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84955751356
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G. Becker, H. Freudenblum, O. Mundt, M. Reti, M. Sachs, in: Brauer, Handbook of Preparative Inorganic Chemistry (Ed.: W. A. Herrmann), in press.
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in: Brauer, Handbook of Preparative Inorganic Chemistry
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Becker, G.1
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8
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84955698804
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H. H. Karsch, F. Bienlein, T. Rupprich, F. Uhlig, E. Herrmann, M. Scheer, in: Brauer, Handbook of Preparative Inorganic Chemistry (Ed.: W. A. Herrmann), in press.
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in: Brauer, Handbook of Preparative Inorganic Chemistry
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Karsch, H.H.1
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9
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84984066642
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G. Becker, H.-M. Hartmann, W. Schwarz, Z. Anorg. Allg. Chem. 1989, 577, 9.
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16
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84984075148
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G. Becker, W. Schwarz, N. Seidler, M. Westerhausen, Z. Anorg. Allg. Chem. 1992, 612, 72; and references therein.
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0002591778
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G. Becker, G. Gresser, W. Uhl, Z. Naturforsch. 1981, B36, 16.
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0003114210
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27
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0001068184
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see, however: J.-C. Guillemin, L. Lassalle, P. Dréan, G. Wlodarczak, J. Demaison, J. Am. Chem. Soc. 1994, 116, 8930.
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34
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0002714978
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G. Becker, W. Becker, R. Knebl, H. Schmidt, U. Weeber, M. Westerhausen, Nova Acta Leopoldina, Neue Folge No. 264, 1985, 59, 55.
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84987214888
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Gaumont, A.C.1
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R. Bartsch, A. Gelessus, P. B. Hitchcock, J. F. Nixon, J. Organomet. Chem. 1992, 430, C10; and references therein.
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59
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-
84955632331
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-
Since alkylidene- and alkylidynephosphanes show an alkene- or alkyne-like chemical reactivity, they are often called phosphaalkenes and phosphaalkynes
-
Since alkylidene- and alkylidynephosphanes show an alkene- or alkyne-like chemical reactivity, they are often called phosphaalkenes and phosphaalkynes.
-
-
-
-
60
-
-
84955655768
-
-
The homologous trimethylstannyl compound recently prepared according to Eq. 7 turned out to be much more
-
The homologous trimethylstannyl compound recently prepared according to Eq. 7 turned out to be much more.
-
-
-
-
61
-
-
84955719785
-
-
Phosphaallyl anions are also being studied in the research groups of, e.g., Niecke [33] and Denis [34]
-
Phosphaallyl anions are also being studied in the research groups of, e.g., Niecke [33] and Denis [34].
-
-
-
-
62
-
-
84955749268
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-
Similar results have been obtained by Karsch and coworkers [42]. The group of Lappert was able to isolate dimeric lithium bis(trimethylsilyliminobenzoyl)methanide [43]
-
Similar results have been obtained by Karsch and coworkers [42]. The group of Lappert was able to isolate dimeric lithium bis(trimethylsilyliminobenzoyl)methanide [43].
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