MANSOUR ET AL.
19 of 20
[26] T. Ketike, V. Ramana, K. Velpula, V. Rao Madduluri,
S. R. Kamaraju, D. R. Burri, Chemistry Select. 2018, 3, 7164.
[27] P. Gautam, B. M. Bhanage, J. Org. Chem. 2015, 80, 7810.
[28] N. Touj, A. S. Al-Ayed, M. Sauthier, L. Mansour, A. Harrath,
J. Al-Tamimi, I. Özdemir, S. Yas¸are, N. Hamdi, RSC Adv. 2019,
9, 675.
Centre, CCDC No 1918071. A copy of this information
may be obtained free of charge from The Director,
CCDC, 12 Union Road, Cambridge, CB21EZ, UK (Fax:
[29] D.-H. Lee, J.-T. Hahn, D.-L. Jung, Green Sustain. Chem. 2013,
3, 15.
ORCID
[30] J.-R. Niu, X. Huo, F.-W. Zhang, H.-B. Wang, P. Zhao,
W.-Q. Hu, Chem. Cat. Chem. 2013, 5, 349.
[31] J. Niu, M. Liu, P. Wang, Y. Long, M. Xie, R. Li, J. Ma, New
J. Chem. 2014, 38, 1471.
[32] C. Zhang, J. Liu, C. Xia, Org. Biomol. Chem. 2014, 12, 9702.
[33] M. He, J. R. Struble, J. W. Bode, J. Am. Chem. Soc. 2006, 128,
8418.
[34] T. Wang, H. Xie, L. Liu, W. X. Zhao, J. Organomet. Chem.
2016, 804, 73.
[35] V. H. Nguyen, M. B. Ibrahim, W. W. Mansour, B. M. El Ali,
H. V. Huynh, Organometallics 2017, 36, 2345.
[36] W. Tao, X. Wang, S. Ito, K. Nozaki, JPolym. Sci., Part A:
Polym. Chem, 2019, 57, 474.
REFERENCES
[1] B. Huangab, X. Ban, K. Sun, Z. Ma, Y. Mei, K. Suna, W. Jiang,
B. Lin, Y. Sun, Dyes Pigm. 2016, 133, 380.
[2] K. M. Bjerglund, T. Skrydstrup, G. A. Molander, Org. Lett.
2014, 16, 1888.
[3] E. Graham, S. Rymarchyk, M. Wood, Y. Cen, ACS Chem. Biol.
2018, 13, 782.
[4] M. R. Guy, P. A. Illarionov, S. S. Gurcha, L. G. Dover,
K. J. Gibson, P. W. Smith, D. E. Minnikin, G. S. Besra,
Biochem. J. 2004, 382, 905.
[5] S. Youn Lee, T. Yasuda, Y. S. Yang, Q. Zhang, C. Adachi,
Angew. Chem. 2014, 126, 6520.
[6] Y. Cui, X. Guo, Y. Wang, X. Guo, Chinese J. Catal. 2015,
36, 322.
[7] P. J. Tambade, Y. P. Patil, A. G. Panda, B. M. Bhanage, Eur.
J. Org. Chem. 2009, 2009, 3022.
[8] N. De Kimpe, M. Keppens, G. Froncg, Chem. Commun. 1996,
635, 635.
[37] A. Y. Kostyukovich, A. M. Tsedilin, E. D. Sushchenko,
D. B. Eremin, A. S. Kashin, M. A. Topchiy, A. F. Asachenko,
M. S. Nechaevbc, V. P. Ananikov, Inorg. Chem. Front. 2019,
6, 482.
[38] A. Aktas¸a, D. Barut, C. Ruya, K. Parham, T. Yetkin,
_
G. Muhittin, A. I. Gülçinc, Polyhedron 2019, 159, 345.
[39] M. Xueji, W. Hangxiang, C. Wanzhi, J. Org. Chem. 2014, 79,
8652.
[40] F. Rajabi, W. R. Thiel, Adv. Synth. Catal. 2014, 356, 1873.
[41] M. N. Hopkinson, C. Richter, M. Schedler, F. Glorius, Nature
2014, 510, 485.
[42] D. J. Nelson, S. P. Nolan, Chem. Soc. Rev. 2013, 42, 6723.
[43] H. V. Huynh, J. Ramasamy, J. Organomet. Chem. 2011, 696,
3369.
[9] Y. Hatanaka, T. Hiyama, Chem. Lett. 1989, 18, 2049.
