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J Org Chem ; 87(15): 10462-10466, 2022 08 05.
Article in English | MEDLINE | ID: mdl-35862248

ABSTRACT

Syntheses of two natural products derived from the ent-kaurene kaurenoic acid are described for the first time using regio- and diastereoselective oxidations. Palladium- and manganese-mediated oxidations were used to accomplish the syntheses of two ent-beyerane metabolites. The use of the White-Gormisky-Zhao catalyst Mn(CF3-PDP) enabled the first application of a nondirected metal-catalyzed oxidation in an unactivated C-H bond in a total synthesis.


Subject(s)
Diterpenes, Kaurane , Diterpenes, Kaurane/chemistry , Oxidation-Reduction
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