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see also 1g
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see also 1g.
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23
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0035915369
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For a note on oxygen-tolerance of ruthenium-catalyzed alkene-alkyne coupling, see:
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For a note on oxygen-tolerance of ruthenium-catalyzed alkene-alkyne coupling, see:. Trost B.M., Pinkerton A.B., Toste F.D., and Sperrle M. J. Am. Chem. Soc. 123 (2001) 12504
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48249091659
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For accounts on air-tolerant alkene metathesis, see:
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For accounts on air-tolerant alkene metathesis, see:. Lin Y.A., Chalker J.M., Floyd N., Bernardes G.J., and Davis B.G. J. Am. Chem. Soc. 130 (2008) 9642
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For ruthenium-catalyzed oxidative coupling of alkenes with arenes, see:
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Foltynowicz, Z.1
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For ruthenium-catalyzed oxidative coupling of phenols leading to biaryls in the presence of molecular oxygen, see:
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For ruthenium-catalyzed oxidative coupling of phenols leading to biaryls in the presence of molecular oxygen, see:. Irie R., Masutani K., and Katsuki T. Synlett (2000) 1433
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66949148414
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note
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We note that processes 16+14→17 and 16+21→23 in DCE are not stopped in the presence of strongly acidic or basic environments (i.e., 34 mM TFA, and 17 mM DBU, respectively).
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55
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For C-C bond formation via π-allylruthenium intermediates, see:. Murahashi S.-I. (Ed), Wiley-VCH, Weinheim
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For a related process in the presence of water under an inert atmosphere, see:
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For a related process in the presence of water under an inert atmosphere, see:. Monnier F., Vovard-Le Bray C., Castillo D., Aubert V., Dérien S., Dixneuf P.H., Toupet L., Lenco A., and Mealli C. J. Am. Chem. Soc. 129 (2007) 6037
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66949127635
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of note is the discussion of air stability relating to isolated ruthenium complexes in 16a.
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of note is the discussion of air stability relating to isolated ruthenium complexes in 16a.
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68
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