Selective oxidation of lupeol by iodosylbenzene catalyzed by manganese porphyrins
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文摘

A selective route to semi-synthetic derivatives of lupeol is proposed.

Oxidation at lupeol takes place without protection of the hydroxyl group at C3.

A selective oxidative cleavage of Cdouble bond; length as m-dashC bond on lupane skeleton was performed.

A metalloporphyrin-catalyzed oxidation of lupeol was developed.

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