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1
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78649524705
-
-
For recent perspectives in this area, see
-
For recent perspectives in this area, see
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-
-
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3
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40849097418
-
-
Michalek, R. D., Nelson, K., Jisolbrook, B., Poole, L. B., and Nelson, K. J. Curr. Opin. Chem. Biol. 2008, 12, 18
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Michalek, R.D.1
Nelson, K.2
Jisolbrook, B.3
Poole, L.B.4
Nelson, K.J.5
-
4
-
-
78649525403
-
-
The best studied examples to date are peroxiredoxins, (3) hydrogenases, (4) NADH peroxidases, (5) and nitrile and thiocyanate hydrolases (6)
-
The best studied examples to date are peroxiredoxins, (3) hydrogenases, (4) NADH peroxidases, (5) and nitrile and thiocyanate hydrolases (6)
-
-
-
-
5
-
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78649522272
-
-
For a recent review, see
-
For a recent review, see
-
-
-
-
6
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-
64149085448
-
-
Hall, A., Karplus, P. A., and Poole, L. B. FEBS J. 2009, 276, 2469
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(2009)
FEBS J.
, vol.276
, pp. 2469
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Hall, A.1
Karplus, P.A.2
Poole, L.B.3
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7
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20044370126
-
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Volbeda, A., Martin, L., Cavazza, C., Matho, M., Faber, B. W., Roseboom, W., Albracht, S. P., Garcin, E., Rousset, M., and Fontecilla-Camps, J. C. J. Biol. Inorg. Chem. 2005, 10, 239
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J. Biol. Inorg. Chem.
, vol.10
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Volbeda, A.1
Martin, L.2
Cavazza, C.3
Matho, M.4
Faber, B.W.5
Roseboom, W.6
Albracht, S.P.7
Garcin, E.8
Rousset, M.9
Fontecilla-Camps, J.C.10
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8
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78649518492
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For a review, see
-
For a review, see
-
-
-
-
9
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1342281240
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Poole, L. B., Karplus, P. A., and Claiborne, A. Annu. Rev. Pharmacol. Toxicol. 2004, 44, 325
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(2004)
Annu. Rev. Pharmacol. Toxicol.
, vol.44
, pp. 325
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Poole, L.B.1
Karplus, P.A.2
Claiborne, A.3
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10
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70350043513
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Arakawa, T., Kawano, Y., Katayama, Y., Nakayama, H., Dohmae, N., Yohda, M., and Odaka, M. J. Am. Chem. Soc. 2009, 131, 14838
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(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 14838
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Arakawa, T.1
Kawano, Y.2
Katayama, Y.3
Nakayama, H.4
Dohmae, N.5
Yohda, M.6
Odaka, M.7
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12
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77955385753
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Dansette, P. M., Thébault, S., Bertho, G., and Mansuy, D. Chem. Res. Toxicol. 2010, 23, 1268
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(2010)
Chem. Res. Toxicol.
, vol.23
, pp. 1268
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-
Dansette, P.M.1
Thébault, S.2
Bertho, G.3
Mansuy, D.4
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13
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62249112083
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Dansette, P. M., Libraire, J., Bertho, G., and Mansuy, D. Chem. Res. Toxicol. 2009, 22, 369
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(2009)
Chem. Res. Toxicol.
, vol.22
, pp. 369
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Dansette, P.M.1
Libraire, J.2
Bertho, G.3
Mansuy, D.4
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15
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74849097198
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Kubec, R., Cody, R. B., Dane, A. J., Musah, R. A., Schraml, J., Vattekkatte, A., and Block, E. J. Agric. Food Chem. 2010, 58, 1121
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(2010)
J. Agric. Food Chem.
, vol.58
, pp. 1121
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Kubec, R.1
Cody, R.B.2
Dane, A.J.3
Musah, R.A.4
Schraml, J.5
Vattekkatte, A.6
Block, E.7
-
16
-
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58249101189
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Vaidya, V., Ingold, K. U., and Pratt, D. A. Angew. Chem., Int. Ed. 2009, 48, 157
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(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 157
-
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Vaidya, V.1
Ingold, K.U.2
Pratt, D.A.3
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17
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78649507023
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Several chapters of a recent volume of Methods in Enzymology is devoted to this topic. See, in particular
-
Several chapters of a recent volume of Methods in Enzymology is devoted to this topic. See, in particular
-
-
-
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18
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77956210622
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Nelson, K. J., Klomsiri, C., Codreanu, S. G., Soito, L., Liebler, D. C., Rogers, L. C., Daniel, L. W., and Poole, L. B. Methods Enzymol. 2010, 473, 95
-
(2010)
Methods Enzymol.
