863016-80-2

Upstream product

• 176298-48-9 N-(2-hydroxy-1, 2-diphenylethyl)-4-methylbenzenesulfonamide 
• 1019853-28-1 (S)-N-methoxy-N-methyl-2-(4-methylphenylsulfonamido)-2-phenylacetamide 
• 100-58-3 phenylmagnesium bromide 
• 98-59-9 p-toluenesulfonyl chloride 
• 127-65-1 chloroamine-T 
• 23190-16-1 (1R,2S)-2-Amino-1,2-diphenylethanol 
• 645-49-8 cis-stilben 
• 176706-54-0 N-((1S,2R)-2-hydroxy-1,2-diphenylethyl)-4-methylbenzene sulfonamide 

Downstream Products

• 1019853-30-5 1(R),2(S),5(S)-diphenyltetrahydro-1aH-oxireno[2,3-c]pyrrol-3-yl (4-methylphenyl) sulfone 
• 1261245-17-3 N-((2S,3R)-3-hydroxy-3-phenylhex-5-en-2-yl)-4-methylbenzenesulfonamide 
• 1383950-76-2 (1S,2S)-1-(4-methylphenylsulfonamido)-1,2,4-triphenylbut-3-yn-2-yl benzoate 
• 1383950-53-5 N-((1S,2S)-2-hydroxy-1,2,4-triphenylbut-3-yn-1-yl)-4-methylbenzenesulfonamide 
• 176706-54-0 N-((1S,2R)-2-hydroxy-1,2-diphenylethyl)-4-methylbenzene sulfonamide 
• 176298-48-9 N-(2-hydroxy-1, 2-diphenylethyl)-4-methylbenzenesulfonamide 

Relevant academic research and scientific papers

Copper(II) triflate-catalyzed intramolecular hydroamination of homoallylic amino alcohols as an expedient route to trans-2,5-dihydro-1H-pyrroles and 1,2-dihydroquinolines

A new efficient synthetic route to trans-2,5-dihydro-1H-pyrroles and 1,2-dihydroquinolines that relies on copper(II) triflate-catalyzed intramolecular hydroamination of homoallylic amino alcohols under mild and operationally straightforward conditions is

Epoxy-annulations by reactions of α-amido ketones with vinyl sulfonium salts. Reagent versus substrate control and kinetic resolution

(Chemical Equation Presented) Diphenyl vinyl sulfonium salt and chiral amido-ketones undergo highly diastereoselective epoxy-annulation reactions in good yield. The use of a chiral vinyl sulfonium salt dominates the stereochemical outcome of the annulatio

First osmium-catalysed ketamination of alkenes

Conditions for a first oxidative conversion of alkenes into 2-amino ketones are described, which yield racemic products within a direct oxidation pathway and 2-amino ketones with up to 99% enantiomeric excess from the corresponding enantiopure amino alcohols. The Royal Society of Chemistry 2005.

A Lewis acid promoted asymmetric umpolung reaction with chiral N-sulfinyl imines as the electrophiles

An new asymmetric umpolung reaction has been developed by reacting N-sulfinyl imines with 2-lithio-2-phenyl-1,3-dithiane. The reaction was conducted at between -20 and -25°C in THF in the presence of Et 2AlCl as the Lewis acid promoter. Excelle

Katalytische asymmetrische Aminohydroxylierung (AA) von Olefinen

Keywords: β-Aminoalkohole; Asymmetrische Aminohydroxylierung; Chloramin T; Osmiumverbindungen; Taxolseitenkette