-
1
-
-
20544450502
-
-
(Eds: A. deMeijere, F. Diederich), Wiley-VCH, Weinheim, 2 nd edn
-
Metal-catalyzed Cross-Coupling Reactions, (Eds:, A. deMeijere, F. Diederich,), Wiley-VCH, Weinheim, 2 nd edn., 2004.
-
(2004)
Metal-catalyzed Cross-Coupling Reactions
-
-
-
2
-
-
78649589132
-
-
Reviews
-
Reviews
-
-
-
-
8
-
-
41149131770
-
-
M. Carril, R. SanMartin, E. Domínguez, Chem. Soc. Rev. 2008, 37, 639
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 639
-
-
Carril, M.1
Sanmartin, R.2
Domínguez, E.3
-
14
-
-
51049095122
-
-
G. Evano, N. Blanchard, M. Toumi, Chem. Rev. 2008, 108, 3054
-
(2008)
Chem. Rev.
, vol.108
, pp. 3054
-
-
Evano, G.1
Blanchard, N.2
Toumi, M.3
-
15
-
-
77149151216
-
-
V. F. Slagt, A. H. M. deVries, J. G. deVries, R. M. Kellog, Org. Process Res. Dev. 2010, 14, 30
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 30
-
-
Slagt, V.F.1
Devries, A.H.M.2
Devries, J.G.3
Kellog, R.M.4
-
17
-
-
78649561577
-
-
For selected contributions, see
-
For selected contributions, see
-
-
-
-
18
-
-
65249101511
-
-
(In, Zn, Sc, Bi)
-
V. P. Reddy, K. Swapna, A. V. Kumar, K. R. Rao, J. Org. Chem. 2009, 74, 3189 (In, Zn, Sc, Bi)
-
(2009)
J. Org. Chem.
, vol.74
, pp. 3189
-
-
Reddy, V.P.1
Swapna, K.2
Kumar, A.V.3
Rao, K.R.4
-
19
-
-
65349124752
-
-
(In)
-
V. P. Reddy, A. V. Kumar, K. Swapna, K. R. Rao, Org. Lett. 2009, 11, 1697 (In)
-
(2009)
Org. Lett.
, vol.11
, pp. 1697
-
-
Reddy, V.P.1
Kumar, A.V.2
Swapna, K.3
Rao, K.R.4
-
20
-
-
53849117807
-
-
(Cd)
-
L. Rout, P. Saha, S. Jammi, T. Punniyamurthy, Adv. Synth. Catal. 2008, 350, 395 (Cd)
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 395
-
-
Rout, L.1
Saha, P.2
Jammi, S.3
Punniyamurthy, T.4
-
21
-
-
78650351501
-
-
early view, DOI:.1002/adsc.200900691 (La)
-
S. N. Murthy, B. Madhav, V. P. Reddy, Y. V. D. Nageswar, Adv. Synth. Catal. 2010, 352, early view, DOI: 10.1002/adsc.200900691 (La)
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 10
-
-
Murthy, S.N.1
Madhav, B.2
Reddy, V.P.3
Nageswar, Y.V.D.4
-
22
-
-
70849094970
-
-
(La)
-
S. N. Murthy, B. Madhav, V. P. Reddy, Y. V. D. Nageswar, Eur. J. Org. Chem. 2009, 5902 (La)
-
(2009)
Eur. J. Org. Chem.
, pp. 5902
-
-
Murthy, S.N.1
Madhav, B.2
Reddy, V.P.3
Nageswar, Y.V.D.4
-
23
-
-
70349445423
-
-
(Fe)
-
K. Swapna, A. V. Kumar, V. P. Reddy, K. R. Rao, J. Org. Chem. 2009, 74, 7514 (Fe)
-
(2009)
J. Org. Chem.
, vol.74
, pp. 7514
-
-
Swapna, K.1
Kumar, A.V.2
Reddy, V.P.3
Rao, K.R.4
-
25
-
-
53549116324
-
-
For copper-catalyzed arylations in DMSO with KOH as base, see L. Rout, T. K. Sen, T. Punniyamurthy, Angew. Chem. 2007, 119, 5679
-
(2007)
Angew. Chem.
