Simple and Practical Synthesis of Various New Nickel Boride-Based Nanocomposites and their Applications for the Green and Expeditious Reduction of Nitroarenes to Arylamines under Wet-Solvent-Free Mechanochemical Grinding
Hossein Mousavi A B , Behzad Zeynizadeh A , Reza Younesi A and Mozhgan Esmati AA Department of Organic Chemistry, Faculty of Chemistry, Urmia University, Urmia, Iran.
B Corresponding author. Email: 1hossein.mousavi@gmail.com
Australian Journal of Chemistry 71(8) 595-609 https://doi.org/10.1071/CH18200
Submitted: 2 May 2018 Accepted: 25 July 2018 Published: 22 August 2018
Abstract
In this paper, we report a simple synthesis of four new nickel boride-based nanocomposites, namely Ni2B@ZrCl4, Ni2B@Cu2O, Ni2B@CuCl2 and Ni2B@FeCl3, from commercially available and cheap starting materials. All of the new Ni2B-based nanocomposites were well characterized by Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. Further, the catalytic applications of these new nanocomposites were successfully evaluated in the wet-solvent-free reduction of aromatic nitro compounds to arylamines with sodium borohydride (NaBH4) at room temperature by a mechanochemical grinding technique. All the introduced catalytic systems provide excellent yields of arylamines in very short reaction times for a wide range of substrates. Also, recoverability and reusability of the new nanocomposites were investigated.
References
[1] (a) H. C. Erythropel, J. B. Zimmerman, T. M. de Winter, L. Petitjean, F. Melnikov, C. H. Lam, A. W. Lounsbury, K. E. Mellor, N. Z. Janković, Q. Tu, L. N. Pincus, M. M. Falinski, W. Shi, P. Coish, D. L. Plata, P. T. Anastas, Green Chem. 2018, 20, 1929.| Crossref | GoogleScholarGoogle Scholar |
(b) D. Azarifar, M. Ghaemi, Appl. Organomet. Chem. 2017, 31,
| Crossref | GoogleScholarGoogle Scholar |
(c) M. G. Dekamin, M. Azimoshan, L. Ramezani, Green Chem. 2013, 15, 811.
| Crossref | GoogleScholarGoogle Scholar |
(d) M. G. Dekamin, M. Eslami, Green Chem. 2014, 16, 4914.
| Crossref | GoogleScholarGoogle Scholar |
(e) R. A. Sheldon, Green Chem. 2014, 16, 950.
| Crossref | GoogleScholarGoogle Scholar |
(f) J. Ma, L. Zhong, X. Peng, R. Sun, Green Chem. 2016, 18, 1738.
| Crossref | GoogleScholarGoogle Scholar |
(g) R. A. Sheldon, Chem. Soc. Rev. 2012, 41, 1437.
| Crossref | GoogleScholarGoogle Scholar |
(h) R. Ghorbani-Vaghei, J. Mahmoodi, A. Shahriari, Y. Maghbooli, Appl. Organomet. Chem. 2017, 31,
| Crossref | GoogleScholarGoogle Scholar |
(i) M. Rimaz, J. Khalafy, H. Mousavi, Res. Chem. Intermed. 2016, 42, 8185.
| Crossref | GoogleScholarGoogle Scholar |
(j) S. Zhaleh, N. Hazeri, M. R. Faghihi, M. T. Maghsoodlou, Res. Chem. Intermed. 2016, 42, 8069.
| Crossref | GoogleScholarGoogle Scholar |
(k) M. Zakeri, M. M. Nasef, T. Kargaran, A. Ahmad, E. Abouzari-Lotf, J. Asadi, Res. Chem. Intermed. 2017, 43, 717.
| Crossref | GoogleScholarGoogle Scholar |
(l) C.-W. Lü, J.-J. Wang, F. Li, S.-J. Yu, Y. An, Res. Chem. Intermed. 2018, 44, 1035.
| Crossref | GoogleScholarGoogle Scholar |
(m) M. Rimaz, H. Mousavi, P. Keshavarz, B. Khalili, Curr. Chem. Lett. 2015, 4, 159.
| Crossref | GoogleScholarGoogle Scholar |
(n) A. Yaghoubi, M. G. Dekamin, ChemistrySelect 2017, 2, 9236.
| Crossref | GoogleScholarGoogle Scholar |
(o) N. Azizi, M. Shahiri Haghayegh, ChemistrySelect 2017, 2, 8870.
| Crossref | GoogleScholarGoogle Scholar |
(p) M. Rimaz, H. Mousavi, M. Behnam, B. Khalili, Curr. Chem. Lett. 2016, 5, 145.
| Crossref | GoogleScholarGoogle Scholar |
(q) D. Ngo, M. Kalala, V. Hogan, R. Manchanayakage, Tetrahedron Lett. 2014, 55, 4496.
| Crossref | GoogleScholarGoogle Scholar |
(r) M. Rimaz, H. Mousavi, B. Khalili, F. Aali, J. Chin. Chem. Soc. 2018, in press.
| Crossref | GoogleScholarGoogle Scholar |
(s) A. Kumar, M. S. Rao, I. Ahmad, B. Khungar, Aust. J. Chem. 2009, 62, 322.
| Crossref | GoogleScholarGoogle Scholar |
[2] (a) M. Rimaz, J. Khalafy, H. Mousavi, S. Bohlooli, B. Khalili, J. Heterocycl. Chem. 2017, 54, 3174.
| Crossref | GoogleScholarGoogle Scholar |
(b) N. R. Modugu, P. K. Pittala, Tetrahedron Lett. 2017, 58, 3859.
| Crossref | GoogleScholarGoogle Scholar |
(c) A. Kumar, Y. E. Jad, A. El-Faham, B. G. de la Torre, F. Albericio, Tetrahedron Lett. 2017, 58, 2986.
| Crossref | GoogleScholarGoogle Scholar |
(d) A. A. Ali, M. Konwar, M. Chetia, D. Sarma, Tetrahedron Lett. 2016, 57, 5661.
| Crossref | GoogleScholarGoogle Scholar |
[3] (a) A. L. Garay, A. Pichon, S. L. James, Chem. Soc. Rev. 2007, 36, 846.
| Crossref | GoogleScholarGoogle Scholar |
(b) A. Shaabani, R. Mohammadian, S. E. Hooshmand, A. Hashemzadeh, M. M. Amini, ChemistrySelect 2017, 2, 11906.
| Crossref | GoogleScholarGoogle Scholar |
(c) A. Sarkar, S. Santra, S. K. Kundu, A. Hajra, G. V. Zyryanov, O. N. Chupakhin, V. N. Charushin, A. Majee, Green Chem. 2016, 18, 4475.
