6533b854fe1ef96bd12ae861
RESEARCH PRODUCT
Syntheses with organoboranes. Part 14: Enolization–aldolization of conjugated cyclohexenones via dienolborinates
Wojciech SokolAndrzej WojtczakMarek ZaidlewiczPiotr NeumannMaija Nissinensubject
Organic ChemistryAcetaldehydechemistry.chemical_elementKeto–enol tautomerismConjugated systemBiochemistryMedicinal chemistryBenzaldehydechemistry.chemical_compoundDeprotonationchemistryDrug DiscoveryLithiumSelectivitydescription
Abstract Enolization of cyclohex-2-enone ( 1 ), 3-methyl- ( 2 ), 3,5-dimethyl- ( 3 ), 3,5,5-trimethyl- ( 4 ), and 3,4,5,5-tetramethylcyclohex-2-enone ( 5 ) with chlorodicyclohexylborane proceeds by deprotonation at the 6-position. Aldolization of the dienolborinates with benzaldehyde, and acetaldehyde, provides the corresponding anti aldols with 87–95% selectivity. Ketones 4 and 5 undergo competitive deprotonation at the 3-methyl group and aldolization at the 2-position. In contrast, lithium dienolates derived from 4 and 5 gave syn aldols with 95% selectivity.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2002-05-01 | Tetrahedron Letters |