76548-06-6

Upstream product

• 14086-78-3 Benzoic acid (1S,2R,3S,4R,6R)-2,3,4-triacetoxy-6-methanesulfonyloxy-cyclohexyl ester 
• 14086-77-2 Benzoic acid (1S,2R,3R,4S,6S)-2,3,4-triacetoxy-6-hydroxy-cyclohexyl ester 
• 488-73-3 (+/-)-cyclohexane-1r,2c,3t,4c,5t-pentaol 
• 108-24-7 acetic anhydride 
• 75419-36-2 3-amino-2,3-dideoxy-D-myo-inositol 
• 28978-34-9 5,6-dideoxy-1,2-O-isopropyledine-6-nitro-α-D-xylo-hexofuranose 
• 108311-23-5 (1R,2S,3S,5S)-5-Nitro-cyclohexane-1,2,3,4-tetraol 
• 4969-33-9 3-O-acetyl-5,6-dideoxy-1,2-O-isopropylidene-6-C-nitro-α-D-xylo-hex-5-enofuranose 
• 56707-67-6 Acetic acid (3aR,5R,6S,6aR)-2,2-dimethyl-5-(2-nitro-ethyl)-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 
• 108311-24-6 2,3-dideoxy-3-nitro-D-myo-inositol-1,4,5,6-tetraacetate 
• 108391-63-5 N-acetyl-2-deoxy-scyllo-inosamine 

Downstream Products

• 75419-36-2 3-amino-2,3-dideoxy-D-myo-inositol 
• 6216-30-4 N-((1R,2S,3R,4R,5S)-2,3,4,5-Tetrahydroxy-cyclohexyl)-acetamide 

Relevant academic research and scientific papers

Isolation of nabscessin C from nocardia abscessus IFM 10029T and A study on biosynthetic pathway for nabscessins

A new aminocyclitol derivative, designated nabscessin C (1), was isolated from Nocardia abscessus IFM 10029T. Nabcessin C is an isomer of nabscessins A (2) and B (3) with different positioning of the acyl group. Absolute configuration of nabscessin A was determined by conversion into the 2-deoxy-scyllo-inosamine pentaacetyl derivative (4) by hydrolysis and acetylation of 2. The biosynthetic pathway of nabscessins is proposed based on gene expression analysis.

Synthetic Study and Conformational Analysis of O-Benzylated Aminocyclitols

DL-(1,3/2)-3-Acetamido-1,2-di-O-benzylcyclohex-4-enediol (IIIa) and DL-(1,3/4)-1-acetamido-3,4-di-O-benzylcyclohex-5-enediol (IIIb) were synthesized from DL-trans-1,2-di-O-benzylcyclohex-3-enediol (I) via the corresponding azide derivatives (IIa-b) prepar