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Oppenauer oxidation,
named after Rupert Viktor Oppenauer [de], is a
gentle method for
selectively oxidizing secondary alcohols to ketones. The reaction...
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Alcohol oxidation is a
collection of
oxidation reactions in
organic chemistry that
convert alcohols to aldehydes, ketones,
carboxylic acids, and esters...
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isopropoxide is used in MPV
reductions of
ketones and
aldehydes and the
Oppenauer oxidation of
secondary alcohols. In
these reactions, it is ****umed that...
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benzophenone in
presence of pot****ium tert
butoxide or
aluminium tert
butoxide (
Oppenauer oxidation). The 6
ketone group may be
replaced with a
methylene group...
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aldehydes to give α-hydroxy
ketones Meerwein–Ponndorf–Verley
reduction and
Oppenauer oxidation -
related interconversions of
ketones and
secondary alcohols...
- 1016/j.resuscitation.2016.07.238. PMID 27521472.
Arrich J, Schütz N,
Oppenauer J,
Vendt J,
Holzer M,
Havel C,
Herkner H (May 2023). "Hypothermia for...
- reduction. This method, however, has the
ability to
undergo the
reverse Oppenauer oxidation due to the
proximity of the two reagents. Thus the reaction...
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oxidation of
alcohols to
aldehydes Pyridinium chlorochromate Jones oxidation Oppenauer oxidation Pfitzner–Moffatt
oxidation Parikh–Doering
oxidation Albright-Goldman...
- Library.
Retrieved October 22, 2017. Arrich, Jasmin; Schütz, Nikola;
Oppenauer, Julia; Vendt, Janne; Holzer, Michael; Havel, Christof; Herkner, Harald...
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converted to the
dioxirane using oxone. It
serves as an
oxidizing agent in
Oppenauer oxidation.
Trifluoracetone is also used in a
synthesis of 2-trifluoromethyl-7-azaindoles...
