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4
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15444367668
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C.D. Edlin, J. Faulkner, D. Fengas, C.K. Knight, J. Parker, I. Preece, P. Quayle, and S.N. Richards Synlett 2005 572 576
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Edlin, C.D.1
Faulkner, J.2
Fengas, D.3
Knight, C.K.4
Parker, J.5
Preece, I.6
Quayle, P.7
Richards, S.N.8
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7
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4143094838
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F. Lopez, A. Delgado, J.R. Rodriguez, L. Castedo, and J.L. Mascarenas J. Am. Chem. Soc. 126 2004 10262 10263
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Lopez, F.1
Delgado, A.2
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Mascarenas, J.L.5
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11
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0037420362
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T.M. Trnka, J.P. Morgan, M.S. Sanford, T.E. Wilhelm, M. Scholl, T.-L. Choi, S. Ding, M.W. Day, and R.H. Grubbs J. Am. Chem. Soc. 125 2003 2546 2558
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Trnka, T.M.1
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Choi, T.-L.6
Ding, S.7
Day, M.W.8
Grubbs, R.H.9
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12
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7744223654
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For a theoretical treatment see: W.J. van Rensburg, P.J. Steynberg, W.H. Meyer, M.M. Kirk, and G.S. Forman J. Am. Chem. Soc. 126 2004 14332 14333
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Van Rensburg, W.J.1
Steynberg, P.J.2
Meyer, W.H.3
Kirk, M.M.4
Forman, G.S.5
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13
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17844396965
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J. Faulkner, C.D. Edlin, D. Fengas, I. Preece, P. Quayle, and S.N. Richards Tetrahedron Lett. 46 2005 2381 2385
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Faulkner, J.1
Edlin, C.D.2
Fengas, D.3
Preece, I.4
Quayle, P.5
Richards, S.N.6
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23
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0037590608
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For dual reactivity (ATRP and metathesis) see: L. Delaude, S. Delfosse, A. Richel, A. Demonceau, and A.F. Noels Chem. Commun. 2003 1526 1527 and references cited therein
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Delaude, L.1
Delfosse, S.2
Richel, A.3
Demonceau, A.4
Noels, A.F.5
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24
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30544437289
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note
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The copper(I)-dHbipy system affords 7 as a 1:1 mixture of diastereoisomers.
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26
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0037620216
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A. Fürstner, O.R. Thiel, L. Ackermann, H.-J. Schanz, and S.P. Nolan J. Org. Chem. 65 2000 2204 2207
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Fürstner, A.1
Thiel, O.R.2
Ackermann, L.3
Schanz, H.-J.4
Nolan, S.P.5
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28
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0042703435
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This may be due to the formation of stable, metathetically inactive, chelated complexes. For discussion see: M. Zaja, S.J. Connon, A.M. Dunne, M. Rivand, N. Buschmann, J. Jiricek, and S. Blechert Tetrahedron 59 2003 6545 6558
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Tetrahedron
, vol.59
, pp. 6545-6558
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Zaja, M.1
Connon, S.J.2
Dunne, A.M.3
Rivand, M.4
Buschmann, N.5
Jiricek, J.6
Blechert, S.7
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30
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4344610661
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A.M.M. Castro Chem. Rev. 104 2004 2939 3002 and references cited therein
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Chem. Rev.
, vol.104
, pp. 2939-3002
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Castro, A.M.M.1
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31
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0037716294
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See: M. Rivard, and S. Blechert Eur. J. Org. Chem. 2003 2225 2228 for an example of the activating effect of Cu(I) salts in CM reactions
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Eur. J. Org. Chem.
, pp. 2225-2228
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Rivard, M.1
Blechert, S.2
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40
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0035944162
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M.G. Bolster, B.M.F. Lagnel, B.J.M. Jansen, C. Morin, and A. de Groot Tetrahedron 57 2001 8369 8379
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(2001)
Tetrahedron
, vol.57
, pp. 8369-8379
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Bolster, M.G.1
Lagnel, B.M.F.2
Jansen, B.J.M.3
Morin, C.4
De Groot, A.5
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42
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84987486268
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The suprafacial 1,3-allylic interconversion of i and ii has been desrcibed (Chiche, L.; Christol, H.; Coste, J.; Pietrasanta, F.; Plénat, F. Can. J. Chem. 1981, 59, 164-174), as has their conversion into the lactone iii.
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H.-R. Känel, and C. Ganter Helv. Chim. Acta 68 1985 1226 1234 The suprafacial 1,3-allylic interconversion of i and ii has been desrcibed (Chiche, L.; Christol, H.; Coste, J.; Pietrasanta, F.; Plénat, F. Can. J. Chem. 1981, 59, 164-174), as has their conversion into the lactone iii.
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(1985)
Helv. Chim. Acta
, vol.68
, pp. 1226-1234
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Känel, H.-R.1
Ganter, C.2
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43
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30544441904
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note
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13C NMR, IR, mass spectrometry (low and high resolution) and/or combustion microanalysis.
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