Please do not adjust margins
Green Chemistry
Page 6 of 8
DOI: 10.1039/C7GC00192D
COMMUNICATION
Journal Name
6
7
8
9
S. Chikkali and S. Mecking Angew. Chem. Int. Ed. 2012, 51
5802-5808.
P. B. Van Dam, M. C. Mittelmeijer and C. J. Boelhouer Chem. 37 D. G. Gusev ACS Catal. 2016,
Soc. Chem. Commun. 1972, 1221.
Handbook of Methatesis (Ed.: R. H. Grubbs), Wiley-VCH,
Weinheim, 2003.
,
36 X. Miao, C. Fischmeister, P. H. Dixneuf, C. Bruneau, J.-L.
Dubois and J.-L. Couturier Green Chem. 2012, 14, 2179-2183.
6 (10), 6967-6981.
38 J. Pritchard, G. A. Filonenko, R. Van Putten, E. J. M.Hensen,
E.A. Pidko Chem. Soc. Rev. 2015, 44 (11), 3808-3833.
39 P. A. Dub and T. Ikariya, ACS Catal. 2012, 2, 1718-1741.
Olefin Metathesis Theory and Practice (Ed.: K. Grela), John 40 S. Werkmeister, K. Junge and M. Beller Org. Process Res.
Wiley & Sons, Inc., Hoboken, NY, 2014. Chem. 2014, 18, 289-302.
10 Adv. Synth. Catal. 2007, 349, 1-268 (Special Issue: Olefin 41 M. L. Clarke Catal. Sci. Technol. 2012,
2
, 2418-2423.
Metathesis).
11 R. H. Grubbs Tetrahedron 2004, 60, 7117-7140
12 T. M. Trnka and R. H. Grubbs Acc. Chem. Res. 2001, 34, 18-
29.
42 S. Elangovan, M. Garbe, H. Jiao, A. Spannenberg, K. Junge, M.
Beller Angew. Chem. Int. Ed. 2016, 55, 15364-15368
43 O. Ogata, Y. Nakayama, H. Nara, M. Fujiwhara, Y. Kayaki Org.
Lett. 2016, 18, 3894-3897.
13 H. Mutlu, R. Hofsäβ, R. E. Montenegro and M. A. R. Meier 44 D. Kim, L. Le, M. J. Drance, K. H. Jensen, K. Bogdanovski, T. N.
RSC Adv. 2013,
14 A. Nickel, T. Ung, G. Mkrtumyan, J. Uy, C. Woo Lee, D.
3
, 4927-4934.
Cervarich, M. G. Barnard, N. J. Pudalov, S. M. M. Knapp, A. R.
Chianese Organometallics 2016, 35, 982-989.
Stoianova, J. Papazian, W.-H. Wei, A. Mallari, Y. Schrodi and 45 S. Elangovan, B. Wendt, C. Topf, S. Bachmann, M. Scalone, A.
R. L. Pederson Top Catal. 2012, 55, 518-523.
15 A. Rybak and M. A. R. Meier Green Chem. 2007,
1361.
16 R. Malacea, C. Fischmeister, C. Bruneau, J.-L. Dubois, J.-
L. Couturier and P. H. Dixneuf Green Chem. 2009, 11, 152-
155.
17 T. Jacobs, A. Rybak and M. A. R. Meier Appl. Catal. A :
General 2009, 353, 32-35.
18 A. Behr, S. Toepell and S. Harmuth RSC Adv. 2014, 4, 16320-
Spannenberg, H. Jiao, W. Baumann, K. Junge, M. Beller Adv.
Synth. Catal. 2016, 358, 820-825.
46 P. Gajewski, A. Gonzalez-de-Castro, M. Renom-Carrasco, U.
Piarulli, C. Gennari, J. G. de Vries, L. Lefort, L. Pignataro
ChemCatChem 2016, 8, 3431-3435.
47 T. J. Korstanje, J. I. Van Der Vlugt, C. J. Elsevier, B. De Bruin
Science 2015, 350 (6258), 298-302.
48 D. Srimani, A. Mukherjee, A. F. G. Goldberg, G. Leitus, Y.
Diskin-Posner, L. J. W. Shimon, Y.; Ben-David and D. Milstein,
Angew. Chem. Int. Ed. 2015, 54, 12357-12360.
9, 1356-
16326.
19 H. Bonin, A. Keraani, J.-L. Dubois, M. Brandhorst, C. 49 G. A. Filonenko, M. J. B. Aguila, E. N. Schulpen, R. vanPutten,
J. Wiecko, C. Müller, L. Lefort, E. J. M. Hensen and E. A.
Fischmeister and C. Bruneau Eur. J. Lipid Sci. Technol. 2015,
117, 209-216.
20 P. Vignon, T. Vancompernolle, J.-L. Couturier, J.-L. Dubois, A.
Mortreux and R. M. Gauvin Chem. Sus. Chem. 2015, 8, 1143-
1146.
21 S. J. McLain, S. D. Arthur, E. Hauptman, J. Feldman, W. A.
Pidko, J. Am. Chem. Soc. 2015, 137, 7620-7623.
