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4243159924
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For recent review on the privileged structure concept, see:
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For recent review on the privileged structure concept, see:. DeSimone R.W., Currie K.S., Mitchell S.A., Darrow J.W., and Pippin D.A. Comb. Chem. High Throughput Screening 7 (2004) 473-494
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33847377928
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For selective recent examples, see:
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For selective recent examples, see:. Hodous B.L., Geuns-Meyer S.D., Hughes P.E., Albrecht B.K., Bellon S., Bready J., Caenepeel S., Cee V.J., Chaffee S.C., Coxon A., Emery M., Fretland J., Gallant P., Gu Y., Hoffman D., Johnson R.E., Kendall R., Kim J.L., Long A.M., Morrison M., Olivieri P.R., Patel V.F., Polverino A., Rose P., Tempest P., Wang L., Whittington D.A., and Zhao H. J. Med. Chem. 50 (2007) 611-626
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Coxon, A.10
Emery, M.11
Fretland, J.12
Gallant, P.13
Gu, Y.14
Hoffman, D.15
Johnson, R.E.16
Kendall, R.17
Kim, J.L.18
Long, A.M.19
Morrison, M.20
Olivieri, P.R.21
Patel, V.F.22
Polverino, A.23
Rose, P.24
Tempest, P.25
Wang, L.26
Whittington, D.A.27
Zhao, H.28
more..
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Triazoles 5 are structurally closely related to a phosphate-containing 1,4-disubstituted thiazole which is an inhibitor of the Grb2-SH2 domain, see:
-
Triazoles 5 are structurally closely related to a phosphate-containing 1,4-disubstituted thiazole which is an inhibitor of the Grb2-SH2 domain, see:. Caravatti G., Rahuel J., Gay B., and Furet P. Bioorg. Med. Chem. Lett. 9 (1999) 1973-1978
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34250726632
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The synthesis of a phosphine oxide containing-triazole was recently reported using a modular flow reactor by Ley and co-workers, see:
-
The synthesis of a phosphine oxide containing-triazole was recently reported using a modular flow reactor by Ley and co-workers, see:. Smith C.D., Baxendale I.R., Lanners S., Hayward J.J., and Smith S.C. Org. Biomol. Chem. 5 (2007) 1559-1561
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40149107624
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For the synthesis of piperidine-functionalized 1,4-disubstituted-1,2,3-triazoles and their coupling with the triazine backbone, to form bivalent β-turn mimics, see:
-
For the synthesis of piperidine-functionalized 1,4-disubstituted-1,2,3-triazoles and their coupling with the triazine backbone, to form bivalent β-turn mimics, see:. Angell Y., Chen D., Brahimi F., Saragovi H.U., and Burgess K. J. Am. Chem. Soc. 130 (2008) 556-565
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Lynch, M.A.4
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34848859255
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For an example of click chemistry involving pentafluorosulfanylacetylene and 2,4-diazido-6-diazomethyl-1,3,5-triazine, see:
-
For an example of click chemistry involving pentafluorosulfanylacetylene and 2,4-diazido-6-diazomethyl-1,3,5-triazine, see:. Ye C., Gard G.L., Winter R.W., Syvret R.G., Twamley B., and Shreeve J.M. Org. Lett. 9 (2007) 3841-3844
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Shreeve, J.M.6
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