J IRAN CHEM SOC
2
‑Hydroxybenzophenone (Table 2, entry 6)
158.02, 147.77, 140.86, 133.85, 133.46, 132.95, 132.04,
27.96, 127.58, 120.01.
1
1
H-NMR (250 MHz, CDCl ) δ ppm: 11.98 (s, 1H), 7.56–
3
1
3
Acknowledgments We gratefully acknowledge the support of this
study by Persian Gulf University Research Council.
7
.48 (m, 7H), 6.96–6.92 (m, 1H), 6.77–6.71 (m, 1H); C-
NMR (62.9 MHz, CDCl ) δ ppm: 197.03, 139.70, 137.26,
3
1
1
34.33, 129.67, 129.20, 119.61 (overlap, two peaks),
19.29 (overlap, two peaks).
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1
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1
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3
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1
H-NMR (250 MHz, CDCl ) δ ppm: 11.78 (s, 1H), 8.35–
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3
1
3
8
1
NMR (62.9 MHz, CDCl ) δ ppm: 204.77, 136.88, 132.97,
3
1
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(
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1
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3
1
1
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7
.54–7.37 (m, 4H), 7.10 (d, 2H, J = 8.0 Hz), 6.96 (t, 1H,
13
J = 7.8 Hz), 6.88–6.84 (m, 1H), 2.44 (s, 3H); C-NMR
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3
96, 224 (2015)
(
(
62.9 MHz, CDCl ) δ ppm: 201.72, 163.10, 142.83, 136.07
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3
1
1
2
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4
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(
(
2‑Hydroxyphenyl)‑naphthalen‑1‑yl‑methanone
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1
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3
1
3
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7
.83 (m, 3H), 7.46–7.17 (m, 7H), 7.04–6.67 (m, 1H); C-
2
2
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(
1
(
3
York, 1992)
overlap, two peaks), 133.00, 131.69, 131.49, 130.75,
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2
2
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3
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(
(
5‑Bromo‑2‑hydroxyphenyl)(phenyl)methanone
Table 2, entry 11)
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(
1
33. I. Cobo, M.I. Matheu, S. Castillon, O. Boutureira, B.G. Davis,
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3
Org. Lett. 14, 1728 (2012)
7
.45 (d, 1H, J = 8.4 Hz, Ar), 7.19 (m, 1H, Ar), 7.06 (d, 1H,
J = 8.4 Hz, Ar), 6.90 (m, 2H, Ar), 6.79 (s, 1H, Ar), 6.63
m, 2H, Ar); C-NMR (62.9 MHz, CDCl ) δ ppm: 200.00,
3
4. P. Cyr, S.T. Deng, J.M. Hawkins, K.E. Price, Org. Lett. 15, 4342
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1
3
(
3
1
3