, vol.119
, pp. 5679
-
-
Rout, L.1
Sen, T.K.2
Punniyamurthy, T.3
-
27
-
-
34548152778
-
-
L. Rout, S. Jammi, T. Punniyamurthy, Org. Lett. 2007, 9, 3397
-
(2007)
Org. Lett.
, vol.9
, pp. 3397
-
-
Rout, L.1
Jammi, S.2
Punniyamurthy, T.3
-
28
-
-
64249134236
-
-
S. Jammi, S. Sakthivel, L. Rout, T. Mukherjee, S. Mandal, R. Mitra, P. Saha, T. Punniyamurthy, J. Org. Chem. 2009, 74, 1971
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1971
-
-
Jammi, S.1
Sakthivel, S.2
Rout, L.3
Mukherjee, T.4
Mandal, S.5
Mitra, R.6
Saha, P.7
Punniyamurthy, T.8
-
29
-
-
70449635493
-
-
P. Saha, T. Ramana, N. Purkait, A. Ali, R. Paul, T. Punniyamurthy, J. Org. Chem. 2009, 74, 8719
-
(2009)
J. Org. Chem.
, vol.74
, pp. 8719
-
-
Saha, P.1
Ramana, T.2
Purkait, N.3
Ali, A.4
Paul, R.5
Punniyamurthy, T.6
-
30
-
-
55049092392
-
-
J. Zhang, Z. Zhang, Y. Wang, X. Zheng, Z. Wang, Eur. J. Org. Chem. 2008, 5112
-
(2008)
Eur. J. Org. Chem.
, pp. 5112
-
-
Zhang, J.1
Zhang, Z.2
Wang, Y.3
Zheng, X.4
Wang, Z.5
-
31
-
-
62749122280
-
-
V. P. Reddy, A. V. Kumar, K. Swapna, K. Rao, Org. Lett. 2009, 11, 951
-
(2009)
Org. Lett.
, vol.11
, pp. 951
-
-
Reddy, V.P.1
Kumar, A.V.2
Swapna, K.3
Rao, K.4
-
32
-
-
77955159291
-
-
D. Singh, A. M. Deobald, L. R. S. Camargo, G. Tabarelli, O. E. D. Rodrigues, A. L. Braga, Org. Lett. 2010, 12, 3288
-
(2010)
Org. Lett.
, vol.12
, pp. 3288
-
-
Singh, D.1
Deobald, A.M.2
Camargo, L.R.S.3
Tabarelli, G.4
Rodrigues, O.E.D.5
Braga, A.L.6
-
33
-
-
78649589627
-
-
C.-K. Chen, Y.-W. Chen, C.-H. Lin, H.-P. Lin C.-F. Lee, Chem. Commun. 2010, 46, 281
-
(2010)
Chem. Commun.
, vol.46
, pp. 281
-
-
Chen, C.-K.1
Chen, Y.-W.2
Lin, C.-H.3
Lee, H.-P.L.C.-F.4
-
34
-
-
77049116355
-
-
D. Zhao, N. Wu, S. Zhang, P. Xi, X. Su, J. Lan, J. You, Angew. Chem. 2009, 121, 8885
-
(2009)
Angew. Chem.
, vol.121
, pp. 8885
-
-
Zhao, D.1
Wu, N.2
Zhang, S.3
Xi, P.4
Su, X.5
Lan, J.6
You, J.7
-
36
-
-
77049091885
-
-
A. Tlili, N. Xia, F. Monnier, M. Taillefer, Angew. Chem. 2009, 121, 8881
-
(2009)
Angew. Chem.
, vol.121
, pp. 8881
-
-
Tlili, A.1
Xia, N.2
Monnier, F.3
Taillefer, M.4
-
38
-
-
78649626773
-
-
Selected examples of metal-free N-arylations
-
Selected examples of metal-free N-arylations
-
-
-
-
39
-
-
33947466604
-
-
J. D. Roberts, D. A. Semenow, H. E. Simmons Jr., L. A. Carlsmith, J. Am. Chem. Soc. 1956, 78, 601
-
(1956)