| Crossref | GoogleScholarGoogle Scholar |
(d) R. A. Sheldon, Green Chem. 2005, 7, 267.
| Crossref | GoogleScholarGoogle Scholar |
(e) M. Leonardi, M. Villacampa, J. C. Mendéz, Chem. Sci. 2018, 9, 2042.
| Crossref | GoogleScholarGoogle Scholar |
(f) R. Ghorbani-Vaghei, S. Alavinia, Z. Merati, V. Izadkhah, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(g) E. Colacino, A. Porcheddu, I. Halasz, C. Charnay, F. Delogu, R. Guerra, J. Fullenwarth, Green Chem. 2018, 20, 2973.
| Crossref | GoogleScholarGoogle Scholar |
[4] (a) Z. T. Bhutia, A. Das, M. Biswas, A. Cheterjee, M. Banerjee, Eur. J. Org. Chem. 2018, 506.
| Crossref | GoogleScholarGoogle Scholar |
(b) D. Tan, T. Friščić, Eur. J. Org. Chem. 2018, 18.
| Crossref | GoogleScholarGoogle Scholar |
(c) J. Li, D.-N. Jiang, J.-X. Chen, M. C. Liu, J. C. Ding, H.-Y. Wu, J. Heterocycl. Chem. 2011, 48, 403.
| Crossref | GoogleScholarGoogle Scholar |
(d) V. Štrukil, Synlett 2018, 1281.
| Crossref | GoogleScholarGoogle Scholar |
[5] (a) F. Toda, K. Tanaka, K. Hamai, J. Chem. Soc., Perkin Trans. 1 1990, 3207.
| Crossref | GoogleScholarGoogle Scholar |
(b) C. L. Raston, J. L. Scott, Green Chem. 2000, 2, 49.
| Crossref | GoogleScholarGoogle Scholar |
(c) A. F. M. M. Rahman, R. Ali, Y. Jahng, A. A. Kadi, Molecules 2012, 17, 571.
| Crossref | GoogleScholarGoogle Scholar |
(d) A. A. Napoleon, F.-R. Nawaz Khan, E. D. Jeong, E. H. Chung, Chin. Chem. Lett. 2015, 26, 567.
| Crossref | GoogleScholarGoogle Scholar |
(e) N. M. Rateb, H. F. Zohdi, Synth. Commun. 2009, 39, 2789.
| Crossref | GoogleScholarGoogle Scholar |
[6] A. K. Bose, S. Pednekar, S. N. Ganguly, G. Chakraborty, M. S. Manhas, Tetrahedron Lett. 2004, 45, 8351.
| Crossref | GoogleScholarGoogle Scholar |
[7] (a) E. Kashani, N. Noroozi Pesyan, T. Tunç, E. Shahin, J. Chin. Chem. Soc. 2015, 62, 249.
| Crossref | GoogleScholarGoogle Scholar |
(b) Z. Ren, W. Cao, W. Ding, W. Shi, Synth. Commun. 2004, 34, 4395.
| Crossref | GoogleScholarGoogle Scholar |
[8] F. Toda, T. Suzuki, S. Higa, J. Chem. Soc., Perkin Trans. 1 1998, 3521.
| Crossref | GoogleScholarGoogle Scholar |
[9] F. Toda, H. Takumi, H. Yamaguchi, Chem. Express 1989, 4, 507.
[10] (a) S. Kumar, P. Sharma, K. K. Kapoor, M. S. Hundal, Tetrahedron 2008, 64, 536.
| Crossref | GoogleScholarGoogle Scholar |
(b) A. M. Zonouz, D. Moghani, Synth. Commun. 2011, 41, 2152.
| Crossref | GoogleScholarGoogle Scholar |
[11] (a) S. Gupta, J. M. Khurana, Green Chem. 2017, 19, 4153.
| Crossref | GoogleScholarGoogle Scholar |
(b) A. Kumar, S. Sharma, Green Chem. 2011, 13, 2017.
| Crossref | GoogleScholarGoogle Scholar |
(c) T. Lohar, A. Mane, S. Kamat, A. Kumbahar, R. Salunkhe, Res. Chem. Intermed. 2018, 44, 1919.
| Crossref | GoogleScholarGoogle Scholar |
(d) B. Sakram, B. Sonyanaik, K. Ashok, S. Rambabu, D. Ravi, A. Kurumanna, P. Shyam, Res. Chem. Intermed. 2017, 43, 1881.
| Crossref | GoogleScholarGoogle Scholar |
(e) H. Naeimi, H. Foroughi, Res. Chem. Intermed. 2016, 42, 3999.
| Crossref | GoogleScholarGoogle Scholar |
(f) K. Ravi, B. Krishankumar, M. Sawminathan, Res. Chem. Intermed. 2015, 41, 5353.
| Crossref | GoogleScholarGoogle Scholar |
(g) Q.-S. Ding, J.-L. Zhang, J.-X. Chen, M.-C. Liu, J.-C. Ding, H.-Y. Wu, J. Heterocycl. Chem. 2012, 49, 375.
| Crossref | GoogleScholarGoogle Scholar |
(h) D. Zhou, Z. Ren, W. Cao, J. Chen, H. Deng, J. Heterocycl. Chem. 2008, 45, 1865.
| Crossref | GoogleScholarGoogle Scholar |
(i) S. I. Bhat, A. R. Choudhury, D. R. Trivedi, RSC Adv. 2012, 2, 10556.
| Crossref | GoogleScholarGoogle Scholar |
(j) B. Lee, P. Kang, K. H. Lee, J. Chao, W. Nam, W. K. Lee, N. H. Hur, Tetrahedron Lett. 2013, 54, 1384.
| Crossref | GoogleScholarGoogle Scholar |
(k) K. Longhi, D. N. Moreira, M. R. B. Marzari, V. M. Floss, H. G. Bonacorso, N. Zanatta, M. A. P. Martins, Tetrahedron Lett. 2010, 51, 3193.
| Crossref | GoogleScholarGoogle Scholar |
(l) Z. T. Bhutia, G. Prasannakumar, A. Das, M. Biswas, A. Chatterjee, M. Banerjee, ChemistrySelect 2017, 2, 1183.
| Crossref | GoogleScholarGoogle Scholar |
(m) S. Kuntikana, C. Bhat, M. Kongot, S. I. Bhat, A. Kumar, ChemistrySelect 2016, 1, 1723.
| Crossref | GoogleScholarGoogle Scholar |
[12] R. Ghahremanzadeh, S. Ahadi, G. I. Shakibaei, A. Bazgir, Tetrahedron 2010, 51, 499.
