62422-95-1

Upstream product

• 4122-57-0 3-methoxy-3H-isobenzofuran-1-one 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 873962-34-6 1,3-di-p-tolyl-4,7-dihydro-isobenzofuran 
• 5465-41-8 ditoluylethylene 
• 64-17-5 ethanol 
• 42211-60-9 1,2-phenylenebis(p-tolylmethanone) 
• 74322-72-8 [2-Diethylamino-6-(4-methyl-benzoyl)-cyclohex-3-enyl]-p-tolyl-methanone 

Downstream Products

• 95793-16-1 [2-(2,2-Dichloro-1-p-tolyl-vinyl)-phenyl]-p-tolyl-methanone 
• 42211-60-9 1,2-phenylenebis(p-tolylmethanone) 
• 1054569-43-5 1,3-di(p-tolyl)benzo[c]selenophene 
• 1610619-60-7 5,13-di-p-tolyl-12H-dibenzo[b,h]fluoren-12-one 
• 1610619-65-2 5,13-diphenyl-6,11-di-p-tolyl-12H-dibenzo[b,h]fluoren-12-one 
• 78237-42-0 5,10-bis(4-methoxyphenyl)-11H-benzo[b]-fluoren-11-one 
• 1610619-48-1 6,11-di-p-tolylbenzo[b]naphtho[2,3-d]thiophene S,S-dioxide 
• 1610619-70-9 6,11-di-p-tolylbenzo[d]naphtho[2,3-b]thiophene 
• 1012085-51-6 1,4-di(p-tolyl)naphthalene 

Relevant academic research and scientific papers

Synthesis and characterization of 1,3-diarylbenzo[c]selenophenes

A series of 1,3-diarylbenzo[c]selenophenes (symmetrical/unsymmetrical) have been synthesized involving a selenium transfer reaction of keto-alcohol/benzo[c]furan using Woollins reagent. The optical and electrochemical studies of these diarylbenzo[c]selenophenes are correlated with their structures.

A single-step synthesis of symmetrical 1,3-diarylisobenzofurans

A convenient single-step synthesis of various symmetrically substituted 1,3-diarylisobenzofurans from readily available 3-methoxy-3H-isobenzofuran-1-one (1a) and two equivalents of aryl Grignard reagents is described. The title compounds are obtained in medium to high isolated yields. Crude isobenzofuran has also been trapped by maleimide, furnishing pure Diels-Alder adduct almost quantitatively. Georg Thieme Verlag Stuttgart.