Asymmetric synthesis of both enantiomers of 2.5-hexane diol and 2.6-heptane diol induced by chiral sulfoxides

Tetrahedron Letters

Volumn 35, Issue 29, 1994, Pages 5297-5300

  Solladié, Guy ^a   Huser, Nathalie ^a   Garcia Ruano, José Luis ^b   Adrio, Javier ^b   Carreño, M Carmen ^b   Tito, Amelia ^b  

^a CNRS   (France)

^b UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

HEPTANOL; HEXANOL; SULFOXIDE;

ARTICLE; CHEMICAL REACTION; CHIRALITY; ENANTIOMER; STEREOCHEMISTRY; SYNTHESIS;

EID: 0028237291     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)77089-4     Document Type: Article

References (22)

1. An Optimized Synthesis of (2S,5S)-2,5-Dimethylpyrrolidine
2. Combined Chemical and Enzymatic Synthesis of (S,S)-2,5-Dimethylpyrrolidine
3. Reduction of .beta.-keto sulfoxides: a highly efficient asymmetric synthesis of both enantiomers of allylic alcohols
4. Reduction of chiral .beta.-hydroxy sulfoxides: application to the synthesis of both enantiomers of 4-substituted butenolides
5. Stereoselective reductions of 2-keto sulfoxides with hydrides
6. Asymmetric synthesis of chiral spiroacetals from chiral diketodisulfoxides: 2,8-dimethyl-1,7-dioxaspiro [5,5] undecane.
7. Improved Preparation of Optically Active Methylp-Tolyl Sulfoxide
8. Asymmetric synthesis of (S)-zearalenone dimethyl ether, an orsellinic acid type macrolide