| Crossref | GoogleScholarGoogle Scholar |
[13] M. A. Pasha, B. Datta, J. Saudi Chem. Soc. 2014, 18, 47.
| Crossref | GoogleScholarGoogle Scholar |
[14] S. I. Bhat, D. R. Trivedi, Environ. Chem. Lett. 2013, 11, 91.
| Crossref | GoogleScholarGoogle Scholar |
[15] (a) Z. Ren, W. Cao, W. Tong, Synth. Commun. 2002, 32, 3475.
| Crossref | GoogleScholarGoogle Scholar |
(b) S.-X. Wang, J.-T. Li, W.-Z. Yang, Y.-H. Yin, Z.-H. Xie, Synth. Commun. 2004, 34, 829.
| Crossref | GoogleScholarGoogle Scholar |
[16] K. Tanaka, S. Kishigami, F. Toda, J. Org. Chem. 1991, 56, 4333.
| Crossref | GoogleScholarGoogle Scholar |
[17] P. Chauhan, S. S. Chimni, Asian J. Org. Chem. 2012, 1, 138.
| Crossref | GoogleScholarGoogle Scholar |
[18] K. Sato, T. Ozu, N. Takenaga, Tetrahedron Lett. 2013, 54, 661.
| Crossref | GoogleScholarGoogle Scholar |
[19] R. Eisavi, S. Alifam, Phosphorus Sulfur Silicon Relat. Elem. 2018, 193, 211.
| Crossref | GoogleScholarGoogle Scholar |
[20] N. Zhao, Y. Li, Y. Wang, J. Wang, J. Sulfur Chem. 2006, 27, 427.
| Crossref | GoogleScholarGoogle Scholar |
[21] B. Karami, M. Taei, S. Khodabakhshi, M. Jamshidi, J. Sulfur Chem. 2012, 33, 65.
| Crossref | GoogleScholarGoogle Scholar |
[22] Z. Zhang, X. Wang, Z. Li, Synth. Commun. 2004, 34, 1407.
| Crossref | GoogleScholarGoogle Scholar |
[23] L. Rong, H. Han, H. Jiang, S. Tu, Synth. Commun. 2008, 38, 3530.
| Crossref | GoogleScholarGoogle Scholar |
[24] L. Rong, H. Han, H. Jiang, D. Shi, S. Tu, Synth. Commun. 2008, 38, 1044.
| Crossref | GoogleScholarGoogle Scholar |
[25] D. Wu, Z. Ren, Synth. Commun. 2005, 35, 3157.
| Crossref | GoogleScholarGoogle Scholar |
[26] J.-T. Li, H.-G. Dai, D. Liu, T.-S. Li, Synth. Commun. 2006, 36, 794.
[27] S. Wang, P. He, J.-M. Zhang, H. Jiang, S.-Z. Zhu, Synth. Commun. 2005, 35, 1803.
| Crossref | GoogleScholarGoogle Scholar |
[28] H. Hagiwara, K. Morohashi, T. Suzuki, M. Ando, I. Yammamoto, M. Kato, Synth. Commun. 1998, 28, 2001.
| Crossref | GoogleScholarGoogle Scholar |
[29] W. Bai, J. Lin, Synth. Commun. 2011, 41, 903.
| Crossref | GoogleScholarGoogle Scholar |
[30] Z. Quan, Z. Zhang, X. Wang, Z. Li, Phosphorus Sulfur Silicon Relat. Elem. 2006, 181, 1397.
| Crossref | GoogleScholarGoogle Scholar |
[31] A. R. Kiasat, B. Mokhtari, F. Kazemi, S. Yousefi, M. Javaherian, J. Sulfur Chem. 2007, 28, 171.
| Crossref | GoogleScholarGoogle Scholar |
[32] V. P. Jejurkar, C. K. Khatri, G. U. Chaturbhuj, S. Saha, ChemistrySelect 2017, 2, 11693.
| Crossref | GoogleScholarGoogle Scholar |
[33] N. Noroozi-Pesyan, J. Khalafy, Z. Malekpoor, J. Chin. Chem. Soc. 2009, 56, 1018.
| Crossref | GoogleScholarGoogle Scholar |
[34] L.-Y. Zhu, Z. Lou, J. Lin, W. Zheng, C. Zhang, J.-D. Lou, Res. Chem. Intermed. 2013, 39, 4315.
| Crossref | GoogleScholarGoogle Scholar |
[35] (a) F. Toda, K. Kiyoshige, M. Yagi, Angew. Chem. Int. Ed. Engl. 1989, 101, 329.
| Crossref | GoogleScholarGoogle Scholar |
(b) L. Sadighnia, B. Zeynizadeh, J. Iran. Chem. Soc. 2015, 12, 873.
| Crossref | GoogleScholarGoogle Scholar |
(c) B. Zeynizadeh, S. Sorkhabi, J. Chem. Soc. Pak. 2016, 38, 679.
[36] (a) M. Hassani, M. R. Naimi-Jamal, L. Panahi, ChemistrySelect 2018, 3, 666.
| Crossref | GoogleScholarGoogle Scholar |
(b) P. Rai, M. Srivastava, J. Singh, J. Singh, New J. Chem. 2014, 38, 3181.
| Crossref | GoogleScholarGoogle Scholar |
(c) A. R. Hajipour, P. Abdolfathi, New J. Chem. 2017, 41, 2386.
| Crossref | GoogleScholarGoogle Scholar |
(d) A. R. Hajipour, S. M. Hosseini, S. Jajarmi, New J. Chem. 2017, 41, 7447.
| Crossref | GoogleScholarGoogle Scholar |
(e) A. El Kadib, ChemSusChem 2015, 8, 217.
| Crossref | GoogleScholarGoogle Scholar |
(f) S. Rostamnia, E. Doustkhah, RSC Adv. 2014, 4, 28238.
| Crossref | GoogleScholarGoogle Scholar |
(g) B. Sakthivel, A. Dhakshinamoorthy, J. Colloid Interface Sci. 2017, 485, 75.
| Crossref | GoogleScholarGoogle Scholar |
(h) Z. Li, X. Liu, Y. Yin, Y. Li, J. Wang, X. Yu, ChemistrySelect 2018, 3, 599.
| Crossref | GoogleScholarGoogle Scholar |
(i) M. G. Dekamin, Z. Karimi, Z. Latifidoost, S. Ilkhanizadeh, H. Daemi, M. R. Naimi-Jamal, M. Barikani, Int. J. Biol. Macromol. 2018, 108, 1273.
