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Dalton Transactions
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DOI: 10.1039/C7DT04326K
ARTICLE
4 (a) A. Iturmendi, N. García, E. A. Jaseer, J. Munárriz, P. J.
Journal Name
Wei, D. Xue, Q. Lei, C. Wang and J. Xiao, Green Chem.
,
Sanz Miguel, V. Polo, M. Iglesias and L. A. Oro, Dalton
Trans, 2016, 45, 12835–12845; (b) M. V. Jiménez, J.
2013, 15, 629; (d) D. Talwar, X. Wu, O. Saidi, N. P. Salguero
and J. Xiao, Chem. ꢀ Eur. J., 2014, 20, 12835–12842.
FernándezꢀTornos, J. J. PérezꢀTorrente, F. J. Modrego, S. 14 (a) O. Prakash, K. N. Sharma, H. Joshi, P. L. Gupta and A. K.
Winterle, C. Cunchillos, F. J. Lahoz and L. A. Oro,
Organometallics, 2011, 30, 5493–5508; (c) A. Pontes da
Costa, M. Viciano, M. Sanaú, S. Merino, J. Tejeda, E. Peris
Singh, Organometallics, 2014, 33, 2535−2543. (b) O.
Prakash, K. N. Sharma, H. Joshi, P. L. Gupta, and A. K.
Singh, Organometallics, 2014, 33, 983−993.
and B. Royo, Organometallics, 2008, 27, 1305–1309; (d) F. 15 (a) M. H. S. A. Hamid, P. A. Slatford and J. M. J. Williams,
E. Hahn, C. Holtgrewe, T. Pape, M. Martin, E. Sola and L. A.
Oro, Organometallics, 2005, 24, 2203–2209; (e) A. C.
Hillier, H. M. Lee, E. D. Stevens and S. P. Nolan,
Organometallics, 2001, 20, 4246–4252; (f) I. Kownacki, M.
Adv. Synth. Catal., 2007, 349, 1555–1575; (b) T. D. Nixon,
M. K. Whittlesey and J. M. J. Williams, Dalton Trans, 2009,
753–762; (c) G. E. Dobereiner and R. H. Crabtree, Chem.
Rev., 2010, 110, 681–703; (d) G. E. Dobereiner and R. H.
Crabtree, Chem. Rev. 2010, 110, 681–703; (e) A. J. A.
Watson, and J. M. J. Williams, Science, 2010, 329, 635–636.
Kubicki, K. Szubert and B. Marciniec, J. Organomet. Chem.
,
2008, 693, 321–328; (g) G.ꢀM. Zhao, H.ꢀl. Liu, X.ꢀr. Huang,
D.ꢀd. Zhanga, X. Yang, RSC Adv. 2015, 5, 22996–23008; (h) 16 (a) K. Fujita, Z. Li, N. Ozeki and R. Yamaguchi, Tetrahedron
O. Saidi, J. M. J. Williams, Top. Organomet. Chem. 2011, 34,
Lett., 2003, 44, 2687–2690; (b) Y.ꢀH. Chang, C.ꢀF. Fu, Y.ꢀH.
77–106.
Liu, S.ꢀM. Peng, J.ꢀT. Chen and S.ꢀT. Liu, Dalton Trans
2009, 861–867; (c) A. Prades, R. Corberan, M. Poyatos, and
E. Peris, Chem. Eur. J., 2008, 14, 11474–11479.
,
5
(a) A. Prades, R. Corberán, M. Poyatos and E. Peris, Chem. ꢀ
Eur. J., 2008, 14, 11474–11479; (b) Y.ꢀH. Chang, Y.
Nakajima and F. Ozawa, Organometallics, 2013, 32, 2210– 17 (a) S. Mukhopadhyay, R. K. Gupta, R. P. Paitandi, N. K.
2215; (c) Zhu, M.; Fujita, K.ꢀi.; Yamaguchi, R.; Org. Lett.,
2010, 12, 1336–1339; (d) R. Yamaguchi, S. Kawagoe, C.
