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Anciaux, A. J.; Hubert, A. J.; Noels, A. F.; Petiniot, N.; P. Teyssié, P. J. Org. Chem. 1980, 45, 695.
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(1980)
J. Org. Chem.
, vol.45
, pp. 695
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Anciaux, A.J.1
Hubert, A.J.2
Noels, A.F.3
Petiniot, N.4
Teyssié, P.P.5
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0002586214
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Top
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a) Maas, G. Top. Curr. Chem. 1987, 137, 77. -
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Maas, G.1
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Doyle, M. P.; Eismont, M. Y.; Bergbreiter, D. E.; Gray, H. N. J. Org. Chem. 1992, 57, 6103.
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Doyle, M.P.1
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Bergbreiter, D.E.3
Gray, H.N.4
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0000852249
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Juliette, J. J. J.; Horváth, I. T.; Gladysz, J. A. Angew. Chem. 1997, 109, 1682;
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Juliette, J.J.J.1
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0032505207
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Betzemeier, B.; Lhermitte, F.; Knochel, P. Tetrahedron Lett. 1998, 39, 6667.
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Betzemeier, B.1
Lhermitte, F.2
Knochel, P.3
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0031029886
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Studer, A.; Hadida, S.; Ferritto, R.; Kim, S.-Y.; Jeger. P.; Wipf, P.; Curran, D. P. Science 1997, 275, 823
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Studer, A.1
Hadida, S.2
Ferritto, R.3
Kim, S.-Y.4
Jeger, P.5
Wipf, P.6
Curran, D.P.7
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0025877971
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Bergbreiter, D. E.; Morvant, M.; Chen, B. Tetrahedron Lett. 1991, 32, 2731.
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Bergbreiter, D.E.1
Morvant, M.2
Chen, B.3
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1842640868
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The use of complex 2a to catalyze C-H insertion of alkoxycarbonylcarbenes into C-H bonds of alkanes was mentioned, but its preparation and properties have not been described
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The use of complex 2a to catalyze C-H insertion of alkoxycarbonylcarbenes into C-H bonds of alkanes was mentioned, but its preparation and properties have not been described: Demonceau, A.; Noels, A. F.; Hubert, A. J.; Teyssié, P. J. Chem. Soc., Chem. Commun. 1981, 688.
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(1981)
J. Chem. Soc., Chem. Commun.
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Demonceau, A.1
Noels, A.F.2
Hubert, A.J.3
Teyssié, P.4
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0009580269
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note
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3CN ligands and formation of 2a).
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0009615845
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2 (4 ml) was added during 8 h with a syringe pump. After an additional time of 4 h the solvent and most of the alkene were removed at 40 °C/500 mbar. The liquid residue was stirred for 15 min with perfluoro(methylcyclohexane) (0.6 ml). After phase separation the dark-green fluorous phase was removed and the liquid residue was distilled at 100°C/ 0.1 mbar to afford 5d
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2 (4 ml) was added during 8 h with a syringe pump. After an additional time of 4 h the solvent and most of the alkene were removed at 40 °C/500 mbar. The liquid residue was stirred for 15 min with perfluoro(methylcyclohexane) (0.6 ml). After phase separation the dark-green fluorous phase was removed and the liquid residue was distilled at 100°C/ 0.1 mbar to afford 5d.
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a) Doyle, M. P.; Bagheri, V.; Wandless, T. J.; Harn, N. K.; Blinker, D. A.; Eagle, C. T.; Loh, K.-L. J. Am. Chem. Soc. 1990, 112, 1906. -
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Doyle, M.P.1
Bagheri, V.2
Wandless, T.J.3
Harn, N.K.4
Blinker, D.A.5
Eagle, C.T.6
Loh, K.-L.7
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0000234509
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b) Doyle, M. P.; Westrum, L. J., Wolthuis, W. N. E.; See, M. M.; Boone, W. P.; Bagheri, V.; Pearson, M. M. J. Am. Chem. Soc. 1993, 115, 958.
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Doyle, M.P.1
Westrum, L.J.2
Wolthuis, W.N.E.3
See, M.M.4
Boone, W.P.5
Bagheri, V.6
Pearson, M.M.7
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28
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0001432893
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Anciaux, A. J.; Demonceau, A.; Noels, A. F.; Hubert, A. J.; Warin, R.; Teyssié, P. J. Org. Chem. 1981, 46, 873.
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(1981)
J. Org. Chem.
, vol.46
, pp. 873
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Anciaux, A.J.1
Demonceau, A.2
Noels, A.F.3
Hubert, A.J.4
Warin, R.5
Teyssié, P.6
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