79854-87-8

Upstream product

• 103539-11-3 (S)-3-((R)-2-Hydroxy-1-phenyl-ethylamino)-nonan-2-ol 
• 111-25-1 1-bromo-hexane 
• 103539-09-9 (3S,5R)-3-Hexyl-2-methyl-5-phenyl-morpholin-2-ol 
• 103539-08-8 (S)-2-((R)-4-Phenyl-oxazolidin-3-yl)-octanenitrile 

Downstream Products

• 130573-54-5 erythro-1-(2-hydroxy-3-nonyl)imidazole-4-carboxamide 
• 95273-59-9 9-[(R)-1-((R)-1-Hydroxy-ethyl)-heptyl]-1,9-dihydro-purin-6-one 
• 95273-61-3 Erythro-9-(2-hydroxy-3-nonyl)hypoxanthine 
• 103539-12-4 N-[(S)-1-((R)-1-Hydroxy-ethyl)-heptyl]-benzamide 
• 87871-08-7 erythro-9-(2-hydroxy-3-nonyl)-1-deazaadenine 
• 87871-09-8 erythro-9-(2-hydroxy-3-nonyl)-3-deazaadenine 
• 103298-51-7 erythro-9-(2-hydroxy-3-nonyl)-7-deazadenine 
• 111209-68-8 erythro-1-<(2-hydroxy-3-nonyl)amino>-2,3-dinitrobenzene 

Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS VII1: ENANTIOSPECIFIC PREPARATION OF β-AMINOALCOHOLS FROM THE N-CYANOMETHYL-4-PHENYL-1,3-OXAZOLIDINE SYNTHON

(-)-N-cyanomethyl-4-phenyl-1,3-oxazolidine 1 has been investigated as chiral template for the enantiospecific synthesis of β-aminoalcohols. (-)-2(R)-hydroxy-3(S)-nonylamine 5a was chosen as a target molecule of the new method.