J. Am. Chem. Soc.
, vol.78
, pp. 601
-
-
Roberts, J.D.1
Semenow, D.A.2
Simmons Jr., H.E.3
Carlsmith, L.A.4
-
41
-
-
33947333255
-
-
H. Bader, A. R. Hansen, F. J. McCarty, J. Org. Chem. 1966, 31, 2319
-
(1966)
J. Org. Chem.
, vol.31
, pp. 2319
-
-
Bader, H.1
Hansen, A.R.2
McCarty, F.J.3
-
42
-
-
0035936728
-
-
M. Beller, C. Breindl, R. H. Riermeier, A. Tillack, J. Org. Chem. 2001, 66, 1403
-
(2001)
J. Org. Chem.
, vol.66
, pp. 1403
-
-
Beller, M.1
Breindl, C.2
Riermeier, R.H.3
Tillack, A.4
-
43
-
-
0345255658
-
-
L. Shi, M. Wang, C.-A. Fan, F.-M. Zhang, Y.-Q. Tu, Org. Lett. 2003, 5, 3515
-
(2003)
Org. Lett.
, vol.5
, pp. 3515
-
-
Shi, L.1
Wang, M.2
Fan, C.-A.3
Zhang, F.-M.4
Tu, Y.-Q.5
-
44
-
-
4143053592
-
-
R. Varala, E. Ramu, M. M. Alam, S. R. Adapa, Synlett 2004, 1747
-
(2004)
Synlett
, pp. 1747
-
-
Varala, R.1
Ramu, E.2
Alam, M.M.3
Adapa, S.R.4
-
47
-
-
77952398665
-
-
M. Poirier, S. Goudreau, J. Poulin, J. Savole, P. L. Beaulieu, Org. Lett. 2010, 12, 2334.
-
(2010)
Org. Lett.
, vol.12
, pp. 2334
-
-
Poirier, M.1
Goudreau, S.2
Poulin, J.3
Savole, J.4
Beaulieu, P.L.5
-
48
-
-
78649570171
-
-
Selected examples of metal-free O-arylations
-
Selected examples of metal-free O-arylations
-
-
-
-
52
-
-
0347176375
-
-
T. Yamatani, M. Yasunami, K. Takase, Tetrahedron Lett. 1970, 20, 1725
-
(1970)
Tetrahedron Lett.
, vol.20
, pp. 1725
-
-
Yamatani, T.1
Yasunami, M.2
Takase, K.3
-
55
-
-
78649545638
-
-
G. Bartoli, F. Ciminale, P. E. Todesco, J. Org. Chem. 1975, 40, 1975
-
(1975)
J. Org. Chem.
, vol.40
, pp. 1975
-
-
Bartoli, G.1
Ciminale, F.2
Todesco, P.E.3
-
57
-
-
78649577761
-
-
Selected examples of metal-free S-arylations
-
Selected examples of metal-free S-arylations
-
-
-
-
58
-
-
33947090254
-
-
J. S. Bradshaw, E. Y. Chen, R. H. Hales, J. A. South, J. Org. Chem. 1972, 37, 2051
-
(1972)
J. Org. Chem.
, vol.37
, pp. 2051
-
-
Bradshaw, J.S.1
Chen, E.Y.2
Hales, R.H.3
South, J.A.4
-
59
-
-
14844303984
-
-
R. Varala, E. Ramu, M. M. Alam, S. R. Adapa, Chem. Lett. 2004, 33, 1614.
-
(2004)
Chem. Lett.
, vol.33
, pp. 1614
-
-
Varala, R.1
Ramu, E.2
Alam, M.M.3
Adapa, S.R.4
-
60
-
-
78649576217
-
-
Selected examples of metal-free C-arylations
-
Selected examples of metal-free C-arylations
-
-
-
-
61
-
-
0038818627
-
-
R. Zhang, F. Zhao, M. Sato, Y. Ikushima, Chem. Commun. 2003, 1548
-
(2003)
Chem. Commun.
, pp. 1548
-
-
Zhang, R.1
Zhao, F.2
Sato, M.3
Ikushima, Y.4
-
62
-
-
0141630561
-
-
F. Li, Q. Wang, Z. Ding, F. Tao, Org. Lett. 2003, 5, 2169
-
(2003)
Org. Lett.