50 D. Spasyuk, C. Vicent and D. G. Gusev, J. Am. Chem. Soc.
2015, 137, 3743-3746.
51 T. Chen, H. Li, S. Qu, B. Zheng, L. He, Z. Lai, Z.-X. Wang, K.-W.
Huang, Organometallics 2014, 33, 4152-4155.
Nugent, L. K. Johnson, S. Mecking and M. Brookhart Polym. 52 W. Li, J.-H. Xie, M.-L. Yuan and Q.-L. Zhou Green Chem. 2014,
Mater. Sci. Eng. 1997, 76, 246-247. 16, 4081-4085.
22 J. Louie, C. W. Bielawski and R. H. Grubbs J. Am. Chem. Soc. 53 X. Tan, Y. Wang, Y. Liu, F. Wang, L. Shi, K.-H. Lee, Z. Lin, H. Lv
2001, 123, 11312-11313.
23 M. D. Watson, K. B. Wagener Macromolecules 2000, 33
3196-3201.
and X. Zhang Org. Lett. 2015, 17, 454-457.
54 K. Junge, B. Wendt, H. Jiao and M. Beller ChemCatChem.
2014, 6, 2810-2814.
,
24 S. E. Lehman Jr., K. B. Wagener, L. S. Baugh, S. P. Rucker, D.
N. Schulz, M. Varma-Nair, E. Berluche Macromolecules 2007,
40, 2643-2656.
55 S. Werkmeister, K. Junge, B. Wendt, E. Alberico, H. Jiao, W.
Baumann, H. Junge, F. Gallou and M. Beller Angew. Chem.
Int. Ed. 2014, 53, 8722-8726.
25 S. D. Drouin, F. Zamanian, D. E. Fogg Organometallics 2001,
20, 5495-5487.
56 T. Zell, Y. Ben-David and D. Milstein Angew. Chem. Int. Ed.
2014, 53, 4685-4689.
57 G. A. Filonenko, E. Cosimi, L. Lefort, M. P. Conley, C. Copéret,
M. Lutz, E. J. M. Hensen and E. A. Pidko ACS Catal. 2014, 4,
2667-2671.
58 Cooperative & Redox Non-Innocent Ligands in Directing
Organometallic Reactivity (Cluster Issue) Eur. J. Inorg. Chem.
2012, 3, 340-580.
59 H. A. Younus, N. Ahmad, W. Su and F. Verpoort Coord. Chem.
Rev. 2014, 276, 112-152.
26 U. L. Dharmasena, H. M. Foucault, E. N. dos Santos, D. E.
Fogg, S. P. Nolan Organometallics 2005, 24, 1056-1058.
27 K. D. Camm, N. M. Castro, Y. Liu, P. Czechura, J. L. Snelgrove,
D. E. Fogg J. Am. Chem. Soc. 2007, 129, 4168-4169.
28 G. C. Zielinski, C. Samojlowice, T. Wdowik and K. Grela, Org.
Biomol. Chem. 2015, 13, 2684-2688.
29 B. Schmidt Pure Appl. Chem. 2006, 78, 469-476.
30 V. Dragutan and I. Dragutan, J. Organomet. Chem. 2006, 691
,
5129-5147.
31 S. Kotha, S. Misra, G. Sreevani and B. V. Babu, Curr. Org.
Chem. 2013, 17, 2776-2795.
60 J. R. Khusnutdinova, D. Milstein Angew. Chem. Int. Ed. 2015,
54, 12236-12273.
61 L. A. Saudan, C. M. Saudan, C. Debieux and P. Wyss Angew.
Chem. Int. Ed. 2007, 46, 7473-7476.
32 B. Alcaide, P. Almendros and A. Luna Chem. Rev. 2009, 109
,
3817-3858.
33 Ru hydrides and Ru dihydrogen complexes were identified
62 M. B. Dinger and J. C. Mol Organometallics 2003, 22, 1089-
1095.
as active hydrogenation species after treatment of Ru 63 M. B. Dinger and J. C. Mol Eur. J. Inorg. Chem. 2003, 2827-
metathesis catalysts with H2: S. D. Drouin, G. P. A. Yap, D. E.
Fogg Inorg. Chem. 2000, 39, 5412-5414.
34 X. Miao, C. Fischmeister, C. Bruneau, P. H. Dixneuf,
2833.
64 N. J. Beach, K. D. Camm and D. E. Fogg Organometallics
2010, 29, 5450-5455.
ChemSusChem. 2009,
35 X. Miao, C. Fischmeister, C. Bruneau, P. H. Dixneuf, , J.-L.
2
, 542-545.
65 N. J. Beach, J. A. M. Lummiss, J. M. Bates and D. E. Fogg
Organometallics 2012, 31, 2349-2356.
Dubois and J.-L. Couturier ChemSusChem. 2012,
1414.
5, 1410-
6 | J. Name., 2012, 00, 1-3
This journal is © The Royal Society of Chemistry 20xx
Please do not adjust margins