Green Chemistry
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ARTICLE
Journal Name
4
4
5
5
5
8
9
0
1
2
D. Sriram, Bioorg. Med. Chem. Lett., 2007, 17, 6459-6462. Dai, J. Appl. Polym. Sci., 2020, 137, 47
M. Kidwai, R. Poddar, S. Bhardwaj, S. Singh and P. M. Luthra, 76 L. Zhang, H. Wu, M. Wei, Z. Zheng, D. D. Vu, T. T. X. Bui and
Eur. J. Med. Chem., 2010, 45, 5031-5038. X. Huang, J. Coat. Technol. Res., 2018, 15, 1343-1356.
D. Kumar, V. B. Reddy, S. Sharad, U. Dube and S. Kapur, Eur. 77 V. H. Pham, H. D. Pham, T. T. Dang, S. H. Hur, E. J. Kim, B. S.
D
7
O 10.1039/D0GC01274B
10I:
.
J. Med. Chem., 2009, 44, 3805-3809.
Kong, S. Kim and J. S. Chung, J. Mater. Chem., 2012, 22,
10530-10536.
A. Tanabe, H. Nakashima, O. Yoshida, N. Yamamoto, O.
Tenmyo and T. Oki, J. Antibiotics, 1988, 41, 1708-1710.
A. Bolognese, G. Correale, M. Manfra, A. Lavecchia, O.
78 D. Bouša, J. Luxa, V. Mazanek, O. Jankovský, D. Sedmidubský,
K. Klímová and Z. Sofer, RSC Adv., 2016, 6, 66884-66892.
Mazzoni, E. Novellino and R. Loddo, J. Med. Chem., 2004, 47, 79 M. Frey, R. K. Zenn, S. Warneke, K. Müller, A. Hintennach, R. E.
8
49-858.
Dinnebier and M. R. Buchmeiser, ACS Energy Lett., 2017, 2, 595-
604.
80 J. Zheng, H. T. Liu, B. Wu, C. A. Di, Y. L. Guo, T. Wu and D. B.
Zhu, Sci. Rep., 2012, 2, 662.
5
5
3
4
O. Rosati, A. Pelosi, A. Temperini, V. Pace and M. Curini,
Synthesis, 2016, 48, 1533-1540.
K. Niknam, M. Khataminejad and F. Zeyaei, Tetrahedron Lett.,
2
016, 57, 361-365.
81 M. K. Rabchinskii, A. T. Dideikin, D. A. Kirilenko, M. V.
Baidakova, V. V. Shnitov, F. Roth and N. M. Lebedeva, Sci.
Rep., 2018, 8, 14154.
5
5
5
6
A. Molla and S. Hussain, RSC Adv., 2016, 6, 5491-5502.
D. Azarifar, S. M. Khatami and R. Nejat-Yami, J. Chem. Sci.,
2
014, 126, 95-101.
82 W. Zhang, S. Wang, J. Ji, Y. Li, G. Zhang, F. Zhang and X. Fan,
Nanoscale, 2013, 5, 6030-6033.
83 A. M. Dimiev, L. B. Alemany and J. M. Tour, ACS nano,
2013, 7, 576-588.
5
5
5
6
6
6
6
6
7
8
9
0
1
2
3
4
K. S. Pandit, P. V. Chavan, U. V. Desai, M. A. Kulkarni and P. P.
Wadgaonkar, New J. Chem., 2015, 39, 4452-4463.
H. Kiyani and F. Ghorbani, Res. Chem. Inter., 2015, 41, 7847-
7
882.
84 Y. Wan, W. W. Liu, Q. C. Zhan, H. Cui, Q. Zhang, S. N. Yue and
H. Wu, Lett. Org. Chem., 2015, 12, 538-543.
85 N. M. Abd El-Rahman, A. A. El-Kateb and M. F. Mady, Synth.
Commun., 2007, 37, 3961-3970.
86 L. M. Wang, J. H. Shao, H. Tian, Y. H. Wang and B. Liu, J.
Fluorine Chem., 2006, 127, 97-100.
87 M. R. Yousefi, O. Goli-Jolodar and F. Shirini, Bioorg. Chem.,
2018, 81, 326-333.
