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1. (a) Chatgilialoglu, C.; Ferreri, C.; Lucarini, M. Chem. Eur. J. 1997, 3, 376.
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(c) Crich, D.; Chen, C., Hwang, J. T.; J. Am. Chem. Soc. 1994, 116, 8937.
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3. (a) Bachi, M. D.; Melman, A.; Barner, N. J. Org. Chem., 1997, 62, 1896.
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0000874522
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(b) Bachi, M. D.; Balanov, A.; Barner, N. Ibid. 1994, 59, 7752.
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15
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0001362069
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6. N-alkyl substituted carbamoyl radicals are known to exist as a mixture of the respective E- and Z-conformers: Sutcliffe, R.; Ingold, K. U. J. Am. Chem. Soc. 1981, 103, 7686.
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Sutcliffe, R.1
Ingold, K.U.2
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16
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33751499942
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7. Curran has noted a temperature effect on the yields of atom-transfer cyclizations of α-amide radicals that is presumably a reflection of the rate of conformer interconversion: Curran, D. P.; Tamine, J. J. Org. Chem. 1991, 56, 2746.
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Tamine, J.2
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0010396897
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note
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13C NMR, IR) and analytical (HRMS) data fully consistent with the assigned structure.
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19
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0010356665
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note
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3SnH.
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21
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0010358539
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3SnH afforded primarily decarbonylated products at higher concentrations: Bachi, M. D.; Balanov, A.; Bar-Ner, N.; Bosch, E.; Denenmark, D.; Mizhiritskii, M. Pure & Appl. Chem. 1993, 65, 595.
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Bachi, M.D.1
Balanov, A.2
Bar-Ner, N.3
Bosch, E.4
Denenmark, D.5
Mizhiritskii, M.6
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22
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0000221903
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13. For radical cyclizations wherein the electronic nature of the N-substituent influences the course of reaction, see: Padwa, A.; Nimmesgarn, H.; Wong, G. S. K. J. Org. Chem. 1985, 50, 5620.
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Padwa, A.1
Nimmesgarn, H.2
Wong, G.S.K.3
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24
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0000863049
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15. 5-Exo cyclizations of substrates with terminal diphenylethenyl acceptors are known to be approximately two orders of magnitude faster than cyclizations involving terminal alkenes: Newcomb, M.; Horner, J. H.; Filipkowski, M. A.; Ha, C.; Park, S. U. J. Am. Chem. Soc. 1995, 117, 3674.
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Newcomb, M.1
Horner, J.H.2
Filipkowski, M.A.3
Ha, C.4
Park, S.U.5
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0000812146
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16. Simakov, P. A.; Martinez, F. N.; Horner, J. H.; Newcomb, M. J. Org. Chem. 1998, 63, 1226.
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Simakov, P.A.1
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