-
3
-
-
14344266665
-
-
For organotin reagents in cross-coupling reactions Eds.: A. DeMeijere, F. Diederich, Wiley-VCH, Weinheim.
-
c)For organotin reagents in cross-coupling reactions, see: T. N. Mitchel in Metal-Catalyzed Cross-Coupling Reactions, Vol.1 (Eds.: A. DeMeijere, F. Diederich), Wiley-VCH, Weinheim., 2004, pp. 125-161;
-
(2004)
Metal-Catalyzed Cross-Coupling Reactions
, vol.1
, pp. 125-161
-
-
Mitchel, T.N.1
-
5
-
-
4644245555
-
-
Angew. Chem. Int. Ed. 2004, 43, 4704-4734.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 4704-4734
-
-
-
6
-
-
50249143998
-
-
a) F. Chimenti, E. Maccioni, D. Secci, A. Bolasco, P. Chimenti, A. Granese, S. Carradori, S. Alcaro, F. Ortuso, M. Yáñez, F. Orallo, R. Cirilli, R. Ferretti, F. La Torre, J. Med Chem. 2008, 51, 4874-4880;
-
(2008)
J. Med Chem.
, vol.51
, pp. 4874-4880
-
-
Chimenti, F.1
Maccioni, E.2
Secci, D.3
Bolasco, A.4
Chimenti, P.5
Granese, A.6
Carradori, S.7
Alcaro, S.8
Ortuso, F.9
Yáñez, M.10
Orallo, F.11
Cirilli, R.12
Ferretti, R.13
La Torre, F.14
-
7
-
-
30444455608
-
-
b) S. C. Goodacre, L. J. Street, D. J. Hallett, J. M. Crawforth, S. Kelly, A. P. Owens, W. P. Blackaby, R. T. Lewis, J. Stanley, A. J. Smith, P. Ferris, B. Sohal, S. M. Cook, A. Pike, N. Brown, K. A. Wafford, G. Marshall, J. L. Castro, J. R. Atack, J. Med Chem. 2006, 49, 35-38.
-
(2006)
J. Med Chem.
, vol.49
, pp. 35-38
-
-
Goodacre, S.C.1
Street, L.J.2
Hallett, D.J.3
Crawforth, J.M.4
Kelly, S.5
Owens, A.P.6
Blackaby, W.P.7
Lewis, R.T.8
Stanley, J.9
Smith, A.J.10
Ferris, P.11
Sohal, B.12
Cook, S.M.13
Pike, A.14
Brown, N.15
Wafford, K.A.16
Marshall, G.17
Castro, J.L.18
Atack, J.R.19
-
8
-
-
0032491270
-
-
a) R. W Friesen, C. Brideau, C. C. Chan, S. Charleson, D. Deschênes, D. Dubé, D. Ethier, R. Fortin, J. Gauthier, Y. Girard, R. Gordon, G. M. Greig, D. Riendeau, C. Savoie, Z. Wang, E. Wong, D. Visco, L. J. Xu, R. N. Young, Bioorg. Med. Chem. Lett. 1998, 8, 2777-2782;
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2777-2782
-
-
Friesen, R.W.1
Brideau, C.2
Chan, C.C.3
Charleson, S.4
Deschênes, D.5
Dubé, D.6
Ethier, D.7
Fortin, R.8
Gauthier, J.9
Girard, Y.10
Gordon, R.11
Greig, G.M.12
Riendeau, D.13
Savoie, C.14
Wang, Z.15
Wong, E.16
Visco, D.17
Xu, L.J.18
Young, R.N.19
-
9
-
-
0242300219
-
-
b) J. Quirk, M. Thornton, E. Kirkpatrick, Nature. 2003, 2, 769-770;
-
(2003)
Nature.
, vol.2
, pp. 769-770
-
-
Quirk, J.1
Thornton, M.2
Kirkpatrick, E.3
-
10
-
-
0036635291
-
-
c) R. Capdeville, E. Buchdunger, J. Zimmermann, A. Matter, Nature. 2002, 1, 493-502.
-
(2002)
Nature.
, vol.1
, pp. 493-502
-
-
Capdeville, R.1
Buchdunger, E.2
Zimmermann, J.3
Matter, A.4
-
11
-
-
67749093252
-
-
J. Clayden, S. P. Fletcher, J. J. W. McDouall, S. J. M. Rowbottom, J. Am. Chem. Soc. 2009, 131, 5331-5341.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5331-5341
-
-
Clayden, J.1
Fletcher, S.P.2
McDouall, J.J.W.3
Rowbottom, S.J.M.4
-
12
-
-
0000419106
-
-
S. Choppin, P. Gros, Y. Fort, Org. Lett. 2000, 2, 803-805.
-
(2000)
Org. Lett.
