References
- Brase, S.; Gil, C.; Knepper, K.; Zimmermann, V. Angew. Chem. Int. Ed. 2005, 44, 5188 https://doi.org/10.1002/anie.200400657
- Huisgen, R.; Szeimies, G.; Moebius, L. Chem. Ber. 1967, 100, 2494 https://doi.org/10.1002/cber.19671000806
- Huisgen, R. 1,3-Dipolar Cycloaddition Chemistry; Wiley: New York, 1984
- Huisgen, R. Pure Appl. Chem. 1989, 61, 613 https://doi.org/10.1351/pac198961040613
- Katritzky, A. R.; Zhang, Y.; Singh, S. K. Heterocycles 2003, 60, 1225 https://doi.org/10.3987/REV-02-562
- Wang, Z.-X.; Qin, H.-L. Chem. Commun. 2003, 2450
- Radi, S.; Lazrek, H. B. Bull. Korean Chem. Soc. 2002, 23, 437 https://doi.org/10.5012/bkcs.2002.23.3.437
- Palacios, F.; Ochoa de Retana, A. M.; Pagalday, J.; Sanchez, J. M. Org. Prep. Proced. Int. 1995, 27, 603 https://doi.org/10.1080/00304949509458517
- Hlasta, D. J.; Ackerman, J. H. J. Org. Chem. 1994, 59, 6184 https://doi.org/10.1021/jo00100a019
- Mock, W. L.; Irra, T. A.; Wepsiec, J. P.; Adhya, M. J. Org. Chem. 1989, 54, 5302 https://doi.org/10.1021/jo00283a024
- Peng, W.; Zhu, S. Synlett 2003, 187
- Li, Z.; Seo, T. S.; Ju, J. Tetraheron Lett. 2004, 45, 3143 https://doi.org/10.1016/j.tetlet.2004.02.089
- Suarez, P. L.; Gandara, Z.; Gomez, G.; Fall, Y. Tetraheron Lett. 2004, 45, 4619 https://doi.org/10.1016/j.tetlet.2004.04.117
- Bodine, K. D.; Jin, D. Y.; Gin, M. S. J. Am. Chem. Soc. 2004, 126, 1638 https://doi.org/10.1021/ja039374t
- Wu, Y.-M.; Deng, J.: Li, Y.; Chen, Q.-Y. Synthesis 2005, 1314
- Kacprzak, K. Synlett 2005, 943
- Manetsch, R.; Krasinnski, A.; Radiæ, Z.; Raushel, J.; Taylor, P.; Sharpless, K. B.; Kolb, H. C. J. Am. Chem. Soc. 2004, 126, 12809 https://doi.org/10.1021/ja046382g
- Kolb, H. C.; Sharpless, K. B. Drug Discovery Today 2003, 8, 1128 https://doi.org/10.1016/S1359-6446(03)02933-7
- Fu, X.; Albermann, C.; Zhang, C.; Thorson, J. S. Org. Lett. 2005, 7, 1513 https://doi.org/10.1021/ol0501626
- Punna, S.; Kuzelka, J.; Wang, Q.; Finn, M. G. Angew. Chem. Int. Ed. 2005, 44, 2215 https://doi.org/10.1002/anie.200461656
- Wang, Q.; Chan, T. R.; Hilgraf, R.; Fokin, V. V.; Sharpless, K. B.; Finn, M. G. J. Am. Chem. Soc. 2003, 125, 3192 https://doi.org/10.1021/ja021381e
- Meng, J.- C.; Siuzdak, G.; Finn, M. G. Chem. Commun. 2004, 2108
- Link, A. J.; Vink, M. K. S.; Tirrell, D. A. J. Am. Chem. Soc. 2004, 126, 10598 https://doi.org/10.1021/ja047629c
- Sivakumar, K.; Xie, F.; Cash, B. M.; Long, S.; Barnhill, H. N.; Wang, Q. Org. Lett. 2004, 6, 4603 and references therein https://doi.org/10.1021/ol047955x
- Parent, M.; Mongin, O.; Kamada, K.; Katan, C.; Blanchard- Desce, M. Chem. Commun. 2005, 2029
- Englert, B. C.; Bakbak, S.; Bunz, U. H. F. Macromolecules 2005, 38, 5868 https://doi.org/10.1021/ma050484p
- Diaz, D. D.; Punna, S.; Holzer, P.; McPherson, A. K.; Sharpless, K. B.; Fokin, V. V.; Finn, M. G. J. Polym. Sci., Part A 2004, 42, 4392 https://doi.org/10.1002/pola.20330
