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0013577752
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note
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1H-COSY NMR experiments. Enhancements, shown in Figure II, were proofs of the proposed structure. This result indicates that the ratio of the products (13 and 14) depends on the stability of the intermediates (7 and 9) in the equilibration. Figure II (equation presented).
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-
-
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23
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0004035319
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Wiley-VCH, New York
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a) N. L. Bauld, Radicals, Ion Radicals, and Triplets: The Spin-Bearing Intermediates of Organic Chemistry, Wiley-VCH, New York, 1997, p. 14;
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Bauld, N.L.1
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Kumar, P.P.5
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25
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0013609085
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At this stage, the other products such as monocyclized unsaturated compound were oxidized to give the corresponding carbonyl compounds. Although 35% yield, the isolation of the monobenzyl-substituted cyclopropane product is a rare case
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At this stage, the other products such as monocyclized unsaturated compound were oxidized to give the corresponding carbonyl compounds. Although 35% yield, the isolation of the monobenzyl-substituted cyclopropane product is a rare case.
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