Please do not adjust margins
Dalton Transactions
Page 12 of 13
ARTICLE
Journal Name
Chem., 2010, 63, 3688-3696; (e) K. C. Gupta and A. K. Sutar,
Coord. Chem. Rev., 2008, 252, 1420-1450; (f) C. Rocaboy
and J. A. Gladysz, Org. Lett., 2002, , 1993-1996.
Methods in Chemistry; Springer: NewDYOoI:r1k01.19093V91ie/,wC(7AbDrt)iTcC0le4.O6Ln3eli5neAe,
W. Yang and R. G. Parr, Phys. Rev., 1988, B37, 785-789.
4
13 (a) P. Gogoi, M. Kalita and P. Barman, Synlett, 2014, 25, 866-
870; (b) M. Iwasaki, M. Iyanaga, Y. Tsuchiya, Y. Nishimura,
W. Li, Z. Li and Y. Nishihara, Chem. Eur. J., 2014, 20, 2459-
2462.
36 H. B. Schlegel, J. Comput. Chem., 1982,
37 L. Skripnikov, Chemissian v4. 36, A computer program to
analyse and visualize quantum-chemical calculations 2015
3, 214-218.
.
38 U. Das, P. Pattanayak, D. Patra, P. Brandão, V. Felix and S.
Chattopadhyay, Polyhedron 2016, 110, 165-171.
14 (a) J. Li, C. Li, S. Yang, Y. An, W. Wu and H. Jiang, J. Org.
Chem., 2016, 81, 7771-7783; (b) Y. Chen, C.-H. Cho, F. Shi,
and R. C. Laroc, J. Org. Chem., 2009, 74, 6802-6811
15 P. P. Kumar, Y. D. Reddy, Ch. V. R. Reddy, B. R. Devi and P. K.
Dubey, J. Sulfur Chem., 2014, 35, 356-361.
39 M. Kalita, P. Gogoi, P. Barman and B. Sarma, J. Coord.
Chem., 2014, 67, 2445-2454.
40 D. Vidovic, A. Radulovic and V. Jevtovic, Polyhedron, 2011,
30, 16-21.
16 (a) Z. Wu, Y.-C. Li, W.-z. Ding, T. Zhu, S.-Z. Liu, X. Ren and L.-
41 P. Pattanayak, J. L. Pratihar, D. Patra, P. Brandao and V.
Felix, Inorganica Chimica Acta, 2014, 418, 171-179.
42 (a) P. Kar, S. Verma, A. Sen, A. Das, B. Ganguly and H.N.
Ghosh, Inorg. Chem., 2010, 49, 4167-4174; (b) S. I. Orysyk,
O. O. Zholob, V. V. Bon, V. V. Nikulina, V. V. Orysyk, T. V.
Nikolaienko, L. V. Garmanchuk, Y. L. Zborovskii, G. M.
Tolstanova, N. M. Khranovska, V. I. Pekhnyo and M. V. Vovk,
Polyhedron, 2015, 85, 208-220; (c) S. Naiya, S. Biswas, M. G.
B. Drew and A. Ghosh, Polyhedron, 2012, 34, 67-73; (d) V.
M. Leovac, L. S. Jovanovic´, V. Divjakovic´, A. Pevec, I. Leban
and T. Armbruster, Polyhedron, 2007, 26, 49-58; (e) P.
Pratihar, S. Jha, T. K. Mondal, G. Mostafa and C. Sinha.
Polyhedron, 2007, 26, 4328-4344.
H. Zou, Asian J. Org. Chem., 2016, 5, 625-628; (b) H. Liao, Y.
Yang, W-mei Li, C. Shen and P. Zhang, Curr. Org. Chem.,
2017, 21, 2509-2513; (c) N. Golzar, N. Nowrouzi, M. Abbasi
and A. M. Mehranpour, New J. Chem., 2017, 41, 11921-
11925. (d) Z. Li, J. Hong and X. Zhou, Tetrahedron, 2011, 67
3690-3697; (e) S. Ranjit, R. Lee, D. Heryadi, C. Shen, E. Wu,
P. Zhang, K.- W. Huang and X. Liu, J. Org. Chem. 2011, 76
,
,
8999-9007; (f) Z. Li, L. Hong, R. Liu, J. Shen and X. Zhou,
Tetrahedron Lett., 2011, 52, 1343-1347.
17 (a) X.-L. Fang, R.-Y. Tang, P. Zhong and J.-H. Li, Synthesis,
2009, 4183-4189; (b)J. S. Yadav, B. V. S. Reddy, Y. J. Reddy
and K. Praneeth, Synthesis, 2009, 1520-1524.
18 M. Chen, Z.-T. Huang and Q.-Y. Zheng, Chem. Commun.,
2012, 48, 11686-1168.
43 M. Kalita, P. Gogoi, P. Barman, B. Sarma, A. K. Buragohain and
R. D. Kalita, Polyhedron, 2014, 74, 93-98.
44 S. Acharya, A. Kejriwal, A. N. Biswas, P. Das, D. N. Neogi and
P. Bandyopadhyay, Polyhedron, 2012, 38, 50-57.
19 M. Tudge, M. Tamiya, C. Savarin and G. R. Humphrey, Org.
Lett., 2006, 8, 565-568.
