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6
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0034672069
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Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York; Chapter 1
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For a review, see: (a) Negishi, E. I. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York, 1998; Chapter 1; (b) Negishi, E.; King, A. O.; Okukado, N. J. Org. Chem. 1977, 42, 1821-1823; (c) Erdik, E. Tetrahedron 1992, 48, 9577-9648; (d) Boudier, A.; Bromm, L. O.; Lotz, M.; Knochel, P. Angew. Chem., Int. Ed. 2000, 39, 4414-4435.
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Negishi, E.I.1
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7
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33847088408
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For a review, see: (a) Negishi, E. I. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York, 1998; Chapter 1; (b) Negishi, E.; King, A. O.; Okukado, N. J. Org. Chem. 1977, 42, 1821-1823; (c) Erdik, E. Tetrahedron 1992, 48, 9577-9648; (d) Boudier, A.; Bromm, L. O.; Lotz, M.; Knochel, P. Angew. Chem., Int. Ed. 2000, 39, 4414-4435.
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Negishi, E.1
King, A.O.2
Okukado, N.3
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8
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0026458587
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For a review, see: (a) Negishi, E. I. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York, 1998; Chapter 1; (b) Negishi, E.; King, A. O.; Okukado, N. J. Org. Chem. 1977, 42, 1821-1823; (c) Erdik, E. Tetrahedron 1992, 48, 9577-9648; (d) Boudier, A.; Bromm, L. O.; Lotz, M.; Knochel, P. Angew. Chem., Int. Ed. 2000, 39, 4414-4435.
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Erdik, E.1
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9
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0034672069
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For a review, see: (a) Negishi, E. I. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York, 1998; Chapter 1; (b) Negishi, E.; King, A. O.; Okukado, N. J. Org. Chem. 1977, 42, 1821-1823; (c) Erdik, E. Tetrahedron 1992, 48, 9577-9648; (d) Boudier, A.; Bromm, L. O.; Lotz, M.; Knochel, P. Angew. Chem., Int. Ed. 2000, 39, 4414-4435.
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Angew. Chem., Int. Ed.
, vol.39
, pp. 4414-4435
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Boudier, A.1
Bromm, L.O.2
Lotz, M.3
Knochel, P.4
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10
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18544409180
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Klement I., Rottländer M., Tucker C.E., Majid T.N., Knochel P. Tetrahedron. 52:1996;7201-7220.
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Klement, I.1
Rottländer, M.2
Tucker, C.E.3
Majid, T.N.4
Knochel, P.5
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15
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0037474639
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Liron F., Gervais M., Peyrat J.F., Alami M., Brion J.D. Tetrahdron Lett. 44:2003;2789-2794.
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Liron, F.1
Gervais, M.2
Peyrat, J.F.3
Alami, M.4
Brion, J.D.5
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18
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85031140265
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Ramiandrasoa P., Bréhon B., Thivet A., Alami M., Cahiez G. Tetrahedron Lett. 38:1997;6109-6112.
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Ramiandrasoa, P.1
Bréhon, B.2
Thivet, A.3
Alami, M.4
Cahiez, G.5
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19
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0000488020
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2(dppf) is well-known to depress side reactions particularly β-elimination, see:
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2(dppf) is well-known to depress side reactions particularly β-elimination, see: Hayashi T., Konishi M., Kobori Y., Kumada M., Higuchi T., Hirotsu K. J. Am. Chem. Soc. 106:1984;158-163.
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Hayashi, T.1
Konishi, M.2
Kobori, Y.3
Kumada, M.4
Higuchi, T.5
Hirotsu, K.6
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23
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0034702556
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Ryu I., Ikebe M., Sonod N., Yamato S.Y., Yamamura G.H., Komatsu M. Tetrahedron Lett. 41:2000;5689-5692.
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Ryu, I.1
Ikebe, M.2
Sonod, N.3
Yamato, S.Y.4
Yamamura, G.H.5
Komatsu, M.6
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24
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0007485735
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The beneficial influence of DMPU has already been demonstrated for the Mn-catalyzed alkylation of chloroenynes with Grignard reagents, see:
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The beneficial influence of DMPU has already been demonstrated for the Mn-catalyzed alkylation of chloroenynes with Grignard reagents, see: Alami M., Ramiandrasoa P., Cahiez G. Synlett. 1998;325-327.
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Synlett
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Alami, M.1
Ramiandrasoa, P.2
Cahiez, G.3
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25
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85031140268
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note
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3) δ -5.3, 14.0, 18.3, 22.6, 23.8, 25.9, 28.8, 29.1, 29.2, 29.4, 31.9, 32.9, 62.1, 80.4, 85.2, 109.6, 143.8.
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26
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0033118167
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Crousse B., Mladenova M., Ducept P., Alami M., Linstrumelle G. Tetrahedron. 55:1999;4353-4368.
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(1999)
Tetrahedron
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Crousse, B.1
Mladenova, M.2
Ducept, P.3
Alami, M.4
Linstrumelle, G.5
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