, vol.473
, pp. 95
-
-
Nelson, K.J.1
Klomsiri, C.2
Codreanu, S.G.3
Soito, L.4
Liebler, D.C.5
Rogers, L.C.6
Daniel, L.W.7
Poole, L.B.8
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19
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70349284540
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See also
-
See also: Leonard, S. E., Reddie, K. G., and Carroll, K. S. ACS Chem. Biol. 2009, 4, 783
-
(2009)
ACS Chem. Biol.
, vol.4
, pp. 783
-
-
Leonard, S.E.1
Reddie, K.G.2
Carroll, K.S.3
-
23
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78649526877
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-
Examples include
-
Examples include
-
-
-
-
25
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84945064255
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Tripolt, R., Belaj, F., and Nachbaur, E. Z. Naturforsch, B: Chem. Sci. 1993, 48, 1212
-
(1993)
Z. Naturforsch, B: Chem. Sci.
, vol.48
, pp. 1212
-
-
Tripolt, R.1
Belaj, F.2
Nachbaur, E.3
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26
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0028327681
-
-
Machiguchi, T., Hasegawa, T., and Otani, H. J. Am. Chem. Soc. 1994, 116, 407
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 407
-
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MacHiguchi, T.1
Hasegawa, T.2
Otani, H.3
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27
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33748244638
-
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Goto, K., Tokitoh, N., and Okazaki, R. Angew. Chem., Int. Ed. 1995, 34, 1124
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(1995)
Angew. Chem., Int. Ed.
, vol.34
, pp. 1124
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Goto, K.1
Tokitoh, N.2
Okazaki, R.3
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28
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0030894735
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Goto, K., Holler, M., and Okazaki, R. J. Am. Chem. Soc. 1997, 119, 1460
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 1460
-
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Goto, K.1
Holler, M.2
Okazaki, R.3
-
29
-
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0016385617
-
-
Chou, T. S., Burgtorf, J. R., Ellis, A. L., Lammert, S. R., and Kukolja, S. P. J. Am. Chem. Soc. 1974, 96, 1609
-
(1974)
J. Am. Chem. Soc.
, vol.96
, pp. 1609
-
-
Chou, T.S.1
Burgtorf, J.R.2
Ellis, A.L.3
Lammert, S.R.4
Kukolja, S.P.5
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30
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0032541730
-
-
Fekner, T., Baldwin, J. E., Adlington, R. M., and Schofield, C. J. Tetrahedron Lett. 1998, 39, 6983
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 6983
-
-
Fekner, T.1
Baldwin, J.E.2
Adlington, R.M.3
Schofield, C.J.4
-
32
-
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0030482396
-
-
Ishii, A., Komiya, K., and Nakayama, J. J. Am. Chem. Soc. 1996, 118, 12836
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 12836
-
-
Ishii, A.1
Komiya, K.2
Nakayama, J.3
-
33
-
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0010392885
-
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Yoshimura, T., Tsukurimichi, E., Yamazaki, S., Soga, S., Shimasaki, C., and Hasegawa, K. J. Chem. Soc., Chem. Commun. 1992, 18, 1337
-
(1992)
J. Chem. Soc., Chem. Commun.
, vol.18
, pp. 1337
-
-
Yoshimura, T.1
Tsukurimichi, E.2
Yamazaki, S.3
Soga, S.4
Shimasaki, C.5
Hasegawa, K.6
-
34
-
-
78649495707
-
-
33S (S = 3/2; a = 1.72 G) was also visible
-
33S (S = 3/2; a = 1.72 G) was also visible.
-
-
-
-
35
-
-
78649508125
-
-
3SO was generated via photolysis of either (a) a solution of dimethyl sulfide, isopropyl alcohol, and di- tert -butylperoxide or (b) a mixture of methanethiol, di- tert -butylperoxide, and ethylene. See
-
3SO was generated via photolysis of either (a) a solution of dimethyl sulfide, isopropyl alcohol, and di- tert -butylperoxide or (b) a mixture of methanethiol, di- tert -butylperoxide, and ethylene. See
-
-
-
-
36
-
-
0142110344
-
-
Kawamura, T., Krusic, P. J., and Kochi, J. K. Tetrahedron Lett. 1972, 13, 4075
-
(1972)
Tetrahedron Lett.
