Product Information
The mechanism of the cyclobutanone cleavage reaction is a sequential intramolecular process in which the first step is a cyclobutanol intermediate that undergoes an expansion to form a six-membered ring with two unsaturated bonds. The second step involves bond cleavage and is triggered by the presence of palladium. This sequence can be used to synthesize 3-(2-chlorophenyl)cyclobutan-1-one.
Chemical properties
Technical inquiry about: 3D-FTB63635 3-(2-Chlorophenyl)cyclobutan-1-one
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