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Oxidation, enzymic with lead tetraacetate

More recently, the preparative value of VOCl3 and VOF3-TFA in chemical oxidation has been demonstrated (see Section III, on the pro-aporphine and promorphinane alkaloids) (415,462). Some other authors used the purified enzyme horseradish peroxidase (463). By this method the aporphine base (besides the quaternary dibenzopyrrocoline) is readily obtained from (S)-( + )-laudanosoline hydrobromide or from (/ )-(—)-laudanosoline methiodide with retention of the absolute configuration. The synthesis of 6a,7-dehydroaporphine bases was also carried out by making use of the benzyne reaction (439). Reduction of these substances affords the corresponding aporphine bases (439). The synthesis of isoquinoline alkaloids by lead tetraacetate oxidation was reviewed by Umezawa and Hoshino (343). [Pg.419]


See other pages where Oxidation, enzymic with lead tetraacetate is mentioned: [Pg.322]    [Pg.208]    [Pg.120]    [Pg.547]    [Pg.117]    [Pg.131]    [Pg.267]    [Pg.267]   


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Enzyme oxidation

Enzymes Oxidation with

Enzymes oxidizing

Lead oxidation

Lead tetraacetate

Lead tetraacetate oxidation

Lead tetraacetate oxidative

Oxidants lead tetraacetate

Oxidation with lead tetraacetate

Oxidative enzymes

Tetraacetate

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