139299-89-1

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 210833-99-1 phenyl 2,3,4-tri-O-benzyl-1-thio-D-glucopyranoside 
• 2936-70-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 100-39-0 benzyl bromide 
• 143436-69-5 phenyl 6-O-(tert-butyldiphenylsilyl)-1-thio-β-D-glucopyranoside 

Downstream Products

• 127570-64-3 N-acetyl-2,3,4-tri-O-benzyl-N-(benzyl N-benzyloxycarbonyl-L-β-aspartyl)-6-O-tert-butyldiphenylsilyl-α-D-glucopyranosylamine 
• 127570-61-0 2,3,4-tri-O-benzyl-N-(benzyl N-benzyloxycarbonyl-L-β-aspartyl)-α-D-glucopyranosylamine 
• 147556-23-8 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-(((tert-butyldiphenylsilyl)oxy)methyl)tetrahydro-2H-pyran-2-one 
• 885314-16-9 C₄₈H₅₆O₆Si₂ 
• 885314-12-5 C₃₂H₃₄O₈S 
• 885314-11-4 C₃₁H₃₁BrO₅S 
• 885314-18-1 C₃₁H₃₂O₅S 
• 885314-17-0 C₃₀H₃₂O₇S 
• 885314-10-3 C₂₉H₃₀O₅ 
• 885314-08-9 C₄₆H₅₀O₈Si 
• 885314-07-8 C₄₅H₄₇BrO₅Si 
• 885314-06-7 C₄₅H₄₈O₅Si 
• 885314-05-6 C₄₈H₅₆O₅Si₂ 

Relevant academic research and scientific papers

Synthesis of the bicyclic core of tagetitoxin

A synthesis of the 9-oxa-3-thiabicyclo[3.3.1]nonane ring system, which constitutes the core of the RNA polymerase inhibitor tagetitoxin, has been achieved through cyclisation of a thiol onto an electrophilic ketone. The Royal Society of Chemistry 2006.

Stereoselective glycosylation using the long-range effect of a [2-(4-phenylbenzyl)oxycarbonyl]benzoyl group

Highly α-selective glucosylation was effected by virtue of the solvent effect of cyclopentyl methyl ether and the long-range assistance of bulky 6-O-protective groups. Higher α-selectivity was obtained by the use of this solvent in comparison to conventio

Sulfated glyceroglucolipids as inhibitors of bacterial adherence

The subject invention involves pharmaceutical compositions comprising a sulfated glyceroglucolipid having the structure: STR1 wherein n is an integer of from 1 to about 5, R is hydrogen or C1 -C24 acyl or alkyl, R' is hydrogen or C1 -C24 acyl or alkyl, and M+ is a cationic moiety, and methods of treating or preventing gastroduodenal diseases or disorders caused by or associated with H. pylori by administering such compounds.

An Efficient and Stereocontrolled Synthesis of the Nephritogenoside Core Structure

An efficient and stereocontrolled synthesis of the core trisaccharide 2 of nephritogenic glycopeptide, nephritogenoside 1 is described.Key to our synthetic strategy was β-selective glycosylation without neighboring group participation. Key words: nephrito