651031-29-7

Upstream product

• 651031-27-5 3-[(2S)-2-(tert-butoxycarbonylamino)-3-(benzyloxy)propanoxy]-(2R)-1-(benzyloxy)-2-(tert-butyldimethylsilyloxy)propane 
• 651031-26-4 (2R)-3-benzyloxy-2-tert-butyldimethylsilyloxypropyl trifluoromethanesulfonate 
• 126181-46-2 (2R)-methyl 2-((tert-butoxycarbonyl)amino)-3-((tetrahydro-2H-pyran-2-yl)oxy)propanoate 
• 100-39-0 benzyl bromide 
• 95715-85-8 2-(tert-butoxycarbonylamino)-3-hydroxypropionic acid methyl ester 
• 79069-15-1 N-(tert-butyloxycarbonyl)-O-benzyl-L-serinol 
• 17325-85-8 (2S)-3-(benzyloxy)propane-1,2-diol 
• 124-63-0 methanesulfonyl chloride 
• 651031-28-6 3-[(2S)-2-(tert-butoxycarbonylamino)-3-(benzyloxy)propanoxy]-(2R)-1-(benzyloxy)propan-2-ol 

Downstream Products

• 651031-30-0 (3S,5S)-3,5-bis(benzyloxymethyl)morpholine 

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