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1
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0000081750
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1. For a recent review of carbene chemistry, see Regitz, M. Angew. Chem. 1996, 108, 791; Angew, Chem. Int. Ed. Engl. 1996, 35, 725.
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Regitz, M.1
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2
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33748217333
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1. For a recent review of carbene chemistry, see Regitz, M. Angew. Chem. 1996, 108, 791; Angew, Chem. Int. Ed. Engl. 1996, 35, 725.
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(1996)
Angew, Chem. Int. Ed. Engl.
, vol.35
, pp. 725
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3
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0001923773
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2. (a) Coleman, A. W.; Hitchcock, P. B.; Lappert, M. F.; Maskell, R. K.; Müller, J. H. J. Organomet. Chem. 1983, 250, C9;
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Coleman, A.W.1
Hitchcock, P.B.2
Lappert, M.F.3
Maskell, R.K.4
Müller, J.H.5
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4
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0000798797
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(b) Coleman, A. W.; Hitchcock, P. B.; Lappert, M. F; Maskell, R. K.; Müller, J. H. ibid. 1985, 296, 173.
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J. Organomet. Chem.
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Coleman, A.W.1
Hitchcock, P.B.2
Lappert, M.F.3
Maskell, R.K.4
Müller, J.H.5
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5
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0030512868
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3. (a) Herrmann, W. A.; Gooßen, L. J.; Köcher, C.; Artus, G. R. J. Angew. Chem. 1996, 108, 2980; Angew. Chem. Int. Ed. Engl. 1996, 35, 2805;
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Angew. Chem.
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, pp. 2980
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Herrmann, W.A.1
Gooßen, L.J.2
Köcher, C.3
Artus, G.R.J.4
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6
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0030512868
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3. (a) Herrmann, W. A.; Gooßen, L. J.; Köcher, C.; Artus, G. R. J. Angew. Chem. 1996, 108, 2980; Angew. Chem. Int. Ed. Engl. 1996, 35, 2805;
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Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 2805
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7
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0001382354
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(b) Herrmann, W. A.; Gooßen, L. J.; Artus, G. R. J.; Köcher, C. Organometallics 1997, 16, 2472.
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Organometallics
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Herrmann, W.A.1
Gooßen, L.J.2
Artus, G.R.J.3
Köcher, C.4
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8
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0000868901
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4. (a) Enders, D.; Gielen, H.; Raabe, G.; Runsink, J.; Teles, J. H. Chem. Ber. 1996, 129, 1483;
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Chem. Ber.
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Enders, D.1
Gielen, H.2
Raabe, G.3
Runsink, J.4
Teles, J.H.5
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9
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33745395811
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(b) Enders, D.; Gielen, H.; Raabe, G.; Runsink, J.; Teles, J. H. Chem. Ber./Recueil 1997, 130, 1253.
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Chem. Ber./Recueil
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Enders, D.1
Gielen, H.2
Raabe, G.3
Runsink, J.4
Teles, J.H.5
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11
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85036685115
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The new complexes 1-3 gave appropriate spectroscopic data (IR, NMR, MS, HR-MS)
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6. The new complexes 1-3 gave appropriate spectroscopic data (IR, NMR, MS, HR-MS).
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12
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85036676615
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2O=2:1), the enantiomeric excess of the product alcohol was determined by gas chromatography (LIPODEX E, CP-CHIRASIL-DEX CB, 7-CD PERME)
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2O=2:1), the enantiomeric excess of the product alcohol was determined by gas chromatography (LIPODEX E, CP-CHIRASIL-DEX CB, 7-CD PERME).
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14
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0001101060
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9. (a) Buschmann, H.; Scharf, H.-D.; Hoffmann, N.; Esser, P. Angew. Chem. 1991, 103, 480; Angew. Chem. Int. Ed. Engl. 1991, 30, 477;
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(1991)
Angew. Chem.
, vol.103
, pp. 480
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Buschmann, H.1
Scharf, H.-D.2
Hoffmann, N.3
Esser, P.4
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15
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0025780257
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9. (a) Buschmann, H.; Scharf, H.-D.; Hoffmann, N.; Esser, P. Angew. Chem. 1991, 103, 480; Angew. Chem. Int. Ed. Engl. 1991, 30, 477;
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(1991)
Angew. Chem. Int. Ed. Engl.
, vol.30
, pp. 477
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