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The regioselectivity observed with aryl-substituted amino-cyclopropanes may be explained by a productive interaction of the aryl-Pd(II)I intermediate through the less hindered approach of the cyclopropyl ring. Further insights into the potential electronic effects of the aryl moiety should be addressed by comparison with alkyl-substituted cyclo-propanes.
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The regioselectivity observed with aryl-substituted amino-cyclopropanes may be explained by a productive interaction of the aryl-Pd(II)I intermediate through the less hindered approach of the cyclopropyl ring. Further insights into the potential electronic effects of the aryl moiety should be addressed by comparison with alkyl-substituted cyclo-propanes.
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A direct Pd-catalyzed activation-functionalization of the C-H bond of cyclopropanes is possible when directing groups are present. For a review, see
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A direct Pd-catalyzed activation-functionalization of the C-H bond of cyclopropanes is possible when directing groups are present. For a review, see:, Kubota A, Sanford M S., Synthesis 2011 2579
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