-
1
-
-
85042994825
-
-
Selected reviews
-
Selected reviews:
-
-
-
-
3
-
-
78149432679
-
-
A. Zamfir, S. Schenker, M. Freund, B. S. Tsogoeva, Org. Biomol. Chem. 2010, 8, 5262–5276;
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 5262-5276
-
-
Zamfir, A.1
Schenker, S.2
Freund, M.3
Tsogoeva, B.S.4
-
4
-
-
80053992962
-
-
M. Rueping, A. Kuenkel, I. Atodiresei, Chem. Soc. Rev. 2011, 40, 4539–4549;
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 4539-4549
-
-
Rueping, M.1
Kuenkel, A.2
Atodiresei, I.3
-
5
-
-
84908249055
-
-
D. Parmar, E. Sugiono, S. Raja, M. Rueping, Chem. Rev. 2014, 114, 9047–9153.
-
(2014)
Chem. Rev.
, vol.114
, pp. 9047-9153
-
-
Parmar, D.1
Sugiono, E.2
Raja, S.3
Rueping, M.4
-
6
-
-
85043017734
-
-
For selected examples, see
-
For selected examples, see:
-
-
-
-
8
-
-
0040017910
-
-
P. J. Lu, X. Z. Zhou, M. H. Shen, K. P. Lu, Science 1999, 283, 1325–1328.
-
(1999)
Science
, vol.283
, pp. 1325-1328
-
-
Lu, P.J.1
Zhou, X.Z.2
Shen, M.H.3
Lu, K.P.4
-
9
-
-
85042954261
-
-
Selected reviews
-
Selected reviews:
-
-
-
-
10
-
-
0034614490
-
-
T. Hunter, Cell 2000, 100, 113–127;
-
(2000)
Cell
, vol.100
, pp. 113-127
-
-
Hunter, T.1
-
12
-
-
85042978507
-
-
Selected examples
-
Selected examples:
-
-
-
-
13
-
-
81355138382
-
-
A. Dermenci, P. S. Selig, R. A. Domaoal, K. A. Spasov, K. S. Anderson, S. J. Miller, Chem. Sci. 2011, 2, 1568–1572;
-
(2011)
Chem. Sci.
, vol.2
, pp. 1568-1572
-
-
Dermenci, A.1
Selig, P.S.2
Domaoal, R.A.3
Spasov, K.A.4
Anderson, K.S.5
Miller, S.J.6
-
15
-
-
85043002237
-
-
Selected reports
-
Selected reports:
-
-
-
-
16
-
-
33746269442
-
-
M. Rueping, A. P. Antonchick, T. Theissmann, Angew. Chem. Int. Ed. 2006, 45, 3683–3686;
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 3683-3686
-
-
Rueping, M.1
Antonchick, A.P.2
Theissmann, T.3
-
17
-
-
33750175116
-
-
Angew. Chem. 2006, 118, 3765–3768;
-
(2006)
Angew. Chem.
, vol.118
, pp. 3765-3768
-
-
-
18
-
-
38349018738
-
-
Q. S. Guo, D. M. Du, J. T. Xu, Angew. Chem. Int. Ed. 2008, 47, 759–762;
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 759-762
-
-
Guo, Q.S.1
Du, D.M.2
Xu, J.T.3
-
19
-
-
53549126171
-
-
Angew. Chem. 2008, 120, 771–774;
-
(2008)
Angew. Chem.
, vol.120
, pp. 771-774
-
-
-
20
-
-
77955656206
-
-
M. Rueping, M. Stoechel, E. Sugiono, T. Theissmann, Tetrahedron 2010, 66, 6565–6568;
-
(2010)
Tetrahedron
, vol.66
, pp. 6565-6568
-
-
Rueping, M.1
Stoechel, M.2
Sugiono, E.3
Theissmann, T.4
-
21
-
-
80052692148
-
-
M. Rueping, T. Theissmann, M. Stoeckel, A. P. Antonchick, Org. Biomol. Chem. 2011, 9, 6844–6850;
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 6844-6850
-
-
Rueping, M.1
Theissmann, T.2
Stoeckel, M.3
Antonchick, A.P.4
-
22
-
-
84879462165
-
-
X. F. Cai, M. W. Chen, Z. S. Ye, R. N. Guo, L. Shi, Y. Q. Li, Y. G. Zhou, Chem. Asian J. 2013, 8, 1381–1385;
-
(2013)
Chem. Asian J.
