80065-53-8

Upstream product

• 69982-70-3 3,4-di-O-acetyl-2,6-dibromo-2,6-dideoxy-5a-carba-β-DL-glucopyranosyl bromide 
• 140854-93-9 DL-(1,3/2,4,6)-3-Acetamido-1,2-di-O-acetyl-4-bromo-6-bromomethyl-1-,2-cyclohexanediol 
• 80065-34-5 (1RS)-3,4-di-O-acetyl-(1,2,4/3,5)-5-bromomethyl-2-(p-toluenesulfonamido)-1,3,4-cyclohexanetriol 
• 101924-30-5 <(1S)-(1,2,4/3,5)-5-Bromomethyl-3,4-dihydroxy-2-(p-toluenesulfonamido)-1-cyclohexyl> β-<*>-glucopyranoside hexaacetate 
• 140854-92-8 (+/-)-2-exo-(p-tolylsulfonylamino)-4,8-dioxatricyclo<4.2.1.0^3,7>nonane 
• 80065-34-5 DL-3,4-di-O-acetyl-(1,2,4/3,5)-5-bromomethyl-2-(toluene-p-sulfonamido)-1,3,4-cyclohexanetriol 
• 74766-78-2 3,4-di-O-acetyl-1,5-anhydro-6-bromo-2,6-dideoxy-5a-carba-DL-arabino-hex-1-enitol 
• 108-24-7 acetic anhydride 

Downstream Products

• 140855-00-1 DL-(1,2,4,5/3)-4-Acetamido-1,2,3,5-tetra-O-acetyl-1-C-acetoxymethyl-1,2,3,5-cyclohexanetetrol 
• 140924-59-0 DL-(1,3/2,4,5)-4-Acetamido-1,2,3,5-tetra-O-acetyl-1-C-acetoxymethyl-1,2,3,5-cyclohexanetetrol 
• 140924-58-9 DL-(1,3/2,4,5)-4-Acetamido-2,3,5-tri-O-acetyl-1-C-acetoxymethyl-1,2,3,5-cyclohexanetetrol 
• 140854-99-5 DL-(1,2,4,5/3)-4-Acetamido-2,3,5-tri-O-acetyl-1-C-acetoxymethyl-1,2,3,5-cyclohexanetetrol 
• 140855-05-6 DL-(1,3/2,4,5)-4-Amino-1-C-hydroxymethyl-1,2,3,5-cyclohexanetetrol 
• 141039-91-0 DL-(1,2,4,5/3)-4-Amino-1-C-hydroxymethyl-1,2,3,5-cyclohexanetetrol 
• 140855-01-2 DL-(1,2,4,5/3)-2-Acetamido-5-C-acetoxymethyl-1,3,4-tri-O-acetyl-5-bromo-1,3,4-cyclohexanetriol 
• 140855-04-5 DL-(1,2,4/3)-2-Acetamido-5-acetoxymethyl-1,3,4-tri-O-acetyl-cyclohexene-1,3,4-triol 
• 140855-02-3 DL-(1,2,4,5/3)-2-Acetamido-1,3,4-tri-O-acetyl-5-bromo-5-C-bromomethyl-1,3,4-cyclohexanetriol 
• 140855-03-4 DL-(1,2,4/3)-2-Acetamido-1,3,4-tri-O-acetyl-5-bromomethyl-5-cyclohexene-1,3,4-triol 
• 140854-91-7 DL-(1,2,4/3)-2-Amino-5-(hydroxymethyl)-5-cyclohexene-1,3,4-triol 
• 140854-97-3 DL-(1,2,4/3)-2-Acetamido-1,3,4-tri-O-acetyl-5-methylene-1,3,4-cyclohexanetriol 

Relevant academic research and scientific papers

New Synthesis of 2-Amino-5a-carba-2-deoxy-&α-DL-glucopyranose and Its Transformation into Valienamine and Valiolamine Analogues

The positional isomers 2, 4, and 6 of respective validamine (1), valiolamine (3), and valienamine (5), derived from 2-amino-5a-carba-2-deoxy-α-D-glucopyranose, were synthesized as racemates from DL-(1,3/2,4,6)-3-acetamido-1,2-di-O-acetyl-4-bromo-6-bromome

Pseudo-sugars. VII. Synthesis of Pseudo-hexopyranose Derivatives with α- and β-Gluco Configurations

Several derivatives of pseudo-hexopyranose (5-hydroxymethyl-1,2,3,4-cyclohexanetetrol) with α-gluco, (1,2,4/3,5), and β-gluco, (1,3,5/2,4), configurations were synthesized starting from the compounds obtained by cis-hydroxylation and oxyamination of DL-di