129729-12-0

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 1253692-55-5 2,3,4,2',3',4'-hexa-O-benzyl-α,α-trehalose 
• 125177-97-1 [(2R,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yl]-methanol 

Downstream Products

• 129729-13-1 2,3,4-tri-O-benzyl-6-deoxy-α-D-gluco-heptopyranosylurononitrile 2,3,4-tri-O-benzyl-6-deoxy-α-D-gluco-heptopyranosidurononitrile 
• 129729-14-2 2,3,4-tri-O-benzyl-6-deoxy-α-D-gluco-heptopyranosyluronamide 2,3,4-tri-O-benzyl-6-deoxy-α-D-gluco-heptopyranosiduronamide 
• 171815-52-4 2,2',3,3',4,4'-hexabenzyl-6,6'-bis(diphenylphosphinyl)-6,6'-dideoxy-α-D-trehalose 
• 1017579-22-4 2,3,4-tri-O-benzyl-6-deoxy-6-N-(tetrazol-1-yl)-α-D-glucopyranosyl 2,3,4-tri-O-benzyl-6-deoxy-6-N-(tetrazol-2-yl)-α-D-glucopyranoside 
• 1017579-21-3 2,3,4-tri-O-benzyl-6-deoxy-6-N-(tetrazol-2-yl)-α-D-glucopyranosyl 2,3,4-tri-O-benzyl-6-deoxy-6-N-(tetrazol-2-yl)-α-D-glucopyranoside 
• 1017579-23-5 2,3,4-tri-O-benzyl-6-deoxy-6-N-(5-phenyltetrazol-2-yl)-α-D-glucopyranosyl 2,3,4-tri-O-benzyl-6-deoxy-6-N-(5-phenyltetrazol-2-yl)-α-D-glucopyranoside 
• 1017579-25-7 2,3,4-tri-O-benzyl-6-deoxy-6-N-(5-phenyltetrazol-1-yl)-α-D-glucopyranosyl 2,3,4-tri-O-benzyl-6-deoxy-6-N-(5-phenyltetrazol-2-yl)-α-D-glucopyranoside 
• 76790-48-2 6,6'-diamino-2,3,4,2',3',4'-hexa-O-benzyl-6,6'-dideoxy-α,α-trehalose 
• 827026-07-3 6,6'-dideoxy-6,6'-di(monoheptaminoacetyl)amino-2,2',3,3',4,4'-hexa-O-benzyl-α-D-trehalose 
• 827026-03-9 6,6'-dioctylcarbamoylamino-2,2',3,3',4,4'-hexa-O-benzyl-6,6'-dideoxy-α-D-trehalose 
• 827026-06-2 6,6'-dideoxy-6,6'-di(monobromoacetyl)amino-2,2',3,3',4,4'-hexa-O-benzyl-α-D-trehalose 
• 76790-47-1 6,6'-diazido-2,3,4,2',3',4'-hexa-O-benzyl-6,6'-dideoxy-α,α-trehalose 

Relevant academic research and scientific papers

Synthesis of new heterocyclic derivatives of α,α-trehalose

Several novel N-1, N-2, and S-5 tetrazole and 1,3,4-oxadiazole derivatives of α,α-trehalose disubstituted at C-6,6′, with potential synthetic and pharmacological interest were prepared from commercial tetrazoles and 1,3,4-oxadiazoles in reaction with hexa

Synthesis of trehalose-based compounds and their inhibitory activities against Mycobacterium smegmatis

The synthesis of a library of trehalose-based compounds has been accomplished, and their activities against Mycobacterium smegmatis have been determined. A preliminary structure-activity relationship (SAR) is reported. Despite not having a potent lead, on

Synthesis of a trehalose homolog, 6-deoxy-α-D-gluco-heptopyranosyl 6-deoxy-α-D-gluco-heptopyranoside, and the corresponding bis(heptosiduronic acid)

Crystalline 6-deoxy-α-D-gluco-heptopyranosyl 6-deoxy-α-D-gluco-heptopyranoside (8) and (6-deoxy-α-D-gluco-heptopyranosyluronic acid) 6-deoxy-α-D-gluco-heptopyranosiduronic acid (7) were synthesized from α,α-trehalose (1).Reaction of 2,3,4,2',3',4'-hexa-O-