, vol.8
, pp. 1381-1385
-
-
Cai, X.F.1
Chen, M.W.2
Ye, Z.S.3
Guo, R.N.4
Shi, L.5
Li, Y.Q.6
Zhou, Y.G.7
-
23
-
-
84890793338
-
-
J. Stemper, K. Isaac, J. Pastor, G. Frison, P. Retailleau, A. Voituriez, J. F. Betzer, A. Marinetti, Adv. Synth. Catal. 2013, 355, 3613–3624;
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 3613-3624
-
-
Stemper, J.1
Isaac, K.2
Pastor, J.3
Frison, G.4
Retailleau, P.5
Voituriez, A.6
Betzer, J.F.7
Marinetti, A.8
-
24
-
-
84902085643
-
-
A. Aillerie, V. Lemau de Talancé, A. Moncomble, T. Bousquet, L. Pélinski, Org. Lett. 2014, 16, 2982–2985;
-
(2014)
Org. Lett.
, vol.16
, pp. 2982-2985
-
-
Aillerie, A.1
Lemau de Talancé, V.2
Moncomble, A.3
Bousquet, T.4
Pélinski, L.5
-
25
-
-
84900854230
-
-
X. F. Cai, R. N. Guo, G. S. Feng, B. Wu, Y. G. Zhou, Org. Lett. 2014, 16, 2680–2683.
-
(2014)
Org. Lett.
, vol.16
, pp. 2680-2683
-
-
Cai, X.F.1
Guo, R.N.2
Feng, G.S.3
Wu, B.4
Zhou, Y.G.5
-
26
-
-
85043011851
-
-
Selected reports of asymmetric reductions of 1,10-disubstituted phenanthrolines
-
Selected reports of asymmetric reductions of 1,10-disubstituted phenanthrolines:
-
-
-
-
27
-
-
0036828173
-
-
K. Skupinska, E. J. McEachern, R. T. Skerlj, G. J. Bridgr, J. Org. Chem. 2002, 67, 7890–7893;
-
(2002)
J. Org. Chem.
, vol.67
, pp. 7890-7893
-
-
Skupinska, K.1
McEachern, E.J.2
Skerlj, R.T.3
Bridgr, G.J.4
-
29
-
-
84880153569
-
-
T. Wang, F. Chen, J. Qin, Y.-M. He, Q.-H. Fan, Angew. Chem. Int. Ed. 2013, 52, 7172–7176;
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 7172-7176
-
-
Wang, T.1
Chen, F.2
Qin, J.3
He, Y.-M.4
Fan, Q.-H.5
-
30
-
-
84885968565
-
-
Angew. Chem. 2013, 125, 7313–7317.
-
(2013)
Angew. Chem.
, vol.125
, pp. 7313-7317
-
-
-
31
-
-
85042974823
-
-
Seminal reports
-
Seminal reports:
-
-
-
-
33
-
-
2342570203
-
-
T. Akiyama, J. Itoh, K. Yokota, K. Fuchibe, Angew. Chem. Int. Ed. 2004, 43, 1566–1568;
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 1566-1568
-
-
Akiyama, T.1
Itoh, J.2
Yokota, K.3
Fuchibe, K.4
-
34
-
-
6044226554
-
-
Angew. Chem. 2004, 116, 1592–1594.
-
(2004)
Angew. Chem.
