Indexed keywords
CROSS-COUPLING REACTIONS;
NEGISHI REACTION;
ORGANOZINC COMPOUNDS;
CATALYSTS;
ORGANIC COMPOUNDS;
PALLADIUM;
PHASE TRANSITIONS;
REACTION KINETICS;
AMINES;
2 BROMO 3 HEPTYLPYRIDINE;
2 BROMO 5 HEPTYLPYRIDINE;
2 BROMO 6 (2,5 DIMETHYL 1H PYRROL 1 YL)PYRIDINE;
2 BROMOPYRIDINE DERIVATIVE;
2 CHLOROPYRIDINE DERIVATIVE;
2,2' BIPYRIDINE DERIVATIVE;
3 HEPTYLPYRIDINE;
4 (2,5 DIMETHYL 1H PYRROL 1 YL) 6' METHOXY 2,2' BIPYRIDINE;
4,6' DIMETHOXY 2,2' BIPYRIDINE;
4,6' DIMETHYL 2,2' BIPYRIDINE;
5 (2,5 DIMETHYL 1H PYRROL 1 YL) 2,2' BIPYRIDINE;
5 (4 HYDROXYPHENYL) 2,2' BIPYRIDINE;
5 (4 METHOXYPHENYL) 2,2' BIPYRIDINE;
5 (4 METHOXYPHENYL) 5' METHYL 2,2' BIPYRIDINE;
5 [(TRIMETHYLSILYL)ETHYNYL] 2,2' BIPYRIDINE;
5 BROMO 5' HEPTYL 2,2' BIPYRIDINE;
5 HEPTYL 5' (4 HYDROXYPHENYL) 2,2' BIPYRIDINE;
5 HEPTYL 5' (4 METHOXYPHENYL) 2,2' BIPYRIDINE;
5 METHOXY 2,2' BIPYRIDINE;
5 METHYL 2,2' BIPYRIDINE;
5 METHYL 5' [(TRIMETHYLSILYL)ETHYNYL] 2,2' BIPYRIDINE;
6' (2,5 DIMETHYL 1H PYRROL 1 YL) 4 METHOXY 2,2' BIPYRIDINE;
METHYL 2,2' BIPYRIDINE 5 CARBOXYLATE;
METHYL 5' [(TRIMETHYLSILYL)ETHYNYL] 2,2' BIPYRIDINE 5 CARBOXYLATE;
METHYL 5' HEPTYL 2,2' BIPYRIDINE 5 CARBOXYLATE;
METHYL 6' (2,5 DIMETHYL 1H PYRROL 1 YL) 2,2' BIPYRIDINE 4 CARBOXYLATE;
METHYL 6' (2,5 DIMETHYL 1H PYRROL 1 YL) 2,2' BIPYRIDINE 6 CARBOXYLATE;
PALLADIUM;
PYRIDINE DERIVATIVE;
TRIPHENYLPHOSPHINE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL STRUCTURE;
CROSS COUPLING REACTION;
DEMETHYLATION;
SONOGASHIRA REACTION;
SUBSTITUTION REACTION;
SYNTHESIS;
1
0034299604
(a) Kaes, C.; Katz, A.; Hosseini, M. W. Chem. Rev. 2000, 100, 3553.
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Chem. Rev
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Kaes, C.1
Katz, A.2
Hosseini, M.W.3
2
84891024683
(b) Newkome, G. R.; Patri, A. K.; Holder, E.; Schubert, U. S. Eur. J. Org. Chem. 2002, 235.
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Eur. J. Org. Chem
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Newkome, G.R.1
Patri, A.K.2
Holder, E.3
Schubert, U.S.4
3
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Piguet, C.; Bernadinelli, G.; Hopfgartner, G. Chem. Rev. 1997, 97, 2005.
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Chem. Rev
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Piguet, C.1
Bernadinelli, G.2
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4
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Juris, A.; Balzani, V.; Barigelletti, F.; Campagna, S.; Belser, P.; von Zelewsky, A. Coord. Chem. Rev. 1998, 84, 85.
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Coord. Chem. Rev
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Juris, A.1
Balzani, V.2
Barigelletti, F.3
Campagna, S.4
Belser, P.5
von Zelewsky, A.6
7
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Hassan, J.; Sévignon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Chem. Rev. 2002, 102, 1359.
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Chem. Rev
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Hassan, J.1
Sévignon, M.2
Gozzi, C.3
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Lemaire, M.5
9
0029089889
Some examples, see: a
Some examples, see: (a) Romero, F.; Ziessel, R. Tetrahedron Lett. 1995, 36, 6471.