, vol.5
, pp. 2169
-
-
Li, F.1
Wang, Q.2
Ding, Z.3
Tao, F.4
-
63
-
-
58449085051
-
-
S. Yanagisawa, K. Ueda, T. Taniguchi, K. Itami, Org. Lett. 2008, 10, 4673
-
(2008)
Org. Lett.
, vol.10
, pp. 4673
-
-
Yanagisawa, S.1
Ueda, K.2
Taniguchi, T.3
Itami, K.4
-
65
-
-
78049346852
-
-
DOI: 10.1021/ja103050x
-
W. Liu, H. Cao, H. Zhang, H. Zhang, K. H. Chung, C. He, H. Wang, F. Y. Kwong, A. Lei, J. Am. Chem. Soc. 2010, 132, 0000, DOI: 10.1021/ja103050x.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 0000
-
-
Liu, W.1
Cao, H.2
Zhang, H.3
Zhang, H.4
Chung, K.H.5
He, C.6
Wang, H.7
Kwong, F.Y.8
Lei, A.9
-
66
-
-
0003467672
-
-
3rd edn., Wiley-Interscience, New York, p
-
J. March, Advanced Organic Chemistry, 3rd edn., Wiley-Interscience, New York, 1985, p 576.
-
(1985)
Advanced Organic Chemistry
, pp. 576
-
-
March, J.1
-
69
-
-
84943884675
-
-
C. F. Bernasconi, M. Kaufmann, H. Zollinger, Helv. Chim. Acta 1966, 49, 2563.
-
(1966)
Helv. Chim. Acta
, vol.49
, pp. 2563
-
-
Bernasconi, C.F.1
Kaufmann, M.2
Zollinger, H.3
-
70
-
-
0000264238
-
-
(Eds.: B.M. Trost, I. Fleming), Pergamon Press, p
-
For reviews see S. V. Kessar, in: Comprehensive Organic Synthesis, Vol. 4, (Eds.:, B.M. Trost, I. Fleming,), Pergamon Press, 1991, p 483
-
(1991)
Comprehensive Organic Synthesis
, vol.4
, pp. 483
-
-
Kessar, S.V.1
-
72
-
-
0010954389
-
-
For a review, see:, and references therein
-
For a review, see:, B. A. Trofimov, Sulfur Rep. 1992, 11, 207 and references therein.
-
(1992)
Sulfur Rep.
, vol.11
, pp. 207
-
-
Trofimov, B.A.1
-
73
-
-
0344039811
-
-
For reviews see P. A. A. Klusener, L. Brandsma, H. D. Verkruijsse, P. von R. Schleyer, T. Friedl, R. Pi, Angew. Chem. 1986, 98, 458
-
(1986)
Angew. Chem.
, vol.98
, pp. 458
-
-
Klusener, P.A.A.1
Brandsma, L.2
Verkruijsse, H.D.3
Schleyer, P.V.R.4
Friedl, T.5
Pi, R.6
-
75
-
-
84987246060
-
-
L. Brandsma, A. G. Mal'kina, L. Lochmann, P. V. Schleyer, Recl. Trav. Chim. Pays-Bas 1994, 113, 529
-
(1994)
Recl. Trav. Chim. Pays-Bas
, vol.113
, pp. 529
-
-
Brandsma, L.1
Mal'kina, A.G.2
Lochmann, L.3
Schleyer, P.V.4
-
77
-
-
0000308330
-
-
For the use of superbases in organocatalysis, see
-
P. Caubere, Chem. Rev. 1993, 93, 2317. For the use of superbases in organocatalysis, see
-
(1993)
Chem. Rev.
, vol.93
, pp. 2317
-
-
Caubere, P.1
-
78
-
-
84889285302
-
-
(Ed. T. Ishikawa), John Wiley and Sons, Ltd., West Sussex, UK
-
Superbases for Organic Synthesis, (Ed., T. Ishikawa,), John Wiley and Sons, Ltd., West Sussex, UK, 2009.
-
(2009)
Superbases for Organic Synthesis
-
-
-
79
-
-
78649565408
-
-
Recently, cross-couplings with ppm quantities of metal salts have been reported. For examples, see
-
Recently, cross-couplings with ppm quantities of metal salts have been reported. For examples, see
-
-
-
-
82
-
-
71949123493
-
-
P.-F. Larsson, A. Correa, M. Carril, P.-O. Norrby, C. Bolm, Angew. Chem. 2009, 121, 5801
-
(2009)
Angew. Chem.
