-
1
-
-
2042507954
-
-
For general reviews on the Suzuki coupling reaction, see: (a) Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457-2483
-
(1995)
Chem. Rev.
, vol.95
, pp. 2457-2483
-
-
Miyaura, N.1
Suzuki, A.2
-
2
-
-
0036589259
-
-
(b) Hassan, J.; Sevignon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Chem. Rev. 2002, 102, 1359-1469.
-
(2002)
Chem. Rev.
, vol.102
, pp. 1359-1469
-
-
Hassan, J.1
Sevignon, M.2
Gozzi, C.3
Schulz, E.4
Lemaire, M.5
-
3
-
-
4444264948
-
-
For general reviews on the Heck reaction, see: (a)
-
For general reviews on the Heck reaction, see: (a) Heck, R. F. Acc. Chem. Res. 1979, 12, 146-151
-
(1979)
Acc. Chem. Res.
, vol.12
, pp. 146-151
-
-
Heck, R.F.1
-
5
-
-
75749144221
-
-
For example, see: (a) Bonazzi, S.; Eidam, O.; Guttinger, S.; Wach, J.-Y.; Zemp, I.; Kutay, U.; Gademann, K. J. Am. Chem. Soc. 2010, 132, 1432-1442
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 1432-1442
-
-
Bonazzi, S.1
Eidam, O.2
Guttinger, S.3
Wach, J.-Y.4
Zemp, I.5
Kutay, U.6
Gademann, K.7
-
8
-
-
25444515688
-
-
(d) Alcaide, B.; Almendros, P.; Rodriguez-Acebes, R. Chem.-Eur J. 2005, 11, 5708-5712
-
(2005)
Chem.-eur J.
, vol.11
, pp. 5708-5712
-
-
Alcaide, B.1
Almendros, P.2
Rodriguez-Acebes, R.3
-
11
-
-
0000718373
-
-
(g) Pu, L. Chem. Rev. 1998, 98, 2405-2494.
-
(1998)
Chem. Rev.
, vol.98
, pp. 2405-2494
-
-
Pu, L.1
-
13
-
-
24044470646
-
-
(b) Li, C.-J. Chem. Rev. 2005, 105, 3095-3165
-
(2005)
Chem. Rev.
, vol.105
, pp. 3095-3165
-
-
Li, C.-J.1
-
17
-
-
0000586886
-
-
Badone, D.; Baroni, M.; Cardamone, R.; Ielmini, A.; Guzzi, U. J. Org. Chem. 1997, 62, 7170-7173.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7170-7173
-
-
Badone, D.1
Baroni, M.2
Cardamone, R.3
Ielmini, A.4
Guzzi, U.5
-
18
-
-
0030600195
-
-
(a) Reetz, M. T.; Breinbauer, R.; Wanninger, K. Tetrahedron Lett. 1996, 37, 4499-4502
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4499-4502
-
-
Reetz, M.T.1
Breinbauer, R.2
Wanninger, K.3
-
19
-
-
0030576421
-
-
(b) Beller, M.; Fischer, H.; Kühlein, K.; Reisinger, C.-P.; Herrmann, W. A. J. Organomet. Chem. 1996, 520, 257-259
-
(1996)
J. Organomet. Chem.
, vol.520
, pp. 257-259
-
-
Beller, M.1
Fischer, H.2
Kühlein, K.3
Reisinger, C.-P.4
Herrmann, W.A.5
-
22
-
-
17844409826
-
-
(a) Bhattacharya, S.; Srivastava, A.; Sengupta, S. Tetrahedron Lett. 2005, 46, 3557-3560
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 3557-3560
-
-
Bhattacharya, S.1
Srivastava, A.2
Sengupta, S.3
-
23
-
-
58149494116
-
-
(b) Saha, D.; Chattopadhyay, K.; Ranu, B. C. Tetrahedron Lett. 2009, 50, 1003-1006.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 1003-1006
-
-
Saha, D.1
Chattopadhyay, K.2
Ranu, B.C.3
-
25
-
-
49149102096
-
-
Wei, G.; Zhang, W.; Wen, F.; Wang, Y.; Zhang, M. J. Phys. Chem. C 2008, 112, 10827-10832.
-
(2008)
J. Phys. Chem. C
, vol.112
, pp. 10827-10832
-
-
Wei, G.1
Zhang, W.2
Wen, F.3
Wang, Y.4
Zhang, M.5
-
26
-
-
76149145705
-
-
(a)Anraku, Y.;Kishimura, A.;Oba, M.;Yamasaki, Y.;Kataoka, K.J. Am. Chem. Soc. 2010, 132, 1631-1636
-
(2010)
.J. Am. Chem. Soc.
, vol.132
, pp. 1631-1636
-
-
Anraku, Y.1
Kishimura, A.2
Oba, M.3
Yamasaki, Y.4
Kataoka, K.5
-
27
-
-
77149166966
-
-
(b) Akagi, T.; Watanabe, K.; Kim, H.; Akashi, M. Langmuir 2010, 26, 2406-2413
-
(2010)
Langmuir
, vol.26
, pp. 2406-2413
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Akagi, T.1
Watanabe, K.2
Kim, H.3
Akashi, M.4
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30
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85030588375
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When the preparation of PIC-PdNPs was performed with reduced amount of PAA (1 equiv of AA unit for each ammonium unit in 2b), the signals of polymer 2b were confirmed by 1H NMR in aqueous phase after pH treatment
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When the preparation of PIC-PdNPs was performed with reduced amount of PAA (1 equiv of AA unit for each ammonium unit in 2b), the signals of polymer 2b were confirmed by 1H NMR in aqueous phase after pH treatment.
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31
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85030584456
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No polymer was confirmed by 1H NMR in aqueous phase
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No polymer was confirmed by 1H NMR in aqueous phase.
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33
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85030584748
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When the recycling experiment was performed with 1 equiv of p-methyl-phenylboronic acid, the gradual decrease in yield was observed (first run: 97%, second run: 76%, third run: 58%)
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When the recycling experiment was performed with 1 equiv of p-methyl-phenylboronic acid, the gradual decrease in yield was observed (first run: 97%, second run: 76%, third run: 58%).
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34
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71749098056
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Similar results have been reported. (a) Sin, E.; Yi, S.-S.; Lee, Y.-S. J. Mol. Catal. A 2010, 315, 99-104
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(2010)
J. Mol. Catal. A
, vol.315
, pp. 99-104
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Sin, E.1
Yi, S.-S.2
Lee, Y.-S.3
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35
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34548051126
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(b) Yi, S.-S.; Lee, D.-H.; Sin, E.; Lee, Y.-S. Tetrahedron Lett. 2007, 48, 6771-6775.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 6771-6775
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Yi, S.-S.1
Lee, D.-H.2
Sin, E.3
Lee, Y.-S.4
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36
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85030590522
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It was reported that a biphenyl compound poisoned an active site of PVP-Pd and decreased the product yield (see Ref. 15). However, no biphenyl by-products were observed in the Heck reaction
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It was reported that a biphenyl compound poisoned an active site of PVP-Pd and decreased the product yield (see Ref. 15). However, no biphenyl by-products were observed in the Heck reaction.
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