參考文獻 |
[1] Moss, G. P.; Smith, P. A. S.; Tavernier, D. “Glossary of class names of organic compounds and reactive itermediates based on structure.” Pure Appl. Chem. 1995, 67, 1307‒1375.
[2] Bhalla, V.; Grimm, P. C.; Chertow, G. M.; Pao, A. C. “Melamine nephrotoxicity: an emerging epidemic in an era of globalization.” Kidney Int. 2009, 75, 774‒779.
[3] Chien, C. Y.; Wu, C. F.; Liu, C. C.; Chen, B. H.; Huang, S. P.; Chou, Y. H.; Chang, A. W.; Lee, H. H.; Pan, C. H.; Wu, W. J.; Shen, J. T.; Chang, M. Y.; Huang, C. H.; Shiea, J.; Hsieh, T. J.; Wu, M. T. “High melamine migration in daily-use melamine-made tableware.” J. Hazard. Mater. 2011, 188, 350‒356.
[4] Huthmacher, K.; Most, D. “Cyanuric Acid and Cyanuric Chloride.” In Ullmann′s Encyclopedia of Industrial Chemistry, 7th ed.; Wiley-VCH: Weinheim, Germany, 2006.
[5] El-Faham, A.; Osman, S. M.; Al-Lohedan, H. A.; El-Mahdy, G. A. “Hydrazino-methoxy-1,3,5-triazine derivatives excellent corrosion organic inhibitors of steel in acidic chloride solution.” Molecules 2016, 21, 714-727.
[6] Zhao, Y.; King, G.; Kwan, M. H. T.; Blacker, A. J. “A mild and selective method for the catalytic hydrodeoxygenation of cyanurate activated phenols in multiphasic continuous flow.” Org. Process Res. Dev. 2016, 20, 2012‒2018.
[7] Shi, B.; Lewis, W.; Campbell, I. B.; Moody, C. J. “A concise route to pyridines from hydrazides by metal carbene N−H insertion, 1,2,4-Triazine Formation, and Diels−Alder Reaction.” Org. Lett. 2009, 11, 3686‒3688.
[8] Quiñones, R. E.; Glinkerman, C. M.; Zhu, K.; Boger, D. L. “Direct synthesis of β-aminoenals through reaction of 1,2,3-triazine with secondary amines.” Org. Lett. 2017, 19, 3568‒3571.
[9] Anderson, E. D.; Boger, D. L. “Inverse electron demand Diels–Alder reactions of 1,2,3-triazines: pronounced substituent effects on reactivity and cycloaddition Scope.” J. Am. Chem. Soc. 2011, 133, 12285‒12292.
[10] Itoh, T.; Ohsawa, A.; Okada, M.; Kaihoh, T.; Igeta, H. “Reaction of 1,2,3-triazine with dieneophile.” Chem. Pharm. Bull. 1985, 33, 3050‒3052.
[11] Okatani, T.; Koyama, J.; Tagahara, K.; Suzuta, Y. “Synthesis of sesquiterpene alkaloids, guaipyridine: epiguaipyridine and related compounds.” Heterocycles 1987, 26, 595‒597.
[12] Okatani, T.; Koyama, J.; Suzuta, Y.; Tagahara, K. “The effects of solvent and temperature on the orientation of cycloaddition reaction of 1,2,3-triazine with enamines: its application to the synthesis of alkaloids. onychine and 6-methoxyonychine.” Heterocycles 1988, 27, 2213‒2217.
[13] Okatani, T.; Koyama, J.; Tagahara, K. “Modified synthesis of monocyclic 1,2,3-triazine and cycloaddition reaction with enamine: the application to the synthesis of alkaloids, tortuosamine, N-formyltortuosamine and N-acetyltortuosamine.” Heterocycles 1989, 29, 1809‒1814.
[14] Itoh, T.; Okada, M.; Nagata, K.; Yamaguchi, K.; Ohsawa, A. “The ring transformation of 1, 2, 3-triazines.” Chem. Pharm. Bull. 1990, 38, 2108‒2111.
[15] Anderson, E. D.; Duerfeldt, A. S.; Zhu, K.; Glinkerman, C. M.; Boger, D. L. “Cycloadditions of noncomplementary substituted 1,2,3-triazines.” Org. Lett. 2014, 16, 5084‒5087.
