79646-67-6

Upstream product

• 6752-49-4 (4aR,6S,8aR)-6-Methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one 

Downstream Products

• 79607-48-0 2,2,2-Trichloro-acetimidic acid 2-[(4aR,6S,8aS)-6-methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-(8E)-ylidene]-ethyl ester 
• 79607-50-4 2,2,2-Trichloro-N-((4aR,6S,8S,8aS)-8-formyl-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-acetamide 
• 79607-49-1 2,2,2-Trichloro-N-((4aR,6S,8R,8aS)-6-methoxy-2-phenyl-8-vinyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-acetamide 
• 88901-92-2 methyl 4,6-O-benzylidene-3-C-(carbomethoxy-methylene)-2,3-didesoxy-α-D-ribo-hexapyranoside 
• 79607-47-9 2-[(4aR,6S,8aS)-6-Methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-(8E)-ylidene]-ethanol 

Relevant academic research and scientific papers

UNVERZWEIGTE UND R-C-N-VERZWEIGTE AMINOZUCKER DURCH TRICHLORACETIMIDAT-UMLAGERUNG

Trichloroacetimidates from carbohydrates with an endo- or an exocyclic allylic alcohol grouping rearrange under thermal conditions with formation of unbranched or R-C-N branched amino sugars.