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V. Rajpara et al.
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1,4-Dimethyl-2-(4-nitrobenzyl)benzene (Table 1, Entry 3)
1H NMR (200 MHz, CDCl3): d = 2.18 (s, 3 H), 2.3 (s, 3 H), 4.05 (s,
2 H), 6.9–7.1 (m, 3 H), 7.2–7.3 (d, J = 9.8 Hz, 2 H), 8.1–8.2 (d,
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1,4-Dimethyl-2-[(2E)-3-phenylprop-2-en-1-yl]benzene(Table1,
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1H NMR (200 MHz, CDCl3): d = 2.25 (s, 3 H), 2.3 (s, 3 H), 3.25–
3.3 (d, 2 H), 6.35–6.4 (m, 2 H), 6.9–7.1 (m, 3 H), 7.2–7.5 (m, 5 H).
2-(Diphenylmethyl)-1,4-dimethylbenzene (Table 1, Entry 9)
1H NMR (200 MHz, CDCl3): d = 2.15 (s, 3 H), 2.2 (s, 3 H), 5.65 (s,
1 H), 6.9–7.4 (m, 13 H).
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1-(2,5-Dimethylbenzyl)naphthalene (Table 1, Entry 10)
1H NMR (200 MHz, CDCl3): d = 2.2 (s, 3 H), 2.25 (s, 3 H), 4.35 (s,
2 H), 6.8 (s, 1 H), 6.9–7.1 (m, 2 H), 7.2–7.55 (m, 4 H), 7.65–8.1 (m,
3 H).
1-Methoxy-4-methyl-2-(1-phenylethyl)benzene (Table 1, Entry
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This work has been supported by the Director, Office of Science,
Office of Biological & Environmental Research, Biological Sys-
tems Science Division, of the U.S. Department of Energy under
Contract No. DE-FG02-08ER64624, NSF (EPSCoR Grant No.
0554609 and MRI Grant No. 0722632 for acquisition of an XRD
powder diffractometer) and by the State of South Dakota.
(19) Liu, C.; Li, M.; Yang, C.; Tian, S. Chem. Eur. J. 2008, 15,
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Synthesis 2010, No. 16, 2835–2840 © Thieme Stuttgart · New York