| Crossref | GoogleScholarGoogle Scholar |
(j) K. Nikoofar, Z. Khademi, Res. Chem. Intermed. 2016, 42, 3929.
| Crossref | GoogleScholarGoogle Scholar |
(k) M. G. Dekamin, S. Z. Peyman, Z. Karimi, S. Javanshir, M. R. Naimi-Jamal, M. Barikani, Int. J. Biol. Macromol. 2016, 87, 172.
| Crossref | GoogleScholarGoogle Scholar |
(l) N. Daneshvar, F. Shirini, M. Safarpoor Nikoo Langarudi, R. Karimi-Chayjani, Bioorg. Chem. 2018, 77, 68.
| Crossref | GoogleScholarGoogle Scholar |
(m) X. Xiong, Z. Tang, S. Sun, X. Meng, S. Song, Z. Quan, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(n) S. B. Bhagat, V. N. Telvekar, Synlett 2018, 874.
| Crossref | GoogleScholarGoogle Scholar |
(o) M. Shoeb, M. Mobin, A. Ali, S. Zaman, A. H. Naqavi, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
[37] (a) A. R. Hajipour, F. Rezaei, Z. Khorsandi, Green Chem. 2017, 19, 1353.
| Crossref | GoogleScholarGoogle Scholar |
(b) H. Ghafuri, B. Ghorbani, A. Rashidizadeh, M. Talebi, M. Roshani, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(c) S. Sajjadifar, S. Rezayati, S. Shahriari, S. Abbaspou, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(d) S. F. Hojati, A. Amiri, N. MoeiniEghbali, S. Mohamadi, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(e) Y. K. Tailor, S. Khandelwal, R. Gopal, E. Rushell, A. Prajapati, M. Kumar, ChemistrySelect 2017, 2, 11055.
| Crossref | GoogleScholarGoogle Scholar |
(f) M. Gholami Dehbalaei, N. Foroughifar, H. Pasdar, A. Khajeh-Amiri, New J. Chem. 2018, 42, 327.
| Crossref | GoogleScholarGoogle Scholar |
(g) D. Azarifar, M. Ghaemi, R. Karamian, Y. Abbasi, F. Ghasemlou, M. Asadbegi, New J. Chem. 2018, 42, 1796.
| Crossref | GoogleScholarGoogle Scholar |
(h) F. Asghari-Haji, K. Rad-Moghadam, N. O. Mahmoodi, T. Tonekaboni, N. Rahimi, Appl. Organomet. Chem. 2017, 31,
| Crossref | GoogleScholarGoogle Scholar |
(i) D. Azarifar, O. Badalkhani, Y. Abbasi, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(j) K. Sapkota, S. S. Han, New J. Chem. 2017, 41, 5395.
| Crossref | GoogleScholarGoogle Scholar |
(k) S. Taheri, H. Veisi, M. Hekmati, New J. Chem. 2017, 41, 5075.
| Crossref | GoogleScholarGoogle Scholar |
(l) A. Mohammadinezhad, B. Akhlaghinia, Aust. J. Chem. 2018, 71, 32.
| Crossref | GoogleScholarGoogle Scholar |
(m) L. M. Rossi, N. J. C. Costa, F. P. Silva, R. Wojcieszak, Green Chem. 2014, 16, 2906.
| Crossref | GoogleScholarGoogle Scholar |
(n) P. Paul, P. Bhanja, N. Salam, U. Mandi, A. Bhaumik, S. M. Alam, S. M. Islam, J. Colloid Interface Sci. 2017, 493, 206.
| Crossref | GoogleScholarGoogle Scholar |
(o) Z. Nasresfahani, M. Z. Kassaee, ChemistrySelect 2017, 2, 9642.
| Crossref | GoogleScholarGoogle Scholar |
(p) D. Elhamifar, Z. Ramazani, M. Norouzi, R. Mirbagheri, J. Colloid Interface Sci. 2018, 511, 392.
| Crossref | GoogleScholarGoogle Scholar |
(q) A. Maleki, N. Hamidi, S. Maleki, J. Rahimi, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(r) R. Maleki, N. Koukabi, E. Kolvari, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(s) L. Shiri, S. Zarei, M. Kazemi, D. Sheikh, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(t) L. Shiri, A. Ghorbani-Choghamarani, M. Kazemi, Aust. J. Chem. 2017, 70, 9.
| Crossref | GoogleScholarGoogle Scholar |
(u) S. Memar Masjed, B. Akhlaghinia, M. Zarghani, M. Razavi, Aust. J. Chem. 2017, 70, 33.
(v) A. Ghorbani-Choghamarani, Z. Taherinia, Aust. J. Chem. 2017, 70, 1127.
| Crossref | GoogleScholarGoogle Scholar |
(w) L. Shiri, M. Kazemi, Res. Chem. Intermed. 2017, 43, 4813.
| Crossref | GoogleScholarGoogle Scholar |
(x) M. R. Nabid, Y. Bide, Z. Habibi, RSC Adv. 2015, 5, 2258.
| Crossref | GoogleScholarGoogle Scholar |
(y) N. Iranpoor, H. Firouzabadi, S. Motevalli, K. Rajabi, Aust. J. Chem. 2015, 68, 926.
| Crossref | GoogleScholarGoogle Scholar |
(z) R. Tayebee, A. Pejhan, H. Ramshini, B. Maleki, M. Erfaninia, Z. Tabatabaie, E. Esmaeili, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
[38] (a) D. Wang, D. Astruc, Chem. Soc. Rev. 2017, 46, 816.
| Crossref | GoogleScholarGoogle Scholar |
(b) M. B. Gawande, A. Goswami, F.-X. Felpin, T. Asefa, X. Huang, R. Silva, X. Zou, R. Zboril, R. S. Varma, Chem. Rev. 2016, 116, 3722.
| Crossref | GoogleScholarGoogle Scholar |
(c) V. K. Akkilagunta, R. R. Kakulapati, J. Org. Chem. 2011, 76, 6819.
| Crossref | GoogleScholarGoogle Scholar |
(d) S. Asghari, M. Mohammadnia, Res. Chem. Intermed. 2017, 43, 7193.
| Crossref | GoogleScholarGoogle Scholar |
(e) N. Basavegowda, K. B. S. Magar, K. Mishra, Y. R. Lee, New J. Chem. 2014, 38, 5415.
| Crossref | GoogleScholarGoogle Scholar |
(f) D. Cantillo, M. Baghbanzadeh, C. O. Kappe, Angew. Chem. Int. Ed. 2012, 51, 10190.
