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Kim, P.1
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10
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33745000875
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Bened A., Durand R., Pioch D., Geneste P., Guimon C., Guillouzo G.P., Declercq J.-P., Germain G., Briard P., Rambaud J., and Roques R. J. Chem. Soc., Perkin Trans. 2 (1984) 1-6
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Declercq, J.-P.7
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11
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0001521459
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12
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0005132348
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Albini F.M., Ceva P., Mascherpa A., Albini E., and Caramella P. Tetrahedron 38 (1982) 3629-3639
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14
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33745005851
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Aziridines cis-2a and trans-2b were prepared following the procedure described in:
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Aziridines cis-2a and trans-2b were prepared following the procedure described in:. Cromwell N.H., and Caughlan J.A. J. Am. Chem. Soc. 67 (1945) 2235-2238
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(1945)
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, vol.67
, pp. 2235-2238
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Cromwell, N.H.1
Caughlan, J.A.2
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15
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0005986993
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aziridines cis-2c, trans-2c, cis-2d and trans-2d were prepared following the procedure described in:
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aziridines cis-2c, trans-2c, cis-2d and trans-2d were prepared following the procedure described in:. Cromwell N.H., and Hoeksema H. J. Am. Chem. Soc. 71 (1949) 708-711
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(1949)
J. Am. Chem. Soc.
, vol.71
, pp. 708-711
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Cromwell, N.H.1
Hoeksema, H.2
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16
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33744979191
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Padwa A., and Pearson W.H. (Eds), J. Wiley and Sons, Hoboken
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Gothelf K.V., and Jørgensen K.A. In: Padwa A., and Pearson W.H. (Eds). Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products (2003), J. Wiley and Sons, Hoboken 820-821
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(2003)
Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products
, pp. 820-821
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Gothelf, K.V.1
Jørgensen, K.A.2
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17
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33744967204
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note
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‡The coupling constants were calculated and assigned to protons 1-H, 3-H, 3a-H and 8b-H from decoupling experiments.
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18
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33744980368
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note
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® Ultra version 8.0.3, Cambridge Soft Corporations, Cambridge, © 1985-2003. MM2 parameters were provided by N. L. Allinger (MM2 parameters), J. W. Ponder (TINKER parameters) and Cambridge Scientific Computing.
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19
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0000002236
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Padwa A. (Ed), J. Wiley and Sons, New York
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Lown J.W. In: Padwa A. (Ed). 1,3-Dipolar Cycloaddition Chemistry Vol. 1 (1984), J. Wiley and Sons, New York 653
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(1984)
1,3-Dipolar Cycloaddition Chemistry
, vol.1
, pp. 653
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Lown, J.W.1
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23
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33744979422
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note
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13C COSY spectra.Crystallographic data (excluding structure factors) for compound 5a have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 606048. These data can be obtained free of charge via www.ccdc.cam.ac.uk/.
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