbon-carbon double bonds. [1]

  7. The Death of Avicii, 6 Years Later: What Happened to the DJ ...

    www.aol.com/death-avicii-6-years-later-151947525...

    Avicii was found dead in the afternoon hours of April 20, 2018, according to a statement from his rep. His tragic death came two years after he announced his retirement from touring in March 2016.

  8. Certain foods may disrupt your body’s fight against cancer ...

    www.aol.com/news/certain-foods-may-disrupt-body...

    Higher levels of omega-6 fatty acids often found in ultraprocessed foods may interfere with the immune system’s fight against cancer cells, a new study says.

  9. Collins reagent - Wikipedia

    en.wikipedia.org/wiki/Collins_reagent

    Collins reagent is especially useful for oxidations of acid sensitive compounds. Primary and secondary alcohols are oxidized respectively to aldehydes and ketones in yields of 87-98%. [5] Like other oxidations by Cr(VI), the stoichiometry of the oxidations is complex because the metal undergoes 3e reduction and the substrate is oxidized by 2 ...