68774-48-1

Upstream product

• 76-83-5 trityl chloride 
• 41107-82-8 2,5-anhydro-D-mannitol 
• 65758-50-1 2,5-anhydro-1,3-O-isoprpylidene-6-O-triphenylmethyl-D-glucitol 

Downstream Products

• 1146544-48-0 2,5-anhydro-3,4,6-tri-O-benzoyl-D-mannitol 
• 1352744-35-4 (2R,3R,4R,5R)-2-(benzoyloxymethyl)-5-(tosyloxymethyl)tetrahydrofuran-3,4-diyl dibenzoate 
• 1472641-27-2 2,5-anhydro-3,4,6-tri-O-benzoyl-1-fluoro-D-mannitol 
• 1472641-26-1 2,5-anhydro-3,4,6-tri-O-benzoyl-1-O-trityl-D-mannitol 
• 84447-07-4 3,4,6-tri-O-acetyl-2,5-anhydro-1-O-tosyl-D-mannitol 
• 130466-42-1 2,5-anhydro-3,4-di-O-benzyl-1-deoxy-1-diethylphosphono-6-O-diphenylphosphono-D-mannitol 
• 130372-43-9 Acetic acid (2R,3R,4S,5S)-3,4-bis-benzyloxy-5-(diethoxy-phosphorylmethyl)-tetrahydro-furan-2-ylmethyl ester 
• 130465-01-9 ((2S,3S,4R,5R)-3,4-Bis-benzyloxy-5-hydroxymethyl-tetrahydro-furan-2-ylmethyl)-phosphonic acid diethyl ester 
• 102292-67-1 2,5-anhydro-3,4,6-tri-O-benzyl-1-deoxy-1-diethoxyphophinoyl-D-mannitol 
• 109065-80-7 2,5-anhydro-3,4,6-tri-O-benzyl-1-deoxy-1-iodo-D-mannitol 
• 102208-55-9 2,5-anhydro-3,4,6-tri-O-benzyl-D-mannitol 
• 84446-96-8 3,4,6-tri-O-acetyl-2,5-anhydro-1-O-trityl-D-mannitol 

Relevant academic research and scientific papers

Synthesis and preliminary evaluation of 1-[18F]Fluoro-1-deoxy-2, 5-anhydro-D-mannitol as a PET radiotracer for breast cancer imaging

1-[18F]Fluoro-1-deoxy-2,5-anhydro-D-mannitol (3, 18F-FDAM) has been synthesized in 6 steps starting from 2,5-anhydro-D-mannitol (2,5-AM) and evaluated as a new radiotracer for PET imaging of MCF-7 breast tumor. The result of PET imag

Stereospecific synthesis of 5-phospho-α-D-arabinosyl-C-phosphonophosphate (pACpp): A stable analogue of the putative mycobacterial cell wall biosynthetic intermediate 5-phospho-D-arabinosyl pyrophosphate (pApp)

The stereospecific synthesis of 5-phospho-α-D-arabinosyl-C-phosphonophosphate (pACpp) from D-glucosamine is described. This compound was evaluated for its ability to serve as a stable analogue of the putative mycobacterial cell wall biosynthetic intermediate 5-phospho-D-arabinosyl pyrophosphate (pApp). The phosphonophosphate proved incapable of interfering with formation of the mycobacterial arabinan precursor decaprenylphospho-arabinose (DpA) in vitro.

Analysis of the linkage positions in D-fructofuranosyl residues by the reductive-cleavage method.

The suitability of the reductive-cleavage method for analysis of the linkage positions in D-fructofuranosyl residues of D-fructans was examined by using sucrose, chicory-root inulin, and Aerobacter levanicum levan as models. Permethylation, and reductive