82586-27-4

Upstream product

• 1618-26-4 2,4-dithiapentane 
• 25226-97-5 3-methoxyphenethyl iodide 
• 79539-10-9 4,4-dimethoxy-1-bromo pentane 

Downstream Products

• 82586-29-6 3-[2-(3-methoxy-phenyl)-ethyl]-cyclohex-2-enone 
• 82586-28-5 3-[2-(3-Methoxy-phenyl)-ethyl]-3-methylsulfanyl-cyclohexanone 
• 82586-30-9 6-[2-(3-Methoxy-phenyl)-ethyl]-7-oxa-bicyclo[4.1.0]heptan-2-one 
• 82586-31-0 3-[2-(3-Methoxy-phenyl)-ethyl]-phenol 
• 82586-26-3 [7-(3-Methoxy-phenyl)-1-methylene-5,5-bis-methylsulfanyl-heptyloxy]-trimethyl-silane 

Relevant academic research and scientific papers

AN APPROACH TO THE PHENANTHRENE NUCLEUS VIA THIONIUM IONS AND EPOXYKETONE CYCLIZATIONS

A sulfur version of a directed aldol-type condensation followed by a cyclization of an α,β-epoxyketone produces the phenanthrene nucleus, common in many natural products.