651031-17-3

Upstream product

• 79069-15-1 N-(tert-butyloxycarbonyl)-O-benzyl-L-serinol 
• 651031-13-9 (2S)-2-(tert-butoxycarbonylamino)-3-(benzyloxy)propanoxy-(4S)-methyl-2,2-dimethyl-[1,3]-dioxolane 
• 651031-14-0 3-[(2S)-2-(tert-butoxycarbonylamino)-3-(benzyloxy)propanoxy]-(2R)-propane-1,2-diol 
• 126181-46-2 (2R)-methyl 2-((tert-butoxycarbonyl)amino)-3-((tetrahydro-2H-pyran-2-yl)oxy)propanoate 
• 95715-85-8 2-(tert-butoxycarbonylamino)-3-hydroxypropionic acid methyl ester 
• 124-63-0 methanesulfonyl chloride 
• 651031-16-2 3-[(2S)-2-(tert-butoxycarbonylamino)-3-(benzyloxy)propanoxy]-(2S)-1-(tert-butyldiphenylsilyloxy)propan-2-ol 

Relevant academic research and scientific papers

Facile Route to 3,5-Disubstituted Morpholines: Enantioselective Synthesis of O-Protected trans-3,5-Bis(hydroxymethyl)morpholines

(Equation presented) trans-3,5-Bis(benzyl/terf-butyldiphenylsilyloxymethyl) morpholines, promising candidates for the C2-symmetric class of chiral reagents, were prepared with excellent optical purity. A key step in the synthesis is the couplin