174271-52-4

Upstream product

• 321658-31-5 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(E)-2-carbomethoxyvinyl>oxazolidine 
• 174271-50-2 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(E)-3-hydroxy-1-propenyl>oxazolidine 
• 174271-51-3 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(E)-2-formylvinyl>oxazolidine 
• 1145-80-8 N-(benzyloxycarbonyl)-L-serine 
• 117833-92-8 (4S)-3-benzyloxycarbonyl-2,2-dimethyloxazolidine-4-carbaldehyde 
• 117833-99-5 N-benzyloxycarbonyl 4(S)-(1'-methoxycarbonyl)-2,2-dimethyl-1,3-oxazolidine 
• 1676-81-9 N-benzyloxycarbonyl-L-serine methyl ester 

Downstream Products

• 174271-53-5 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(1E,5E,3S,4S)-3,4-bis<(tert-butyldimethylsilyl)oxy>-1,5-heptadienyl>oxazolidine 
• 174271-54-6 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(1R,2S,3S,4S,5S,6R)-3,4-bis<(tert-butyldimethylsilyl)oxy>-1,2,5,6-tetrahydroxyheptyl>oxazolidine 
• 76951-87-6 1,2:3,4-di-O-isopropylidene-6--6-deoxy-L-glycero-α-D-galacto-heptopyranose 

Relevant academic research and scientific papers

Stereoselective synthesis of differentially protected derivatives of the higher amino sugars destomic acid and lincosamine from serine and threonine

The aminoheptose destomic acid (3.5) and the aminooctose lincosamine (6.8) were synthesized in protected form by parallel sequences starting from the oxazolidine derivatives 2.4 and 5.1 of N-CBz serinal and N-BOC threoninal. The parallel sequences feature