| Crossref | GoogleScholarGoogle Scholar |
(g) R. Fareghi-Alamdari, N. Zekri, F. Mansouri, Res. Chem. Intermed. 2017, 43, 6537.
| Crossref | GoogleScholarGoogle Scholar |
(h) M. Gholinejad, N. Jeddi, ACS Sustainable Chem. Eng. 2014, 2, 2658.
| Crossref | GoogleScholarGoogle Scholar |
(i) H. Sharghi, R. Khalifeh, M. M. Doroodmand, Adv. Synth. Catal. 2009, 351, 207.
| Crossref | GoogleScholarGoogle Scholar |
(j) G. Molteni, C. L. Bianchi, G. Marinoni, N. Santo, A. Ponti, New J. Chem. 2006, 30, 1137.
| Crossref | GoogleScholarGoogle Scholar |
(k) L. Shiri, A. Ghorbani-Choghamarani, M. Kazemi, Aust. J. Chem. 2016, 69, 585.
| Crossref | GoogleScholarGoogle Scholar |
[39] (a) Y. Zhou, H. Zhou, S. Liu, D. Pi, G. Shen, Tetrahedron 2017, 73, 3898.
| Crossref | GoogleScholarGoogle Scholar |
(b) S. Liu, Y. Wang, J. Jiang, Z. Jin, Green Chem. 2009, 11, 1397.
| Crossref | GoogleScholarGoogle Scholar |
(c) U. Sharma, N. Kumar, P. K. Verma, V. Kumar, B. Singh, Green Chem. 2012, 14, 2289.
| Crossref | GoogleScholarGoogle Scholar |
(d) Z. Sun, Z. Zhao, Y. Xie, R. Tao, H. Zhang, C. Huang, Z. Liu, Green Chem. 2010, 12, 1007.
| Crossref | GoogleScholarGoogle Scholar |
(e) M. Rimaz, B. Khalili, G. Khatyal, H. Mousavi, F. Aali, Aust. J. Chem. 2017, 70, 1274.
| Crossref | GoogleScholarGoogle Scholar |
(f) T. Senthamarai, K. Murugesan, K. Natte, N. V. Kalevaru, H. Neumann, P. C. J. Kamer, R. V. Jagadeesh, ChemCatChem 2018, 10, 1235.
| Crossref | GoogleScholarGoogle Scholar |
(g) C. Yang, W. Xue, H. Yin, Z. Lu, A. Wang, L. Shen, Y. Jiang, New J. Chem. 2017, 41, 3358.
| Crossref | GoogleScholarGoogle Scholar |
(h) P. K. Verma, M. Bala, T. Thakur, U. Sharma, N. Kumar, B. Singh, Catal. Lett. 2014, 144, 1258.
| Crossref | GoogleScholarGoogle Scholar |
(i) C. Gunanathan, D. Milstein, Angew. Chem. Int. Ed. 2008, 47, 8661.
| Crossref | GoogleScholarGoogle Scholar |
(j) D. Cantillo, M. Baghbanzadeh, C. O. Kappe, Angew. Chem. Int. Ed. 2012, 51, 10190.
| Crossref | GoogleScholarGoogle Scholar |
(k) M.-f. Lv, G.-p. Lu, C. Cai, Asian J. Org. Chem. 2015, 4, 141.
| Crossref | GoogleScholarGoogle Scholar |
(l) V. Pandarus, R. Ciriminna, F. Béland, M. Pagliaro, Adv. Synth. Catal. 2011, 353, 1306.
| Crossref | GoogleScholarGoogle Scholar |
(m) R. S. Kokane, V. R. Acham, A. B. Kulal, E. Kemnitz, M. K. Dongare, S. B. Umbarkar, ChemistrySelect 2017, 2, 10618.
| Crossref | GoogleScholarGoogle Scholar |
(n) K. P. Cole, M. D. Johnson, M. E. Laurila, J. R. Stoul, React. Chem. Eng. 2017, 2, 288.
| Crossref | GoogleScholarGoogle Scholar |
(o) M. Liang, J. Chen, Chem. Soc. Rev. 2013, 42, 3453.
| Crossref | GoogleScholarGoogle Scholar |
(p) F. Liu, S. Chen, Y. Gao, J. Colloid Interface Sci. 2017, 506, 236.
| Crossref | GoogleScholarGoogle Scholar |
(q) J. Goscianska, N. A. Fathy, R. M. M. Aboelenin, J. Colloid Interface Sci. 2017, 505, 593.
| Crossref | GoogleScholarGoogle Scholar |
(r) S. Daemi, A. A. Ashkarran, A. Bahari, S. Ghasemi, J. Colloid Interface Sci. 2017, 494, 290.
| Crossref | GoogleScholarGoogle Scholar |
(s) J. Gao, Y. He, X. Zhao, X. Ran, Y. Wu, Y. Su, J. Dai, J. Colloid Interface Sci. 2016, 481, 220.
| Crossref | GoogleScholarGoogle Scholar |
(t) X. Qiu, Q. Liu, M. X. Song, C. Huang, J. Colloid Interface Sci. 2016, 477, 131.
| Crossref | GoogleScholarGoogle Scholar |
(u) Y. Le, D. Guo, B. Cheng, J. Yu, J. Colloid Interface Sci. 2013, 408, 173.
| Crossref | GoogleScholarGoogle Scholar |
(v) C. McManamon, A. M. Burke, J. D. Holmes, M. A. Morris, J. Colloid Interface Sci. 2012, 369, 330.
| Crossref | GoogleScholarGoogle Scholar |
(w) S. J. Tabatabaei Rezaei, A. Mashhadi Malekzadeh, S. Poulaei, A. Ramazani, K. Khorramabadi, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(x) Y. Shi, P. C. J. Kamer, D. J. Cole-Hamilton, Green Chem. 2017, 19, 5460.
| Crossref | GoogleScholarGoogle Scholar |
(y) I. B. Seiple, S. Su, I. S. Young, C. A. Lewis, J. Yamaguchi, P. S. Baran, Angew. Chem. Int. Ed. 2010, 49, 1095.
| Crossref | GoogleScholarGoogle Scholar |
(z) A. Hager, N. Vrielink, D. Hager, J. Lefranc, D. Trauner, Nat. Prod. Rep. 2016, 33, 491.
| Crossref | GoogleScholarGoogle Scholar |
[40] (a) M. Rimaz, H. Mousavi, Turk. J. Chem. 2013, 37, 252.
