50805-40-8

Upstream product

• 67-56-1 methanol 
• 38274-35-0 1,2,3-triphenylindene 
• 117446-52-3 o-(1,2-Diphenyl-3-methoxy-2-propenyl)benzophenone 
• 145430-85-9 2--1,2-diphenylethanone 
• 79023-66-8 1-Azido-1,3,4-triphenyl-1H-isochromene 

Downstream Products

• 117446-52-3 o-(1,2-Diphenyl-3-methoxy-2-propenyl)benzophenone 
• 118599-46-5 1-(1-Phenyl-2-methoxyvinyl)-2-(1,2-diphenyl-3-methoxy-2-propenyl)benzene 
• 89619-51-2 (1S,8R,9S)-1,8,9-Triphenyl-10,11,12-trioxa-tricyclo[7.2.1.0^2,7]dodeca-2,4,6-triene 
• 145430-85-9 2--1,2-diphenylethanone 

Relevant academic research and scientific papers

Ozonolyses of 1,2-Diphenyl- and 2-Phenylindene

Ozonolyses of 1,2-diphenylindene (7), 2-phenylindene (18), and the structurally related acyclic keto olefins 13, 14, 26, and 32 were conducted in MeOH/CH2Cl2 at -70 and 0 deg C.The structure of the indenes, 7 and 18, and the rection temperature, were foun

Ozonolysis of 1-Substituted 2,3-Diphenylindenes and o-(1-Substituted-2-phenyl-3-methoxy-2-propenyl)benzophenones. Remarkable Effects of the Method of Generation of the Carbonyl Oxide Intermediates on the Stereochemistries of Both the Ozonide and the Metha

Ozonolyses of 1-substituted 2,3-diphenylindenes 1a,b and o-(1-substituted-2-phenyl-3-methoxy-2-propenyl)benzophenones 8a,b in methanol-methylene chloride at -70 deg C, which should proceed through common carbonyl oxide intermediates 11a,b, afforded stereo

1-Azidoisochromenes. A New Route to 3,1-benzoxazepines

Nucleophilic attack of sodium azide on isochromylium salts leads to the preparation of 1-azidoisochromenes which when heated lose molecular nitrogen and give 3,1-benzoxazepines.