118468-43-2

Upstream product

• 67-56-1 methanol 
• 896-65-1 (1,2-diphenylcyclopropyl)benzene 
• 120400-29-5 (Z/E)-α-(2-methylthiophenyl)-β-methoxyphenylmethyl styrene 
• 64244-25-3 benzylideneacetophenone dimethyl acetal 
• 119-61-9 benzophenone 
• 100-42-5 styrene 
• 120400-21-7 2,4-diphenyl-1-thio-2H-chromene 
• 98540-20-6 (Z)-1-methoxy-1,3,3-triphenylpropene 
• 86477-16-9 methyl-(1,3,3-triphenyl-allyl)-ether 

Relevant academic research and scientific papers

Synthesis and Reactions of 1-Thianaphthalenes

Treatment of 1-methyl-4-phenyl-1-thio-2H-chromenium perchlorate (2) with sodium hydride yielded a dimeric compound 4 and two rearrangement products 5 and 6 via unstable 1-methyl-4-phenyl-1-thianaphthalene (3).On heating with potassium hydroxide in ethanol

Effects of Aryl Substituents on Electron-Transfer-Mediated Photochemical Addition of Alcohol to 1,1,2-Triarylcyclopropanes

Direct irradiation of 1,1,2-triarylcyclopropanes in alcohol resulted in the formation of all possible products arising from trimethylene biradicals, while DCB-sensitised irradiation gave a novel "anti-Markownikoff" addition product of alcohol almost exclusively.In order to get insight into the nature and fate of intermediates in the reactions, the effects of nucleophiles and aryl substituents are examined.