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The net transformation is identical to that produced by ozonolysis.
During that time he published numerous papers on ozonolysis.
He proposed a reaction mechanism for ozonolysis in 1953.
Ozone attacks all organic matter by ozonolysis and is used in water purification.
Due to their instability, they are rarely isolated during the course of the ozonolysis reaction sequence.
However, the contribution of ozonolysis reactions to the overall photooxidation process is still subject to controversy.
They possess double bonds in their repeat units which are cleaved during ozonolysis.
After addition of the allylsilane, ozonolysis provides the corresponding carbonyl compound.
Usually ozonolysis is carried out in a solution of dichloromethane, at a temperature of 78C.
Such elastomers possess double bonds in their main chains, the group which is attacked during ozonolysis.
His major publication detailing ozonolysis was published in, Liebigs Ann.
The auxiliary cam be removed by ozonolysis or hydrolysis.
Ozonolysis of maleic acid is also effective.
Ozonolysis of oleic acid is an important route to azelaic acid.
Ozonolysis with ozone and triphenylphosphine provided aldehyde 21.
Thiourea is also used in the reductive workup of ozonolysis to give carbonyl compounds.
Azelaic acid is industrially produced by the ozonolysis of oleic acid.
Maleic acid is an industrial raw material for the production of glyoxylic acid by ozonolysis.
Reaction with ozone in ozonolysis leads to the breaking of the double bond, yielding two aldehydes or ketones.
An example is the ozonolysis of eugenol converting the terminal alkene to an aldehyde:
RuO readily cleaves double bonds to yield carbonyl products, in a manner similar to ozonolysis.
DMS is also used in a range of organic syntheses, including as a reducing agent in ozonolysis reactions.
Acridone is N-alkylated and the terminal alkene group is converted into an aldehyde by ozonolysis.
Finally, the alkylated ketone or aldehyde can be regenerated by ozonolysis or hydrolysis.