142559-11-3Relevant articles and documents
Asymmetric synthesis of protected 1,2-amino alcohols using tert-butanesulfinyl aldimines and ketimines
Tang,Volkman,Ellman
, p. 8772 - 8778 (2007/10/03)
tert-Butanesulfinyl aldimines and ketimines bearing an α-benzyloxy or α-silyloxy substituent serve as precursors in the synthesis of protected 1,2-amino alcohols in high yields and diastereoselectivities. General protocols are described for the addition of unbranched alkyl, branched alkyl, and aryl organometallic reagents to N-sulfinyl aldimines 1 and 2 and ketimines 5 and 6. Furthermore, the selective N- or O-deprotection of sulfinamide products 3, 4, 7, and 8 is described, enabling further synthetic transformations of the reaction products.
Resolving agents. Part 1. (R)-(-)-2-amino-1-benzyloxybutane, a new base for the resolution of racemic acids
Touet,Ruault,Brown
, p. 293 - 300 (2007/10/02)
Treatment of the readily available (R)-(-) enantiomer of 2-aminobutan-1- ol 1 with sodium hydride followed by benzyl chloride afforded the O-benzyl base (R)-(-)-2. The latter was successfully used for the resolution of racemic α-methylsuccinic and α-bromo