[10] S. G. Davies, D. Pyatt, C. Thomson, J. Organomet. Chem. 1990,
387, 381.
[11] H. Matsuhashia, M. Kuroboshia, Y. Hatanakab, T. Hiyama,
Tetrahedron Lett. 1994, 35, 6507.
[12] S.-K. Kang, W.-Y. Kim, Y.-T. Lee, S.-K. Ahn, J.-C. Kim,
Tetrahedron Lett. 1998, 15, 2131.
[44] D. Zhang, Y. Hea, J. Tanga, Dalton Trans. 2016, 45, 11699.
[45] S. Sakaguchi, K. S. Yoo, J. O'Neill, J. H. Lee, T. Stewart,
K. W. Jung, Angew. Chem. Int. Ed. 2008, 47, 9326.
[46] M. B. Ibrahim, I. Malik, W. W. Mansour, M. Sharif,
M. Fettouhi, B. El Ali, J. Organomet. Chem. 2018, 859, 44.
[47] M. B. Ibrahim, I. Malik, W. W. Mansour, M. Sharif,
M. Fettouhi, B. El Ali, Appl. Organomet. Chem. 2018, 32, 4280.
[48] S. K. U. Riederer, P. Gigler, M. P. Högerl, E. Herdtweck,
B. Bechlars, W. A. Herrmann, F. E. Kühn, Organometallics
2010, 29, 5681.
[49] A. F. Pozharskii, A. M. Simonov, Zh. Obshch. Khim. 1963,
33, 179.
[50] H. V. Huynh, Y. Han, R. Jothibasu, J. A. Yang, Organometal-
lics 2009, 28, 5395.
[51] Q. Teng, H. V. Huynh, Inorg. Chem. 2014, 53, 10964.
[52] Bruker, APEX2. Bruker AXS Inc., Madison, Wisconsin, USA,
2014.
[53] P. N. Muskawarm, P. K. Sachin, A. A. Pundlik,
R. B. Sellappan, S. Kumar, Arab. J. Chem. 2016, 9, S1765.
[54] Bruker SAINT, Bruker AXS Inc., Madison, USA, 2014.
[55] G. M. Sheldrick, SADABS, Bruker AXS Inc., Madison,
Wisconsin, USA, 2014.
[13] S. Changa, Y. Jina, X. Rong, Z. Yong, B. Sunb, Tetrahedron
Lett. 2016, 16, 2017.
[14] G. Evano, C. Theunissen, Rev. Angew. Chem. Int. Ed. Engl.
2019, 58, 7558.
[15] H. Sharghi, M. Jokar, M. M. Doroodmand, R. Khalifeh, Adv.
Synth. Catal. 2010, 352, 3031.
[16] M. Rueping, J. Boris, N. Beilstein, Rev. J. Org. Chem. 2010, 6, 6.
[17] G. Sartori, R. Maggi, Advances in Friedel-Crafts Acylation
Reactions: Catalytic and Green Processes, 1st ed., CRC Press,
Boca Raton, Florida, USA. 2009.
[18] S. Shi, M. Szostak, Org. Lett. 2016, 18, 5872.
[19] H. Kim, S. Park, Y. Baek, K. Um, G. U. Han, D.-H. Jeon,
S. H. Han, P. H. Lee, J. Org. Chem. 2018, 83, 3486.
[20] T. Ishiyama, H. Kizaki, N. Miyaura, A. Suzuki, Tetrahedron
Lett. 1993, 34, 7595.
[21] D. Mingji, B. Liang, C. Wang, Z. You, J. Xiang, G. Dong,
J. Chen, Z. Yang, Adv. Synth. Catal. 2004, 346, 1669.
[22] S. Zheng, L. Xu, C. Xia, Appl. Organomet. Chem. 2007, 21, 772.
[23] B. Michael O'Keefe, N. Simmons, S. F. Martin, Org. Lett. 2008,
10, 5301.
[24] Z. J. Wang, X. Y. Wang, X. Wang, Z. W. Liang, X. Xu, Cat.
Com. 2017, 101, 10.
[25] Y. Cuiab, X. Guoa, Y. Wanga, X. Guoa, Chinese J. Catal. 2015,
36, 322.
[56] G. M. Sheldrick, Acta Crystallogr. 2015, C71, 3.
[57] L. J. Farrugia, J. Appl. Crystallogr. 1997, 30, 565.