Asai and K. Fujita, Org. Lett., 2008, 10, 181–184.
D. Wang and D. Astruc, Chem. Rev., 2015, 115, 6621–6686.
(a) G. Guillena, D. J. Ramón and M. Yus, Chem. Rev., 2010, 18 (a) T. Nakagawa, H. Seino and Y. Mizobe, Organometallics
Rana, G. Sharma, B. Koch, L. K. Rana, M. S. Hundal and D.
S. Pandey, Organometallics, 2015, 34, 4491–4506; (b) L. B.
Kumbhare, A. P. Wadawale, V. K. Jain, M. Sieger and W.
Kaim, Inorg. Chem. Commun., 2010, 13, 475–478.
6
7
,
110, 1611–1641; (b) Pharmaceuticals: Classes, Therapeutic
Agents, Areas of Application; J. L. McGuire, Ed.; WileyꢀVCH
2000, Vol. 1−4; (c) S. Bähn, S. Imm, L. Neubert, M. Zhang,
H. Neumann and M. Beller, ChemCatChem, 2011, 3, 1853–
1864.
(a) M. Kumar, J. DePasquale, N. J. White, M. Zeller, E. T.
Papish, Organometallics, 2013, 32, 2135−2144; (b) K. A.
Rashid, S. E. Clapham, A. Hadzovic, J. N. Harvey, A. J.
Lough, R. H. Morris, J. Am. Chem. Soc., 2002, 124, 15104ꢀ
15118.
2010, 29, 2254–2259; (b) O. Prakash, H. Joshi, K. N. Sharma,
P. L. Gupta and A. K. Singh, Organometallics, 2014, 33,
3804–3812; (c) X.ꢀQ. Xiao, Y.ꢀJ. Lin and G.ꢀX. Jin, Dalton
Trans., 2008, 2615; (d) Y.ꢀK. Sau, X.ꢀY. Yi, K.ꢀW. Chan, C.ꢀ
S. Lai, I. D. Williams and W.ꢀH. Leung, J. Organomet.
Chem., 2010, 695, 1399–1404; (e) O. Prakash, P. Singh, G.
Mukherjee and A. K. Singh, Organometallics, 2012, 31,
3379–3388; (f) M. Hamdaoui, C. Desrousseaux, H. Habbita
8
9
and
J.ꢀP.
Djukic,
Organometallics
,
2017,
DOI:
10.1021/acs.organomet.7b00749; (g) R. A. Arthurs, P. N.
Horton, S. J. Coles, and C. J. Richards, Eur. J. Inorg. Chem.,
2017, 229–232.
(a) A. Kumar, G. K. Rao, S. Kumar and A. K. Singh, Dalton
Trans., 2013, 42, 5200ꢀ5233; (b) A. Kumar, G. Kumar Rao
and A. K Singh, RSC Adv., 2012, 2, 12552ꢀ12574; (c) A. 19 (a) J.ꢀE. Bäckvall, J. Organomet. Chem., 2002, 652, 105–111;
Kumar, G. K. Rao, F. Saleem and A. K. Singh, Dalton
Trans., 2012, 41, 11949ꢀ11977; (d) G. Kumar Rao, A.
(b) M. J. Palmer and M. Wills, Tetrahedron Asymmetry
1999, 10, 2045–2061.
,
Kumar, B. Kumar and A. K. Singh, Dalton Trans., 2012, 41, 20 (a) J. Campos, U. Hintermair, T. P. Brewster, M. K. Takase,
4306ꢀ4334; (e) G. K. Rao, A. Kumar, B. Kumar, D. Kumar
and A. K. Singh, Dalton Trans, 2012, 41, 1931–1937; (f) G.
K. Rao, A. Kumar, J. Ahmed and A. K. Singh, Chem.
Commun., 2010, 46, 5954ꢀ5956.
R. H. Crabtree, ACS Catal., 2014, 4, 973−985. (b) F. Saleem,
G. K. Rao, A. Kumar, G. Mukherjee, and A. K. Singh,
Organometallics, 2014, 33, 2341−2351.
