(a) Makgwane, P.R.; Ray, S.S. Nanosized ruthenium particles decorated carbon nanofibers as active catalysts for the oxidation of
p-cymene by molecular oxygen.
J. Mol. Catal. Chem., 2013,
373, 1-11.
[
http://dx.doi.org/10.1016/j.molcata.2013.02.017]
(b) Naota, T.; Takaya, H.; Murahashi, S-I. Ruthenium-catalyzed reactions for organic synthesis.
Chem. Rev., 1998,
98(7), 2599-2660.
[
http://dx.doi.org/10.1021/cr9403695] [PMID:
11848973]
(c) Murahashi, S-I.; Takaya, H.; Naota, T. Ruthenium catalysis in organic synthesis.
Pure Appl. Chem., 2002,
74, 19-24.
[
http://dx.doi.org/10.1351/pac200274010019]
(d) Kim, Y-H.; Hwang, S-K.; Kim, J.W.; Lee, Y-S. Zirconia supported ruthenium catalyst for efficient aerobic oxidation of alcohols to aldehyde.
Ind. Eng. Chem. Res., 2014,
53, 12548-12552.
[
http://dx.doi.org/10.1021/ie5009794]
(e) Murahashi, S-I.; Takaya, H. Low-valent ruthenium and iridium hydride complexes as alternatives to Lewis acid and base catalysts.
Acc. Chem. Res., 2000,
33, 225-233.
[
http://dx.doi.org/10.1021/ar980085x]
(f) Murahashi, S-I.; Naota, T. A new way for efficient catalysis by using low valent ruthenium complexes as redox Lewis acid and base catalysts.
Bull. Chem. Soc. Jpn., 1996,
69, 1805-1824.
[
http://dx.doi.org/10.1246/bcsj.69.1805]
(g) Grubbs, R.H. Olefin-metathesis catalysts for the preparation of molecules and materials (Nobel lecture).
Angew. Chem. Int. Ed., 2006,
45, 3760-3765.
[
http://dx.doi.org/10.1002/anie.200600680]
(h) Nguyen, S.T.; Grubbs, R.H.; Ziller, J.W. Synthesis and activities of new single-component, ruthenium-based olefin metathesis catalysts.
J. Am. Chem. Soc., 1993,
115, 9858-9859.
[
http://dx.doi.org/10.1021/ja00074a086]
(i)Schwab, P.; Grubbs, R.H.; Ziller, J.W. Synthesis and applications of RuCl
2(CHR’)(PR
3)
2: The influence of the alkylidene moiety on metathesis activity.
J. Am. Chem. Soc., 1996,
118, 100-110.
[
http://dx.doi.org/10.1021/ja952676d]
(j)Nguyen, S.T.; Johnson, L.K.; Grubbs, R.H.; Ziller, J.W. Ring-opening metathesis polymerization (ROMP) of norbornene by a group VIII carbene complex in protic media.
J. Am. Chem. Soc., 1992,
114, 3974-3975.
[
http://dx.doi.org/10.1021/ja00036a053]
(k)Ferguson, M.L.; O’Leary, D.J.; Grubbs, R.H.; Grubbs, R.H. Ring-closing metathesis synthesis of
N-Boc-3-pyrroline.
Org. Synth., 2003,
80, 85-92.
[
http://dx.doi.org/10.15227/orgsyn.080.0085]
(l)Andrade, R.B.; Plante, O.J.; Melean, L.G.; Seeberger, P.H. Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents.
Org. Lett., 1999,
1(11), 1811-1814.
[
http://dx.doi.org/10.1021/ol991071+] [PMID:
10836038]
(m)Burdett, K.A.; Harris, L.D.; Margl, P.; Maughon, B.R.; Mokhtar-Zadeh, T.; Saucier, P.C.; Wasserman, E.P. Renewable monomer feedstocks
via olefin metathesis: fundamental mechanistic studies of methyl oleate ethenolysis with the first-generation Grubbs catalyst.
Organometallics, 2004,
23, 2027-2047.
[
http://dx.doi.org/10.1021/om0341799]
(n)Blackwell, H.E.; O’Leary, D.J.; Chatterjee, A.K.; Washenfelder, R.A.; Bussmann, D.A.; Grubbs, R.H. New approaches to olefin cross-metathesis.
J. Am. Chem. Soc., 2000,
122, 58-71.
[
http://dx.doi.org/10.1021/ja993063u]
(o)France, M.B.; Paciello, R.A.; Grubbs, R.H. Initiation of ring-opening metathesis polymerization in protic media. Extension of [Ru(H
2O)
6]
2+ catalyzed polymerizations to less-strained cyclic monomers.
Macromolecules, 1993,
26, 4739-4741.
[
http://dx.doi.org/10.1021/ma00070a001]
(p)Johnson, L.K.; Grubbs, R.H.; Ziller, J.W. Synthesis of tungsten vinyl alkylidene complexes
via the reactions of WCl
2(NAr)(PX
3)
3 (X = R, OMe) precursors with 3,3-disubstituted cyclopropenes.
J. Am. Chem. Soc., 1993,
115, 8130-8145.
[
http://dx.doi.org/10.1021/ja00071a026]
(q)Dias, E.L.; Nguyen, S.T.; Grubbs, R.H. Well-defined ruthenium olefin metathesis catalysts: Mechanism and activity.
J. Am. Chem. Soc., 1997,
119, 3887-3897.
[
http://dx.doi.org/10.1021/ja963136z]
(r)Binger, P.; Müller, P.; Benn, R.; Mynott, R. Vinylcarbene complexes of titanocene.
Angew. Chem. Int. Ed. Engl., 1989,
28, 610-611.
[
http://dx.doi.org/10.1002/anie.198906101]