(b) S. Mor, R. Mohil, S. Nagoria, A. Kumar, K. Lal, D. Kumar, V. Singh, J. Heterocycl. Chem. 2017, 54, 1327.
| Crossref | GoogleScholarGoogle Scholar |
(c) S. Uppuluri, S. E. Keinath, D. A. Tomalia, P. R. Dvornic, Macromolecules 1998, 31, 4498.
| Crossref | GoogleScholarGoogle Scholar |
(d) A. Komáromi, G. L. Tolnai, Z. Novák, Tetrahedron Lett. 2008, 49, 7294.
| Crossref | GoogleScholarGoogle Scholar |
(e) S. F. Vasilevsky, M. P. Davydova, V. I. Mamatyuk, N. Tsvetkov, A. Hughes, D. S. Baranov, I. V. Alabugin, Aust. J. Chem. 2017, 70, 421.
| Crossref | GoogleScholarGoogle Scholar |
(f) G. Gudes de la Cruz, B. Svobodova, M. Lichtenegger, O. Tiapko, K. Groschner, T. Glasnov, Synlett 2017, 695.
[41] (a) Y. Kuninobu, Y. Nishina, M. Shouho, K. Takai, Angew. Chem. 2006, 118, 2832.
| Crossref | GoogleScholarGoogle Scholar |
(b) S. Cavalli, D. Carbajo, M. Acosta, S. Lope-Piedrafita, A. P. Candiota, C. Arús, M. Royo, F. Albericio, Chem. Commun. 2012, 5322.
| Crossref | GoogleScholarGoogle Scholar |
(c) A. Guerry, J. Bernard, E. Samain, E. Fleury, S. Cottaz, S. Halila, Bioconjug. Chem. 2013, 24, 544.
| Crossref | GoogleScholarGoogle Scholar |
(d) R. Ramesh, R. Madhesh, J. G. Malecki, A. Lalitha, ChemistrySelect 2016, 1, 5196.
| Crossref | GoogleScholarGoogle Scholar |
(e) M. Rimaz, Z. Jalalian, H. Mousavi, R. H. Prager, Tetrahedron Lett. 2016, 57, 105.
| Crossref | GoogleScholarGoogle Scholar |
(f) M. Rimaz, H. Mousavi, M. Behnam, L. Sarvari, B. Khalili, Curr. Chem. Lett. 2017, 6, 55.
| Crossref | GoogleScholarGoogle Scholar |
(g) S. E. Denmark, G. L. Beutner, Angew. Chem. Int. Ed. 2008, 47, 1560.
| Crossref | GoogleScholarGoogle Scholar |
(h) B. Singh, K. R. Mote, C. S. Gopinath, P. K. Madhu, V. Polshettiwar, Angew. Chem. Int. Ed. 2015, 54, 5985.
| Crossref | GoogleScholarGoogle Scholar |
(i) P. Melchiorre, Angew. Chem. Int. Ed. 2012, 51, 9748.
| Crossref | GoogleScholarGoogle Scholar |
(j) A. Saeed, P. A. Channar, J. Heterocycl. Chem. 2017, 54, 780.
| Crossref | GoogleScholarGoogle Scholar |
(k) C. Rougeot, H. Situ, B. H. Cao, V. Vlachos, J. E. Hein, React. Chem. Eng. 2017, 2, 226.
| Crossref | GoogleScholarGoogle Scholar |
(l) L. D. White, C. P. Tripp, J. Colloid Interface Sci. 2000, 232, 400.
| Crossref | GoogleScholarGoogle Scholar |
(m) J. Ou-Yang, Y. Zhao, H. Jiang, L. Meng, X. Li, X. Jia, Aust. J. Chem. 2015, 68, 1599.
| Crossref | GoogleScholarGoogle Scholar |
(n) J. Duan, P. Li, Catal. Sci. Technol. 2014, 4, 311.
| Crossref | GoogleScholarGoogle Scholar |
(o) M. Rimaz, H. Mousavi, L. Nikpey, B. Khalili, Res. Chem. Intermed. 2017, 43, 3925.
| Crossref | GoogleScholarGoogle Scholar |
[42] S. U. Nandanwar, M. Chakraborty, Chin. J. Catal. 2012, 33, 1532.
| Crossref | GoogleScholarGoogle Scholar |
[43] (a) M. Barbero, S. Cadamuro, S. Dughera, Org. Biomol. Chem. 2016, 14, 1437.
| Crossref | GoogleScholarGoogle Scholar |
(b) F. Mo, D. Quin, Y. Zhang, J. Wang, Acc. Chem. Res. 2018, 51, 496.
| Crossref | GoogleScholarGoogle Scholar |
(c) A. Pourjavadi, N. Keshavarzi, F. Matloubi Moghaddam, S. H. Hosseini, ChemistrySelect 2018, 3, 2716.
| Crossref | GoogleScholarGoogle Scholar |
(d) X. Zhao, X. Zheng, M. Tian, Y. Tong, B. Yang, X. Wei, D. Qiu, K. Lu, Org. Chem. Front. 2018, in press.
| Crossref | GoogleScholarGoogle Scholar |
(e) F. Korte, Methodicum Chimicum, Vol. 6 1975 (Georg Thieme: Stuttgart).
[44] (a) X. Chen, Z. Zhou, Y. Chen, Z. Dong, Y. Gao, C. Qian, C. He, Res. Chem. Intermed. 2012, 38, 2255.
| Crossref | GoogleScholarGoogle Scholar |
(b) B. Zeynizadeh, D. Setamdideh, Synth. Commun. 2006, 36, 2699.
| Crossref | GoogleScholarGoogle Scholar |
(c) B. Zeynizadeh, H. Ghasemi, J. Chem. Res. 2006, 2006, 542.
| Crossref | GoogleScholarGoogle Scholar |
(d) B. Zeynizadeh, K. Zahmatkesh, J. Chin. Chem. Soc. 2003, 50, 267.
| Crossref | GoogleScholarGoogle Scholar |
(e) P. K. Verma, M. Bala, K. Thakur, U. Sharma, N. Kumar, B. Singh, Catal. Lett. 2014, 144, 1258.
| Crossref | GoogleScholarGoogle Scholar |
(f) J. Spencer, N. Anjum, H. Patel, R. P. Rathnam, J. Verma, Synlett 2007, 2557.
| Crossref | GoogleScholarGoogle Scholar |
(g) L. Pehlivan, E. Métay, S. Laval, W. Dayoub, P. Demonchaux, G. Mignani, M. Lemaire, Tetrahedron Lett. 2010, 51, 1939.
| Crossref | GoogleScholarGoogle Scholar |
(h) Y. Motoyama, K. Kamo, H. Nagashima, Org. Lett. 2009, 11, 1345.
| Crossref | GoogleScholarGoogle Scholar |
(i) H. Min, S. Lee, M. Park, J. Hwang, H. M. Jung, S. Lee, J. Organomet. Chem. 2014, 755, 7.
