71787-00-3

Upstream product

• 70719-51-6 methyl 2,4-dimethoxy-6-<(phenylthio) methyl>-benzoate 
• 70719-39-0 2,4-Dimethoxy-6-phenylsulfanylmethyl-benzoic acid 

Downstream Products

• 111649-53-7 4-<2-(4-methanesulfonyloxybutyl)-1,3-dithian-2-yl>-1-methylbutyl-2,4-dimethoxy-6-<(phenylthio) methyl> benzoate 
• 111649-56-0 4-<2-(4-methanesulfonyloxy butyl)-1,3-dioxalan-2-yl>-1-methylbutyl-2,4-dimethoxy-6-<(phenylthio) methyl> benzoate 
• 111649-54-8 9-methanesulfonyloxy-1-methyl-5-oxo-nonyl-2,4-dimethoxy-6-<(phenylthio) methyl> benzoate 
• 111649-58-2 2,4-Dimethoxy-6-phenylsulfanylmethyl-benzoic acid 4-[2-(4-iodo-butyl)-[1,3]dithian-2-yl]-1-methyl-butyl ester 
• 111649-52-6 2,4-Dimethoxy-6-phenylsulfanylmethyl-benzoic acid 4-[2-(4-hydroxy-butyl)-[1,3]dithian-2-yl]-1-methyl-butyl ester 
• 111649-55-9 2,4-Dimethoxy-6-phenylsulfanylmethyl-benzoic acid 9-hydroxy-1-methyl-5-oxo-nonyl ester 
• 73127-59-0 4-<2-(4-iodobutyl)-1,3-dioxalan-2-yl>-1-methylbutyl-2,4-dimethoxy-6-<(phenylthio) methyl> benzoate 

Relevant academic research and scientific papers

SYNTHESIS OF (+/-)-ZEARALENONE

The aliphatic portion of (+/-)-zearalenone has been synthesised by a new simple route starting from 2,3-dihydropyran and 2-acetyl-γ-butyrolactone by employing dithiane for C-C bond formation.The final condensation of this segment with the aromatic part and subsequent transformations led to (+/-)-zearalenone.