, vol.121
, pp. 5801
-
-
Larsson, P.-F.1
Correa, A.2
Carril, M.3
Norrby, P.-O.4
Bolm, C.5
-
85
-
-
77954811022
-
-
2O 8ppm of Pd, <1ppm of Cu, 1ppm of Ni. From all available data we have no indication that such trace metal amounts have an effect on the reported transformations under the given conditions
-
2O 8ppm of Pd, <1ppm of Cu, 1ppm of Ni. From all available data we have no indication that such trace metal amounts have an effect on the reported transformations under the given conditions.
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1577
-
-
Bonnamour, J.1
Piedrafita, M.2
Bolm, C.3
-
86
-
-
77952403309
-
-
While this manuscript was in preparation, a related system for C-S cross-couplings based on the use of KOH and polyethylene glycol was reported
-
While this manuscript was in preparation, a related system for C-S cross-couplings based on the use of KOH and polyethylene glycol was reported., Z. Duan, S. Ranjit, X. Liu, Org. Lett. 2010, 12, 2430.
-
(2010)
Org. Lett.
, vol.12
, pp. 2430
-
-
Duan, Z.1
Ranjit, S.2
Liu, X.3
-
87
-
-
78649568407
-
-
3)
-
3).
-
-
-
-
88
-
-
78649564403
-
-
Rao reported the formation of diphenyl disulfide under these conditions
-
Rao reported the formation of diphenyl disulfide under these conditions.
-
-
-
-
89
-
-
78649578735
-
-
2O in DMSO at 120°C starting from aryl halides and thiols
-
2O in DMSO at 120°C starting from aryl halides and thiols.
-
-
-
-
91
-
-
0001240204
-
-
F. G. Bordwell, R. J. McCallum, W. N. Olmstead, J. Org. Chem. 1984, 49, 1424
-
(1984)
J. Org. Chem.
, vol.49
, pp. 1424
-
-
Bordwell, F.G.1
McCallum, R.J.2
Olmstead, W.N.3
-
92
-
-
33847086202
-
-
W. N. Olmstead, Z. Margolin, F. G. Bordwell, J. Org. Chem. 1980, 45, 3295
-
(1980)
J. Org. Chem.
, vol.45
, pp. 3295
-
-
Olmstead, W.N.1
Margolin, Z.2
Bordwell, F.G.3
-
95
-
-
0000564185
-
-
F. G. Bordwell, G. E. Drucker, H. E. Fried, J. Org. Chem. 1981, 46, 632.
-
(1981)
J. Org. Chem.
, vol.46
, pp. 632
-
-
Bordwell, F.G.1
Drucker, G.E.2
Fried, H.E.3
-
96
-
-
0012724767
-
-
For a discussion on the formation of aryl methyl thioethers in reactions of halonaphthalenes with tert-butoxide in a tert-butanol/DMSO medium at 140°C, see:,. Also in reactions of iodobenzene with allyl alcohol, allylamine or dimethyl sulfide in KOH/DMSO mixtures at elevated temperatures we detected thioethers
-
For a discussion on the formation of aryl methyl thioethers in reactions of halonaphthalenes with tert-butoxide in a tert-butanol/DMSO medium at 140°C, see:, R. H. Hales, J. S. Bradshaw, D. R. Pratt, J. Org. Chem. 1971, 36, 314. Also in reactions of iodobenzene with allyl alcohol, allylamine or dimethyl sulfide in KOH/DMSO mixtures at elevated temperatures we detected thioethers.
