-
2
-
-
85052165526
-
-
Synthetic Chemistry of Stable Nitroxides (Eds.: L. B. Volodarsky, V. A. Reznikov, V. I. Ovcharenko), CRC Press, 1994.
-
b) Synthetic Chemistry of Stable Nitroxides (Eds.: L. B. Volodarsky, V. A. Reznikov, V. I. Ovcharenko), CRC Press, 1994.
-
-
-
-
3
-
-
0003439271
-
-
Ed, L. J. Berliner, Academic Press, New York
-
Spin Labeling: Theory and Application (Ed.: L. J. Berliner), vol. 2, Academic Press, New York, 1979.
-
(1979)
Spin Labeling: Theory and Application
, vol.2
-
-
-
5
-
-
36949035784
-
-
E. K. Y. Chen, D. Chan-Seng, P. O. Otieno, R. G. Hicks, M. K. Georges, Macromolecules 2007, 40, 8609.
-
(2007)
Macromolecules
, vol.40
, pp. 8609
-
-
Chen, E.K.Y.1
Chan-Seng, D.2
Otieno, P.O.3
Hicks, R.G.4
Georges, M.K.5
-
6
-
-
0034614865
-
-
For selected examples: a
-
For selected examples: a) D. J. R. Brook, S. Fornell, J. E. Stevens, B. Noll, T. H. Koch, W. Eisfeld, Inorg. Chem. 2000, 39, 562;
-
(2000)
Inorg. Chem
, vol.39
, pp. 562
-
-
Brook, D.J.R.1
Fornell, S.2
Stevens, J.E.3
Noll, B.4
Koch, T.H.5
Eisfeld, W.6
-
7
-
-
0038447968
-
-
b) J.-Z. Wu, E. Bouwman, J. Reedijk, A. M. Mills, A. L. Spek, Inorg. Chim. Acta 2003, 361, 326;
-
(2003)
Inorg. Chim. Acta
, vol.361
, pp. 326
-
-
Wu, J.-Z.1
Bouwman, E.2
Reedijk, J.3
Mills, A.M.4
Spek, A.L.5
-
8
-
-
33745662830
-
-
c) J. B. Gilroy, B. D. Koivisto, R. McDonald, M. J. Ferguson, R. G. Hicks, J. Mater. Chem. 2006, 16, 2618.
-
(2006)
J. Mater. Chem
, vol.16
, pp. 2618
-
-
Gilroy, J.B.1
Koivisto, B.D.2
McDonald, R.3
Ferguson, M.J.4
Hicks, R.G.5
-
9
-
-
0003916113
-
-
Eds, A. Padwa, W. H. Pearson, John Wiley & Sons, New York
-
Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Towards Heterocycles and Natural Products (Eds.: A. Padwa, W. H. Pearson), John Wiley & Sons, New York, 2002.
-
(2002)
Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Towards Heterocycles and Natural Products
-
-
-
10
-
-
50549178107
-
-
a) R. Huisgen, R. Fleischmann, A. Eckell, Tetrahedron Lett. 1960, 1, 1;
-
(1960)
Tetrahedron Lett
, vol.1
, pp. 1
-
-
Huisgen, R.1
Fleischmann, R.2
Eckell, A.3
-
12
-
-
84980140232
-
-
c) R. Huisgen, R. Fleischmann, A. Eckell, Chem. Ber. 1977, 110, 500;
-
(1977)
Chem. Ber
, vol.110
, pp. 500
-
-
Huisgen, R.1
Fleischmann, R.2
Eckell, A.3
-
13
-
-
53849086700
-
-
d) R. Huisgen, R. Fleischmann, A. Eckell, Chem. Ber. 1977, 110, 514;
-
(1977)
Chem. Ber
, vol.110
, pp. 514
-
-
Huisgen, R.1
Fleischmann, R.2
Eckell, A.3
-
18
-
-
0002959272
-
-
i) A. Eckell, M. V. Georges, R. Huisgen, A. S. Kende, Chem. Ber. 1977, 110, 578.
