120401-20-9

Upstream product

• 6752-49-4 (4aR,6S,8aR)-6-Methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one 
• 1826-67-1 vinyl magnesium bromide 

Downstream Products

• 20880-50-6 [(4aR,6S,8aS)-6-Methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-(8E)-ylidene]-acetic acid methyl ester 
• 79607-47-9 2-[(4aR,6S,8aS)-6-Methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-(8E)-ylidene]-ethanol 
• 120401-22-1 Acetic acid 1-acetoxy-2-[(4aR,6S,8aS)-6-methoxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-(8E)-ylidene]-ethyl ester 
• 120401-23-2 [(Z)-2-((4aR,6S,8aS)-6-Methoxy-2-phenyl-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-yl)-vinyl]-dimethyl-amine 
• 120401-21-0 methyl 4,6-O-benzylidene-2,3-dideoxy-3-C-(formylmethylene)-α-D-erythro-hexopyranoside 

Relevant academic research and scientific papers

Efficient routes to pyranosidic homologated conjugated enals and dienes from monosaccharides

Three new processes for the obtention of pyranosidic dienes type B, and D and homologated conjugated enals A, have been designed in the context of the preparation of useful chiral building blocks from monosaccharides. Addition of vinylmagnesium bromide on

A Synthetic Approach to Actinobolin Analogs from D-Glucose

Synthesis of methyl 4,6-O-benzylidene-2,3-dideoxy-3-C--α-D-arabino-hexopyranoside (22), a common intermediate for the synthesis of actinobolin (1a), bactobolin (1b), ramulosin (2a) and 6-hydroxyramulosin (2b) from D-glucose