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9
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Zhang L., Chen X., Xue P., Sun H.H.Y., Williams I.D., Sharpless K.B., Fokin V.V., and Jia G. J. Am. Chem. Soc. 127 (2005) 15998
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Jia, G.8
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10
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-
0021840547
-
-
For reports on the synthesis of 2-sulfonyl-1,2,3-triazoles, see
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For reports on the synthesis of 2-sulfonyl-1,2,3-triazoles, see. Abdel-Halim A.M., Abdel-Rahman R.M., and Mohamed E.A. Acta Pharm. Jugosl. 35 (1985) 89
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Abdel-Halim, A.M.1
Abdel-Rahman, R.M.2
Mohamed, E.A.3
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11
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0035746329
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Potapova I.A., Purygin P.P., Lipatov I.S., Belousova Z.P., Yakimova N.A., Tezikov Y.V., and Selezneva E.S. Pharm. Chem. J. 35 (2001) 588
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Potapova, I.A.1
Purygin, P.P.2
Lipatov, I.S.3
Belousova, Z.P.4
Yakimova, N.A.5
Tezikov, Y.V.6
Selezneva, E.S.7
-
13
-
-
0037448384
-
-
For reports on the pharmaceutical activity of 2,4-disubstituted triazoles, see
-
For reports on the pharmaceutical activity of 2,4-disubstituted triazoles, see. Balle T., Perregaard J., Ramirez M.T., Larsen A.K., Liljefors T., and Andersen K. J. Med. Chem. 46 (2003) 265
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Balle, T.1
Perregaard, J.2
Ramirez, M.T.3
Larsen, A.K.4
Liljefors, T.5
Andersen, K.6
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14
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-
4444283656
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-
Roppe J., Smith N.D., Huang D., Tehrani L., Wang B., Anderson J., Brodkin J., Chung J., Jiang X., King C., Munoz B., Varney M.A., Prasit P., and Cosford N.D.P. J. Med. Chem. 47 (2004) 4645
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Roppe, J.1
Smith, N.D.2
Huang, D.3
Tehrani, L.4
Wang, B.5
Anderson, J.6
Brodkin, J.7
Chung, J.8
Jiang, X.9
King, C.10
Munoz, B.11
Varney, M.A.12
Prasit, P.13
Cosford, N.D.P.14
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15
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61349086057
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and references therein
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Liu Y., Yan W., Chen Y., Petersen J.L., and Shi X. Org. Lett. 10 (2008) 5389 and references therein
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Liu, Y.1
Yan, W.2
Chen, Y.3
Petersen, J.L.4
Shi, X.5
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16
-
-
57349191194
-
-
2 afforded a mixture of 1-tosyl and 2-tosyl triazoles (80%, l-tosyl:2-tosyl = 82:18). See also
-
2 afforded a mixture of 1-tosyl and 2-tosyl triazoles (80%, l-tosyl:2-tosyl = 82:18). See also. Horneff T., Chuprakov S., Chernyak N., Gevorgyan V., and Fokin V.V. J. Am. Chem. Soc. 130 (2008) 14972
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Horneff, T.1
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Chernyak, N.3
Gevorgyan, V.4
Fokin, V.V.5
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23
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0002884076
-
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For sulfonyl group rearrangement of other heterocycles, see
-
For sulfonyl group rearrangement of other heterocycles, see. Kohori K., Kinoshita H., and Inomata K. Chem. Lett. (1995) 799
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(1995)
Chem. Lett.
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Kohori, K.1
Kinoshita, H.2
Inomata, K.3
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26
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34248146410
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-
Yoo E.J., Ahlquist M., Kim S.H., Bae I., Fokin V.V., Sharpless K.B., and Chang S. Angew. Chem. Int. Ed. 46 (2007) 1730
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(2007)
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Yoo, E.J.1
Ahlquist, M.2
Kim, S.H.3
Bae, I.4
Fokin, V.V.5
Sharpless, K.B.6
Chang, S.7
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27
-
-
76949097994
-
-
note
-
2 were also effective for the rearrangement of sulfonyl group.
-
-
-
-
28
-
-
76949093002
-
-
note
-
+ 300.0807. Found m/z 300.0801.
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