270076-02-3

Upstream product

• 538-37-4 dibenzyl phosphochloridate 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 1146540-71-7 3-O-benzoyl-5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose 

Downstream Products

• 1146540-72-8 3-O-acetyl-5-O-dibenzylphosphono-1,2-O,O-isopropylidene-α-D-xylofuranose 
• 270076-05-6 3-O-benzyl-1,2-O-isopropylidene-3-C-methyl-α-D-ribofuranose 5-dibenzylphosphate 
• 270076-08-9 2-O-benzyl-2-C-methyl-D-erythritol 4-dibenzylphosphate 
• 270076-07-8 2-O-benzyl-2-C-methyl-D-erythrose 4-dibenzylphosphate 
• 270076-04-5 1,2-O-isopropylidene-3-C-methyl-α-D-ribofuranose 5-dibenzylphosphate 
• 270076-03-4 1,2-O-isopropylidene-α-D-erythro-pentofuranose-3-ulose 5-dibenzylphosphate 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of 4-diphosphocytidyl-2-C-methyl-d-erythritol: a substrate for IspE

Enantiomerically pure 2-C-methyl-d-erythritol 4-phosphate 1 (MEP) is synthesized from 1,2-O-isopropylidene-α-d-xylofuranose via facile benzylation in good yield. Subsequently, 1 is used for enzymatic synthesis of 4-diphosphocytidyl-2-C-methyl-d-erythritol

Synthesis of simple adenosine diphosphate ribose analogues

(Chemical Equation Presented) The synthesis of analogues of adenosine diphosphate ribose and acetylated adenosine diphosphate ribose, modified at the northern pentose, is reported. The stereochemistry at the acetylated centers was chosen to minimize acety

Chemical synthesis of enantiopure 2-C-methyl-D-erythritol 4-phosphate, the key intermediate in the mevalonate-independent pathway for isoprenoid biosynthesis

Optically pure 2-C-methyl-D-erythritol 4-phosphate, a key intermediate in the mevalonate-independent route for isoprenoid biosynthesis, is conveniently synthesized from 1,2-O-isopropylidene-α-D-xylofuranose, including the possibility of radiolabeling of t