99322-26-6

Upstream product

• 690-12-0 (2-chloroethyl)phosphonic dichloride 
• 100-51-6 benzyl alcohol 
• 112-72-1 1-Tetradecanol 
• 111-77-3 2-(2-methoxyethoxy)ethyl alcohol 

Downstream Products

• 99322-48-2 dibenzyl 4,5,6-tri-O-benzyl-8-O-(dibenzyloxyphosphoryl)-1,2,3-trideoxy-3-nitro-α-D-altro-3-octulopyranose-1-phosphonate 
• 99322-49-3 dibenzyl 4,5,6-tri-O-benzyl-8-O-(dibenzyloxyphosphoryl)-1,2-dideoxy-D-altro-3-octulopyranose-1-phosphonate 
• 99322-47-1 dibenzyl 4,5,6-tri-O-benzyl-1,2,3-trideoxy-3-nitro-α-D-altro-octulopyranose-1-phosphonate 

Relevant academic research and scientific papers

An Improved Access to Phosphonic Acids and Their Mono- and Diesters

The reaction of phosphonic dichlorides with a mixture of benzyl alcohol and an aliphatic alcohol affords a mixture of the corresponding dibenzyl phosphonate, dialkyl phosphonate, and alkyl benzyl phosphonate which is easily separated by column chromatogra

89. Deoxy-nitrosugars. 10th Communication. Synthesis of Isosteric Phosphonate Analogues of Ulose-1-Phosphates

A general approach to isosteric phosphonate analogues of ulose-1-phosphates is described.A base-catalysed chain elongation via a Michael addition of 1-deoxy-1-nitro-sugars 4, 8, and 16 to the vinylphosphonate 18 followed by hydrolysis of the nitro adducts