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1
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34249305313
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For monographs, see:
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3
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0003760097
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Sapse A.M., and von Ragué Schleyer P. (Eds), J. Wiley & Sons, New York, NY
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In: Sapse A.M., and von Ragué Schleyer P. (Eds). Lithium Chemistry: A Theoretical and Experimental Overview (1995), J. Wiley & Sons, New York, NY
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(1995)
Lithium Chemistry: A Theoretical and Experimental Overview
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4
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0002148313
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Abel E.W., Stone F.G.A., Wilkinson G., and McKillop A. (Eds), Pergamon, Oxford
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Gray M., Tinkel M., and Snieckus V. In: Abel E.W., Stone F.G.A., Wilkinson G., and McKillop A. (Eds). Comprehensive Organometallic Chemistry II Vol. 11 (1995), Pergamon, Oxford 1-92
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(1995)
Comprehensive Organometallic Chemistry II
, vol.11
, pp. 1-92
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Gray, M.1
Tinkel, M.2
Snieckus, V.3
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6
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0037503118
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Rappoport Z., and Marek I. (Eds), Wiley, Chichester, UK
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In: Rappoport Z., and Marek I. (Eds). The Chemistry of Organolithium Compounds (2004), Wiley, Chichester, UK
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(2004)
The Chemistry of Organolithium Compounds
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7
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34249283933
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For reviews, see:
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10
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34249295357
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See, for instance:
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18
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34249300287
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For leading references, see:
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22
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33645037635
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For a recent application of this stoichiometric lithiation reaction, see:
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For a recent application of this stoichiometric lithiation reaction, see:. Deng K., Bensari-Bouguerra A., Whetstone J., and Cohen T. J. Org. Chem. 71 (2006) 2360
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(2006)
J. Org. Chem.
, vol.71
, pp. 2360
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Deng, K.1
Bensari-Bouguerra, A.2
Whetstone, J.3
Cohen, T.4
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23
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34249326007
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For reviews, see:
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28
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33748199260
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Rappoport Z., and Marek I. (Eds), J. Wiley & Sons, Chichester, UK Part 2, Chapter 11; For mechanistic studies, see:
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Yus M. In: Rappoport Z., and Marek I. (Eds). The Chemistry of Organolithium Compounds Vol. 1 (2004), J. Wiley & Sons, Chichester, UK Part 2, Chapter 11; For mechanistic studies, see:
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(2004)
The Chemistry of Organolithium Compounds
, vol.1
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Yus, M.1
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33
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0037505267
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For a polymer supported arene-catalysed version of this reaction, see:
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Yus M., Herrera R.P., and Guijarro A. Tetrahedron Lett. 44 (2003) 5025 For a polymer supported arene-catalysed version of this reaction, see:
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(2003)
Tetrahedron Lett.
, vol.44
, pp. 5025
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Yus, M.1
Herrera, R.P.2
Guijarro, A.3
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39
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34249331465
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For different examples from our group, see:
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44
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0033939071
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Alonso F., Falvello L.R., Fanwick P.E., Lorenzo E., and Yus M. Synthesis (2000) 949
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(2000)
Synthesis
, pp. 949
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Alonso, F.1
Falvello, L.R.2
Fanwick, P.E.3
Lorenzo, E.4
Yus, M.5
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47
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34249313147
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These intermediates are functionalised organolithium compounds, which are very unstable species even at low temperatures that decompose either by elimination processes or by proton abstraction from the reaction medium. For reviews on this type of compounds, see:
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56
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34249329391
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See also the special issue of Tetrahedron Symposium-in-Print (Nájera, C., Yus, M., Eds.,) devoted to 'Functionalised Organolithium Compounds'
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See also the special issue of Tetrahedron Symposium-in-Print (Nájera, C., Yus, M., Eds.,) devoted to 'Functionalised Organolithium Compounds',. Tetrahedron 61 (2005)
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(2005)
Tetrahedron
, vol.61
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60
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34249332538
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Some of the results included in this study have been preliminary communicated: Abou, A.; Foubelo, F.; Yus, M. 10th International Electronic Conference on Synthetic Organic Chemistry (ESOC-10) 2006, Comm. A029.
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62
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0345426367
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Maleczka R.E., Terrell L.R., Clark D.H., Whitehead S.L., Gallagher W.P., and Terstiege I. J. Org. Chem. 64 (1999) 5958
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(1999)
J. Org. Chem.
, vol.64
, pp. 5958
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Maleczka, R.E.1
Terrell, L.R.2
Clark, D.H.3
Whitehead, S.L.4
Gallagher, W.P.5
Terstiege, I.6
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64
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1542530558
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For a report on lithiation of bromo olefins (bromine-lithium exchange versus α-deprotonation) using t-BuLi, see:
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For a report on lithiation of bromo olefins (bromine-lithium exchange versus α-deprotonation) using t-BuLi, see:. Bonnet B., Plé G., and Duhamel L. Synlett (1996) 221
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(1996)
Synlett
, pp. 221
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Bonnet, B.1
Plé, G.2
Duhamel, L.3
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