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b) Huisgen, R. "1,3-Dipolar Cycloaddition Chemistry: 1,3-Dipolar Cycloadditions-Introduction, Survey, Mechanism," ed. by Padwa, A. Wiley-Interscience, New York, 1984, vol. 1, pp. 1-176;
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c) Huisgen, R. "Advances in Cycloaddition: Steric Course and Mechanism of 1,3-Dipolar Cycloadditions", ed. by Curran, D. P., JAI Press, Greenwich, CT, 1988, Vol. 1, pp. 1-31, Potts, K. T.;
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d) "1,3-Dipolar Cycloaddition Chemistry: Mesoionic Ring Systems", ed. by Padwa, A. Wiley-Interscience, New York, 1984, vol. 2, pp. 1-82.
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Bianchi, G.1
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19
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85030208303
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note
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13C NMR, HETCOR, FT-IR, mass spectra and HRMS).
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20
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85030200436
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note
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3H.
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21
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85030201648
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note
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5 = 158 °. The authors thank Tom Wilson for help obtaining this data and helpful discussions.
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22
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0011878207
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No semicarbazide 7 was formed upon reaction of benzylhydrazine (18) with p-Br-Ph-NCO
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Satchell, D. P. N.; Satchell, R. S. Chem. Soc. Rev. 1975, 4, 231. No semicarbazide 7 was formed upon reaction of benzylhydrazine (18) with p-Br-Ph-NCO.
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(1975)
Chem. Soc. Rev.
, vol.4
, pp. 231
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Satchell, D.P.N.1
Satchell, R.S.2
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24
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85030200796
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note
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The closest literature precedent is Tilles, H. (Stauffer Chemical Co.) US Patent 3712914, date 730123.
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