7330-17-8

Upstream product

• 5382-00-3 Diphenyl phosphorochloridite 
• 67-63-0 isopropyl alcohol 
• 14747-96-7 diphenyl-N,N-diethylphosphoramidite 
• 108-95-2 phenol 
• 19620-78-1 O,O-diphenyl N-dimethylamidophosphite 

Downstream Products

• 934619-27-9 methyl 2-O-benzyl-6-deoxy-6-diphenoxyphosphinyl-3,4-O-isopropylidene-β-D-galactoside 
• 135052-86-7 [(3aR,4S,6S,7R,7aS)-6-Methoxy-7-(4-methoxy-benzyloxy)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethyl]-phosphonic acid diphenyl ester 
• 135052-85-6 ((3aR,5S,5aR,8aS,8bR)-2,2,7,7-Tetramethyl-tetrahydro-bis[1,3]dioxolo[4,5-b;4',5'-d]pyran-5-ylmethyl)-phosphonic acid diphenyl ester 

Relevant academic research and scientific papers

Galactose-derived phosphonate analogues as potential inhibitors of phosphatidylinositol biosynthesis in mycobacteria

Galactose-based phosphonate analogues of myo-inositol-1-phosphate and phosphatidylinositol have been synthesized from methyl β-d- galactopyranoside. Michaelis-Arbuzov reaction of isopropyl diphenyl phosphite or triisopropyl phosphite with a 6-iodo-3,4-iso

Synthesis of Phosphonates: a Modified Arbuzov Procedure

Reactions of 6-iodogalactosides with either methyl or isopropyl diphenyl phosphite lead to diphenylphosphoryl derivatives; these can be converted by ester exchange into dibenzylphosphoryl derivatives, which are convenient precursors of carbohydrate phosphonic acids.