6533b825fe1ef96bd12828a5
RESEARCH PRODUCT
Regioselective Epoxide Ring Opening. Steroselective Synthesis of a Tetrahydropyran Ring
Michelangelo GruttadauriaSerena RielaRenato Notosubject
StereochemistryOrganic ChemistryALUMINUM HYDRIDERegioselectivityEpoxideTetrahydropyranSettore CHIM/06 - Chimica OrganicaRing (chemistry)Stereocenterchemistry.chemical_compoundchemistryepoxideStereoselectivityTetrahydrofurandescription
The stereoselective synthesis of a 2-substituted tetrahydropyran with adjacent alkoxy-bearing stereogenic centre is described. The key steps of this synthesis were the stereoselective epoxidation of an allylic alcohol and the regioselective epoxide ring opening by lithium aluminum hydride. The regio and stereoselective synthesis of a trihydroxyselenide and a trihydroxysulfide is also described. The latter compounds are not suitable for cyclization to tetrahydrofuran ring.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 1998-07-01 |