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Collect. Czech. Chem. Commun. 1999, 64, 633-648
https://doi.org/10.1135/cccc19990633

Are 1,4-Dihydropyrazines Antiaromatic? Ab initio Study of 1,4-Dihydropyrazines and Their Tetrahydro Derivatives

Pavel Vlčeka, Zdeněk Havlasb,* and Zdeněk Pavlíčeka

a Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University, Hlavova 2030, 120 00 Prague 2, Czech Republic
b Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Flemingovo nám. 2, 166 10 Prague 6, Czech Republic

Crossref Cited-by Linking

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  • Saito Teruhiko, Nishiyama Haruka, Tanahashi Hiromasa, Kawakita Kento, Tsurugi Hayato, Mashima Kazushi: 1,4-Bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadienes as Strong Salt-Free Reductants for Generating Low-Valent Early Transition Metals with Electron-Donating Ligands. J. Am. Chem. Soc. 2014, 136, 5161. <https://doi.org/10.1021/ja501313s>
  • Vashchenko A. V., Pavlova T. O., Chuvashev N. F.: Quantum-chemical study of the relative stability of conformers of 1,4-dihydropyrazine and 1,4-dihydro-1,4-diphosphinine. Russ J Gen Chem 2013, 83, 1094. <https://doi.org/10.1134/S1070363213060157>
  • Nakai Shunichiro, Yasui Masanori, Nakazato Masaki, Iwasaki Fujiko, Maki Shojiro, Niwa Haruki, Ohashi Mamoru, Hirano Takashi: Fundamental Studies on the Structures and Spectroscopic Properties of Imidazo[1,2-a]pyrazin-3(7H)-one Derivatives. BCSJ 2003, 76, 2361. <https://doi.org/10.1246/bcsj.76.2361>
  • Fruit Corinne, Turck Alain, Plé Nelly, Mojovic Ljubica, Quéguiner Guy: Syntheses and metalation of pyridazinecarboxamides and thiocarboxamides. Diazines. Part 32. Tetrahedron 2002, 58, 2743. <https://doi.org/10.1016/S0040-4020(02)00176-X>
  • New Convulsive Compounds, Brasiliamides A and B, from Penicillium brasilianum Batista JV-379. Biosci Biotechnol Biochem 2002, 66, 1697. <https://doi.org/10.1271/bbb.66.1697>