Rearrangement of the Grignard reagent from 1-methylcyclobutylmethyl bromide: origins of the methyl substituent effect
EA Hill, MW Hallade
Index: Hill, E. Alexander; Hallade, Marc W. Journal of Organometallic Chemistry, 1988 , vol. 352, p. 263 - 272
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Abstract
Abstract 1-Methyl substitution leads to a small decrease (ca. 0.45) in the rate of the ring cleavage rearrangement of cyclobutylmethylmagnesium bromide. Comparison with literature data for 3-and 5-membered rings indicates that the methyl substituent shifts the equilibrium in the direction of ring cleavage, mostly by stabilization of the double bond of the open isomer, and possibly partly by destabilization of the organometallic function of the ...
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