Publication | Closed Access
Asymmetric Synthesis of 2‐Substituted Dihydrobenzofurans and 3‐Hydroxydihydrobenzopyrans through the Enantioselective Epoxidation of <i>O</i>‐Silyl‐Protected <i>ortho</i>‐Allylphenols
28
Citations
42
References
2010
Year
Chemical EngineeringEngineeringAsymmetric SynthesisOrganic ChemistryStereoselective SynthesisChemistryEnantioselective EpoxidationShi‐type EpoxidationNatural Product SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringO ‐Allylphenols
Abstract The Shi‐type epoxidation of O ‐ tert‐ butyldiphenylsilyl (TBDPS) protected o ‐allylphenols serves as an efficient strategy to construct the dihydrobenzofurans and dihydrobenzopyrans in up to 97% ee . This methodology led to the enantioselective synthesis of (+)‐marmesin, (−)‐(3′ R )‐decursinol, and (+)‐lomatin.
| Year | Citations | |
|---|---|---|
Page 1
Page 1