321658-31-5

Upstream product

• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 117833-92-8 (4S)-3-benzyloxycarbonyl-2,2-dimethyloxazolidine-4-carbaldehyde 
• 1145-80-8 N-(benzyloxycarbonyl)-L-serine 
• 1676-81-9 N-benzyloxycarbonyl-L-serine methyl ester 
• 117833-99-5 N-benzyloxycarbonyl 4(S)-(1'-methoxycarbonyl)-2,2-dimethyl-1,3-oxazolidine 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 

Downstream Products

• 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 
• 174271-53-5 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(1E,5E,3S,4S)-3,4-bis<(tert-butyldimethylsilyl)oxy>-1,5-heptadienyl>oxazolidine 
• 174271-52-4 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(1E,5E,3S,4S)-4-<(tert-butyldimethylsilyl)oxy>-3-hydroxy-1,5-heptadienyl>oxazolidine 
• 174271-51-3 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(E)-2-formylvinyl>oxazolidine 
• 76951-87-6 1,2:3,4-di-O-isopropylidene-6--6-deoxy-L-glycero-α-D-galacto-heptopyranose 
• 321658-32-6 (R)-4-((E)-4-tert-Butoxycarbonylamino-4-ethoxycarbonyl-3-oxo-but-1-enyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 1027290-06-7 (R)-4-((E)-2-Chlorocarbonyl-vinyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 500109-19-3 (R)-4-((E)-2-Carboxy-vinyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 
• 174271-50-2 (R)-3-(benzyloxycarbonyl)-2,2-dimethyl-4-<(E)-3-hydroxy-1-propenyl>oxazolidine 

Relevant academic research and scientific papers

A synthetic azinomycin analogue with demonstrated DNA cross-linking activity: Insights into the mechanism of action of this class of antitumor agent

An efficient synthesis of simplified azinomycin A and B analogues 1 and 2 (see picture) is described, and it is demonstrated that only 1, bearing both the epoxide and aziridine, induces interstrand cross-links in double-stranded DNA. Remarkably, a compoun

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