233666-39-2Relevant academic research and scientific papers
A revised mechanism for chemoselective reduction of esters with borane-dimethyl sulfide complex and catalytic sodium tetrahydroborate directed by adjacent hydroxyl group
Saito,Ishikawa,Kuroda,Koga,Moriwake
, p. 4067 - 4086 (2007/10/02)
The plausible mechanism for the reduction of the ester groups with a strong preference for one located α to the hydroxyl groups of (S)-malates and (R,R)-tartrate-based derivatives has been proposed together with some results with regard to its applications to the syntheses of chiral synthons.
SYNTHESIS OF THE OPTICALLY ACTIVE FORMS OF 4,10-DIHYDROXY-1,7-DIOXASPIROUNDECANE AND THEIR CONVERSION TO THE ENANTIOMERS OF 1,7-DIOXASPIROUNDECANE, THE OLIVE FLY PHEROMONE
Mori, Kenji,Uematsu, Tamon,Yanagi, Kazunori,Minobe, Masao
, p. 2751 - 2758 (2007/10/02)
Both the enantiomers of 1,7-dioxaspiroundecane, the major component of the pheromone of the olive fly (Dacus oleae), were synthesized from (S)-malic acid.
