INFORMAZIONI SU QUESTO ARTICOLO

Cita

1. Hu, C., Guo, X., Jing, Y., Chen, J., Zhang, C. & Huang, J. (2014). Structure and mechanical properties of crosslinked glycidyl azide polymers via click chemistry as potential binder of solid propellant. J. Appl. Polym. Sci.131 (16), 318-323. DOI: 10.1002/app.40636.10.1002/app.40636Open DOISearch in Google Scholar

2. Lee, D.H., Kim, K.T., Jang, Y., Lee, S., Jeon, H.B. & Paik, H.J., et al. (2014). 1,2,3-triazole crosslinked polymers as binders for solid rocket propellants. J. Appl. Polym. Sci. 131 (15), 4401-4404. DOI: 10.1002/app.40594.10.1002/app.40594Open DOISearch in Google Scholar

3. Ajaz, A.G. (1995). Hydroxyl-terminated polybutadiene telechelic polymer (htpb): binder for solid rocket propellants. Rubber Chem. & Technol. 68 (3), 481-506.10.5254/1.3538752Search in Google Scholar

4. Se kkar, V., Alex, A.S., Kumar, V., & Bandyopadhyay, G.G.(2017). Pot life extension of hydroxyl terminated polybutadiene based solid propellant binder system by tailoring the binder polymer microstructure. J. Macromol. Sci. Part A - Chemistry, 54 (3), 171-175. DOI: 10.1080/10601325.2017.1265403.10.1080/10601325.2017.1265403Open DOISearch in Google Scholar

5. Cornille, A., Auvergne, R., Figovsky, O., Boutevin, B. & Caillol, S. (2017). A perspective approach to sustainable routes for non-isocyanate polyurethanes. European Polym. J. 87, 535-552. http: //dx.doi.org/10.1016/j.eurpolymj.2016.11.02710.1016/j.eurpolymj.2016.11.027Open DOISearch in Google Scholar

6. Reshmi, S., Hemanth, H., Gayathri, S. & Nair, C.P.R. (2016). Polyether triazoles: an effective binder for ‘green’ gas generator solid propellants. Polymer, 92, 201-209. http: //dx.doi. org/10.1016/j.polymer.2016.03.006.10.1016/j.polymer.2016.03.006Open DOISearch in Google Scholar

7. Krishnan, S.G., KavithaAyyaswamy, & Nayak, S.K. (2013). Hydroxy terminated polybutadiene: chemical modifi cations and applications. J. Macromol. Sci. Part A Pure & Applied Chemistry, 50 (1), 128-138. DOI: 10.1080/10601325.2013.736275.10.1080/10601325.2013.736275Open DOISearch in Google Scholar

8. Ruechardt, C., Sauer, J. & Sustmann, R. (2005). Rolf huisgen: some highlights of his contributions to organic chemistry. Cheminform,36 (40). DOI: 10.1002/hlca.200590098.10.1002/hlca.200590098Search in Google Scholar

9. Sexton, T.M., Freindorf, M., Kraka, E. & Cremer, D. (2016). A reaction valley investigation of the cycloaddition of 1,3-dipoles with the dipolarophiles ethene and acetylene - solution of a mechanistic puzzle. J. Physical Chem. A. DOI: 10.1021/acs.jpca.6b07975.10.1021/acs.jpca.6b0797527690469Open DOISearch in Google Scholar

10. Binder, W.H. & Sachsenhofer, R. (2010). Polymersome/ silica capsules by ‘click’-chemistry. Die Unterrichtspraxis/teaching German, 29 (12-13), 1097-1103. DOI: 10.1002/marc.200800119.10.1002/marc.200800119Search in Google Scholar

11. Mlostoń, G., Kowalski, M.K., Obijalska, E. & Heimgartner, H. (2017). Effi cient synthesis of fl uoroalkylated 1,4,2-oxathiazoles via regioselective [3+2]-cycloaddition of fl uorinated nitrile oxides with thioketones. J. Fluor. Chem. 199: 92-96.https: //doi.org/10.1016/j.jfl uchem. 2017.04.11.10.1016/j.jfluchem.2017.04.11Open DOISearch in Google Scholar

12. Majumder, S. & Bhuyan, P.J. (2012). Stereoselective synthesis of novel annulated thiopyrano indole derivatives from simple oxindole via intramolecular 1,3-dipolar cycloaddition reactions of nitrone and nitrile oxide. Tetrahedron Lett. 53 (7), 762-764. DOI: 10.1016/j.tetlet.2011.11.13610.1016/j.tetlet.2011.11.136Open DOISearch in Google Scholar

13. Woodward, R.B. & Hoffmann, R. (1965). Stereochemistry of electrocyclic reactions. J. Amer. Chem. Soc. 87 (2), 395-397.10.1021/ja01080a054Search in Google Scholar

14. Breslow D.S., Gardens M. US Patent 3390204 1968.Search in Google Scholar

15. Lin, B., Yu, P., He, C.Q. & Houk, K.N. (2016). Origins of regioselectivity in 1,3-dipolar cycloadditions of nitrile oxides with alkynylboronates. Bioorg. & Medic. Chem. 24(20), 4787-4790.https: //doi.org/10.1016/j.bmc.2016.07.03210.1016/j.bmc.2016.07.03227501912Open DOISearch in Google Scholar

