-
5
-
-
0034839247
-
-
(e) Pease, A. R.: Jeppesen, J. O.; Stoddart, J. F.; Luo, Y.; Collier, C. P.; Heath, J. R. Acc. Chem. Res. 2001, 34, 433.
-
(2001)
Acc. Chem. Res.
, vol.34
, pp. 433
-
-
Pease, A.R.1
Jeppesen, J.O.2
Stoddart, J.F.3
Luo, Y.4
Collier, C.P.5
Heath, J.R.6
-
7
-
-
0032569172
-
-
(g) Tour, J. M.; Kozaky, M.; Seminario, J. M. J. Am. Chem. Soc. 1998, 120, 8486.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 8486
-
-
Tour, J.M.1
Kozaky, M.2
Seminario, J.M.3
-
9
-
-
0034607434
-
-
(b) Seminario, J. M.; Zacarias, A. G.; Tour, J. M. J. Am. Chem. Soc. 2000, 122, 3015.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 3015
-
-
Seminario, J.M.1
Zacarias, A.G.2
Tour, J.M.3
-
10
-
-
0033584805
-
-
(c) Chen, J.; Reed, M.-A.; Rawlett, A. M.; Tour, J. M. Science 1999, 286, 1550.
-
(1999)
Science
, vol.286
, pp. 1550
-
-
Chen, J.1
Reed, M.-A.2
Rawlett, A.M.3
Tour, J.M.4
-
11
-
-
0035844685
-
-
(a) Dirk, S. M.; Price, D. W. Jr.; Chanteau, S.; Kosynkin, D. V.; Tour, J. M. Tetrahedron 2001, 5109.
-
(2001)
Tetrahedron
, pp. 5109
-
-
Dirk, S.M.1
Price D.W., Jr.2
Chanteau, S.3
Kosynkin, D.V.4
Tour, J.M.5
-
14
-
-
0003086428
-
-
Nerenz, H.; Meier, M.; Grahn, W.; Reisner, A.; Schmälzlin, E.; Standler, S.; Meerholz, K.; Bräuchle, C.; Jones, P. G. J. Chem. Soc., Perkin Trans. 2 1998, 437.
-
(1998)
J. Chem. Soc., Perkin Trans. 2
, pp. 437
-
-
Nerenz, H.1
Meier, M.2
Grahn, W.3
Reisner, A.4
Schmälzlin, E.5
Standler, S.6
Meerholz, K.7
Bräuchle, C.8
Jones, P.G.9
-
16
-
-
0001186913
-
-
Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford, Chap. 3.4
-
(b) Farina, F. Comprehensive Organometallic Chemistry II, Vol. 12; Abel, E. W.; Stone, F. G. A.; Wilkinson, G., Eds.; Pergamon Press: Oxford, 1995, Chap. 3.4, 161.
-
(1995)
Comprehensive Organometallic Chemistry II
, vol.12
, pp. 161
-
-
Farina, F.1
-
23
-
-
0001200278
-
-
Barchín, B. M.; Valenciano, J.; Cuadro, A. M.; Alvarez-Builla, J.; Vaquero, J. J. Org. Lett. 1999, 1, 545.
-
(1999)
Org. Lett.
, vol.1
, pp. 545
-
-
Barchín, B.M.1
Valenciano, J.2
Cuadro, A.M.3
Alvarez-Builla, J.4
Vaquero, J.J.5
-
24
-
-
0011372135
-
-
Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York, Chap. 4
-
(a) Mitchell, T. N. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: New York, 1998, Chap. 4.
-
(1998)
Metal-Catalyzed Cross-Coupling Reactions
-
-
Mitchell, T.N.1
-
25
-
-
0000802361
-
-
(b) Farina, V.; Krishnamurthy, V.; Scott, W. J. Org. React. 1997, 50, 1.
-
(1997)
Org. React.
, vol.50
, pp. 1
-
-
Farina, V.1
Krishnamurthy, V.2
Scott, W.J.3
-
26
-
-
0002079003
-
-
Liebeskind, L. S., Ed.; JAI Press. Inc.: Greenwich
-
(c) Farina, V.; Roth, G. P. Advances in Metal-Organic Chemistry, Vol. 5; Liebeskind, L. S., Ed.; JAI Press. Inc.: Greenwich, 1996. 1.
-
(1996)
Advances in Metal-Organic Chemistry
, vol.5
, pp. 1
-
-
Farina, V.1
Roth, G.P.2
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30
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note
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4 (0.0165 mmol, 15.1 mg). The reaction mixture was heated at 80°C or stirred at r.t. (as indicated) and then filtered through a small pad of celite and washed with methanol. The solvent was removed and the residue was triturated with EtOAc. Purification of the crude product by column chromatography on silica gel (reverse phase), using water as the eluent yielded the coupling product.
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0011319635
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note
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3 (0.0165 mmol, 5 mg) were slowly added followed by the corresponding stannane (1.3 equiv, 0.429 mmol). The mixture was stirred at r.t. and the work-up procedure, which was similar to Method A, yielded the coupling product.
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(b) Majeed, A. J.; Antonsen, O.; Beneche, T.; Undheim, K. Tetrahedron 1989, 45, 993.
-
(1989)
Tetrahedron
, vol.45
, pp. 993
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Majeed, A.J.1
Antonsen, O.2
Beneche, T.3
Undheim, K.4
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note
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3 (0.0165 mmol, 5 mg) and 1.3 equiv KF (0.429 mmol, 24.9 mg) were slowly added followed by 1.3 equiv of the corresponding stannane (0.429 mmol). The reaction mixture was heated at 80°C (as indicated), the residue was triturated with acetonitrile and the liquid was purified by column chromatography on silica gel (reverse phase) using water as the eluent.
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