-
2
-
-
0014663969
-
-
Gotto, Antonio M.; Shore, B. Nature 1969, 224, 69.
-
Gotto, Antonio M.; Shore, B. Nature 1969, 224, 69.
-
-
-
-
4
-
-
0034691565
-
-
(a) Maritan, A.; Micheletti, C.; Trovato, A.; Banavar, J. R. Nature 2000, 406, 287.
-
(2000)
Nature
, vol.406
, pp. 287
-
-
Maritan, A.1
Micheletti, C.2
Trovato, A.3
Banavar, J.R.4
-
5
-
-
0033168451
-
-
(b) Zhu, S.; Liu, Y.; Rafailovich, M. H.; Sokolov, J.; Gersappe, D.; Winesett, D. A.; Ade, H. Nature 1999, 400, 49.
-
(1999)
Nature
, vol.400
, pp. 49
-
-
Zhu, S.1
Liu, Y.2
Rafailovich, M.H.3
Sokolov, J.4
Gersappe, D.5
Winesett, D.A.6
Ade, H.7
-
7
-
-
0031929837
-
-
(a) Rowan, A. E.; Nolte, R. J. M. Angew. Chem., Int. Ed. 1998, 37, 63.
-
(1998)
Angew. Chem., Int. Ed
, vol.37
, pp. 63
-
-
Rowan, A.E.1
Nolte, R.J.M.2
-
9
-
-
0032164163
-
-
(c) Amabilino, D. B.; Ramos, E.; Serrano, J.-L.; Veciana, J. Adv. Mater. 1998, 10, 1001.
-
(1998)
Adv. Mater
, vol.10
, pp. 1001
-
-
Amabilino, D.B.1
Ramos, E.2
Serrano, J.-L.3
Veciana, J.4
-
10
-
-
0032577361
-
-
(d) Cornelissen, J. J. L. M.; Fischer, M.; Sommerdijk, N. A. J. M.; Nolte, R. J. M. Science 1998, 280, 1427.
-
(1998)
Science
, vol.280
, pp. 1427
-
-
Cornelissen, J.J.L.M.1
Fischer, M.2
Sommerdijk, N.A.J.M.3
Nolte, R.J.M.4
-
11
-
-
0004074521
-
-
Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: Berlin
-
(a) Comprehensive Asymmetric Catalysts; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; Vol. 1-3.
-
(1999)
Comprehensive Asymmetric Catalysts
, vol.1-3
-
-
-
12
-
-
0003779363
-
-
Beller, M, Bolm, C, Ed, VCH; Weinheim, Germany
-
(b) Transition Metals for Organic Synthesis; Beller, M., Bolm, C., Ed.; VCH; Weinheim, Germany, 1998.
-
(1998)
Transition Metals for Organic Synthesis
-
-
-
14
-
-
0003544583
-
-
Ojima, I, Ed, VCH: New York, II
-
(d) Catalytic Asymmetric Synthesis: Ojima, I., Ed.; VCH: New York, 1993, 2000; Vol. 1, II.
-
(1993)
Catalytic Asymmetric Synthesis
, vol.1
-
-
-
16
-
-
22844441238
-
-
Zhang, J.; Albelda, M. T.; Liu, Y.; Canary, J. W. Chirality 2005, 17, 404.
-
(2005)
Chirality
, vol.17
, pp. 404
-
-
Zhang, J.1
Albelda, M.T.2
Liu, Y.3
Canary, J.W.4
-
17
-
-
0035980278
-
-
and references therein
-
Kobayashi, N.; Fukuda, T.; Ueno, K.; Ogino, H. J. Am. Chem. Soc. 2001, 123, 10740 and references therein.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 10740
-
-
Kobayashi, N.1
Fukuda, T.2
Ueno, K.3
Ogino, H.4
-
19
-
-
33747588552
-
-
and references therein
-
(b) Grote, Z.; Bonazzi, S.; Scopelliti, R.; Severin, K. J. Am. Chem. Soc. 2006, 128, 10382 and references therein.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 10382
-
-
Grote, Z.1
Bonazzi, S.2
Scopelliti, R.3
Severin, K.4
-
20
-
-
0033552261
-
-
This type of nonplanar topology can be found in the naturally occurring bilirubin and its synthetic analogues. However, the corresponding helical conformations are unstable. See, for example: Chen, Q, Huggins, M. T, Lightner, D. A, Norona, W, McDonagh, A. F. J. Am. Chem. Soc. 1999, 121, 9253 and references therein
-
This type of nonplanar topology can be found in the naturally occurring bilirubin and its synthetic analogues. However, the corresponding helical conformations are unstable. See, for example: Chen, Q.; Huggins, M. T.; Lightner, D. A.; Norona, W.; McDonagh, A. F. J. Am. Chem. Soc. 1999, 121, 9253 and references therein.