, vol.13
, pp. 4075
-
-
Kawamura, T.1
Krusic, P.J.2
Kochi, J.K.3
-
37
-
-
78649495923
-
-
The tert -butyl sulfinyl radicals were generated by photolysis of di- tert -butylperoxide containing solutions of t -BuSOH formed in situ from the thermolysis of di- tert -butyl sulfoxide. See
-
The tert -butyl sulfinyl radicals were generated by photolysis of di- tert -butylperoxide containing solutions of t -BuSOH formed in situ from the thermolysis of di- tert -butyl sulfoxide. See
-
-
-
-
39
-
-
78649501146
-
-
2, have been observed in frozen aqueous samples. See
-
2, have been observed in frozen aqueous samples. See
-
-
-
-
40
-
-
0023229060
-
-
Sevilla, M. D., Becker, D., Swarts, S., and Herrington, J. Biochem. Biophys. Res. Commun. 1987, 144, 1037
-
(1987)
Biochem. Biophys. Res. Commun.
, vol.144
, pp. 1037
-
-
Sevilla, M.D.1
Becker, D.2
Swarts, S.3
Herrington, J.4
-
41
-
-
78649494091
-
-
2-SR
-
2-SR.
-
-
-
-
42
-
-
78649516445
-
-
-9 at 298 K
-
-9 at 298 K.
-
-
-
-
43
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0028120449
-
-
Lucarini, M., Pedulli, G. F., and Cipollone, M. J. Org. Chem. 1994, 59, 5063
-
(1994)
J. Org. Chem.
, vol.59
, pp. 5063
-
-
Lucarini, M.1
Pedulli, G.F.2
Cipollone, M.3
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44
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0037424392
-
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Amorati, R., Lucarini, M., Mugnaini, V., and Pedulli, G. F. J. Org. Chem. 2003, 68, 1747
-
(2003)
J. Org. Chem.
, vol.68
, pp. 1747
-
-
Amorati, R.1
Lucarini, M.2
Mugnaini, V.3
Pedulli, G.F.4
-
45
-
-
78649509106
-
-
The calculated electronic structure in PhSO suggests no delocalization of spin from the sulfinyl radical. See
-
The calculated electronic structure in PhSO suggests no delocalization of spin from the sulfinyl radical. See
-
-
-
-
46
-
-
0031235363
-
-
Darmanyan, A. P., Gregory, D. D., Guo, Y., and Jenks, W. S. J. Phys. Chem. A 1997, 101, 6855
-
(1997)
J. Phys. Chem. A
, vol.101
, pp. 6855
-
-
Darmanyan, A.P.1
Gregory, D.D.2
Guo, Y.3
Jenks, W.S.4
-
48
-
-
78649501500
-
-
3H could not catalyze the condensation of the sulfenic acid to the corresponding thiosulfinate
-
3H could not catalyze the condensation of the sulfenic acid to the corresponding thiosulfinate.
-
-
-
-
49
-
-
0000095341
-
-
Jovanovic, S. V., Jankovic, I., and Josimovic, L. J. Am. Chem. Soc. 1992, 114, 9018
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 9018
-
-
Jovanovic, S.V.1
Jankovic, I.2
Josimovic, L.3
-
50
-
-
78649524341
-
-
2O at 20°C. See
-
2O at 20°C. See
-
-
-
-
51
-
-
84986409546
-
-
Okuyama, T., Miyake, K., Fueno, T., Yoshimura, T., Soga, S., and Tsukurimichi, E. Heteroat. Chem. 1992, 3, 577
-
(1992)
Heteroat. Chem.
, vol.3
, pp. 577
-
-
Okuyama, T.1
Miyake, K.2
Fueno, T.3
Yoshimura, T.4
Soga, S.5
Tsukurimichi, E.6
-
52
-
-
78649496297
-
-
This was the maximum reliable value we could obtain with our pH probe
-
This was the maximum reliable value we could obtain with our pH probe.
-
-
-
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