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General synthetic approach to functionalized dihydrooxepines.


ABSTRACT: A three-step sequence to access functionalized 4,5-dihydrooxepines from cyclohexenones has been developed. This approach features a regioselective Baeyer-Villiger oxidation and subsequent functionalization via the corresponding enol phosphate intermediate.

SUBMITTER: Nicolaou KC 

PROVIDER: S-EPMC3653422 | biostudies-literature | 2013 Apr

REPOSITORIES: biostudies-literature

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General synthetic approach to functionalized dihydrooxepines.

Nicolaou K C KC   Yu Ruocheng R   Shi Lei L   Cai Quan Q   Lu Min M   Heretsch Philipp P  

Organic letters 20130404 8


A three-step sequence to access functionalized 4,5-dihydrooxepines from cyclohexenones has been developed. This approach features a regioselective Baeyer-Villiger oxidation and subsequent functionalization via the corresponding enol phosphate intermediate. ...[more]

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