-
-
-
-
21
-
-
27544463710
-
-
(a) Soloshonok, V. A.; Cai, C.; Yamada, T.; Ueki, H.; Ohfune, Y.; Hruby, V. J. J. Am. Chem. Soc. 2005, 127, 15296.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 15296
-
-
Soloshonok, V.A.1
Cai, C.2
Yamada, T.3
Ueki, H.4
Ohfune, Y.5
Hruby, V.J.6
-
22
-
-
33750437425
-
-
(b) Ellis, T. K.; Ueki, H.; Yamada, T.; Ohfune, Y.; Soloshonok, V. A. J. Org. Chem. 2006, 71, 8572.
-
(2006)
J. Org. Chem
, vol.71
, pp. 8572
-
-
Ellis, T.K.1
Ueki, H.2
Yamada, T.3
Ohfune, Y.4
Soloshonok, V.A.5
-
23
-
-
0034930295
-
-
This reaction includes the reaction of the enolate, derived from 3, with molecular oxygen followed by the C-N bond cleavage, leading to the formation the tridentate ligands 4. For mechanistic details, see: (a) Ooi, T, Takeuchi, M, Ohara, D, Maruoka, K. Synlett 2001, 1185
-
This reaction includes the reaction of the enolate, derived from 3, with molecular oxygen followed by the C-N bond cleavage, leading to the formation the tridentate ligands 4. For mechanistic details, see: (a) Ooi, T.; Takeuchi, M.; Ohara, D.; Maruoka, K. Synlett 2001, 1185.
-
-
-
-
24
-
-
37049087681
-
-
(b) Easton, C. J.; Eichinger, S. K.; Pitt, M. J. J. Chem. Soc., Chem. Commun. 1992, 1295.
-
(1992)
J. Chem. Soc., Chem. Commun
, pp. 1295
-
-
Easton, C.J.1
Eichinger, S.K.2
Pitt, M.J.3
-
25
-
-
0030977240
-
-
(c) Easton, C. J.; Eichinger, S. K.; Pitt, M. J. Tetrahedron 1997, 53, 5609.
-
(1997)
Tetrahedron
, vol.53
, pp. 5609
-
-
Easton, C.J.1
Eichinger, S.K.2
Pitt, M.J.3
-
26
-
-
0036027102
-
-
(d) Bull, S. D.; Davis, S. G.; Garner, A. C.; O'Shea, M. D.; Savory, E. D.; Snow, E. J. J. Chem. Soc., Perkin Trans. 1 2002, 2442.
-
(2002)
J. Chem. Soc., Perkin Trans. 1
, pp. 2442
-
-
Bull, S.D.1
Davis, S.G.2
Garner, A.C.3
O'Shea, M.D.4
Savory, E.D.5
Snow, E.J.6
-
27
-
-
1242339721
-
-
(e) Green, B. J.; Tesfai, T. M.; Xie, Y.; Margerum, D. W. Inorg. Chem. 2004, 43, 1463.
-
(2004)
Inorg. Chem
, vol.43
, pp. 1463
-
-
Green, B.J.1
Tesfai, T.M.2
Xie, Y.3
Margerum, D.W.4
-
28
-
-
33847686640
-
-
On the nature of the Ni(II)-Ni(II) bond, see: Banks. C. V.; Anderson. S. J. Am. Chem. Soc. 1962, 84, 1486.
-
On the nature of the Ni(II)-Ni(II) bond, see: Banks. C. V.; Anderson. S. J. Am. Chem. Soc. 1962, 84, 1486.
-
-
-
-
29
-
-
0007843763
-
-
The range of the reported in literature Ni(II)-Ni(II) bonds is 2.38-2.81 Å. See. for example: Peng, S.-M.; Goedken, V. L. J. Am. Chem. Soc. 1976, 98, 8500 and references therein.
-
The range of the reported in literature Ni(II)-Ni(II) bonds is 2.38-2.81 Å. See. for example: Peng, S.-M.; Goedken, V. L. J. Am. Chem. Soc. 1976, 98, 8500 and references therein.
-
-
-
-
30
-
-
33847637488
-
-
See the Supporting Information
-
See the Supporting Information.
-
-
-
|