Examples of 'pyridinium chlorochromate' in a sentence
Meaning of "pyridinium chlorochromate"
Pyridinium chlorochromate: a chemical compound commonly used as an oxidizing agent in organic chemistry reactions. It is known for its ability to convert primary and secondary alcohols into aldehydes and ketones
How to use "pyridinium chlorochromate" in a sentence
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pyridinium chlorochromate
Pyridinium chlorochromate and manganese dioxide.
Oxidation steps are typically carried out using pyridinium chlorochromate.
Pyridinium chlorochromate or dimethyl sulfoxide e . g.
Suitable reagents include pyridinium chromate and pyridinium chlorochromate.
Of these, we prefer pyridinium chlorochromate or dimethyl sulphoxide / oxalyl chloride.
The above oxidation can also be performed using pyridinium chlorochromate.
Chromium compounds contain pyridinium chlorochromate and potassium dichromate, which are powerful oxidizing agents.
The resulting allylic alcohol is then oxidized to the aldehyde by pyridinium chlorochromate.
Added 1 g pyridinium chlorochromate and stirred at RT overnight.
Thus for example the oxidation may be carried out using pyridinium chlorochromate.
Concentrated filtrates . Suspect pyridinium chlorochromate also eluted judged by dark color.
The oxidizing agent for this reaction may suitably be dimethylsulfoxide or pyridinium chlorochromate.
Of pyridinium chlorochromate is dissolved in 250 ml of methylene chloride.
Oxidation of the compound of formula VI is accomplished by means of pyridinium chlorochromate.
Oxidation with pyridinium chlorochromate produces the ketones 68.
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In some embodiments, the stoichiometric oxidant is pyridinium chlorochromate.
Of pyridinium chlorochromate and 120 g of molecular sieve are introduced into 1 liter of dichloromethane.
Oxidation of compound 11 was accomplished by reaction with pyridinium chlorochromate.
Another 3 g of pyridinium chlorochromate was added and the reaction mixture further stirred for 30 min.
Specific examples of the oxidizing agent include manganese dioxide, hydrogen peroxide, and pyridinium chlorochromate.
Of pyridinium chlorochromate ( PCC ) at room temperature.
The protected sugars 5a, b were oxidized in high yields into the keto sugars 6a, b with pyridinium chlorochromate.
Such salts include pyridinium chlorochromate ( PCC ) and dichlorochromate.
In some embodiments, the oxidizing agent is pyridinium chlorochromate ( PCC ).
Pyridinium chlorochromate ( PCC ) is a yellow-orange salt with the formula.
A preferable reagent for Step ( f ) is pyridinium chlorochromate ( PCC ) in methylene chloride.
Pyridinium chlorochromate oxidation of 9 gave 10.
Oxidation of the secondary alcohol with pyridinium chlorochromate on alumina22 provided the B-keto amide.
It can be efficiently cleaved to form the C17 ketone compound using pyridinium chlorochromate ( PCC ).
Oxidation of the benzyl alcohol ( 18 ) with pyridinium chlorochromate in dichloromethane affords the benzaldehyde ( 6 ).
Celite and pyridinium chlorochromate ( 430 mg ) were added and the mixture was stirred at room temperature.
Next, 200 mg of pyridinium chlorochromate ( TCI America ) was added to the solution and stirred overnight.
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Pharmaceutical compositions of pyridinium and quinolinium derivatives
The pyridinium cation is isoelectronic with benzene