21 K. Fujita, S. Furukawa and R. Yamaguchi, J. Organomet.
Chem., 2002, 649, 289–292.
10 (a) U. Kumar, P. Dubey, V. V. Singh, O. Prakash and A. K.
Singh, RSC Adv, 2014, 4, 41659–41665; (b) P. Singh and A. 22 (a) D. S. Glueck, L. J. N. Winslow and R. G. Bergman,
K. Singh, Organometallics, 2010, 29, 6433–6442; (c) P.
Singh and A. K. Singh, Inorg. Chim. Acta 2012, 387, 441–
445; (d) P. Dubey, S. Gupta and A. K. Singh, Dalton Trans.,
Organometallics, 1991, 10, 1462–1479; (b) R. Kawahara, K.
Fujita and R. Yamaguchi, Adv. Synth. Catal., 2011, 353,
1161–1168.
2017
11 (a) G. Zassinovich, G. Mestroni and S. Gladiali, Chem. Rev.
1992, 92, 1051–1069; (b) R. Noyori and S. Hashiguchi, Acc. 24 (a) P. Foley, R. DiCosimo and G. M. Whitesides, J. Am.
,
46,
13065–13076
.
23 B. J. Boro, E. N. Duesler, K. I. Goldberg and R. A. Kemp,
,
Inorg. Chem., 2009, 48, 5081–5087.
Chem. Res., 1997, 30, 97–102; (c) K. Everaere, A. Mortreux
and J.ꢀF. Carpentier, Adv. Synth. Catal., 2003, 345, 67–77; (d)
S. E. Clapham, A. Hadzovic and R. H. Morris, Coord. Chem.
Rev., 2004, 248, 2201–2237; (e) S. Gladiali and E. Alberico,
Chem Soc Rev, 2006, 35, 226–236; (f) J. S. M. Samec, J.ꢀE.
Chem. Soc. 1980, 102, 6713–6725; (b) D. R. Anton and R. H.
Crabtree, Organometallics, 1983, 2, 855–859; (c) M. R.
Eberhard, Org. Lett., 2004, 6, 2125–2128; (d) J. A. Widegren
and R. G. Finke, J. Mol. Catal. Chem., 2003, 198, 317–341;
(e) E. Bayram, J. C. Linehan, J. L. Fulton, J. A. S. Roberts, N.
K. Szymczak, T. D. Smurthwaite, S. Özkar, M.
Balasubramanian and R. G. Finke, J. Am. Chem. Soc., 2011,
133, 18889–18902.
Bäckvall, P. G. Andersson and P. Brandt, Chem. Soc. Rev.
,
2006, 35, 237; (g) C. Wang, X. Wu, and J. Xiao, Chem.ꢀAsian
J., 2008, 3, 1750–1770; (i) R. Noyori, M. Yamakawa, and S.
Hashiguchi, J. Org. Chem., 2001, 66, 7931–7944.
12 T. Ikariya and A. J. Blacker, Acc. Chem. Res., 2007, 40, 25 (a) Bruker (2015). APEX3 and SAINT. Bruker–Nonius AXS
1300–1308.
Inc., Madison, Wisconsin, USA; (b) G. M. Sheldrick,
SHELXTL Version 2014/7; (c) http://shelx.uniꢀ
ac.gwdg.de/SHELX/index.php.
13 (a) X.ꢀH. Zhu, L.ꢀH. Cai, C.ꢀX. Wang, Y.ꢀN. Wang, X.ꢀQ.
Guo and X.ꢀF. Hou, J. Mol. Catal. Chem., 2014, 393, 134–
141; (b) H. VázquezꢀVilla, S. Reber, M. A. Ariger and E. M. 26 M. A. Bennett and A. K. Smith, J. Chem. Soc. Dalton Trans.
,
Carreira, Angew. Chem. Int. Ed., 2011, 50, 8979–8981; (c) Y.
1974, 233–241.
10 | J. Name., 2012, 00, 1-3
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