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1
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0035476406
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For examples, see the following review
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For examples, see the following review: J. Eames and M. Watkinson. Angew. Chem., Int. Ed. 40, 3567 (2001).
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(2001)
Angew. Chem., Int. Ed
, vol.40
, pp. 3567
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Eames, J.1
Watkinson, M.2
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2
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33947464577
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Copper: M.S. Kharasch and G. Sosnovsky. J. Am. Chem. Soc. 80, 756 (1958);
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(a) Copper: M.S. Kharasch and G. Sosnovsky. J. Am. Chem. Soc. 80, 756 (1958);
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3
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33847089541
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Selenium: M.A. Umbreit and K.B. Sharpless. J. Am. Chem. Soc. 99, 5526 (1977).
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(b) Selenium: M.A. Umbreit and K.B. Sharpless. J. Am. Chem. Soc. 99, 5526 (1977).
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4
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0001091976
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II: B.M. Trost and P.J. Metzner. J. Am. Chem. Soc. 102, 3572 (1980);
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II: B.M. Trost and P.J. Metzner. J. Am. Chem. Soc. 102, 3572 (1980);
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5
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33747838053
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DMSO-promoted selective stoichiometric oxidation of 1-butene to but-2-enyl acetate: W. Kitching, Z. Rappoport, S. Winstein, and W.G. Young. J. Am. Chem. Soc. 88, 2054 (1966).
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(b) DMSO-promoted selective stoichiometric oxidation of 1-butene to but-2-enyl acetate: W. Kitching, Z. Rappoport, S. Winstein, and W.G. Young. J. Am. Chem. Soc. 88, 2054 (1966).
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6
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0037454309
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Pd-catalyzed selective oxidations of α,β-enones (or ketals) to 1,4-enediones: J.-Q. Yu and E.J. Corey. J. Am. Chem. Soc. 125, 3232 (2003).
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Pd-catalyzed selective oxidations of α,β-enones (or ketals) to 1,4-enediones: J.-Q. Yu and E.J. Corey. J. Am. Chem. Soc. 125, 3232 (2003).
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8
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0025356808
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(b) S. Hansson, A. Heumann, T. Rein, and B. Akermark. J. Org. Chem. 55, 975 (1990);
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(1990)
J. Org. Chem
, vol.55
, pp. 975
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Hansson, S.1
Heumann, A.2
Rein, T.3
Akermark, B.4
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13
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30444437460
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(b) T. Mitsudome, T. Umetani, N. Nosaka, K. Mori, T. Mizugaki, K. Ebitani, and K. Kaneda. Angew. Chem., Int. Ed. 45, 481 (2006).
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(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 481
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Mitsudome, T.1
Umetani, T.2
Nosaka, N.3
Mori, K.4
Mizugaki, T.5
Ebitani, K.6
Kaneda, K.7
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14
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18744372130
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M.S. Chen, N. Prabagaran, N.A. Labenz, and M.C. White. J. Am. Chem. Soc. 127, 6970 (2005).
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(2005)
J. Am. Chem. Soc
, vol.127
, pp. 6970
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Chen, M.S.1
Prabagaran, N.2
Labenz, N.A.3
White, M.C.4
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16
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33746094649
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K.J. Fraunhoffer, N. Prabagaran, L.E. Sirois, and M.C. White. J. Am. Chem. Soc. 128, 9032 (2006).
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(2006)
J. Am. Chem. Soc
, vol.128
, pp. 9032
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Fraunhoffer, K.J.1
Prabagaran, N.2
Sirois, L.E.3
White, M.C.4
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17
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33645451955
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N. Marion, O. Navarro, J.-G. Mei, E.D. Stevens, N.M. Scott, and S.P Nolan. J. Am. Chem. Soc. 128, 4101 (2006).
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(2006)
J. Am. Chem. Soc
, vol.128
, pp. 4101
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Marion, N.1
Navarro, O.2
Mei, J.-G.3
Stevens, E.D.4
Scott, N.M.5
Nolan, S.P.6
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18
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2942699370
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W. Kitching, T. Sakakiyama, Z. Rappoport, PD. Sleezer, S. Winstein, and W.G. Young. J. Am. Chem. Soc. 94, 2329 (1972).
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(1972)
J. Am. Chem. Soc
, vol.94
, pp. 2329
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Kitching, W.1
Sakakiyama, T.2
Rappoport, Z.3
Sleezer, P.D.4
Winstein, S.5
Young, W.G.6
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20
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67650861294
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tBu-Box, and (S)-(-)-BINAP
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tBu-Box, and (S)-(-)-BINAP
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21
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2942699370
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W. Kitching, T. Sakakiyama, Z. Rappoport, PD. Sleezer, S. Winstein, and W.G. Young. J. Am. Chem. Soc. 94, 2329 (1972).
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(1972)
J. Am. Chem. Soc
, vol.94
, pp. 2329
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Kitching, W.1
Sakakiyama, T.2
Rappoport, Z.3
Sleezer, P.D.4
Winstein, S.5
Young, W.G.6
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22
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67650922750
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A small amount of 1-phenylallyl acetate (∼9%) is also formed during the reaction. More detailed mechanistic studies are underway to reconcile this observation with the proposed mechanism.
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A small amount of 1-phenylallyl acetate (∼9%) is also formed during the reaction. More detailed mechanistic studies are underway to reconcile this observation with the proposed mechanism.
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24
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0001490103
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A similar equilibrium was also proposed for (PCy3)Pd(allyl)(OAc): T. Yamamoto, O. Saito, and A. Yamamoto. J. Am. Chem. Soc. 103, 5600 (1981).
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A similar equilibrium was also proposed for (PCy3)Pd(allyl)(OAc): T. Yamamoto, O. Saito, and A. Yamamoto. J. Am. Chem. Soc. 103, 5600 (1981).
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25
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67650890415
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2, BPM, and BQ in acetone forms (BPM)Pd(BQ): RA. Klein, P. Witte, R. van Belzen, J. Fraanje, K. Goubitz, M. Numan, H. Schenk, J.M. Ernsting, and C.J. Elsevier. Eur. J. Inorg. Chem. 319 (1998);
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2, BPM, and BQ in acetone forms (BPM)Pd(BQ): RA. Klein, P. Witte, R. van Belzen, J. Fraanje, K. Goubitz, M. Numan, H. Schenk, J.M. Ernsting, and C.J. Elsevier. Eur. J. Inorg. Chem. 319 (1998);
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26
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67650897314
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BQ could be viewed as an electron-deficient olefin
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(b) BQ could be viewed as an electron-deficient olefin.
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27
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0037425533
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0, see: S.S. Stahl, J.L. Thorman, N. de Silva, I.A. Guzei, and R.W. Clark. J. Am. Chem. Soc. 125, 12 (2003).
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0, see: S.S. Stahl, J.L. Thorman, N. de Silva, I.A. Guzei, and R.W. Clark. J. Am. Chem. Soc. 125, 12 (2003).
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