-
1
-
-
0029837557
-
-
Sträter, N.; Lipscomb, W. N.; Klabunde, T.; Krebs, B. Angew. Chem., Int. Ed. 1996, 35, 2024.
-
(1996)
Angew. Chem., Int. Ed
, vol.35
, pp. 2024
-
-
Sträter, N.1
Lipscomb, W.N.2
Klabunde, T.3
Krebs, B.4
-
2
-
-
5344224096
-
-
Selected examples on chiral bimetallic catalysts: Review: a
-
Review: (a) Ma, J.-A.; Cahard, D. Angew. Chem., Int. Ed. 2004, 43, 4566. Selected examples on chiral bimetallic catalysts:
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 4566
-
-
Ma, J.-A.1
Cahard, D.2
-
3
-
-
23944488799
-
-
(b) Lundgren, S.; Wingstrand, E.; Penhoat, M.; Moberg, C. J. Am. Chem. Soc. 2005, 127, 11592.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 11592
-
-
Lundgren, S.1
Wingstrand, E.2
Penhoat, M.3
Moberg, C.4
-
4
-
-
29244443974
-
-
(c) Kanai, M.; Kato, N.; Ichikawa, E.; Shibasaki, M. Pure Appl. Chem. 2005, 77, 2047.
-
(2005)
Pure Appl. Chem
, vol.77
, pp. 2047
-
-
Kanai, M.1
Kato, N.2
Ichikawa, E.3
Shibasaki, M.4
-
5
-
-
45549083087
-
-
(d) Handa, S.; Nagawa, K.; Sohtome, Y.; Matsunaga, S.; Shibasaki, M. Angew. Chem., Int. Ed. 2008, 47, 3230.
-
(2008)
Angew. Chem., Int. Ed
, vol.47
, pp. 3230
-
-
Handa, S.1
Nagawa, K.2
Sohtome, Y.3
Matsunaga, S.4
Shibasaki, M.5
-
7
-
-
0029798420
-
-
(a) Hansen, K. B.; Leighton, J. L.; Jacobsen, E. N. J. Am. Chem. Soc. 1996, 118, 10924.
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 10924
-
-
Hansen, K.B.1
Leighton, J.L.2
Jacobsen, E.N.3
-
8
-
-
0030860279
-
-
(b) Tokunaga, M.; Larrow, J. F.; Kakiuchi, F.; Jacobsen, E. N. Science 1997, 277, 936.
-
(1997)
Science
, vol.277
, pp. 936
-
-
Tokunaga, M.1
Larrow, J.F.2
Kakiuchi, F.3
Jacobsen, E.N.4
-
9
-
-
1042265088
-
-
Detailed mechanistic study, see: c
-
Detailed mechanistic study, see: (c) Nielsen, L. P. C.; Stevenson, C. P.; Blackmond, D. G.; Jacobsen, E. N. J. Am. Chem. Soc. 2004, 126, 1360.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 1360
-
-
Nielsen, L.P.C.1
Stevenson, C.P.2
Blackmond, D.G.3
Jacobsen, E.N.4
-
10
-
-
0032556244
-
-
(a) Konsler, R. G.; Karl, J.; Jacobsen, E. N. J. Am. Chem. Soc. 1998, 120, 10780.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 10780
-
-
Konsler, R.G.1
Karl, J.2
Jacobsen, E.N.3
-
11
-
-
0037091011
-
-
(b) Ready, J. M.; Jacobsen, E. N. Angew. Chem., Int. Ed. 2002, 41, 1374.
-
(2002)
Angew. Chem., Int. Ed
, vol.41
, pp. 1374
-
-
Ready, J.M.1
Jacobsen, E.N.2
-
12
-
-
0034675617
-
-
(c) Breinbauer, R.; Jacobsen, E. N. Angew. Chem., Int. Ed. 2000, 39, 3604.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 3604
-
-
Breinbauer, R.1
Jacobsen, E.N.2
-
14
-
-
33846783022
-
-
(e) Zheng, X.; Jones, C. W.; Week, M. J. Am. Chem. Soc. 2007, 129, 1105.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 1105
-
-
Zheng, X.1
Jones, C.W.2
Week, M.3
-
15
-
-
8444229360
-
-
(f) Gianneschi, N. C.; Cho, S.-H.; Nguyen, S. T.; Mirkin, C. A. Angew. Chem., Int. Ed. 2004, 43, 5503.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 5503
-
-
Gianneschi, N.C.1
Cho, S.-H.2
Nguyen, S.T.3
Mirkin, C.A.4
-
16
-
-
1242293781
-
-
Reviews on supramolecular catalysts: a
-
Reviews on supramolecular catalysts: (a) Cacciapaglia, R.; Di Stefano, S.; Mandolini, L. Acc. Chem. Res. 2004, 37, 113.
-
(2004)
Acc. Chem. Res
, vol.37
, pp. 113
-
-
Cacciapaglia, R.1
Di Stefano, S.2
Mandolini, L.3
-
18
-
-
1242289460
-
-
Selected examples of supramolecular catalysts using hydrogen-bonding interactions: (a) Ohshima, S.; Tamura, N.; Nabeshima, T.; Yano, Y. Chem. Commun. 1993, 712.
-
Selected examples of supramolecular catalysts using hydrogen-bonding interactions: (a) Ohshima, S.; Tamura, N.; Nabeshima, T.; Yano, Y. Chem. Commun. 1993, 712.
