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• 381-73-7 Difluoroacetic acid 
• 119-62-0 (1R,2R)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol 
• 555-16-8 4-nitrobenzaldehdye 
• 284028-78-0 (2R,3R)-2-Bromo-3-hydroxy-3-(4-nitro-phenyl)-propionic acid tert-butyl ester 
• 284028-81-5 (2R,3R)-2-Amino-3-(tert-butyl-dimethyl-silanyloxy)-3-(4-nitro-phenyl)-propan-1-ol 
• 284028-80-4 2-azido-3-(tert-butyl-dimethyl-silanyloxy)-3-(4-nitro-phenyl)-propionic acid tert-butyl ester 
• 284028-79-1 2-bromo-3-(tert-butyl-dimethyl-silanyloxy)-3-(4-nitro-phenyl)-propionic acid tert-butyl ester 
• 454-31-9 ethyl difluoroacetate 

Relevant academic research and scientific papers

Efficient enantioselective syntheses of chloramphenicol and (D)-threo- and (D)-erythro-sphingosine

The chiral diazaborolidine 1 has been applied to the enantioselective syntheses of chloramphenicol (2) and (D)-threo-N-acetylsphingosine (3), a synthetic precursor of the diastereomeric (D)-sphingosines. (C) 2000 Elsevier Science Ltd.

Synthesis of photo cross linkers, structural analogs of chloramphenicol

With the view of better characterizing chloramphenicol binding site on the bacterial ribosome, different derivatives of this drug have been synthesized and assayed as antibiotics. Then respective affinities for the ribosome have also been measured. From t