-
(1971)
J. Org. Chem.
, vol.36
, pp. 314
-
-
Hales, R.H.1
Bradshaw, J.S.2
Pratt, D.R.3
-
97
-
-
15444370706
-
-
For selected examples of metal-free C-X bond formation leading to heterocyclic compounds see A. Correa, I. Tellitu, E. Domínguez, I. Moreno, R. SanMartin, J. Org. Chem. 2005, 70, 2256
-
(2005)
J. Org. Chem.
, vol.70
, pp. 2256
-
-
Correa, A.1
Tellitu, I.2
Domínguez, E.3
Moreno, I.4
Sanmartin, R.5
-
98
-
-
33750025600
-
-
A. Correa, I. Tellitu, E. Domínguez, R. SanMartin, J. Org. Chem. 2006, 71, 8316
-
(2006)
J. Org. Chem.
, vol.71
, pp. 8316
-
-
Correa, A.1
Tellitu, I.2
Domínguez, E.3
Sanmartin, R.4
-
99
-
-
77954548154
-
-
E. Feng, H. Huang, Y. Zhou, D. Ye, H. Jiang, H. Liu, J. Comb. Chem. 2010, 12, 422
-
(2010)
J. Comb. Chem.
, vol.12
, pp. 422
-
-
Feng, E.1
Huang, H.2
Zhou, Y.3
Ye, D.4
Jiang, H.5
Liu, H.6
-
101
-
-
67149108356
-
-
N. Barbero, R. SanMartin, E. Domínguez, Tetrahedron 2009, 65, 5729
-
(2009)
Tetrahedron
, vol.65
, pp. 5729
-
-
Barbero, N.1
Sanmartin, R.2
Domínguez, E.3
-
102
-
-
58049208387
-
-
R. Martínez, D. J. Ramón, M. Yus, J. Org. Chem. 2008, 73, 9778
-
(2008)
J. Org. Chem.
, vol.73
, pp. 9778
-
-
Martínez, R.1
Ramón, D.J.2
Yus, M.3
-
103
-
-
70449586102
-
-
Y.-X. Chen, L.-F. Qian, W. Zhang, B. Han, Angew. Chem. 2008, 120, 9470
-
(2008)
Angew. Chem.
, vol.120
, pp. 9470
-
-
Chen, Y.-X.1
Qian, L.-F.2
Zhang, W.3
Han, B.4
-
105
-
-
0042367613
-
-
J. Barluenga, H. Vázquez-Villa, A. Ballesteros, J. M. González, J. Am. Chem. Soc. 2003, 125, 9028.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 9028
-
-
Barluenga, J.1
Vázquez-Villa, H.2
Ballesteros, A.3
González, J.M.4
-
106
-
-
78649626772
-
-
3 in DMF at 135°C the un-catalyzed cyclization of 7b gave 8 in 42% yield. At 120°C only trace of 8 were found under those conditions
-
3 in DMF at 135°C the un-catalyzed cyclization of 7b gave 8 in 42% yield. At 120°C only trace of 8 were found under those conditions., J. Bonnamour, C. Bolm, Org. Lett. 2008, 10, 2667.
-
(2008)
Org. Lett.
, vol.10
, pp. 2667
-
-
Bonnamour, J.1
Bolm, C.2
-
107
-
-
78649613384
-
-
[3,4] In some of these studies, DMSO/KOH was reported as being the only successful solvent/base combination. The results presented here demonstrate that under those conditions particular care should be taken and that possible metal-free "background" reactions mediated by the superbase KOH/DMSO should be considered
-
[3,4] In some of these studies, DMSO/KOH was reported as being the only successful solvent/base combination. The results presented here demonstrate that under those conditions particular care should be taken and that possible metal-free "background" reactions mediated by the superbase KOH/DMSO should be considered.
-
-
-
-
108
-
-
23044453131
-
-
J. Clayden, H. Turner, M. Pickworth, T. Adler, Org. Lett. 2005, 7, 3147.
-
(2005)
Org. Lett.
, vol.7
, pp. 3147
-
-
Clayden, J.1
Turner, H.2
Pickworth, M.3
Adler, T.4
-
109
-
-
72549099177
-
-
J. M. Travins, R. C. Bernotas, D. H. Kaufman, E. Quinet, P. Nambi, I. Feingold, C. Huselton, A. Wilhelmsson, A. Goos-Nilsson, J. Wrobel, Bioorg. Med. Chem. Lett. 2010, 20, 526.
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 526
-
-
Travins, J.M.1
Bernotas, R.C.2
Kaufman, D.H.3
Quinet, E.4
Nambi, P.5
Feingold, I.6
Huselton, C.7
Wilhelmsson, A.8
Goos-Nilsson, A.9
Wrobel, J.10
|