Investigation into the Catalytic Performance of Cu(II) Supported Graphene Quantum Dots Modiꢀed…
1
1
23.02,127.82, 128.27, 128.32, 128.37, 128.65, 131.84,
37.85.
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5
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4.6.2 1‑(1,3‑Diphenylprop‑2‑yn‑1‑yl)piperidine (Table 2,
entry 2)
6. Gholinejad M, Ahmadi J, Nájera C, Seyedhamzeh M, Zareh F,
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7
.
1
HNMR (300 MHz, CDCl ): δ = 1.57–1.61 (2H, m),
3
1
.64–1.78 (4H, m), 2.71 (4H, t, J = 5.26), 4.95 (1H,
8. Koli PB, Kapadnis KH, Deshpande UG, Patil MR (2018) J Nano-
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s), 7.38–7.46 (6H, m, 2-Ar), 7.63–7.66 (2H, m, Ar),
1
3
9. Pirhaji JZ, Moeinpour F, Dehabadi AM, Ardakani SAY (2019) J
Mol Liq 112345.
7
2
1
.77–7.79(2H, m, Ar); CNMR (75 Hz, CDCl ): δ=24.56,
3
6.27, 50.79, 62.45, 84.12, 88.02, 123.43,127.61, 128.19,
1
0. Narayanan S, Sathy BN, Mony U, Koyakutty M, Nair SV, Menon
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28.38, 128.67, 131.93, 138.62.
1
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4.6.3 4‑(1‑(4‑Methoxyphenyl)‑3‑phenylprop‑2‑yn‑1‑l)
12. Javid A, Khojastehnezhad A, Eshghi H, Moeinpour F, Bamohar-
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morpholine (Table 2, entry 5)
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1
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4. Khakzad Siuki MM, Bakavoli M, Eshghi H (2019) Appl Orga-
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1
HNMR (300 MHz, CDCl ): δ = 2.67–2.71 (4H, m),
3
3
.77–3.78 (4H, m), 4.78 (1H, s), 6.95–6.98 (d, 2H,
15. Maensiri S, Masingboon C, Boonchom B, Seraphin S (2007)
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J = 8.7, Ar), 7.35–7.38 (2H, m, J = 6.4, Ar), 7.58–7.63
1
3
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(
d, 2H, J = 8.2, Ar); C NMR (75 Hz, CDCl ): δ = 49.88,
3
5
1
5.31, 61.48, 67.21, 85.47, 88.34, 113.63, 123.09, 128.28,
28.37, 129.77, 129.93,131.86, 159.28.
1
1
1
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4.6.4 1‑(3‑Phenyl‑1‑(p‑tolyl)prop‑2‑yn‑1‑yl)piperidine
(
Table 2, entry 8)
9. Pourshojaei Y, Zolala F, Eskandari K, Talebi M, Morsali L, Amiri
M, Khodadadi A, Shamsimeymandi R, Faghih-Mirzaei E, Asadi-
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1
HNMR (300 MHz, CDCl ): δ = 1.57–1.64 (2H, m),
3
1
.65–1.76 (4H, m), 2.47 (3H, s), 2.66 (4H, t, J = 4.9), 7.28
20. Ramachandran S, Sathishkumar M, Kothurkar NK, Senthilkumar
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(
2H, d, J = 8.1), 7.38–7.44 (3H, m), 7.60–7.63 (2H, m),
1
3
7
2
1
.65 (2H, d, J = 8.1); CNMR (75 Hz, CDCl ): δ = 21.25,
3
2
1. Mirabedini M, Motamedi E, Kassaee MZ (2015) Chin Chem Lett
4.57, 29.27, 50.72, 62.23, 86.47, 87.72, 123.51, 128.12,
2
6:1085–1090
28.37, 128.59, 128.87, 131.92, 135.66, 137.14.
22. González-Béjar M, Peters K, Hallett-Tapley GL, Grenier M, Sca-
iano JC (2003) Chem Comm 49:1732–1734
2
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4.6.5 4‑(1‑(Phenylethynyl)cyclohexyl)morpholine (Table 2,
entry 18)
24. Fischer C, Carreira EM (2001) Org Lett 3:4319–4321
2
5. Mandlimath TR, Sathiyanarayanan KI (2016) RSC Adv
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1
HNMR (300 MHz, CDCl ): δ = 1.27–1.78 (8H, m),
3
26. Khojastehnezhad A, Bakavoli M, Javid A, Siuki MMK, Moein-
pour F (2019) Catal Lett 149:713–722
2
.04–2.08 (3H, m), 2.77 (4H, t, J = 4.8 Hz), 3.81 (4H, t,
1
3
2
2
2
7. Khakzad Siuki MM, Bakavoli M, Eshghi H (2018) Appl Orga-
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J = 4.8 Hz), 7.31–7.47 (5H, m); CNMR (75 Hz, CDCl ):
3
δ = 22.78, 25.71, 29.34, 35.46, 46.67, 58.95, 67.50, 86.53,
8. Benítez-Martínez S, Valcárcel M (2015) Anal Chim Act
8
9.78, 123.44, 128.23, 131.74.
8
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Acknowledgements This work is fnancially assisted by the Islamic
Azad University-Bandar Abbas Branch. The authors are grateꢀul ꢀor
that.
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han H (2017) J Mol Liq 242:447–455
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