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48349118709
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15.
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40
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48349093616
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34249288615
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2O) led selectively to the reduction of the C{double bond, long}O group without deprotection (see: Fujiwara, K.; Aki, Y.; Yamamoto, F.; Kawamura, M.; Kobayashi, M.; Okano, A.; Awakura, D.; Shiga, S.; Murai, A.; Kawai, H.; Suzuki, T. Tetrahedron Lett. 2007, 26, 4523-4527).
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2O) led selectively to the reduction of the C{double bond, long}O group without deprotection (see: Fujiwara, K.; Aki, Y.; Yamamoto, F.; Kawamura, M.; Kobayashi, M.; Okano, A.; Awakura, D.; Shiga, S.; Murai, A.; Kawai, H.; Suzuki, T. Tetrahedron Lett. 2007, 26, 4523-4527).
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44
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48349096272
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2O/hexane) was prepared from rac-3a analogously to the enantiomerically pure 9a.
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2O/hexane) was prepared from rac-3a analogously to the enantiomerically pure 9a.
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45
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48349095608
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note
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23c.
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48349107368
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note
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It is worth mentioning that this signal appears as a d and not as the expected dd. This fact shows that the coupling occurs with only one H-atom located at C(5) of the camphor skeleton. It is likely that the effective coupling results from the interaction with the exo-H. The same phenomenon is observed in other camphor derivatives described in this paper.
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48349134736
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note
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CCDC 684655-684657 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre, via www.ccdc.cam.ac.uk/data_request/cif.
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