89762-99-2Relevant academic research and scientific papers
Stereoselective Preparation of Acyclic syn-β-Amino Alcohols from β-Hydroxy Ketones via the Corresponding O-Benzyl Oximes
Narasaka, Koichi,Ukaji, Yutaka,Yamazaki, Shigeru
, p. 525 - 534 (2007/10/02)
Reduction of β-hydroxy ketone O-benzyl oximes with lithium aluminum hydride in the presence of sodium or potassium methoxide afforded the corresponding syn-β-amino alcohols in highly stereoselective manner.A lythraceae alkaloid, lasubine II, was synthesiz
STEREOSELECTIVE PREPARATION OF ACYCLIC syn-1,3-AMINO ALCOHOLS FROM β-HYDROXY KETONES
Narasaka, Koichi,Ukaji, Yutaka
, p. 147 - 150 (2007/10/02)
syn-1,3-Amino alcohols are prepared in good yields by the stereoselective reduction of β-hydroxy-ketone-O-benzyloximes derived from acyclic β-hydroxy ketones with lithium aluminium hydride.
A FACILE METHOD FOR THE STEREOSELECTIVE PREPARATION OF ACYCLIC syn-1,3-AMINO ALCOHOLS FROM β-HYDROXY KETONES
Narasaka, Koichi,Yamazaki, Shigeru,Ukaji, Yutaka
, p. 2065 - 2068 (2007/10/02)
Treatment of acyclic β-hydroxy ketones with O-benzyl-hydroxylamine hydrochloride gave a mixture of stereoisomers of the corresponding O-benzyloximes.The mixture of the both isomers was reduced with lithium aluminum hydride in the presence of sodium or pot
