935693-85-9

Upstream product

• 6738-06-3 phenylethynylmagnesium bromide 
• 16838-89-4 2,3,5-tri-O-benzyl-D-ribofuranose 
• 4440-01-1 lithium phenylacetylide 
• 536-74-3 phenylacetylene 

Downstream Products

• 113889-66-0 1-(2',3',5'-tri-O-benzyl-β-D-ribofuranosyl)-2-phenylacetylene 
• 935693-87-1 (3R,4S,5R,6R)-3,4,5,6,7-pentabenzoxy-1-phenylhept-1-yne 
• 935693-90-6 dimethyl (1'R,2'S,3'R,4'R)-4-(1',2',3',4',5'-pentabenzoxypentyl)-5-phenylpyridazine-3,6-dicarboxylate 
• 935693-94-0 dimethyl (1'R,2'S,3'R,4'R)-3-(1',2',3',4',5'-pentabenzoxypentyl)-4-phenyl-1H-pyrrole-2,5-dicarboxylate 
• 935694-00-1 dimethyl (1'R,2'S,3'R,4'R)-3-(1',2',3',4',5'-pentahydroxypentyl)-4-phenyl-1H-pyrrole-2,5-dicabroxylate 

Relevant academic research and scientific papers

Synthesis of polyhydroxylated pyrano-pyrrole derivatives from carbohydrate precursors

The efficient synthesis of novel polyhydroxy-tetrahydropyrano-pyrroles from acetylenic carbohydrate precursors in three to four steps is described. The methodology involves, as key steps, the ring contraction of pyridazine intermediates obtained by an inv

Synthesis of novel polyhydroxylated tetrahydropyranopyrroles

The stereoselective access to original polyhydroxylated tetrahydropyranopyrroles is described. The key steps involve an inverse-demand Diels-Alder reaction and a ring contraction of a pyridazine heterocycle. Georg Thieme Verlag Stuttgart.