Journal of Organic Chemistry p. 4280 - 4286 (1983)
Update date:2022-08-03
Topics: NMR spectroscopy Kinetic Analysis Steric Retard Internal Rotation 1-Carbomethoxy-1,2-diphenylcyclopropane
Doering, W. von E.
Robertson, L. R.
Ewing, E. E.
The high preference (RA = 13) found by Chmurny and Cram for internal rotation of the hydrogen-phenyl carbon bond over the carbomethoxy-phenyl carbon bond in 1-carbomethoxy-1,2-diphenylcyclopropane appears to originate in a steric effect.There b
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