1448599-76-5

Upstream product

• 558-30-5 2-methyl-1,2-epoxypropane 
• 135663-97-7 1-phenylbut-3-yn-2-ol 

Downstream Products

• 1448599-78-7 5-benzyl-3,3,11,11-tetraethyl-9,9-dimethyl-4,10-dioxa-3,11-disilatridec-6-yne 
• 1448599-70-9 2,2-dimethyl-4-phenethyl-2,4-dihydro-1H-benzo[f]isochromene 
• 1448599-71-0 2,2-dimethyl-4-phenyl-2,4-dihydro-1H-benzo[f]isochromene 
• 1448599-75-4 4-(4-methoxyphenyl)-2,2-dimethyl-2,4-dihydro-1H-benzo[f]isochromene 
• 1448599-74-3 2,2-dimethyl-4-(4-nitrophenyl)-2,4-dihydro-1H-benzo[f]isochromene 
• 1448599-73-2 2,2-dimethyl-4-(4-(trifluoromethyl)phenyl)-2,4-dihydro-1H-benzo[f]isochromene 
• 1448599-72-1 4-(4-bromophenyl)-2,2-dimethyl-2,4-dihydro-1H-benzo[f]isochromene 

Relevant academic research and scientific papers

Electrophilic Cyclization of Phenylalkynediols to Naphthyl(aryl)iodonium Triflates with Chelating Hydroxyls: Preparation and X-ray Analyses

Alkynediols containing one propargylic alcohol as well as a second alcohol, which is propargylic or homopropargylic, react with PhI+CN-OTf (Stang's reagent) or 3,5-(CF3)2C6H3I+CN

Atom economical, one-pot, three-reaction cascade to novel tricyclic 2,4-dihydro-1 H-benzo[ f ]isochromenes

Reaction of 6-methyl-1-phenylhept-3-yne-2,6-diol with various aldehydes under Lewis acid conditions provides an atom economical, two-component cascade reaction sequence to novel 2,4-dihydro-1H-benzo[f]isochromene compounds. Aliphatic aldehydes as well as