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Tetrahedron Lett
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Romero, F.1
Ziessel, R.2
10
0030970482
(b) Newkome, G. R.; Gross, J.; Patri, A. K. J. Org. Chem. 1997, 62, 3013.
(1997)
J. Org. Chem
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Newkome, G.R.1
Gross, J.2
Patri, A.K.3
12
20544450502
2nd ed, de Meijere, A, Diederich, F, Eds, Wiley-VCH: Weinheim
(b) Metal-Catalyzed Cross-Coupling Reactions, 2nd ed.; de Meijere, A.; Diederich, F., Eds.; Wiley-VCH: Weinheim, 2004.
(2004)
Metal-Catalyzed Cross-Coupling Reactions
13
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Miyaura, N, Ed, Springer: Berlin
(c) Cross-Coupling Reactions; Miyaura, N., Ed.; Springer: Berlin, 2002.
(2002)
Cross-Coupling Reactions
14
0013165218
Recent special issue on cross-coupling reactions, see: (d)
Recent special issue on cross-coupling reactions, see: (d) J. Organomet. Chem. 2002, 653, 1-303.
(2002)
J. Organomet. Chem
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18
34247099122
Angew. Chem., 2002, 114, 4350.
(2002)
Chem
, vol.114
, pp. 4350
Angew1
19
0037124694
(a) Lützen, A.; Hapke, M.; Griep-Raming, J.; Haase, D.; Saak, W. Angew. Chem. Int. Ed. 2002, 41, 2086;
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Angew. Chem. Int. Ed
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Lützen, A.1
Hapke, M.2
Griep-Raming, J.3
Haase, D.4
Saak, W.5
20
34147096402
Angew. Chem., 2002, 114, 2190.
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Chem
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Angew1
21
1642365135
(b) Schalley, C. A.; Lützen, A.; Albrecht, M. Chem. Eur. J. 2004, 10, 1072.
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Chem. Eur. J
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Schalley, C.A.1
Lützen, A.2
Albrecht, M.3
23
0242386451
(b) Lützen, A.; Hapke, M.; Staats, H.; Bunzen, J. Eur. J. Org. Chem. 2003, 3948.
(2003)
Eur. J. Org. Chem
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Lützen, A.1
Hapke, M.2
Staats, H.3
Bunzen, J.4
24
0034600318
Littke, A. F.; Dai, C.; Fu, G. C. J. Am. Chem. Soc 2000, 122, 4020.
(2000)
J. Am. Chem. Soc
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Littke, A.F.1
Dai, C.2
Fu, G.C.3
29
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Grave, C.; Lentz, D.; Schaefer, A.; Samori, P.; Rabe, J. P.; Franke, P.; Schlueter, A. D. J. Am. Chem. Soc. 2003, 125, 6907.
(2003)
J. Am. Chem. Soc
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Grave, C.1
Lentz, D.2
Schaefer, A.3
Samori, P.4
Rabe, J.P.5
Franke, P.6
Schlueter, A.D.7
32
0034741009
Fletcher, N. C.; Nieuwenhuyzen, M.; Rainey, S. J. Chem. Soc., Dalton Trans. 2001, 2641.
(2001)
J. Chem. Soc., Dalton Trans
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Fletcher, N.C.1
Nieuwenhuyzen, M.2
Rainey, S.3
33
13944258152
This compound has been described before using a different synthetic approach; however, no NMR or MS data were provided: Kozhevnikov, V. N, Kozhevnikov, D. N, Shabunina, O. V, Rusinov, V. L, Chupakhin, O. N. Tetrahedron Lett. 2005, 46, 1791
This compound has been described before using a different synthetic approach; however, no NMR or MS data were provided: Kozhevnikov, V. N.; Kozhevnikov, D. N.; Shabunina, O. V.; Rusinov, V. L.; Chupakhin, O. N. Tetrahedron Lett. 2005, 46, 1791.
34
0000457166
Grosshenny, V.; Romero, F. M.; Ziessel, R. J. Org. Chem. 1997, 62, 1491.
(1997)
J. Org. Chem
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, pp. 1491
Grosshenny, V.1
Romero, F.M.2
Ziessel, R.3
35
0001186779
This compound has been described before using a different synthetic approach; however, no NMR or MS data were provided: Schubert, U. S, Eschbaumer, C, Heller, M. Org. Lett. 2000, 2, 3373
This compound has been described before using a different synthetic approach; however, no NMR or MS data were provided: Schubert, U. S.; Eschbaumer, C.; Heller, M. Org. Lett. 2000, 2, 3373.