Enantioselective Michael additions to enones in their inclusion crystals with optically active host compounds

Tetrahedron: Asymmetry

Volumn 4, Issue 8, 1993, Pages 1771-1774

  Toda, Fumio ^a   Tanaka, Koichi ^a   Sato, Jin ^a  

^a EHIME UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXANONE DERIVATIVE;

ARTICLE; COMPLEX FORMATION; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0027200958     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/S0957-4166(00)80413-9     Document Type: Article

References (12)

1. Asymmetric synthesis of optically active cyclohexenol derivatives via highly stereoselective reduction of (R)-3-(p-t-butylphenylthio)cyclohexan-1-one.
2. Highly enantioselective Michael addition of thiols to 2-cyclohexenone by using (2S,4S)-2-(anilinomethyl)-1-ethyl-4-hydroxypyrrolidine as a chiral catalyst.
3. Asymmetric Michael addition of thiophenol to maleic acid esters.
4. Preparative Microbial Reduction ofβ-Oxoesters withThermoanaerobium brockii