, vol.2
, pp. 803-805
-
-
Choppin, S.1
Gros, P.2
Fort, Y.3
-
13
-
-
0037024173
-
-
A. Linke, L. Schwarz, G. C. Fu, J. Am. Chem. Soc. 2002, 124, 6343-6348.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 6343-6348
-
-
Linke, A.1
Schwarz, L.2
Fu, G.C.3
-
14
-
-
11444254369
-
-
a)W. Su, S. Urgaonkar, P.A. McLaughlin, J. G. Verkade, J. Am. Chem. Soc. 2004, 126, 16433-16439;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 16433-16439
-
-
Su, W.1
Urgaonkar, S.2
McLaughlin, P.A.3
Verkade, J.G.4
-
15
-
-
2442598164
-
-
b) W. Su, S. Urgaonkar, P. G. Verkade, Org. Lett. 2004, 6, 1421-1424.
-
(2004)
Org. Lett.
, vol.6
, pp. 1421-1424
-
-
Su, W.1
Urgaonkar, S.2
Verkade, P.G.3
-
16
-
-
4644364062
-
-
S. P. H. Mee, V. Lee, J. E. Baldwin, Angew. Chem. 2004, 116, 1152-1156;
-
(2004)
Angew. Chem.
, vol.116
, pp. 1152-1156
-
-
Mee, S.P.H.1
Lee, V.2
Baldwin, J.E.3
-
17
-
-
1842565056
-
-
Angew. Chem. Int. Ed. 2004, 43, 1132-1136.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 1132-1136
-
-
-
20
-
-
38849191003
-
-
b) E. A. B. Kantchev, C. J. O'Brien, M. G. Organ, Angew. Chem. 2007, 119, 2824-2870;
-
(2007)
Angew. Chem.
, vol.119
, pp. 2824-2870
-
-
Kantchev, E.A.B.1
O'Brien, C.J.2
Organ, M.G.3
-
21
-
-
34250797354
-
-
Angew. Chem. Int. Ed. 2007, 46, 2768-2813;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 2768-2813
-
-
-
24
-
-
19544386162
-
-
N. Hadei, E. A. B. Kantchev, C. J. O'Brien, M. G. Organ, Org. Lett. 2005, 7, 1991-1994.
-
(2005)
Org. Lett.
, vol.7
, pp. 1991-1994
-
-
Hadei, N.1
Kantchev, E.A.B.2
O'Brien, C.J.3
Organ, M.G.4
-
25
-
-
76149119399
-
-
a) M. G. Organ, S. Çalimsiz, S.; M. Sayah, K. H. Hoi, A. J. Lough, Angew. Chem. 2009, 121, 2419-2423;
-
(2009)
Angew. Chem.
, vol.121
, pp. 2419-2423
-
-
Organ, M.G.1
Çalimsiz, S.2
Sayah, M.3
Hoi, K.H.4
Lough, A.J.5
-
26
-
-
77950788758
-
-
M. Sayah, K. H. Hoi, A. J. Lough, Angew. Chem. 2009, 121, 2419-2423;
-
(2009)
, vol.121
, pp. 2419-2423
-
-
Sayah, M.1
Hoi, K.H.2
Lough, A.J.3
Chem, A.4
-
27
-
-
70349782152
-
-
Angew. Chem. Int. Ed. 2009, 48, 2383-2387;
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 2383-2387
-
-
-
28
-
-
84961981994
-
-
b) M. G. Organ, G. A. Chass, D.-C. Fang, A. C. Hopkinson, C. Valente, Synthesis 2008, 2776-2797;
-
(2008)
Synthesis
, pp. 2776-2797
-
-
Organ, M.G.1
Chass, G.A.2
Fang, D.-C.3
Hopkinson, A.C.4
Valente, C.5
-
29
-
-
24344504109
-
-
c) C. J. O'Brien, E. A. B. Kantchev, G. A. Chass, N. Hadei, A. C. Hopkinson, M. G. Organ, D. H. Setiadi, T.-H. Tang, D.-C. Fang, Tetrahedron 2005, 61, 9723-9735;
-
(2005)
Tetrahedron
, vol.61
, pp. 9723-9735
-
-
O'Brien, C.J.1
Kantchev, E.A.B.2
Chass, G.A.3
Hadei, N.4
Hopkinson, A.C.5
Organ, M.G.6
Setiadi, D.H.7
Tang, T.-H.8
Fang, D.-C.9
-
30
-
-
84962440466
-
-
d) G. A. Chass, C. J. O'Brien, N. Hadei, E. A. B. Kantchev, W.-H. Mu, D.-C. Fang, A. C. Hopkinson, I. G. Csizmadia, M. G. Organ, Chem. Eur. J. 2009, 15, 4281-4288.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 4281-4288
-
-
Chass, G.A.1
O'Brien, C.J.2
Hadei, N.3
Kantchev, E.A.B.4
Mu, W.-H.5
Fang, D.-C.6
Hopkinson, A.C.7
Csizmadia, I.G.8
Organ, M.G.9
-
31
-
-
68549092330
-
-
M. Pérez-Rodríguez, A. A. Braga, M. Garcia-Melchor, M1 H1 PérezTemprano, J A. Casares, G. Ujaque, A. R. de Lera, R. Alvarez, F. Maseras, P. Espinet, J. Am. Chem. Soc. 2009, 131, 3650-3657.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 3650-3657
-
-
Pérez-Rodríguez, M.1
Braga, A.A.2
Garcia-Melchor, M.3
Péreztemprano, M.H.4
Casares, J.A.5
Ujaque, G.6
De Lera, A.R.7
Alvarez, R.8
Maseras, F.9
Espinet, P.10
-
32
-
-
9344240844
-
-
The term "flexible steric bulk" was first coined by Glorius, a
-
The term "flexible steric bulk" was first coined by Glorius, see: a) G. Altenhoff, R. Goddard, C. W. Lehmann, F. Glorius, J. Am. Chem. Soc. 2004, 126, 15195-15201;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 15195-15201
-
-
Altenhoff, G.1
Goddard, R.2
Lehmann, C.W.3
Glorius, F.4
-
33
-
-
1842717280
-
-
b) G. Altenhoff, R. Goddard, C.W. Lehmann, F. Glorius, Angew. Chem. 2003, 115, 3818-3821;
-
(2003)
Angew. Chem.
