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98
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33750435288
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note
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3 result in lower conversion.
-
-
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-
99
-
-
33750444004
-
-
note
-
Configurations are assigned by analogy with 9R and 15, which were unambiguously determined through chemical correlation with valine and coniine, respectively.
-
-
-
-
100
-
-
33750461356
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note
-
Allyl bromide gave 12% of the allyl adduct. Benzyl bromide led to recovery of the starting hydrazone, and tert-butyl bromide resulted in decomposition.
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33750458760
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note
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·.
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103
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33750456281
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note
-
During preparation of this manuscript, Tomioka et al. have very recently reported some impressive intermolecular radical additions to N-tosylimines using alkyl iodide stoichiometries from 1.5 to 5 equiv. See ref 7a.
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-
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104
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0000434949
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Morrison, J. D., Ed.; Academic Press: New York
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33750492013
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Identical results were observed on ca. a 200 mg or 1 g scale.
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122
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3). Ref 35b.
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33750493021
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The compound 24B was shown by GC to have dr = 94:6.
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33750455215
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note
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(a) A deuterium incorporation experiment is complicated by the potential for NH exchange on processing the reaction product.
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-
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135
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33750470141
-
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note
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5 (a necessary condition for the PRE).
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150
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152
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note
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1H NMR spectrometry, but there was no evidence of a tridecyl adduct.
-
-
-
-
153
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33750427941
-
-
note
-
Although this study is focused on intermolecular addition, precedent suggests applicability to cyclizations (ref 25).
-
-
-
-
154
-
-
33750461717
-
-
note
-
A statement of general experimental procedures is provided in the Supporting Information.
-
-
-
-
155
-
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33750440615
-
-
note
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4, DMF, 75% yield) gave 14 which matched the NMR data of 14 as observed in the mixture of 14 and 2a. Details will be reported elsewhere.
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