66217-71-8

Upstream product

• 2627-86-3 (S)-1-phenyl-ethylamine 
• 100-52-7 benzaldehyde 
• 3129-98-4 (R)-benzylidene-(1-phenylethyl)amine 
• 3129-98-4 (S)-N-benzylidene(1-phenylethylamine) 
• 83171-68-0 O,O-diphenyl α-[((S)-1-phenylethyl)amino]benzylphosphonate 
• 135738-66-8 [Phenyl-((S)-1-phenyl-ethylamino)-methyl]-phosphonic acid dibutyl ester 
• 135738-67-9 [Phenyl-((S)-1-phenyl-ethylamino)-methyl]-phosphonic acid diisobutyl ester 
• 83171-64-6 [Phenyl-((S)-1-phenyl-ethylamino)-methyl]-phosphonic acid diisopropyl ester 
• 249889-44-9 [Phenyl-((S)-1-phenyl-ethylamino)-methyl]-phosphonic acid diethyl ester 
• 135738-65-7 [Phenyl-((S)-1-phenyl-ethylamino)-methyl]-phosphonic acid dimethyl ester 

Downstream Products

• 37714-05-9 (R)-1-amino-1-phenylmethylphosphonic acid 

Relevant academic research and scientific papers

Diastereoselective addition of Di-(trimethylsilyl)phosphite to chiral N-(R)-α-methylbenzyl and N-(1-methoxycarbonyl-iso-pentyl) Schiff bases of various aldehydes

The addition of bis-(trimethylsilyl) phosphite to chiral imines of several aldehydes was diastereoselective. The separation of predominant diastereoisomers of a majority of formed aminophosphonic acids has been observed. Moreover, the ferrocene-derived ac

STUDIES ON ORGANOPHOSPHORUS COMPOUNDS XLVIII STRUCTURAL EFFECT ON THE INDUCED ASYMMETRIC ADDITION OF DIALKYL PHOSPHITE TO CHIRAL ALDIMINE DERIVATIVES

For the evaluation of the predominating factors controlling the stereochemical process of the addition of dialkylphosphite to a chiral Schiffs base resulting from condensation of substituted benzaldehyde and 1-phenylethylamine, various structural effect o

ASYMMETRIC ADDITION OF TRIS(TRIMETHYLSILYL) PHOSPHITE TO CHIRAL ALDIMINES

Addition of tris(trimethylsilyl) phosphite (2) to (+)-(R)-1-phenylethylaldimines (1) and methanolysis of addition products affords(+)-N-(1-phenyethyl)-1-aminoalkanophosphonic acids (3).Chemical yields and diastereomeric composition of 3 vary from 10 to 90