16. Choe, H., Pham, T.T., Lee, J.Y., Latif, M., Park, H. & Kang, Y.K., et al. (2016). Remote stereoinductive intramolecular nitrile oxide cycloaddition: asymmetric total synthesis and structure revision of (-)-11beta-hydroxycurvularin. J. Orga.Chem. 81 (6), 2612 DOI: 10.1021/acs.joc.5b02760.10.1021/acs.joc.5b0276026894643Open DOISearch in Google Scholar

17. Tegeler, J.J. & Diamond, C.J. (2010). Aroylnitrile oxide cyclizations. 2. synthesis of (3-aroylisoxazol-5-yl)alkanoic acids. J. Heteroc. Chem. 24(3), 701-703. DOI: 10.1002/jhet.5570240331.10.1002/jhet.5570240331Open DOISearch in Google Scholar

18. Pan, W., Chen, H., Mu, J., Li, W., Jiang, F. & Weng, G., et al. (2017). Synthesis of high crystalline syndiotactic 1,2-polybutadienes and study on their reinforcing effect on cis-1,4 polybutadiene. Polymer, 111, 20-26. https: //doi.org/10.1016/j.polymer. 2017.01.022.10.1016/j.polymer.2017.01.022Open DOISearch in Google Scholar

19. Iii, J.B.S., Gardner, D.S., Yao, W., Shi, C., Reddy, P. & Tebben, A.J., et al. (2008). From rigid cyclic templates to conformationally stabilized acyclic scaffolds. part i: the discovery of ccr3 antagonist development candidate bms-639623 with picomolar inhibition potency against eosinophil chemotaxis. Bioorg. & Medic. Chem. Lett. 18 (2), 576. https: //doi.org/10.1016/j.bmcl.2007.11.067Search in Google Scholar

20. Liu, K.C., Shelton, B.R. & Howe, R.K. (1980). A particularly convenient preparation of benzohydroximinoyl chlorides (nitrile oxide precursors). J. Org. Chem. 45 (19), 3916-3918.10.1021/jo01307a039Search in Google Scholar

21. Sugium S, Ueno H, Kono M. US, Patent 3778424 1970.Search in Google Scholar

22. Kissane, M., Lynch, D., Chopra, J., Lawrence, S.E. & Maguire, A.R. (2010). The infl uence of reaction conditions on the diels-alder cycloadditions of 2-thio-3-chloroacrylamides; investigation of thermal, catalytic and microwave conditions. Organic & Biomolecular Chemistry, 8 (24), 5602-5613. DOI: 10.1039/C0OB00368A.10.1039/000368Open DOISearch in Google Scholar

23. Zeng, R.T., Wu, Y., Li, Y.D., Wang, M. & Zeng, J.B. (2017). Curing behavior of epoxidized soybean oil with biobased dicarboxylic acids. Polymer Testing, 57, 281-287. https: //doi.org/10.1016/j. polymertesting. 2016.12.007.10.1016/j.polymertesting.2016.12.007Open DOISearch in Google Scholar

24. Mansilla, M.A., Garraza, A.L.R., Silva, L., Salgueiro, W., Macchi, C. & Marzocca, A.J., et al. (2013). Evolution of the free volume and glass transition temperature with the degree of cure of polybutadiene rubbers. Polymer Testing, 32(4), 686-690. rights reserved. http: //dx.doi.org/10.1016/j.polymertesting. 2013.03.001.10.1016/j.polymertesting.2013.03.001Open DOISearch in Google Scholar

25. Ding, J., Peng, W., Luo, T. & Yu, H. (2016). Study on the curing reaction kinetics of a novel epoxy system. Rsc Advances, 7(12). DOI: 10.1039/C6RA25120J.10.1039/C6RA25120JOpen DOISearch in Google Scholar

26. Haddadi, S.A., Kardar, P., Abbasi, F. & Mahdavian, M. (2017). Effects of nano-silica and boron carbide on the curing kinetics of resole resin. J. Therm. Analysis & Calorimetry, 128 (2), 1217-1226. DOI: 10.1007/s 10973-016-5951-3.10.1007/s10973-016-5951-3Open DOISearch in Google Scholar

27. Monteserín, C., Blanco, M., Aranzabe, E., Aranzabe, A. & Vilas, J.L. (2017). Effects of graphene oxide and chemically reduced graphene oxide on the curing kinetics of epoxy amine composites. J. Appl. Polym. Sci. 134 (19) 44803. DOI: 10.1002/app.44803.10.1002/app.44803Search in Google Scholar

28. Sharif, M., Pourabbas, B., Sangermano, M., Sadeghi Moghadam, F., Mohammadi, M. & Roppolo, I., et al. (2017). The effect of graphene oxide on uv curing kinetics and properties of su8 nanocomposites. Polymer International, 66. 405.DOI: 10.1002/pi.5271.10.1002/pi.5271Search in Google Scholar

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