- Helms, B.; Mynar, J. L.; Hawker, C. J.; Frechet, J. M. J. J. Am. Chem. Soc. 2004, 126, 15020 https://doi.org/10.1021/ja044744e
- Opsteen, J. A.; van Hest, J. C. M. Chem. Commun. 2005, 57
- Mantovani, G.; Ladmiral, V.; Tao, L.; Haddleton, D. M. Chem. Commun. 2005, 2089
- Lutz, J.-F.; Borner, H. G.; Weichenhan, K. Macromol. Rapid Commun. 2005, 26, 514 https://doi.org/10.1002/marc.200500002
- Binder, W. H.; Kluger, C. Macromolecules 2004, 37, 9321 https://doi.org/10.1021/ma0480087
- Tsarevsky, N. V.; Sumerlin, B. S.; Matyjaszewski, K. Macromolecules 2005, 38, 3558 https://doi.org/10.1021/ma050370d
- Wu, P.; Feldman, A. K.; Nugent, A. K.; Hawker, C. J.; Scheel, A.; Voit, B.; Pyun, J.; Frechet, J. M. J.; Sharpless, K. B.; Fokin, V. V. Angew. Chem. Int. Ed. 2004, 43, 3928 https://doi.org/10.1002/anie.200454078
- Malkoch, M.; Schleicher, K.; Drockenmuller, E.; Hawker, C. J.; Russell, T. P.; Wu, P.; Fokin, V. V. Macromolecules 2005, 38, 3663 https://doi.org/10.1021/ma047657f
- Joralemon, M. J.; O'Reilly, R. K.; Matson, J. B.; Nugent, A. K.; Hawker, C. J.; Wooley, K. L. Macromolecules 2005, 38, 5436 https://doi.org/10.1021/ma050302r
- Lee, J. W.; Kim, B. K. Bull. Korean Chem. Soc. 2005, 26, 658 https://doi.org/10.5012/bkcs.2005.26.4.658
- Lee, J. W.; Kim, B. K.; Jin, S. H. Bull. Korean Chem. Soc. 2005, 26, 833 https://doi.org/10.1007/s11814-009-0139-1
- Hawker, C. J.; Wooley, K. L.; Frechet, J. M. J. J. Chem. Soc., Chem. Commun. 1994, 925
- Grayson, S. M.; Frechet, J. M. J. Chem. Rev. 2001, 101, 3919
- Tozawa, T. Chem. Commun. 2004, 1904
- Liao, L.-X.; Stellacci, F.; McGrath, D. V. J. Am. Chem. Soc. 2004, 126, 2181 https://doi.org/10.1021/ja036418p
- Hara, M.; Samori, S.; Cai, X.; Tojo, S.; Arai, T.; Momotake, A.; Hayakawa, J.; Uda, M.; Kawai, K.; Endo, M.; Fujitsuka, M.; Majima, T. J. Am. Chem. Soc. 2004, 126, 14217 https://doi.org/10.1021/ja046650a
- Diez-Barra, E.; Gonzalez, R.; Sanchez-Verdu, P.; Tolosa, J. Tetrahedron 2004, 60, 1563 https://doi.org/10.1016/j.tet.2003.12.003
- Momotake, A.; Arai, T. Tetrahedron Lett. 2004, 45, 4131
- Balzani, V.; Ceroni, P.; Giansante, C.; Vicinelli, V.; Klarner, F.-G.; Verhaelen, C.; Vogtle, F.; Hahn, U. Angew. Chem. Int. Ed. 2005, 44, 4574 https://doi.org/10.1002/anie.200501025
- Li, W.-S.; Jiang, D.-L.; Suna, Y.; Aida, T. J. Am. Chem. Soc. 2005, 127, 7700 https://doi.org/10.1021/ja0513335
- Shanahan, C. S.; McGrath, D. V. J. Org. Chem. 2005, 70, 1054 https://doi.org/10.1021/jo0483419
- Lee, J. W.; Kim, B. K.; Jin, S. H. Bull. Korean Chem. Soc. 2005, 26, 715 https://doi.org/10.5012/bkcs.2005.26.5.715
- Uhrich, K. E.; Hawker, C. J.; Frechet, J. M. J. Macromolecules 1992, 25, 4583 https://doi.org/10.1021/ma00044a019
- Stewart, G. M.; Fox, M. A. J. Am. Chem. Soc. 1996, 118, 4354 https://doi.org/10.1021/ja954021i
- Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. Angew. Chem. Int. Ed. 2002, 41, 2596 https://doi.org/10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
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