107977-13-9Relevant academic research and scientific papers
Generation of chromioenamines by reduction of O-acetyloximes with chromium(II) and their application
Takai,Katsura,Kunisada
, p. 1724 - 1725 (2001)
Chromioenamines can be generated by treatment of O-acetyloximes with chromium(II) via two steps of one-electron reduction and successive isomerization, and the species react with aldehydes to give γ-amino alcohols after reduction with LiA1H4.
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
