137271-98-8

Upstream product

• 14233-64-8 tri-O-benzyl-D-arabinolactone 
• 37776-25-3 2,3,5-tri-O-benzyl-D-arabinose 

Downstream Products

• 55781-02-7 3,5-dimethyl-1-(2,3,5-tri-O-benzyl-α-D-arabinofuranosyl)pyrazole 
• 137272-01-6 2,3,5-tri-O-benzyl-4-O-t-butyldimethylsilyl-N,N',N'-tris-t-butyloxycarbonyl-D-arabinonohydrazide 
• 137272-02-7 2,3,5-tri-O-benzyl-N,N',N'-tris-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide 
• 137271-76-2 2,3,5-tri-O-benzyl-N',N'-bis-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide 
• 137272-03-8 2,3,5-tri-O-benzyl-4-O-t-butyldimethylsilyl-N'-t-butyloxycarbonyl-D-arabinonohydrazide 
• 137272-00-5 2,3,5-tri-O-benzyl-N'-t-butyloxycarbonyl-4-O-trimethylsilyl-D-arabinonohydrazide 
• 137272-04-9 2,3,5-O-tribenzyl-N'-trifluoroacetyl-4-deoxy-L-xylono-1,4-hexacyclohydrazide 
• 14233-64-8 tri-O-benzyl-D-arabinolactone 
• 137271-99-9 2,3,5-tri-O-benzyl-N'-t-butyloxycarbonyl-D-arabinonohydrazide 

Relevant academic research and scientific papers

Synthetic approaches toward glidobamine, the core structure of the glidobactin antibiotics

Peptide synthesis method was first employed to synthesize glidobamine, the core structure of the glidobactin antibiotics (2), but in a model study all attempts failed to cyclize the linear precursor 10. Then a N-N bond cleavage method was developed to con

Derivatives of hydrazino-monosaccharides and aldohexoses which are useful as intermediates for preparing compounds or as compounds which lower the uric acid

Substituted hydrazino- and pyrazolo-aldopentoses and aldohexoses, which are useful as intermediates for preparing compounds, as compounds which lower the uric acid level in the blood, and as bactericides, are provided. The substituted hydrazino compounds also enter into chemical reactions which are not possible with their unsubstituted counterparts.