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See, for example: (a) Ortega, M.; Rodríguez, M. A.; Campos, P. J. Tetrahedron 2005, 61, 11686.
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Campos, P.J.3
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7
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23644459999
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(b) Soldevilla, A.; Sampedro, D.; Campos, P. J.; Rodríguez, M. A. J. Org. Chem. 2005, 70, 6976.
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23744466461
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(c) Sampedro, D.; Caro, M.; Campos, P. J.; Rodríguez, M. A. J. Org. Chem. 2005, 70, 6705.
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Sampedro, D.1
Caro, M.2
Campos, P.J.3
Rodríguez, M.A.4
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9
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(d) Sampedro, D.; Soldevilla, A.; Rodríguez, M. A.; Campos, P. J.; Olivucci, M. J. Am. Chem. Soc. 2005, 127, 441.
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Campos, P.J.4
Olivucci, M.5
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12
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84890739336
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EB at the Millenium, Sita Series in Surface Coatings Technology 7; J. Wiley: New York
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(c) Neckers, D. C.; Jager, W. Photoinitiation for Polymerization: UV & EB at the Millenium, Sita Series in Surface Coatings Technology 7; J. Wiley: New York, 1999.
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Neckers, D.C.1
Jager, W.2
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13
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33747278225
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ACS Symposium Series 847, Belfield, K. D., Crivello, J. V., Eds.; American Chemical Society: Washington, DC
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(d) Photoinitiated Polymerization; ACS Symposium Series 847, Belfield, K. D., Crivello, J. V., Eds.; American Chemical Society: Washington, DC, 2003.
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Photoinitiated Polymerization
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14
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0000781366
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Okada, T.; Kawanisi, M.; Nozaki, H. Bull. Chem. Soc. Jpn. 1969, 42, 2981.
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Bull. Chem. Soc. Jpn.
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Okada, T.1
Kawanisi, M.2
Nozaki, H.3
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15
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37049067878
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was used as precursor
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2-Phenylbenzaldehyde oxime, prepared according to Cullen, K. E.; Sharp, J. T. J. Chem. Soc., Perkin Trans. 1 1993, 2961, was used as precursor.
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(1993)
J. Chem. Soc., Perkin Trans. 1
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Cullen, K.E.1
Sharp, J.T.2
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16
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0003444404
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Blackwell: Oxford
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The addition of nitrogen-centered radical should form an azacyclo-hexadienyl radical, from which a hydrogen atom may be abstracted by another radical to gain aromaticity: Parsons, A. F. An Introduction to Free Radical Chemistry; Blackwell: Oxford, 2000; p 68.
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Parsons, A.F.1
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17
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33747313669
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note
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1 led to nondeuterated isoquinoline.
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