Stereoelectronic control in organic chemistry: addition reactions of some 1, 4-benzoquinone 4-(O-methyloximes)
JE Baldwin, RK Norris
Index: Baldwin, Jack E.; Norris, Robert K. Journal of Organic Chemistry, 1981 , vol. 46, # 4 p. 697 - 703
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Citation Number: 24
Abstract
Results Halogen Addition Reactions. The halogen addition products from the methyloximes 1-3 were prepared by addition of bromine (or chlorine) to an equimolar amount of the appropriate methyloxime in carbon tetrachloride, chloroform, or dichloromethane, followed by removal of the solvent. The 'H NMR spectra of the resulting product mixtures were recorded and the resonances assigned to the
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