-
3
-
-
20544450502
-
-
(Eds.: A. de Meijere, F. Diederich), Wiley-VCH, Weinheim, Germany.
-
Metal-Catalyzed Cross-Coupling Reactions (Eds.:, A. de Meijere, F. Diederich,), Wiley-VCH, Weinheim, Germany, 2004.
-
(2004)
Metal-Catalyzed Cross-Coupling Reactions
-
-
-
11
-
-
57549099215
-
-
The use of a 2-dialkylphosphane-1,1′-biphenyl-type framework is another strategy for developing effective phosphane ligands, see.
-
The use of a 2-dialkylphosphane-1,1′-biphenyl-type framework is another strategy for developing effective phosphane ligands, see:, R. Martin, S. L. Buchwald, Acc. Chem. Res. 2008, 41, 1461.
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 1461
-
-
Martin, R.1
Buchwald, S.L.2
-
13
-
-
84860617627
-
-
S. M. Wong, C. M. So, F. Y. Kwong, Synlett 2012, 23, 1132.
-
(2012)
Synlett
, vol.23
, pp. 1132
-
-
Wong, S.M.1
So, C.M.2
Kwong, F.Y.3
-
15
-
-
38849191003
-
-
E. A. B. Kantchev, C. J. O'Brien, M. G. Organ, Angew. Chem. 2007, 119, 2824
-
(2007)
Angew. Chem.
, vol.119
, pp. 2824
-
-
Kantchev, E.A.B.1
O'Brien, C.J.2
Organ, M.G.3
-
17
-
-
44349175441
-
-
M. R. Biscoe, B. P. Fors, S. L. Buchwald, J. Am. Chem. Soc. 2008, 130, 6686
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 6686
-
-
Biscoe, M.R.1
Fors, B.P.2
Buchwald, S.L.3
-
18
-
-
77957698670
-
-
T. Kinzel, Y. Zhang, S. L. Buchwald, J. Am. Chem. Soc. 2010, 132, 14073.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 14073
-
-
Kinzel, T.1
Zhang, Y.2
Buchwald, S.L.3
-
19
-
-
0347385522
-
-
O. Niyomura, M. Tokunaga, Y. Obora, T. Iwasawa, Y. Tsuji, Angew. Chem. 2003, 115, 1325
-
(2003)
Angew. Chem.
, vol.115
, pp. 1325
-
-
Niyomura, O.1
Tokunaga, M.2
Obora, Y.3
Iwasawa, T.4
Tsuji, Y.5
-
21
-
-
33748787121
-
-
T. Iwasawa, T. Komano, A. Tajima, M. Tokunaga, Y. Obora, T. Fujihara, Y. Tsuji, Organometallics 2006, 25, 4665
-
(2006)
Organometallics
, vol.25
, pp. 4665
-
-
Iwasawa, T.1
Komano, T.2
Tajima, A.3
Tokunaga, M.4
Obora, Y.5
Fujihara, T.6
Tsuji, Y.7
-
22
-
-
33846457891
-
-
H. Ohta, M. Tokunaga, Y. Obora, T. Iwai, T. Iwasawa, T. Fujihara, Y. Tsuji, Org. Lett. 2007, 9, 89
-
(2007)
Org. Lett.
, vol.9
, pp. 89
-
-
Ohta, H.1
Tokunaga, M.2
Obora, Y.3
Iwai, T.4
Iwasawa, T.5
Fujihara, T.6
Tsuji, Y.7
-
23
-
-
77950930169
-
-
T. Fujihara, S. Yoshida, H. Ohta, Y. Tsuji, Angew. Chem. 2008, 120, 8434
-
(2008)
Angew. Chem.
, vol.120
, pp. 8434
-
-
Fujihara, T.1
Yoshida, S.2
Ohta, H.3
Tsuji, Y.4
-
25
-
-
66149158165
-
-
T. Fujihara, S. Yoshida, J. Terao, Y. Tsuji, Org. Lett. 2009, 11, 2121.
-
(2009)
Org. Lett.