[16] Glinkerman, C. M.; Boger, D. L. “Cycloadditions of 1,2,3-triazines bearing C5-electron donating substituents: robust pyrimidine synthesis.” Org. Lett. 2015, 17, 4002‒4005.
[17] Ohsawa, A.; Kaihoh, T.; Igeta, H. “The reaction of 1,2,3-triazines with Grignard reagents.” J. Chem. Soc., Chem. Commun. 1985, 20, 1370‒1371.
[18] Itoh, T.; Nagata, K.; Kaihoh, T.; Okada, M.; Kawabata, C.; Arai, H.; Ohnishi, H.; Yamaguchi, K.; Igeta, H.; Ohsawa, A.; Iitaka, Y. “The reactivity of monocyclic 1,2,3-triazine.” Heterocycles 1992, 33, 631‒639.
[19] Cavani, F.; Teles, J. H. “Sustainability in catalytic oxidation: an alternative approach or a structural evolution.” ChemSusChem 2009, 2, 508‒534.
[20] Davies, H. M. L.; Manning, J. R. “Catalytic C–H functionalization by metal carbenoid and nitrenoid insertion.” Nature 2008, 451, 417‒424.
[21] Constable, D. J. C.; Dunn, P. J.; Hayler, J. D.; Humphrey, G. R.; Leazer, Jr. J. L.; Linderman, R. J.; Lorenz, K.; Manley, J.; Pearlman, B. A.; Wells, A.; Zaks, A.; Zhang, T. Y. “Key green chemistry research areas‒a perspective from pharmaceutical manufacturers.” Green Chem. 2007, 9, 411‒420.
[22] Gligorich, K. M.; Sigman, M. S. “Recent advancements and challenges of palladium II-catalyzed oxidation reactions with molecular oxygen as the sole oxidant.” Chem. Commun. 2009, 26, 3854‒3867.
[23] Stahl, S. S. “Palladium-catalyzed oxidation of organic chemicals with O2.” Science 2005, 309, 1824‒1826.
[24] Allen, S. E.; Walvoord, R. R.; Padilla-Salinas, R.; Kozlowski, M. C. “Aerobic copper-catalyzed organic reactions.” Chem. Rev. 2013, 113, 6234‒6458.
[25] Dhakshinamoorthy, A.; Alvaro, M.; Garcia, H. “Metal organic frameworks as efficient heterogeneous catalysts for the oxidation of benzylic compounds with t-butylhydroperoxide.” J. Catal. 2009, 267, 1‒4.
[26] Barton, D. H. R.; Beviere, S. D.; Hill, D. R. “The functionalization of saturated hydrocarbons part XXIX. Application of tert-butyl hydroperoxide and dioxygen using soluble Fe(III) and Cu(II) chelates.” Tetrahedron 1994, 50, 2665‒2670.
[27] Glaser, C. “Beiträge zur kenntniss des acetenylbenzols.” Ber. Dtsch. Chem. Ges. 1869, 2, 422‒424.
[28] Hay, A. S. “Oxidative coupling of acetylenes.” J. Org. Chem. 1962, 27, 3320‒3321.
[29] Hamada, T.; Ye, X.; Stahl, S. S. “Copper-catalyzed aerobic oxidative amidation of terminal alkynes: efficient synthesis of ynamides.” J. Am. Chem. Soc. 2008, 130, 833‒835.
[30] Laouiti, A.; Rammah, M. M.; Rammah, M. B.; Marrot, J.; Couty, F.; Evano, G. “Copper-catalyzed oxidative alkynylation of diaryl imines with terminal alkynes: a facile synthesis of ynimines.” Org. Lett. 2012, 14, 6‒9.
[31] Hynes, J.; Doubleday, W. W.; Dyckman, A. J.; Godfrey, J. D.; Grosso, J. A.; Kiau, S.; Leftheris, K. “N-Amination of pyrrole and indole heterocycles with monochloramine (NH2Cl).” J. Org. Chem. 2004, 69, 1368‒1371.
[32] Mondal, S.; Samanta, S.; Jana, S.; Hajra, A. “(Diacetoxy)iodobenzene-mediated oxidative C−H amination of imidazopyridines at ambient temperature.” J. Org. Chem. 2017, 82, 4504‒4510. |