93000-11-4

Upstream product

• 93000-10-3 benzyl ((2R,4aR,6S,7R,8R,8aS)-8-hydroxy-6-methoxy-2-phenyl hexahydropyrano[3,2-d][1,3]dioxin-7-yl)carbamate 
• 100-39-0 benzyl bromide 
• 60076-41-7 methyl 4,6-O-benzylidene-2-(benzyloxycarbonyl)-amino-2-deoxy-α-D-glucopyranoside 

Downstream Products

• 110236-56-1 methyl N-benzyloxycarbonyl-2-deoxy-3,6-di-O-benzylglucopyranoside 
• 501088-17-1 methyl 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 175978-55-9 methyl 2-azido-3-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 162678-87-7 Methyl 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 139573-22-1 Methyl 2-amino-4,6-O-benzylidene-3-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 185801-19-8 methyl 3,4-di-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside 
• 159489-49-3 {(S)-1-[(3R,4S,6S)-4-Benzyloxy-6-(benzyloxycarbonylamino-methyl)-2-oxo-tetrahydro-pyran-3-ylcarbamoyl]-2-methyl-propyl}-carbamic acid benzyl ester 
• 159489-44-8 {(S)-1-[(2S,3R,4S,6S)-4-Benzyloxy-6-(benzyloxycarbonylamino-methyl)-2-methoxy-tetrahydro-pyran-3-ylcarbamoyl]-2-methyl-propyl}-carbamic acid benzyl ester 
• 159489-39-1 Toluene-4-sulfonic acid (2R,3R,4R,5R,6S)-4-benzyloxy-5-benzyloxycarbonylamino-2-(tert-butoxycarbonylamino-methyl)-6-methoxy-tetrahydro-pyran-3-yl ester 
• 159489-42-6 {(S)-1-[(2S,3R,4S,6S)-4-Benzyloxy-6-(tert-butoxycarbonylamino-methyl)-2-methoxy-tetrahydro-pyran-3-ylcarbamoyl]-2-methyl-propyl}-carbamic acid benzyl ester 
• 159489-36-8 Toluene-4-sulfonic acid (2R,3S,4R,5R,6S)-4-benzyloxy-5-benzyloxycarbonylamino-3-hydroxy-6-methoxy-tetrahydro-pyran-2-ylmethyl ester 
• 159489-38-0 [(2S,3R,4R,5R,6R)-4-Benzyloxy-6-(tert-butoxycarbonylamino-methyl)-5-hydroxy-2-methoxy-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester 
• 159489-40-4 [(2S,3R,4S,6S)-4-Benzyloxy-6-(tert-butoxycarbonylamino-methyl)-2-methoxy-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester 
• 159489-37-9 ((2S,3R,4R,5R,6R)-6-Azidomethyl-4-benzyloxy-5-hydroxy-2-methoxy-tetrahydro-pyran-3-yl)-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Preparation method of fondaparinux sodium monosaccharide intermediate

The invention discloses a preparation method of a fondaparinux sodium monosaccharide intermediate. The preparation method includes using methyl glucose protected by C4 and C6 positions as a raw material to obtain methyl 3-O-benzyl-4,6-O-benzylidene-2-(ben

The revised structure of the antibiotic Tue 1718 B confirmed by synthesis

The revised structure of the dipeptide antibiotic Tue 1718 B was confirmed by synthesis of two possible diastereoisomers of L-valyl-dihydroxylysine 2. Comparison of the NMR spectra of the synthetic and natural products indicates (2S,3S,5S)- or (2S,3R,5S)-

SYNTHESIS OF AN ANTITHROMBIN BINDING HEPARIN-LIKE PENTASACCHARIDE LACKING 6-O SULPHATE AT ITS REDUCING END.

The synthesis of a pentasaccharide of the structure of the antithrombin (AT-III) binding sequence, but lacking the 6-O sulphate group at the reducing end, is described and its α-Xa activity determined.