143738-96-9

Upstream product

• 78-85-3 2-methylpropenal 
• 108591-33-9 N-((1R,2S)-1-hydroxy-1-phenylpropan-2-yl)-4-methylbenzene sulfonamide 

Downstream Products

• 143738-95-8 (2S,4S,5R)-1-<4-methyl-5-phenyl-3-(toluene-4'-sulfonyl)-oxazolidin-2-yl>-ethanone 
• 166189-46-4 (1'S,2''S,4''S,5''R)-toluene-4-sulfonic acid 2'-hydroxy-2'-[4''-methyl-5''-phenyl-3''-(toluene-4'''-sulfonyl)-oxazolidin-2''-yl]-propyl ester 
• 166189-47-5 (2S,4S,5R,1'S)-4-methyl-2-(2'-methyl-oxiran-2-yl)-5-phenyl-3-(toluene-4''-sulfonyl)-oxazolidine 
• 143754-70-5 (2S,2'S,4'S,5'R)-2-<4'-methyl-5'-phenyl-3'-(toluene-4''-sulfonyl)-oxazolidin-2'-yl>-propane-1,2-diol 
• 143754-69-2 (2RS,2'S,4'S,5'R)-2-<4'-methyl-5'-phenyl-3'-(toluene-4''-sulfonyl)-oxazolidin-2'-yl>-propane-1,2-diol 

Relevant academic research and scientific papers

Diastereoselective addition of metal-coordinated and 'naked' nucleophilic reagents to norephedrine derived 2-acyl-N-tosyl-oxazolidines

The addition of tri-s-butyl borohydrides to the 2-acetyl-1,3-oxazolidine 1 could be directed with high selectivity to either the Si or the Re π-carbonyl face under chelating or non-coordinating conditions respectively. Addition of hydrides to the correspo

Diastereoselective Addition of Metal-coordinated and 'Naked' Tri-sec-butylborohydrides to a Norephedrine-derived 2-Acetyloxazolidine

The addition of tri-sec-butylborohydrides to the 2-acetyl-1,3-oxazolidine 1 can be directed with high selectivity to either the Si or the Re ?-carbonyl face under chelating or non-coordinating conditions, respectively.