, vol.11
, pp. 2121
-
-
Fujihara, T.1
Yoshida, S.2
Terao, J.3
Tsuji, Y.4
-
26
-
-
68849102223
-
-
D. J. M. Snelders, G. van Koten, R. J. M. K. Gebbink, J. Am. Chem. Soc. 2009, 131, 11407
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 11407
-
-
Snelders, D.J.M.1
Van Koten, G.2
Gebbink, R.J.M.K.3
-
27
-
-
81255134888
-
-
S. Mom, M. Beaupérin, D. Roy, S. Royer, R. Amardeil, H. Cattey, H. Doucet, J.-C. Hierso, Inorg. Chem. 2011, 50, 11592
-
(2011)
Inorg. Chem.
, vol.50
, pp. 11592
-
-
Mom, S.1
Beaupérin, M.2
Roy, D.3
Royer, S.4
Amardeil, R.5
Cattey, H.6
Doucet, H.7
Hierso, J.-C.8
-
28
-
-
84859589881
-
-
W. K. Chow, O. Y. Yuen, C. M. So, W. T. Wong, F. Y. Kwong, J. Org. Chem. 2012, 77, 3543.
-
(2012)
J. Org. Chem.
, vol.77
, pp. 3543
-
-
Chow, W.K.1
Yuen, O.Y.2
So, C.M.3
Wong, W.T.4
Kwong, F.Y.5
-
29
-
-
0037433563
-
-
Q.-S. Hu, Y. Lu, Z.-Y. Tang, H.-B. Yu, J. Am. Chem. Soc. 2003, 125, 2856
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 2856
-
-
Hu, Q.-S.1
Lu, Y.2
Tang, Z.-Y.3
Yu, H.-B.4
-
30
-
-
84865718276
-
-
T. Yamamoto, Y. Akai, Y. Nagata, M. Suginome, Angew. Chem. 2011, 123, 9006
-
(2011)
Angew. Chem.
, vol.123
, pp. 9006
-
-
Yamamoto, T.1
Akai, Y.2
Nagata, Y.3
Suginome, M.4
-
32
-
-
0000554985
-
-
J.-P. Bezombes, C. Chuit, R. J. P. Corriu, C. Reyé, J. Mater. Chem. 1998, 8, 1749
-
(1998)
J. Mater. Chem.
, vol.8
, pp. 1749
-
-
Bezombes, J.-P.1
Chuit, C.2
Corriu, R.J.P.3
Reyé, C.4
-
33
-
-
0036472211
-
-
J.-P. Bezombes, C. Chuit, R. J. P. Corriu, C. Reyé, J. Organomet. Chem. 2002, 643-644, 453.
-
(2002)
J. Organomet. Chem.
, vol.643-644
, pp. 453
-
-
Bezombes, J.-P.1
Chuit, C.2
Corriu, R.J.P.3
Reyé, C.4
-
34
-
-
77950801448
-
-
N. Fukaya, S. Onozawa, M. Ueda, K. Saitou, Y. Takagi, T. Sakakura, H. Yasuda, Chem. Lett. 2010, 39, 402
-
(2010)
Chem. Lett.
, vol.39
, pp. 402
-
-
Fukaya, N.1
Onozawa, S.2
Ueda, M.3
Saitou, K.4
Takagi, Y.5
Sakakura, T.6
Yasuda, H.7
-
35
-
-
79551468944
-
-
N. Fukaya, S. Onozawa, M. Ueda, T. Miyaji, Y. Takagi, T. Sakakura, H. Yasuda, Chem. Lett. 2011, 40, 212
-
(2011)
Chem. Lett.