-
(1977)
Chem. Ber
, vol.110
, pp. 578
-
-
Eckell, A.1
Georges, M.V.2
Huisgen, R.3
Kende, A.S.4
-
22
-
-
84943039767
-
-
a) T. Eicher, S. Hünig, H. Hansen, Chem. Ber. 1969, 102, 2889;
-
(1969)
Chem. Ber
, vol.102
, pp. 2889
-
-
Eicher, T.1
Hünig, S.2
Hansen, H.3
-
24
-
-
0002527884
-
-
a) R. Grigg, J. Kemp, N. Thompson, Tetrahedron Lett. 1978, 19, 2827;
-
(1978)
Tetrahedron Lett
, vol.19
, pp. 2827
-
-
Grigg, R.1
Kemp, J.2
Thompson, N.3
-
28
-
-
0037146071
-
-
a) S. Kobayashi, H. Shimizu, Y. Yamashita, H. Ishitani, J. Kobayashi, J. Am. Chem. Soc. 2002, 124, 13678;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 13678
-
-
Kobayashi, S.1
Shimizu, H.2
Yamashita, Y.3
Ishitani, H.4
Kobayashi, J.5
-
30
-
-
33749348910
-
-
c) W. Chen, X. H. Yuan, R. Li, W. Du, Y. Wu, L. S. Ding, Y. C. Chen, Adv. Synth. Catal. 2006, 348, 1818;
-
(2006)
Adv. Synth. Catal
, vol.348
, pp. 1818
-
-
Chen, W.1
Yuan, X.H.2
Li, R.3
Du, W.4
Wu, Y.5
Ding, L.S.6
Chen, Y.C.7
-
31
-
-
33846436800
-
-
d) H. Suga, A. Funyu, A. Kakehi, Org. Lett. 2007, 9, 97.
-
(2007)
Org. Lett
, vol.9
, pp. 97
-
-
Suga, H.1
Funyu, A.2
Kakehi, A.3
-
34
-
-
35348990757
-
-
R. Shintani, M. Murakami, T. Hayashi, J. Am. Chem. Soc. 2007, 129, 12356.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 12356
-
-
Shintani, R.1
Murakami, M.2
Hayashi, T.3
-
35
-
-
23844457533
-
-
A. Suarez, W. Downey, G. C. Fu, J. Am. Chem. Soc. 2005, 127, 11244.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 11244
-
-
Suarez, A.1
Downey, W.2
Fu, G.C.3
-
36
-
-
53849083309
-
-
An alternative mechanism to form 6 involving a single-electron transfer (SET) process between two molecules of 1 was disregarded due to the low reduction potential of 1, which makes the SET unlikely to occur. For electrochemical studies on 6-oxoverdazyl radicals, see: J. B. Gilroy, S. D. J. McKinnon, B. D. Koivisto, R. G. Hicks, Org. Lett. 2007, in press
-
An alternative mechanism to form 6 involving a single-electron transfer (SET) process between two molecules of 1 was disregarded due to the low reduction potential of 1, which makes the SET unlikely to occur. For electrochemical studies on 6-oxoverdazyl radicals, see: J. B. Gilroy, S. D. J. McKinnon, B. D. Koivisto, R. G. Hicks, Org. Lett. 2007, in press.
-
-
-
-
37
-
-
53849091919
-
-
A hydrogen abstraction mechanism similar to that proposed for the verdazyl radical also occurs with nitroxide radicals leading to their decomposition, see: D. F. Bowman, I. Gillian, K. U. Ingold, J. Am. Chem. Soc. 1971, 93, 6555
-
A hydrogen abstraction mechanism similar to that proposed for the verdazyl radical also occurs with nitroxide radicals leading to their decomposition, see: D. F. Bowman, I. Gillian, K. U. Ingold, J. Am. Chem. Soc. 1971, 93, 6555.
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-
-
-
38
-
-
84985733610
-
-
The dimer of 1 has been synthesized by treating 1 with formic acid, albeit in low yield F. A. Neugebauer, H. Fischer, R. Siegel, Chem. Ber. 1988, 121, 815.
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The dimer of 1 has been synthesized by treating 1 with formic acid, albeit in low yield F. A. Neugebauer, H. Fischer, R. Siegel, Chem. Ber. 1988, 121, 815.
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