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Functionalization of the naturally occurring linalool and nerol by the palladium catalyzed oxidation of their trisubstituted olefinic bonds
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文摘
Linalool and nerol are bio-renewable substrates found in many essential oils. Pd(OAc)2/p-benzoquinone system catalyses the aerobic oxidation of linalool and nerol. No requirement in auxiliary electron-transfer mediators under 5–10 atm of oxygen. Sterically encumbered internal acyclic olefinic bonds are involved in the oxidation. Fragrant poly-functionalized monoterpenoid compounds are obtained in good yields.

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