103548-19-2Relevant academic research and scientific papers
ASYMMETRIC REDUCTION OF PROCHIRAL HYDROXY KETONES WITH A CHIRAL REDUCING AGENT PREPARED FROM TIN(II) CHLORIDE, A CHIRAL DIAMINE, AND DIISOBUTYLALUMINUM HYDRIDE
Mukaiyama, Teruaki,Tomimori, Koji,Oriyama, Takeshi
, p. 1359 - 1362 (1985)
Asymmetric reduction of prochiral α- and β-hydroxy ketones with a reagent, generated from tin(II) chloride, a chiral diamine, and diisobutylaluminum hydride, afforded the corresponding dihydroxy compounds in good chemical and optical yields.Optical yields depended on the nature of the protective groups of hydroxyl function.
