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For a review see: (a) McMurry, J. E. Chem. Rev. 1989, 89, 1513-1524; (b) Ruell, J. A.; De Clercq, E.; Pannecouque, C.; Witvrouw, M.; Stup, T. L.; Turpin, J. A.; Buckheit, R. W., Jr.; Cushman, M. J. Org. Chem. 1999, 64, 5858-5866; (c) Rubin, V. N.; Ruenitz, P. C.; Boudinot, F. D.; Boyd, J. L. Bioorg. Med. Chem. 2001, 9, 1579-1587.
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For a review see: (a) Cacchi, S. J. Organomet. Chem. 1999, 576, 42-64; (b) Cacchi, S.; Felici, M.; Pietroni, B. Tetrahedron Lett. 1984, 25, 3137-3140; (c) Wu, M. J.; Wei, L. M.; Lin, C. F.; Leou, S. P.; Wei, L. L. Tetrahedron 2001, 57, 7839-7844; (d) Cacchi, S.; Fabrizi, G.; Goggiamani, A.; Moreno-Manas, M.; Vallribera, A. Tetrahedron Lett. 2002, 43, 5537-5540.
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Wu, M.J.1
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For a review see: (a) Cacchi, S. J. Organomet. Chem. 1999, 576, 42-64; (b) Cacchi, S.; Felici, M.; Pietroni, B. Tetrahedron Lett. 1984, 25, 3137-3140; (c) Wu, M. J.; Wei, L. M.; Lin, C. F.; Leou, S. P.; Wei, L. L. Tetrahedron 2001, 57, 7839-7844; (d) Cacchi, S.; Fabrizi, G.; Goggiamani, A.; Moreno-Manas, M.; Vallribera, A. Tetrahedron Lett. 2002, 43, 5537-5540.
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Cacchi, S.1
Fabrizi, G.2
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Cacchi S., Fabrizi G., Marinelli F., Moro L., Pace P. Tetrahedron. 52:1996;10225-10240.
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43
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84992263974
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2 (R=Me, Ph), DMF or NMP, 20°C), no coupling reaction occurred and the starting material was recovered. Increasing the reaction time to 24 h and temperature to 110°C resulted in decomposition of reactant
-
2 (R=Me, Ph), DMF or NMP, 20°C), no coupling reaction occurred and the starting material was recovered. Increasing the reaction time to 24 h and temperature to 110°C resulted in decomposition of reactant.
-
-
-
-
44
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0032576791
-
-
The coupling of a similar stannane compound having the alcohol group protected as MOM ether was reported, see
-
The coupling of a similar stannane compound having the alcohol group protected as MOM ether was reported, see: Quayle P., Wang J., Xu J. Tetrahedron Lett. 39:1998;485-488.
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Quayle, P.1
Wang, J.2
Xu, J.3
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45
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84992278278
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Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York; Chapter 1
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For a review, see: Negishi, E. I. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York, 1998; Chapter 1.
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Metal-Catalyzed Cross-Coupling Reactions
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Negishi, E.I.1
-
46
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84992243677
-
-
1H NMR spectra of the products indicated the presence of one isomer in each cases
-
1H NMR spectra of the products indicated the presence of one isomer in each cases.
-
-
-
-
47
-
-
0032211326
-
-
Although some halo-substituted styrenes have been prepared, the geometrical purities were not satisfactory, see: (a) Muthiah, C.; Kumar, K. P.; Kumaraswamy, S.; Kumara Swamy, K. C. Tetrahedron 1998, 54, 14315-14326; (b) Huang, Z. Z.; Lan, G. C.; Huang, X. Synth. Commun. 1998, 28, 633-637.
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Muthiah, C.1
Kumar, K.P.2
Kumaraswamy, S.3
Kumara Swamy, K.C.4
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48
-
-
0031882634
-
-
Although some halo-substituted styrenes have been prepared, the geometrical purities were not satisfactory, see: (a) Muthiah, C.; Kumar, K. P.; Kumaraswamy, S.; Kumara Swamy, K. C. Tetrahedron 1998, 54, 14315-14326; (b) Huang, Z. Z.; Lan, G. C.; Huang, X. Synth. Commun. 1998, 28, 633-637.
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Huang, Z.Z.1
Lan, G.C.2
Huang, X.3
-
49
-
-
84992275468
-
-
note
-
3) δ 158.5, 143.4, 142.7, 132.1, 130.9, 127.9, 127.2, 126.9, 125.1, 113.5, 62.3, 55.0, 33.2.
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