179677-67-9

Upstream product

• 25145-43-1 2-phenylpropionyl chloride 
• 114763-30-3 (3aR,7aS)-2,2,4-trimethyl-3a,7a-dihydro-1,3-benzodioxole 
• 179677-68-0 (1R,2S,6S,7S)-9-((Z)-1-phenylethylidene)-4,4,7-trimethyl-3,5,8-trioxatricyclo[5.2.2.0^2,6]undec-10-ene 

Downstream Products

• 179677-68-0 (1R,2S,6S,7S)-9-((Z)-1-phenylethylidene)-4,4,7-trimethyl-3,5,8-trioxatricyclo[5.2.2.0^2,6]undec-10-ene 

Relevant academic research and scientific papers

Reactions of diphenylketene and methylphenylketene with some cis-cyclohexa-3,5-diene-1,2-diol derivatives

The reaction of the dienes 1-5 with diphenylketene to give the [2 + 2]-adducts 6-10 and the [4 + 2]-adducts 11-15, respectively, has been found to occur by an ionic mechanism involving the zwitterion 16. The reactions of the dienes 2 and 3 with methylphenylketene (and also cyclohexa-1,3-diene with diphenylketene) proceed in a similar fashion. The enol ether 13 was converted into the polyoxygenated cyclohexane derivatives 33, 35 and 38.