, vol.40
, pp. 212
-
-
Fukaya, N.1
Onozawa, S.2
Ueda, M.3
Miyaji, T.4
Takagi, Y.5
Sakakura, T.6
Yasuda, H.7
-
36
-
-
79953657281
-
-
T. Miyaji, S. Onozawa, N. Fukaya, M. Ueda, Y. Takagi, T. Sakakura, H. Yasuda, J. Organomet. Chem. 2011, 696, 1565
-
(2011)
J. Organomet. Chem.
, vol.696
, pp. 1565
-
-
Miyaji, T.1
Onozawa, S.2
Fukaya, N.3
Ueda, M.4
Takagi, Y.5
Sakakura, T.6
Yasuda, H.7
-
37
-
-
79957970584
-
-
N. Fukaya, M. Ueda, S. Onozawa, K. Bando, T. Miyaji, Y. Takagi, T. Sakakura, H. Yasuda, J. Mol. Catal. A 2011, 342-343, 58
-
(2011)
J. Mol. Catal. A
, vol.342-343
, pp. 58
-
-
Fukaya, N.1
Ueda, M.2
Onozawa, S.3
Bando, K.4
Miyaji, T.5
Takagi, Y.6
Sakakura, T.7
Yasuda, H.8
-
38
-
-
84887121037
-
-
S. Onozawa, T. Miyaji, N. Fukaya, M. Yoshinaga, M. Ueda, Y. Takagi, H. Yasuda, Chem. Lett. 2013, 42, 275.
-
(2013)
Chem. Lett.
, vol.42
, pp. 275
-
-
Onozawa, S.1
Miyaji, T.2
Fukaya, N.3
Yoshinaga, M.4
Ueda, M.5
Takagi, Y.6
Yasuda, H.7
-
39
-
-
84945903019
-
-
For polystyrene-phosphane covalent hybrids, which were effective for producing mono-P-ligated metal complexes, see
-
For polystyrene-phosphane covalent hybrids, which were effective for producing mono-P-ligated metal complexes, see:, T. Iwai, T. Harada, K. Hara, M. Sawamura, Angew. Chem. 2013, 125, 12548
-
(2013)
Angew. Chem.
, vol.125
, pp. 12548
-
-
Iwai, T.1
Harada, T.2
Hara, K.3
Sawamura, M.4
-
41
-
-
0141746190
-
-
A. Ochida, K. Hara, H. Ito, M. Sawamura, Org. Lett. 2003, 5, 2671
-
(2003)
Org. Lett.
, vol.5
, pp. 2671
-
-
Ochida, A.1
Hara, K.2
Ito, H.3
Sawamura, M.4
-
42
-
-
56049107865
-
-
A. Ochida, G. Hamasaka, Y. Yamauchi, S. Kawamorita, N. Oshima, K. Hara, H. Ohmiya, M. Sawamura, Organometallics 2008, 27, 5494.
-
(2008)
Organometallics
, vol.27
, pp. 5494
-
-
Ochida, A.1
Hamasaka, G.2
Yamauchi, Y.3
Kawamorita, S.4
Oshima, N.5
Hara, K.6
Ohmiya, H.7
Sawamura, M.8
-
43
-
-
35948966920
-
-
G. Hamasaka, A. Ochida, K. Hara, M. Sawamura, Angew. Chem. 2007, 119, 5477
-
(2007)
Angew. Chem.
, vol.119
, pp. 5477
-
-
Hamasaka, G.1
Ochida, A.2
Hara, K.3
Sawamura, M.4
-
45
-
-
61849148885
-
-
G. Hamasaka, S. Kawamorita, A. Ochida, R. Akiyama, K. Hara, A. Fukuoka, K. Asakura, W. J. Chun, H. Ohmiya, M. Sawamura, Organometallics 2008, 27, 6495
-
(2008)
Organometallics
, vol.27
, pp. 6495
-
-
Hamasaka, G.1
Kawamorita, S.2
Ochida, A.3
Akiyama, R.4
Hara, K.5
Fukuoka, A.6
Asakura, K.7
Chun, W.J.8
Ohmiya, H.9
Sawamura, M.10
-
46
-
-
61349098845
-
-
S. Kawamorita, G. Hamasaka, H. Ohmiya, K. Hara, A. Fukuoka, M. Sawamura, Org. Lett. 2008, 10, 4697
-
(2008)
Org. Lett.
