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7
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2342492376
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(d) Takahashi T, Seki T, Nitto Y, Saburai M, Rouusset CM, Negishi E. J. Am. Chem. Soc. 1991;113:6266-6268.
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(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6266-6268
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Takahashi, T.1
Seki, T.2
Nitto, Y.3
Saburai, M.4
Rouusset, C.M.5
Negishi, E.6
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10
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85038554174
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note
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23Cl: C, 75.44; H, 9.71. Found: C, 75.40; H, 9.59.
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15
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0000148752
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2Zr(butene) reacts with styrene to form a zirconacyclopentane consisting of butene and styrene units (Swanson DR, Rousset CJ, Negishi E, Takahashi T, Seki T, Saburi M, Uchida Y. J. Org. Chem. 1989;54:3521-3523.), but coupling products of styrene with butene were not detected by GC analysis.
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(1989)
J. Org. Chem.
, vol.54
, pp. 3521-3523
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Swanson, D.R.1
Rousset, C.J.2
Negishi, E.3
Takahashi, T.4
Seki, T.5
Saburi, M.6
Uchida, Y.7
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17
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0000516579
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(b) Takahashi T, Suzuki N, Kageyama M, Nitto Y, Saburi M, Negishi E. Chem. Lett. 1991:1579-1582.
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(1991)
Chem. Lett.
, pp. 1579-1582
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Takahashi, T.1
Suzuki, N.2
Kageyama, M.3
Nitto, Y.4
Saburi, M.5
Negishi, E.6
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18
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2342492376
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(b) Takahashi T, Seki T, Nitto Y, Saburu M, Rousset CJ, Negishi E. J. Am. Chem. Soc. 1991;113:6266-6268.
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(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6266-6268
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Takahashi, T.1
Seki, T.2
Nitto, Y.3
Saburu, M.4
Rousset, C.J.5
Negishi, E.6
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21
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0000038757
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(e) Miqul Y, Igau A, Donnadieu B, Majoral JP, Pirio N, Meunier P. J. Am. Chem. Soc. 1998;120:3504-3505.
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(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 3504-3505
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Miqul, Y.1
Igau, A.2
Donnadieu, B.3
Majoral, J.P.4
Pirio, N.5
Meunier, P.6
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22
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85038552723
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note
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[10] When a THF solution of EtBr (1.09 M) with PhCHMeMgCl (12, 0.35 M) was warmed from O °C to 50 °C in about 5 min and the reaction was quenched with aqueous HCl (1N) , 2-phenylbutane was formed in 79% yield based on 12 indicating that α-substituted benzylmagnesium chlorides readily react with alkyl bromides.
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23
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0010403350
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[11] The reactivities of the alkyl ligands on Zr as β-hydrogen donors decrease in the order: β-methyl > β-methylene > β-methine, see: Negishi E, Nguyen T, Maye JP, Choueiri D, Suzuki N, Takahashi T. Chem. Lett. 1992:2367-2370.
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(1992)
Chem. Lett.
, vol.23
, pp. 67-2370
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Negishi, E.1
Nguyen, T.2
Maye, J.P.3
Choueiri, D.4
Suzuki, N.5
Takahashi, T.6
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24
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85038552169
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in press
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[12] We have reported that a zirconocene complex catalyzes silylation of alkenes with chlorosilanes under similar conditions which affords vinyl- and/or allylsilanes having silyl groups at the terminal carbons: Angew. Chem., Int. Ed. Engl. in press. We have also found that a titanocene complex catalyzes double alkylation of aryl alkenes with alkyl halides to give 1,2-dialkylated products: J. Am. Chem. Soc., in press.
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Angew. Chem., Int. Ed. Engl.
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25
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85038547809
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in press
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[12] We have reported that a zirconocene complex catalyzes silylation of alkenes with chlorosilanes under similar conditions which affords vinyl- and/or allylsilanes having silyl groups at the terminal carbons: Angew. Chem., Int. Ed. Engl. in press. We have also found that a titanocene complex catalyzes double alkylation of aryl alkenes with alkyl halides to give 1,2-dialkylated products: J. Am. Chem. Soc., in press.
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J. Am. Chem. Soc.
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