, vol.116
, pp. 1592-1594
-
-
-
35
-
-
78650359625
-
-
F. Xu, D. Huang, C. Han, W. Shen, X. Lin, Y. Wang, J. Org. Chem. 2010, 75, 8677–8680;
-
(2010)
J. Org. Chem.
, vol.75
, pp. 8677-8680
-
-
Xu, F.1
Huang, D.2
Han, C.3
Shen, W.4
Lin, X.5
Wang, Y.6
-
36
-
-
27844464898
-
-
G. B. Rowland, H. Zhang, E. B. Rowland, S. Chennamadhavuni, Y. Wang, J. C. Antilla, J. Am. Chem. Soc. 2005, 127, 15696–15697.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15696-15697
-
-
Rowland, G.B.1
Zhang, H.2
Rowland, E.B.3
Chennamadhavuni, S.4
Wang, Y.5
Antilla, J.C.6
-
41
-
-
60549099364
-
-
N. Vale, R. Moreira, P. Gomes, Eur. J. Med. Chem. 2009, 44, 937–953;
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 937-953
-
-
Vale, N.1
Moreira, R.2
Gomes, P.3
-
42
-
-
77954309291
-
-
K. Kaur, M. Jain, R. P. Reddy, R. Jain, Eur. J. Med. Chem. 2010, 45, 3245–3264;
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 3245-3264
-
-
Kaur, K.1
Jain, M.2
Reddy, R.P.3
Jain, R.4
-
43
-
-
84857769077
-
-
M. Delves, D. Plouffe, C. Scheurer, S. Meister, S. Wittlin, E. A. Winzeler, R. E. Sinden, D. Lerory, PLOS Med. 2012, 9, e1001169.
-
(2012)
PLOS Med.
, vol.9
, pp. 1001169
-
-
Delves, M.1
Plouffe, D.2
Scheurer, C.3
Meister, S.4
Wittlin, S.5
Winzeler, E.A.6
Sinden, R.E.7
Lerory, D.8
-
44
-
-
0035800352
-
-
M. M. Vasbinder, E. R. Jarvo, S. J. Miller, Angew. Chem. Int. Ed. 2001, 40, 2824–2827;
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 2824-2827
-
-
Vasbinder, M.M.1
Jarvo, E.R.2
Miller, S.J.3
-
45
-
-
0000142558
-
-
Angew. Chem. 2001, 113, 2906–2909;
-
(2001)
Angew. Chem.
, vol.113
, pp. 2906-2909
-
-
-
46
-
-
84907942517
-
-
D. K. Romney, S. M. Colvin, S. J. Miller, J. Am. Chem. Soc. 2014, 136, 14019–14022.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 14019-14022
-
-
Romney, D.K.1
Colvin, S.M.2
Miller, S.J.3
-
48
-
-
38349112828
-
-
E. A. Colby Davie, S. M. Mennen, Y. Xu, S. J. Miller, Chem. Rev. 2007, 107, 5759–5812.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5759-5812
-
-
Colby Davie, E.A.1
Mennen, S.M.2
Xu, Y.3
Miller, S.J.4
-
49
-
-
0000089981
-
-
G. T. Copeland, E. R. Jarvo, S. J. Miller, J. Org. Chem. 1998, 63, 6784–6785.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 6784-6785
-
-
Copeland, G.T.1
Jarvo, E.R.2
Miller, S.J.3
-
51
-
-
85042992529
-
-
See the Supporting Information for structure and details. CCDC 1412999 (7 f) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre
-
See the Supporting Information for structure and details. CCDC 1412999 (7 f) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre.
-
-
-
-
52
-
-
85042982909
-
-
The singlet at 8.7 ppm corresponds to the aromatic CH of HEox, thus showing that, 5 e, converts HEH to HEox.
-
The singlet at 8.7 ppm corresponds to the aromatic CH of HEox, thus showing that 5 e converts HEH to HEox.
-
-
-
-
53
-
-
84989040046
-
-
G. Barbieri, R. Benassi, P. Lazzeretti, L. Schenetti, F. Taddei, Org. Magn. Resonance 1975, 7, 451–454.
-
(1975)
Org. Magn. Resonance
, vol.7
, pp. 451-454
-
-
Barbieri, G.1
Benassi, R.2
Lazzeretti, P.3
Schenetti, L.4
Taddei, F.5
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