20 C. C. Silveira, S. R. Mendes, L. Wolf and G. M. Martins,
Tetrahedron Lett., 2010, 51, 2014-2016.
21 J. Dupont, C. S. Consorti, and J. Spencer, Chem. Rev., 2005,
105, 2527-2572.
22 (a) H. Kim and P. H. Lee, Adv. Synth. Catal., 2009, 351, 2827-
45 (a) R. Rahaman, N. Devi and P. Barman, Tetrahedron Lett.,
2015, 56, 4224; (b) R. Rahaman, N. Devi, K. Sarma and P.
Barman, RSC Adv., 2016,
6, 10873-10879; (c) R. Rahaman, N.
Devi, J. R. Bhagawati and P. Barman, RSC Adv., 2016,
6
,
18929-18935; (d) R. Rahaman and P. Barman, Synlett, 2017,
684-690; (e) N. Devi, R. Rahaman, K. Sarma and P. Barman,
Eur. J. Org. Chem., 2016, 384-388; (f) S. Hazarika, P. Gogoi
2832; (b) R. R. Tykwinski, Angew. Chem. Int. Ed. 2003, 42
,
1566-1568.
23 J. M. Midgley, B. J. Millard, W. B. Whalley and C. J. Smith, J.
and P. Barman, RSC Adv., 2015,
46 (a) J. Aihara, J. Phys. Chem. A, 1999, 103, 7487–7495; (b) J.
Aihara, Phys. Chem. Chem. Phys., 2000, , 3121-3125; (c) Y.
5, 25765-25767.
Chem. Soc. 1971 ,
24 (a) U. Yapuri, S. Vanjivaka, S. Palle, R. Kumar K. and O.
Gudaparthi, Der Pharma Chemica, 2013, , 1 -5; (b) B. T.
C, 19-23.
2
5
Huang, C. Rong, R. Zhang, S. Liu, J. Mol. Model., 2017, 23, 1-
12.
Cho, O. K. Choi and D. J. Kim, Bull. Korean Chem. Soc., 2003,
24, 1023-1025.
47 (a) K. Sarma, N. Devi, M. Kalita, B. Sarma and P. Barman, J.
Coord. Chem., 2015, 68, 3685-3700; (b) P. Gogoi, M. Kalita,
T. Bhattacharjee and P. Barman, Tetrahedron Lett., 2014,
55, 1028-1030.
25 B. M. Trost and G. S. Massiot, J. Am. Chem. Soc., 1977, 99
,
4405-4412.
26 (a) N. Devi, R. Rahaman, K. Sarma, T. Khan and P. Barman,
Eur. J. Org. Chem., 2017, 1520-1525; (b) G. Foray, A. B.
Peñéñory and R. A. Rossi, Tetrahedron Lett., 1997, 38, 2035-
2038; (c) M. L. Scheinbaum, R. B. Woodward and I. J.
Pachter, J. Org. Chem., 1971, 36, 1137-1139.
48 (a) P. J. Dyson and P. G. Jessop, Catal. Sci. Technol., 2016, 6,
3302-3316; (b) A. F. P. Biajoli, C. S. Schwalm, J. Limberger, T. S.
Claudino, and A. L. Monteiro, J. Braz. Chem. Soc., 2014, 25,
2186-2214; (c) C. Amatore and A. Jutand, Acc. Chem. Res.,
2000, 33, 314-321; (d) G. Meng and M. Szostak, Org. Biomol.
Chem., 2016, 14, 5690-5707; (e) C. E. I. Knappke and A. J. von
Wangelin, Chem. Soc. Rev., 2011, 40, 4948–4962; (f) S. J.
Sabounchei, M. Hosseinzadeh, S. Salehzadeh, F. Maleki and R.
W. Gable, Inorg. Chem. Front., 2017, 4, 2107-2118; (g) P.
Gogoi, S. Hazarika, M. J. Sarma, K. Sarma and P. Barman,
Tetrahedron, 2014, 70, 7484-7489.
27 (a) M. Jereb and A. Togni, Org. Lett., 2005, 7, 4041-4043; (b) H.
Pellissier, Tetrahedron, 2008, 64, 10279-10317.
28 D. D. Perrin and W. L. F. Armarego, Purification of
laboratory Chemicals, 3rd ed., Pergamon, New York 1988
.
29 Q. X. Shi, R. W. Lu, Z. X. Zhang and D. F. Zhao, Chin. Chem.
Lett., 2006, 17, 1045-1047.
30 G. M. Sheldrick, ActaCrystallogr. A., 2008, 64, 112-122.
31 (a) G. M. Sheldrick, SHELXS-97 and SHELXL-97, Fortran
Programs for Crystal Structure Solution and Refinement,
University of Gottingen, Gottingen, Germany, (1997); (b)
SMART, SAINT and SADABS; Bruker AXS Inc., Madison,
Wisconsin, USA 2007
.
32 M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M.
A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B.
Mennucci and G. A. Petersson, Gaussian 09, Revision C.01,
Gaussian, Inc., Wallingford, CT 2010
.
33 R. G. Parr and W. Yang, Density Functional Theory in Atoms
and Molecules; Oxford University Press: New York 1989
34 A. D. Becke, J. Chem. Phys., 1993, 98, 5648-5652.
.
12 | J. Name., 2012, 00, 1-3
This journal is © The Royal Society of Chemistry 20xx
Please do not adjust margins