-
-
-
-
22
-
-
17044413342
-
-
(e) Breit, B.; Seiche, W. Angew. Chem., Int. Ed. 2005, 44, 1640.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 1640
-
-
Breit, B.1
Seiche, W.2
-
23
-
-
33645473788
-
-
(f) Weis, M.; Waloch, C.; Seiche, W.; Breit, B. J. Am. Chem. Soc. 2006, 128, 4188.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 4188
-
-
Weis, M.1
Waloch, C.2
Seiche, W.3
Breit, B.4
-
25
-
-
33746334741
-
-
(h) Shi, L.; Wang, X.; Sandoval, C. A.; Li, M.; Qi, Q.; Li, Z.; Ding, K. Angew. Chem., Int. Ed. 2006, 45, 4108.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 4108
-
-
Shi, L.1
Wang, X.2
Sandoval, C.A.3
Li, M.4
Qi, Q.5
Li, Z.6
Ding, K.7
-
26
-
-
33646743586
-
-
(i) Jonsson, S.; Odille, F. G. J.; Norrby, P.-O.; Wärnmark, K. Org. Biomol. Chem. 2006, 4, 1927.
-
(2006)
Org. Biomol. Chem
, vol.4
, pp. 1927
-
-
Jonsson, S.1
Odille, F.G.J.2
Norrby, P.-O.3
Wärnmark, K.4
-
27
-
-
33846684924
-
-
(j) Clarke, M. L.; Fuentes, J. A. Angew. Chem., Int. Ed. 2007, 46, 930.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 930
-
-
Clarke, M.L.1
Fuentes, J.A.2
-
28
-
-
0000138939
-
-
Symmetrical salens are expected to form oligomeric or polymeric aggregates due to their arrays of hydrogen-bonding donors and acceptors. See: Ducharme, Y, Wuest, J. D. J. Org. Chem. 1988, 53, 5787
-
Symmetrical salens are expected to form oligomeric or polymeric aggregates due to their arrays of hydrogen-bonding donors and acceptors. See: Ducharme, Y.; Wuest, J. D. J. Org. Chem. 1988, 53, 5787.
-
-
-
-
29
-
-
57549084127
-
-
See Supporting Information for experimental details
-
See Supporting Information for experimental details.
-
-
-
-
30
-
-
8444252168
-
-
Recent reviews: a
-
Recent reviews: (a) Palomo, C.; Oiarbide, M.; Mielgo, A. Angew. Chem., Int. Ed. 2004, 43, 5442.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 5442
-
-
Palomo, C.1
Oiarbide, M.2
Mielgo, A.3
-
31
-
-
33846593979
-
-
(b) Boruwa, J.; Gogoi, N.; Saikia, P. P.; Barua, N. C. Tetrahedron: Asymmetry 2006, 17, 3315.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 3315
-
-
Boruwa, J.1
Gogoi, N.2
Saikia, P.P.3
Barua, N.C.4
-
33
-
-
4444257618
-
-
(a) Kogami, Y.; Nakajima, T.; Ikeno, T.; Yamada, T. Synthesis 2004, 1947.
-
(2004)
Synthesis
, pp. 1947
-
-
Kogami, Y.1
Nakajima, T.2
Ikeno, T.3
Yamada, T.4
-
34
-
-
36148983364
-
-
(b) Kowalczyk, R.; Sidorowicz, Ł.; Skarżewski, J. Tetrahedron: Asymmetry 2007, 18, 2581.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2581
-
-
Kowalczyk, R.1
Sidorowicz, Ł.2
Skarżewski, J.3
-
35
-
-
57549115658
-
-
The oxidation state of the catalytically active Co species is not clear at this point. More detailed mechanistic study is needed. See ref 3c
-
The oxidation state of the catalytically active Co species is not clear at this point. More detailed mechanistic study is needed. See ref 3c.
-
-
-
-
36
-
-
57549087806
-
-
The formation of a strong heterodimeric species (1b+1c) with two symmetrical structures is more challenging, because more precise control of the tether lengths and the torsion angle is necessary.
-
The formation of a strong heterodimeric species (1b+1c) with two symmetrical structures is more challenging, because more precise control of the tether lengths and the torsion angle is necessary.
-
-
-
-
37
-
-
0030922091
-
-
1H NMR spectroscopy to determine the dimerization constant of strong hydrogen-bonding dimers: (a) Wash, P. L.; Maverick, E.; Chiefari, J.; Lightner, D. A. J. Am. Chem. Soc. 1997, 119, 3802.
-
1H NMR spectroscopy to determine the dimerization constant of strong hydrogen-bonding dimers: (a) Wash, P. L.; Maverick, E.; Chiefari, J.; Lightner, D. A. J. Am. Chem. Soc. 1997, 119, 3802.
-
-
-
-
39
-
-
33646743972
-
-
(c) Lafitte, V. G. H.; Aliev, A. E.; Horton, P. N.; Hursthouse, M. B.; Bala, K.; Golding, P.; Halles, H. C. J. Am. Chem. Soc. 2006, 128, 6544.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 6544
-
-
Lafitte, V.G.H.1
Aliev, A.E.2
Horton, P.N.3
Hursthouse, M.B.4
Bala, K.5
Golding, P.6
Halles, H.C.7
-
40
-
-
57549101445
-
-
The NH signal of 2-pyridone was not observed due to the peak broadening in this solvent system.
-
The NH signal of 2-pyridone was not observed due to the peak broadening in this solvent system.
-
-
-
-
42
-
-
0032567217
-
-
(b) Sigel, R. K. O.; Freisinger, E.; Metzger, S.; Lippert, B. J. Am. Chem. Soc. 1998, 120, 12000.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 12000
-
-
Sigel, R.K.O.1
Freisinger, E.2
Metzger, S.3
Lippert, B.4
|