| Crossref | GoogleScholarGoogle Scholar |
(j) R. Kaplánek, V. Krchňák, Tetrahedron Lett. 2013, 54, 2600.
| Crossref | GoogleScholarGoogle Scholar |
(k) S. Jian, Y. Li, Chin. J. Catal. 2016, 37, 91.
| Crossref | GoogleScholarGoogle Scholar |
(l) J. Feng, S. Handa, F. Gallou, B. H. Lipshutz, Angew. Chem. Int. Ed. 2016, 55, 8979.
| Crossref | GoogleScholarGoogle Scholar |
(m) M. Baron, E. Métay, M. Lemaire, F. Popowycz, Green Chem. 2013, 15, 1006.
| Crossref | GoogleScholarGoogle Scholar |
(n) N. R. Lee, A. A. Bikovtseva, M. Cortes-Clerget, F. Gallou, B. H. Lipshutz, Org. Lett. 2017, 19, 6518.
| Crossref | GoogleScholarGoogle Scholar |
(o) Y. Wang, J. Shi, Z. Zhang, J. Fu, X. Lü, Z. Hou, Chin. J. Catal. 2017, 38, 1909.
| Crossref | GoogleScholarGoogle Scholar |
(p) S. Doherty, J. G. Knight, T. Backhouse, A. Bradford, F. Saunders, R. A. Bourne, T. W. Chamberlain, R. Stones, A. Clayton, K. Lovelock, Catal. Sci. Technol. 2018, 8, 1454.
| Crossref | GoogleScholarGoogle Scholar |
(q) M. S. Takhur, O. S. Nayal, R. Rana, M. Kumar, S. Sharma, N. Kumar, S. M. Maurya, New J. Chem. 2018, 42, 1372.
(r) W. Feng, T. Huang, L. Gao, X. Yang, W. Deng, R. Zhou, H. Liu, RSC Adv. 2018, 8, 6288.
| Crossref | GoogleScholarGoogle Scholar |
(s) X.-L. Chen, B.-R. Ai, Y. Dong, X.-M. Zhang, J.-Y. Wang, Tetrahedron Lett. 2017, 58, 3646.
| Crossref | GoogleScholarGoogle Scholar |
(t) M.-U. Hung, S.-T. Yang, M. Ramanathan, S.-T. Liu, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
(u) Z. Duan, G. Ma, W. Zhang, Bull. Korean Chem. Soc. 2012, 33, 4003.
| Crossref | GoogleScholarGoogle Scholar |
(v) P. L. Gkizis, M. Stratakis, I. N. Lykakis, Catal. Commun. 2013, 36, 48.
| Crossref | GoogleScholarGoogle Scholar |
(w) B. Fischer, L. Sheihet, J. Org. Chem. 1998, 63, 393.
| Crossref | GoogleScholarGoogle Scholar |
(x) C. Peyrot, T. Vivès, L. Legentil, L. Lemiègre, R. Daniellou, ChemistrySelect 2017, 2, 5214.
| Crossref | GoogleScholarGoogle Scholar |
(y) E. Pedrajas, I. Sorribes, A. L. Gushchin, Y. A. Laricheva, K. Junge, M. Beller, R. Llusar, ChemCatChem 2017, 9, 1128.
| Crossref | GoogleScholarGoogle Scholar |
(z) H. K. Kadam, S. G. Tilve, RSC Adv. 2015, 5, 83391.
| Crossref | GoogleScholarGoogle Scholar |
[45] (a) B. Zeynizadeh, F. Sepehraddin, J. Organomet. Chem. 2018, 856, 70.
| Crossref | GoogleScholarGoogle Scholar |
(b) S. Karami, B. Zeynizadeh, Z. Shokri, Cellulose 2018, 25, 3295.
| Crossref | GoogleScholarGoogle Scholar |
(c) B. Zeynizadeh, I. Mohammadzadeh, Z. Shokri, S. A. Hossein, J. Colloid Interface Sci. 2017, 500, 285.
| Crossref | GoogleScholarGoogle Scholar |
(d) Z. Shokri, B. Zeynizadeh, S. A. Hosseini, J. Colloid Interface Sci. 2017, 485, 99.
| Crossref | GoogleScholarGoogle Scholar |
(e) B. Zeynizadeh, F. Sepehraddin, J. Iran. Chem. Soc. 2017, 14, 2649.
| Crossref | GoogleScholarGoogle Scholar |
(f) Z. Shokri, B. Zeynizadeh, J. Iran. Chem. Soc. 2017, 14, 2467.
| Crossref | GoogleScholarGoogle Scholar |
(g) Z. Shokri, B. Zeynizadeh, S. A. Hosseini, B. Azizi, J. Iran. Chem. Soc. 2017, 14, 101.
| Crossref | GoogleScholarGoogle Scholar |
(h) B. Zeynizadeh, M. Zabihzadeh, Z. Shokri, J. Iran. Chem. Soc. 2016, 13, 1487.
| Crossref | GoogleScholarGoogle Scholar |
(i) B. Zeynizadeh, M. Zabihzadeh, J. Iran. Chem. Soc. 2015, 12, 1221.
| Crossref | GoogleScholarGoogle Scholar |
[46] (a) C. A. Brown, H. C. Brown, J. Am. Chem. Soc. 1963, 85, 1003.
| Crossref | GoogleScholarGoogle Scholar |
(b) H. C. Brown, C. A. Brown, J. Am. Chem. Soc. 1963, 85, 1005.
| Crossref | GoogleScholarGoogle Scholar |
[47] F. Taghavi, C. Falamaki, A. Shabanov, L. Bayrami, A. Roumianfar, Appl. Catal. A 2011, 407, 173.
| Crossref | GoogleScholarGoogle Scholar |
[48] G. Ranjani, R. Nagarajan, Org. Lett. 2017, 19, 3974.
| Crossref | GoogleScholarGoogle Scholar |
[49] (a) X. Zhang, Y. Zhang, H. Huang, J. Cai, K. Ding, S. Lin, New J. Chem. 2018, 42, 458.
| Crossref | GoogleScholarGoogle Scholar |
(b) A. L. Gajengi, C. S. Fernandes, B. M. Bhanage, Mol. Catal. 2018, 451, 13.
| Crossref | GoogleScholarGoogle Scholar |
(c) S. Meghana, P. Kabra, S. Chakraborty, N. Padmavathy, RSC Adv. 2015, 5, 12293.
| Crossref | GoogleScholarGoogle Scholar |
(d) C. Qi, J. Zheng, Electroanalysis 2016, 28, 477.
