216021-63-5

Upstream product

• 28143-91-1 (1S,2S)-2-amino-1-phenyl-1,3-diol 
• 100-52-7 benzaldehyde 

Downstream Products

• 68534-64-5 (1S,2S)-(+)-2-(benzylamino)-1-phenylpropane-1,3-diol 
• 294869-55-9 (1S,2S,αR)-2-(α-methylbenzylamino)-1-phenyl-1,3-propanediol 

Relevant academic research and scientific papers

Stereoselective synthesis of 3-mono- and 1,3-disubstituted 4-phenyl- 1,2,3,4-tetrahydroisoquinolines

(1S,2S)-(+)-Thiomicamine was transformed in high yield and with high diastereoselectivity into (3R,4R)-4-phenyl-1,2,3,4-tetrahydroisoquinoline-3- carboxylic acid and enantiomerically pure (3R,4R)-3-hydroxymethyl-4-phenyl- and (1R,3R,4R)-3-hydroxymethyl-1-

Five-component equilibria of ring-chain tautomeric mixtures derived from 2-amino-1-phenyl-1,3-propanediol diastereomers

In the reactions of (1R*,2S*)- or (1S,2S)-2-amino-1-phenyl-1,3- propanediol with aromatic aldehydes, five-component ring-chain tautomerie mixtures were formed, involving C-2 epimers of structurally isomeric oxazolidines and the corresponding Schiff base.