, vol.115
, pp. 3818-3821
-
-
Altenhoff, G.1
Goddard, R.2
Lehmann, C.W.3
Glorius, F.4
-
34
-
-
0042969355
-
-
Angew. Chem. Int. Ed. 2003, 42, 3690-3693.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 3690-3693
-
-
-
35
-
-
0037463809
-
-
J. D. Speake, F. Navas, M. J. Bishop, D. T. Garrison, E. C. Bigham, S. J. Hodson, D. L. Saussy, J. A. Liacos, P. E. Irving, B. Sherman, Bioorg. Med. Chem. Lett. 2003, 13, 1183-1186.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1183-1186
-
-
Speake, J.D.1
Navas, F.2
Bishop, M.J.3
Garrison, D.T.4
Bigham, E.C.5
Hodson, S.J.6
Saussy, D.L.7
Liacos, J.A.8
Irving, P.E.9
Sherman, B.10
-
36
-
-
0004061172
-
-
Eds.: J. A. Joule, K. Mills, Blackwell Science, Maiden
-
a) Heterocyclic Chemistry (Eds.: J. A. Joule, K. Mills), Blackwell Science, Maiden, 2000;
-
(2000)
Heterocyclic Chemistry
-
-
-
39
-
-
77950787717
-
-
For cases in which moderate product conversions were obtained (i.e., ≈75%), the major impurity in the crude mixture was unreacted starting material (i.e., ArX) and allowing these reactions to proceed longer resulted in greater than 90 % conversions on an individual basis.
-
For cases in which moderate product conversions were obtained (i.e., ≈75%), the major impurity in the crude mixture was unreacted starting material (i.e., ArX) and allowing these reactions to proceed longer resulted in greater than 90 % conversions on an individual basis.
-
-
-
-
40
-
-
33746498355
-
-
a) Y. Liu, S. Zhang, P. J. M. Abreu, NAt. Prod. Rep. 2006, 23, 630-651;
-
(2006)
NAt. Prod. Rep.
, vol.23
, pp. 630-651
-
-
Liu, Y.1
Zhang, S.2
Abreu, P.J.M.3
-
43
-
-
35348825460
-
-
a) L. M. Klingensmith, M. M. Bio, G. A. Moniz, Tetrahedron Lett. 2007, 48, 8242-8245;
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 8242-8245
-
-
Klingensmith, L.M.1
Bio, M.M.2
Moniz, G.A.3
-
45
-
-
84987280084
-
-
c) D. Florentin, M. C. Fournie-Zaluski, M. Callanquin, B. P. Roques, J. Heterocycl. Chem. 1976, 13, 1265-1272.
-
(1976)
J. Heterocycl. Chem.
, vol.13
, pp. 1265-1272
-
-
Florentin, D.1
Fournie-Zaluski, M.C.2
Callanquin, M.3
Roques, B.P.4
-
47
-
-
0000271948
-
-
a) C. Johnson, G. Stemp, N. Anand, S. Stephen, T. Gallagher, Synlett 1998, 1025-1927;
-
(1998)
Synlett
, pp. 1025-1927
-
-
Johnson, C.1
Stemp, G.2
Anand, N.3
Stephen, S.4
Gallagher, T.5
-
48
-
-
0001123553
-
-
b) A. Alvarez, A. Guzmen, A. Ruiz, E. Velards, J. Muchowski, J. Org. Chem. 1992, 57, 1653-1656.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 1653-1656
-
-
Alvarez, A.1
Guzmen, A.2
Ruiz, A.3
Velards, E.4
Muchowski, J.5
-
50
-
-
33845953257
-
-
M. G. Organ, M. Abdel-Hadi, S. Avola, N. Hadei, J. Nasielski, C. J. O'Brien, C. Valente, Chem. Eur. J. 2007, 13, 150-157.
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 150-157
-
-
Organ, M.G.1
Abdel-Hadi, M.2
Avola, S.3
Hadei, N.4
Nasielski, J.5
O'Brien, C.J.6
Valente, C.7
|