| Crossref | GoogleScholarGoogle Scholar |
(e) M. Salavati-Niasari, F. Davar, Mater. Lett. 2009, 63, 441.
| Crossref | GoogleScholarGoogle Scholar |
(f) W. Wang, Y. Tu, P. Zhang, G. Zhang, CrystEngComm 2011, 13, 1838.
| Crossref | GoogleScholarGoogle Scholar |
(g) W. Wang, Y. Tu, L. Wang, Y. Liang, H. Shi, Appl. Surf. Sci. 2013, 264, 399.
| Crossref | GoogleScholarGoogle Scholar |
(h) T. Jiang, T. Xie, L. Chen, Z. Fu, D. Wang, Nanoscale 2013, 5, 2938.
| Crossref | GoogleScholarGoogle Scholar |
(i) Y. Bai, W. Zhang, Z. Zhang, J. Zhou, X. Wang, C. Wang, W. Huang, J. Jiang, Y. Xiong, J. Am. Chem. Soc. 2014, 136, 14650.
| Crossref | GoogleScholarGoogle Scholar |
(j) F. Zhang, G. Dong, M. Wang, Y. Zeng, C. Wang, Appl. Surf. Sci. 2018, 444, 559.
| Crossref | GoogleScholarGoogle Scholar |
(k) M. Iqbal, Y. Wang, H. Hu, M. He, A. H. Shah, L. Lin, P. Li, K. Shao, A. R. Woldu, T. He, Appl. Surf. Sci. 2018, 443, 209.
| Crossref | GoogleScholarGoogle Scholar |
[50] S. Yang, Z.-H. Zhang, Q. Chen, M.-Y. He, L. Wang, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
[51] M. L. Kantam, R. Chakravarti, U. Pal, B. Sreedhar, S. Bhargava, Adv. Synth. Catal. 2008, 350, 822.
| Crossref | GoogleScholarGoogle Scholar |
[52] A. R. Kiasat, R. Mirzajani, F. Ataeian, M. Fallah-Mehrjardi, Chin. Chem. Lett. 2010, 21, 1015.
| Crossref | GoogleScholarGoogle Scholar |
[53] R. Rajesh, R. Venkatesan, J. Mol. Catal. Chem. 2012, 359, 88.
| Crossref | GoogleScholarGoogle Scholar |
[54] Z. Zhao, H. Yang, Y. Li, X. Guo, Green Chem. 2014, 16, 1274.
| Crossref | GoogleScholarGoogle Scholar |
[55] H. K. Kadam, S. G. Tilve, RSC Adv. 2012, 2, 6057.
| Crossref | GoogleScholarGoogle Scholar |
[56] P. S. Rathore, R. Patidar, T. Shripathi, S. Thakore, Catal. Sci. Technol. 2015, 5, 286.
| Crossref | GoogleScholarGoogle Scholar |
[57] K. Chaiseeda, S. Nishimura, K. Ebitani, ACS Omega 2017, 2, 7066.
| Crossref | GoogleScholarGoogle Scholar |
[58] S. Mahata, A. Sahu, P. Shukla, A. Rai, M. Singh, V. K. Rai, New J. Chem. 2018, 42, 2067.
| Crossref | GoogleScholarGoogle Scholar |
[59] F. Yang, Y. Cao, Z. Chen, X. He, L. Hou, Y. Li, New J. Chem. 2018, 42, 2718.
| Crossref | GoogleScholarGoogle Scholar |
[60] G. Romanazzi, A. M. Fiore, M. Mali, A. Pizzuti, C. Leonelli, A. Nacci, P. Mastrorilli, M. M. Dell’Anna, Mol. Catal. 2018, 446, 31.
| Crossref | GoogleScholarGoogle Scholar |
[61] M. Pashaei, E. Mehdipour, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
[62] M. Gholinejad, F. Zareh, C. Nájera, Appl. Organomet. Chem. 2018, 32,
| Crossref | GoogleScholarGoogle Scholar |
[63] H. N. Hareesh, K. U. Minchitha, K. Venkatesh, N. Nagarju, N. Kathyayini, RSC Adv. 2016, 6, 82359.
| Crossref | GoogleScholarGoogle Scholar |
[64] H. Veisi, N. Hajimoradian Nasrabadi, P. Mohammadi, Appl. Organomet. Chem. 2016, 30, 890.
| Crossref | GoogleScholarGoogle Scholar |
[65] M. Rajabzadeh, H. Eshghi, R. Khalifeh, M. Bakavoli, RSC Adv. 2016, 6, 19331.
| Crossref | GoogleScholarGoogle Scholar |
[66] B. Wu, P. Lyu, K. Wang, X. Qiu, T. Liu, F. Zhang, H. Li, S. Xiao, Res. Chem. Intermed. 2018, in press.
| Crossref | GoogleScholarGoogle Scholar |
[67] O. Mazaheri, R. J. Kalbasi, RSC Adv. 2015, 5, 34398.
| Crossref | GoogleScholarGoogle Scholar |
[68] P. Fakhri, M. Nasrollahzadeh, B. Jaleh, RSC Adv. 2014, 4, 48691.
| Crossref | GoogleScholarGoogle Scholar |
[69] K. Karami, M. Rahimi, M. Dinari, J. Iran. Chem. Soc. 2018, 15, 281.
| Crossref | GoogleScholarGoogle Scholar |
[70] B. Karimi, F. Mansouri, H. Vali, ChemPlusChem 2015, 80, 1750.
| Crossref | GoogleScholarGoogle Scholar |
[71] P. Supriya, B. T. V. Srinivas, K. Chowdeswari, N. V. S. Naidu, B. Sreedhar, Mater. Chem. Phys. 2018, 204, 27.
| Crossref | GoogleScholarGoogle Scholar |
[72] P. Eskandari, F. Kazemi, J. Photochem. Photobiol. Chem. 2018, 364, 233.
| Crossref | GoogleScholarGoogle Scholar |
[73] P. Veerakumar, I. P. Muthuselvam, C.-T. Hung, K.-C. Chou, S.-B. Liu, ACS Sustainable Chem. Eng. 2016, 4, 6772.
| Crossref | GoogleScholarGoogle Scholar |
[74] F. M. Moghaddam, V. Saberi, P. Kalvani, ChemistrySelect 2018, 3, 6779.
| Crossref | GoogleScholarGoogle Scholar |
[75] M. Madasu, C.-F. Hsia, S. Rej, M. H. Huang, ACS Sustainable Chem. Eng. 2018, 6, 11071.
| Crossref | GoogleScholarGoogle Scholar |