, vol.10
, pp. 4697
-
-
Kawamorita, S.1
Hamasaka, G.2
Ohmiya, H.3
Hara, K.4
Fukuoka, A.5
Sawamura, M.6
-
47
-
-
67849117187
-
-
S. Kawamorita, H. Ohmiya, K. Hara, A. Fukuoka, M. Sawamura, J. Am. Chem. Soc. 2009, 131, 5058
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5058
-
-
Kawamorita, S.1
Ohmiya, H.2
Hara, K.3
Fukuoka, A.4
Sawamura, M.5
-
48
-
-
84862579743
-
-
S. Kawamorita, H. Ohmiya, T. Iwai, M. Sawamura, Angew. Chem. 2011, 123, 8513
-
(2011)
Angew. Chem.
, vol.123
, pp. 8513
-
-
Kawamorita, S.1
Ohmiya, H.2
Iwai, T.3
Sawamura, M.4
-
50
-
-
82555168484
-
-
S. Kawamorita, T. Miyazaki, H. Ohmiya, T. Iwai, M. Sawamura, J. Am. Chem. Soc. 2011, 133, 19310
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 19310
-
-
Kawamorita, S.1
Miyazaki, T.2
Ohmiya, H.3
Iwai, T.4
Sawamura, M.5
-
51
-
-
84874614567
-
-
S. Kawamorita, R. Murakami, T. Iwai, M. Sawamura, J. Am. Chem. Soc. 2013, 135, 2947.
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 2947
-
-
Kawamorita, S.1
Murakami, R.2
Iwai, T.3
Sawamura, M.4
-
53
-
-
0141924569
-
-
D. G. Ho, R. Gao, J. Celaje, H.-Y. Chung, M. Selke, Science 2003, 302, 259
-
(2003)
Science
, vol.302
, pp. 259
-
-
Ho, D.G.1
Gao, R.2
Celaje, J.3
Chung, H.-Y.4
Selke, M.5
-
60
-
-
79959787124
-
-
For an example of room-temperature heterogeneous Pd-catalyzed Suzuki-Miyaura cross-coupling of unactivated chloroarenes, see:, and ref. [12a].
-
For an example of room-temperature heterogeneous Pd-catalyzed Suzuki-Miyaura cross-coupling of unactivated chloroarenes, see:, B. Karimi, P. F. Akhavan, Chem. Commun. 2011, 47, 7686, and ref. [12a].
-
(2011)
Chem. Commun.
, vol.47
, pp. 7686
-
-
Karimi, B.1
Akhavan, P.F.2
-
61
-
-
84864674266
-
-
For applications of Silica-TRIP, see:, For the synthesis and applications of Silica-TRIP, see: ref. [17f].
-
For applications of Silica-TRIP, see:, S. Kawamorita, T. Miyazaki, T. Iwai, H. Ohmiya, M. Sawamura, J. Am. Chem. Soc. 2012, 134, 12924; For the synthesis and applications of Silica-TRIP, see: ref. [17f].
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 12924
-
-
Kawamorita, S.1
Miyazaki, T.2
Iwai, T.3
Ohmiya, H.4
Sawamura, M.5
-
62
-
-
33846381252
-
-
H. Tsuji, T. Inoue, Y. Kaneta, S. Sase, A. Kawachi, K. Tamao, Organometallics 2006, 25, 6142.
-
(2006)
Organometallics
, vol.25
, pp. 6142
-
-
Tsuji, H.1
Inoue, T.2
Kaneta, Y.3
Sase, S.4
Kawachi, A.5
Tamao, K.6
-
63
-
-
84856837521
-
-
For a heterogeneous Pd catalyst system based on a polymeric imidazole support that showed high activity for the Suzuki-Miyaura coupling between chloroarenes and arylboronic acids in water, see.
-
For a heterogeneous Pd catalyst system based on a polymeric imidazole support that showed high activity for the Suzuki-Miyaura coupling between chloroarenes and arylboronic acids in water, see:, Y. M. A. Yamada, S. M. Sarkar, Y. Uozumi, J. Am. Chem. Soc. 2012, 134, 3190.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 3190
-
-
Yamada, Y.M.A.1
Sarkar, S.M.2
Uozumi, Y.3
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