88 M. Hong and C. Cai, J. Chem. Res., 2010, 34, 568-570.
M. Norouzi, D. Elhamifar, R. Mirbagheri and Z. Ramazani, J.
Taiwan Inst. Chem. Eng., 2018, 89, 234-244.
S. Sadjadi, M. M. Heravi, V. Zadsirjan and V. Farzaneh, Appl.
Surface Sci., 2017, 426, 881-889.
H. R. Safaei, M. Shekouhy, A. Shirinfeshan and S. Rahmanpur,
Mol. Divers., 2012, 16, 669-683.
G. Zhang, Y. Zhang, J. Yan, R. Chen, S. Wang, Y. Ma and R.
Wang, J. Org. Chem., 2012, 77, 878-888.
Y. Gao and D. M. Du, Tetrahedron Asymmetry, 2012, 23, 89 S. Balalaie, M. Sheikh-Ahmadi and M. Bararjanian, Catal.
343-1349. Commun., 2007, 8, 1724-1728.
M. G. Dekamin, S. Z. Peyman, Z. Karimi, S. Javanshir, M. R. 90 V. Bhaskar, R. Chowdary, S. R. Dixit and S. D. Joshi, Bioorg.
1
Naimi-Jamal and M. Barikani, Inter. J. Biol. Macromol., 2016,
7, 172-179.
M. Norouzi and D. Elhamifar, Catal. Lett., 2019, 149, 619-628.
A. Yaghoubi and M. G. Dekamin, ChemistrySelect, 2017, 2,
Chem., 2019, 84, 202-210.
8
91 B. Paplal, S. Nagaraju, P. Veerabhadraiah, K. Sujatha, S.
Kanvah, B. V. Kumar and D. Kashinath, RSC Adv., 2014, 4,
54168-54174.
6
6
5
6
9
236-9243.
92 B. C. Ranu, S. Banerjee and S. Roy, Indian J. Chem., 2008, 47B,
1108-1112.
93 F. Tamaddon and D. Azadi, J. Iran. Chem. Soc., 2017, 14,
2077-2086.
94 M. Amirnejad, M. R. Naimi-Jamal, H. Tourani and H. Ghafuri,
Monatsh. Chem., 2013, 144, 1219-1225.
6
6
6
7
7
7
7
8
9
0
1
2
S. N. Maddila, S. Maddila, W. E. van Zyl and S. B.
Jonnalagadda, Chem. Open, 2016, 5, 38-42.
R. L. Magar, P. B. Thorat, B. R. Patil and R. P. Pawar, Current
Organocatal., 2018, 5, 74-81.
S. Sobhani, F. O. Chahkamali and J. M. Sansano, RSC Adv.,
2
019, 9, 1362-1372.
S. Sobhani, Z. 67M. Falatooni and M. Honarmand, RSC Adv.,
014, 4, 15797-15806.
95 M. Mirza-Aghayan, S. Nazmdeh, R. Boukherroub, M.
Rahimifard, A. A. Tarlani and M. Abolghasemi-Malakshah,
Synth. Commun., 2013, 43, 1499-1507.
2
S. Sobhani, H. Hosseini Moghadam, J. Skibsted and J. M. 96 V. Safarifard, S. Beheshti and A. Morsali, CrystEngComm,
Sansano, Green Chem., 2020, 22, 1353-1365. 2015, 17, 1680-1685.
S. Sobhani and R. Jahanshahi, New J. Chem., 2013, 37, 1009- 97 G. Brahmachari and B. Banerjee, ACS Sustain. Chem. Eng.,
015. 2014, 2, 411-422.
S. Sobhani and Z. Ramezani, RSC Adv., 2016, 6, 29237-29244. 98 W. Deng, L. Liu and Y. Peng, Green Process Synth., 2018, 7,
1
7
7
3
4
S. Sobhani and Z. Zeraatkar, Appl. Organomet. Chem., 2016,
0, 12-19.
191-197.
3
99 S. K. Dangolani, F. Panahi, M. Nourisefat and A. Khalafi-
Nezhad, RSC Adv., 2016, 6, 92316-92324.
1
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