Supporting Information
General information, synthesis of triazines I–X and structure determination, spectral data of amides 3, attempted synthesis of I from 6, amide-forming reaction with VI in the absence of NMM, and copies of 1H and 13C NMR spectra of unknown compounds are given.
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Cite the Following Article
Potent triazine-based dehydrocondensing reagents substituted by an amido group
Munetaka Kunishima, Daiki Kato, Nobu Kimura, Masanori Kitamura, Kohei Yamada and Kazuhito Hioki
Beilstein J. Org. Chem. 2016, 12, 1897–1903.
https://doi.org/10.3762/bjoc.12.179
How to Cite
Kunishima, M.; Kato, D.; Kimura, N.; Kitamura, M.; Yamada, K.; Hioki, K. Beilstein J. Org. Chem. 2016, 12, 1897–1903. doi:10.3762/bjoc.12.179
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- Kitamura, M.; Komine, S.; Yamada, K.; Kunishima, M. Trizaine-based dehydrative condensation reagents bearing carbon-substituents. Tetrahedron 2020, 76, 130900. doi:10.1016/j.tet.2019.130900
- Yamada, K.; Kota, M.; Takahashi, K.; Fujita, H.; Kitamura, M.; Kunishima, M. Development of Triazinone-Based Condensing Reagents for Amide Formation. The Journal of organic chemistry 2019, 84, 15042–15051. doi:10.1021/acs.joc.9b01261
- Kitamura, M.; Sasaki, S.; Nishikawa, R.; Yamada, K.; Kunishima, M. Imido-substituted triazines as dehydrative condensing reagents for the chemoselective formation of amides in the presence of free hydroxy groups. RSC advances 2018, 8, 22482–22489. doi:10.1039/c8ra03057j
- Audebert, P.; Clavier, G.; Allain, C. Triazines, Tetrazines, and Fused Ring Polyaza Systems. Progress in Heterocyclic Chemistry; Elsevier, 2017; pp 483–518. doi:10.1016/b978-0-08-102310-5.00014-x
- Kunishima, M.; Kato, D.; Kimura, N.; Kitamura, M.; Yamada, K.; Hioki, K. Potent Triazine-Based Dehydrocondensing Reagents Substituted by an Amido Group. ChemInform 2016, 47. doi:10.1002/chin.201649057
- Audebert, P.; Clavier, G.; Allain, C. Triazines, Tetrazines, and Fused Ring Polyaza Systems. Progress in Heterocyclic Chemistry 2016, 28, 493–521. doi:10.1016/b978-0-08-100755-6.00014-4
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