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1
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0010077452
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Recent reviews: (a)
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Recent reviews: (a) Molander, G.A., Chem. Rev., 1992, 92, 29.
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(1992)
Chem. Rev.
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Molander, G.A.1
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2
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0000421996
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(b) Trost, B.M., Fleming, I., Eds. Pergamon: Oxford
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(b) Inamoto, T., In Comprehensive Organic Synthesis.; Trost, B.M., Fleming, I., Eds. Pergamon: Oxford, 1991, Vol. 4, pp 231-250.
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(1991)
In Comprehensive Organic Synthesis
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Inamoto, T.1
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3
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0000104223
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(c) Eds., Pergamon, Oxford
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(c) Trost, B.M., Fleming, I., Eds., Pergamon, Oxford, 1991, Vol. 4, pp 251-282.
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(1991)
In Comprehensive Organic Synthesis
, vol.4
, pp. 251-282
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Trost, B.M.1
Fleming, I.2
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5
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33751386286
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For the deoxygenation of sulfoxides and epoxides see
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For the deoxygenation of sulfoxides and epoxides see: Hasegawa, E., Curran, D.P., J. Org. Chem., 1993, 58, 5008;
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(1993)
J. Org. Chem.
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Hasegawa, E.1
Curran, D.P.2
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6
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0001055934
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Harada, Y., Inanaga, J., Yamaguchi, M., J. Chem. Soc., Chem. Commun., 1989, 276.;
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(1989)
J. Chem. Soc., Chem. Commun.
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Harada, Y.1
Inanaga, J.2
Yamaguchi, M.3
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7
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33751386648
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For the organohalo compounds see
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For the organohalo compounds see: Wipf, P., Venkatraman, S., J. Org. Chem., 1993, 58, 3455;
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(1993)
J. Org. Chem.
, vol.58
, pp. 3455
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Wipf, P.1
Venkatraman, S.2
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8
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0009851507
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Curran, D.P., Totleben, M.J., J. Am. Chem. Soc., 1992, 114, 6050;
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(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 6050
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Curran, D.P.1
Totleben, M.J.2
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9
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0001490955
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For the homocoupling of allylic or benzylic halides see
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For the homocoupling of allylic or benzylic halides see: Collin, J., Namy, J.L., Dallemer, F., Kagan, H.B., J. Org. Chem., 1991, 56, 3118.
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(1991)
J. Org. Chem.
, vol.56
, pp. 3118
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Collin, J.1
Namy, J.L.2
Dallemer, F.3
Kagan, H.B.4
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11
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0000489207
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Using samarium diiodide see
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Using samarium diiodide see: Girard, P., Couttignal, R., Kagan, H.B., Tetrahedron Lett., 1981, 22, 3959;
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(1981)
Tetrahedron Lett.
, vol.22
, pp. 3959
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Girard, P.1
Couttignal, R.2
Kagan, H.B.3
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12
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0001492779
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Souppe, J., Namy, J-L., Kagan, H.B., Tetrahedron Lett., 1984, 25, 2869;
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(1984)
Tetrahedron Lett.
, vol.25
, pp. 2869
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Souppe, J.1
Namy, J.-L.2
Kagan, H.B.3
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13
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0004063347
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Using pyrophoric lead see
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Using pyrophoric lead see: Meszaros, L., Tetrahedron Lett., 1967, 4951;
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(1967)
Tetrahedron Lett.
, pp. 4951
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Meszaros, L.1
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14
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0011148134
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Using Li/ultrasound see
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Using Li/ultrasound see: Han, H.B., Boudjouk, P., Tetrahedron Lett., 1981, 22, 2757.
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(1981)
Tetrahedron Lett.
, vol.22
, pp. 2757
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Han, H.B.1
Boudjouk, P.2
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17
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84986409344
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Zibuck, R., Seebach, D., Helv. Chim. Acta., 1988, 71, 237; For using zerovalent complexes of nickel see: Flood, T.C., Tetrahedron Lett., 1977, 3861.
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(1988)
Helv. Chim. Acta.
, vol.71
, pp. 237
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Zibuck, R.1
Seebach, D.2
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18
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0002510696
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For using zerovalent complexes of nickel see
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Zibuck, R., Seebach, D., Helv. Chim. Acta., 1988, 71, 237; For using zerovalent complexes of nickel see: Flood, T.C., Tetrahedron Lett., 1977, 3861.
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(1977)
Tetrahedron Lett.
, pp. 3861
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Flood, T.C.1
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20
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37049040965
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Such type of dimerisation of photochemically prepared acyl radicals has been reported see
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Such type of dimerisation of photochemically prepared acyl radicals has been reported see: Barton, D.H.R., George, M.V., Tomoeda, M., J. Chem. Soc., 1962, 17, 1967; For nucleophilic acylation see: Lapkin, I.I., Anvarovs, G.Y., Povarnltsyna, T.N., J. Gen. Chem., USSR. (English trans) 1966, 36, 1945.
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(1962)
J. Chem. Soc.
, vol.17
, pp. 1967
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Barton, D.H.R.1
George, M.V.2
Tomoeda, M.3
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21
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37049040965
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For nucleophilic acylation see
-
Such type of dimerisation of photochemically prepared acyl radicals has been reported see: Barton, D.H.R., George, M.V., Tomoeda, M., J. Chem. Soc., 1962, 17, 1967; For nucleophilic acylation see: Lapkin, I.I., Anvarovs, G.Y., Povarnltsyna, T.N., J. Gen. Chem., USSR. (English trans) 1966, 36, 1945.
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(1966)
J. Gen. Chem., USSR. (English Trans)
, vol.36
, pp. 1945
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Lapkin, I.I.1
Anvarovs, G.Y.2
Povarnltsyna, T.N.3
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