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A.R. Katritzky C.W. Rees Pergamon Oxford
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4
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0004101860
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A. Padwa Wiley New York
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For reviews of 1,3-dipolar cycloadditions see: R. Huisgen A. Padwa 1,3-Dipolar Cycloaddition Chemistry 1984 Wiley New York 1 176 Chapter 1
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1,3-Dipolar Cycloaddition Chemistry
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Huisgen, R.1
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15
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0037099395
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V.V. Rostovtsev, L.G. Green, V.V. Fokin, and K.B. Sharpless Angew. Chem., Int. Ed. 41 2002 2596 2599
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Rostovtsev, V.V.1
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Fokin, V.V.3
Sharpless, K.B.4
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16
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0038541849
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For the Pd(0)-Cu(I) catalyzed synthesis of triazoles from nonactivated terminal alkynes via a three component reaction see: S. Kamijo, T. Jin, Z. Huo, and Y. Yamamoto J. Am. Chem. Soc. 125 2003 7786 7787
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Kamijo, S.1
Jin, T.2
Huo, Z.3
Yamamoto, Y.4
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17
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9444260351
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While this manuscript was in preparation, a microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a three component reaction was reported: P. Appukkuttan, W. Dehaen, V.V. Fokin, and E. Van der Eycken Org. Lett. 6 2004 4223 4225
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Org. Lett.
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Appukkuttan, P.1
Dehaen, W.2
Fokin, V.V.3
Van Der Eycken, E.4
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18
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85030806350
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note
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4 (M+H) 189
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-
-
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19
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85030811742
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note
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3N·HCl. After the reaction was completed, it turned slightly basic (pH = 8)
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20
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0025195705
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For compound 3b, see: G. Biagi, O. Livi, G.L. Ramacciotti, V. Scartoni, L. Bazzichi, M.R. Mazzoni, and A. Lucacchinni Il Farmaco 45 1990 49 57
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Biagi, G.1
Livi, O.2
Ramacciotti, G.L.3
Scartoni, V.4
Bazzichi, L.5
Mazzoni, M.R.6
Lucacchinni, A.7
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21
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0037416892
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For compound 3c, see: B.E. Blass, K.R. Coburn, A.L. Falukner, W.L. Seibel, and A. Srivastava Tetrahedron Lett. 44 2003 2153 2155
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Blass, B.E.1
Coburn, K.R.2
Falukner, A.L.3
Seibel, W.L.4
Srivastava, A.5
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23
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85030816277
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3e, see Ref. 6b. For compounds 3g and 3h, see:
-
For compound 3e, see Ref. 6b. For compounds 3g and 3h, see: R. William, P.D. Leeson, and K.W. Moore PCT Int. Appl. 1996 24 27
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William, R.1
Leeson, P.D.2
Moore, K.W.3
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24
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21844512339
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For compound 3i, see: F. Palacios, A.M. Ochoa de Retana, J. Pagalday, and J.M. Sanchez Org. Prep. Proced. Int. 27 1995 603 612
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Ochoa De Retana, A.M.2
Pagalday, J.3
Sanchez, J.M.4
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25
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0021026229
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For compound 3l, see: A. Da Settimo, O. Livi, G. Biagi, A. Lucacchinii, and S. Caselli Fármaco Edizione Scientifica 38 1983 725 737
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Da Settimo, A.1
Livi, O.2
Biagi, G.3
Lucacchinii, A.4
Caselli, S.5
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27
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85030805806
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note
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The reaction worked successfully even with 0.1 mol % copper. The latter was the lowest stoichiometry tested during this study
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28
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0034692170
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3m, see Ref. 6b. For compound 3n, see:
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For compound 3m, see Ref. 6b. For compound 3n, see: J. Stanslas, D.J. Hagan, M.J. Ellis, C. Turner, J. Carmichael, W. Ward, T.R. Hammonds, and M.F.G. Stevens J. Med. Chem. 43 2000 1563 1572
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Ellis, M.J.3
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Carmichael, J.5
Ward, W.6
Hammonds, T.R.7
Stevens, M.F.G.8
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30
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4444324951
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For the use of aminotriazoles as Cu(I)-stabilizing ligands in catalysis, see: T.R. Chan, R. Hilgraf, K.B. Sharpless, and V.V. Fokin Org. Lett. 6 2004 2853 2855
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Org. Lett.
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Chan, T.R.1
Hilgraf, R.2
Sharpless, K.B.3
Fokin, V.V.4
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34
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0034523334
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I.G. Crivelli, C. Andrade, M.A. Francois, D. Boys, A. Haberland, R. Segura, A.M. Leiva, and B. Loeb Polyhedron 19 2000 2289 2295
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Crivelli, I.G.1
Andrade, C.2
Francois, M.A.3
Boys, D.4
Haberland, A.5
Segura, R.6
Leiva, A.M.7
Loeb, B.8
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35
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0037454346
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The new protocol could have a potential use in bioconjugation since sodium ascorbate was reported to induce subtantial disassembly of proteins: Q. Wang, T.R. Chan, R. Hilgraf, V.V. Fokin, K.B. Sharpless, and M.G. Finn J. Am. Chem. Soc. 125 2003 3192 3193
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Wang, Q.1
Chan, T.R.2
Hilgraf, R.3
Fokin, V.V.4
Sharpless, K.B.5
Finn, M.G.6
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37
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85030813141
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note
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2 (M+H) 289
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