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Collect. Czech. Chem. Commun. 1960, 25, 1318-1323
https://doi.org/10.1135/cccc19601318

Synthetische reaktionen von dimethylformamid VII. Darstellung von triformylmethan

Z. Arnold and J. Žemlička

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  • Rafat Ramin, Nowroozi Alireza: Solvent effects on the molecular stability, intramolecular hydrogen bond, and π-electron delocalization in the simple RAHB systems with different donors and acceptors: a quantum chemical study. Struct Chem 2019, 30, 777. <https://doi.org/10.1007/s11224-018-1221-2>
  • Reber Keith P., Burdge Hannah E.: Synthesis and Applications of Tricarbonylmethane Compounds. Organic Preparations and Procedures International 2018, 50, 2. <https://doi.org/10.1080/00304948.2018.1405332>
  • Mostovich Evgenii A., Mazhukin Dmitrii G., Gatilov Yurii V., Rybalova Tatyana V.: Coupling of 1,2-bis(alkoxyamino)cyclohexanes with 1,3-dicarbonyl compounds: first synthesis of 1,4-dialkoxy-2,3-dihydro-1,4-diazepinium salts. Mendeleev Communications 2007, 17, 48. <https://doi.org/10.1016/j.mencom.2007.01.019>
  • Adams Florian, Gompper Rudolf: Di(4-pyridinio)-, Di(2-benzothiazolio)-, Di(2-[1,3-dithiolylio])- und Diformyl-tetraaza[14]annulene sowie Tetraaza[14]annulenylen-homologe Tetrathiafulvalene. Angewandte Chemie 2006, 101, 1046. <https://doi.org/10.1002/ange.19891010814>
  • Nowroozi Alireza, Raissi Heidar: Strong intramolecular hydrogen bond in triformylmethane ab-initio, AIM and NBO study. Journal of Molecular Structure: THEOCHEM 2006, 759, 93. <https://doi.org/10.1016/j.theochem.2005.10.037>
  • Nowroozi Alireza, Tayyari Sayyed Faramarz, Rahemi Hedayat: Fourier transforms infrared spectra and structure of triformylmethane. A density functional theoretical study. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2003, 59, 1757. <https://doi.org/10.1016/S1386-1425(02)00410-9>
  • Koissi Niangoran, Neuvonen Kari, Munter Tony, Kronberg Leif, Lönnberg Harri: CONDENSATION OF TRIFORMYLMETHANE WITH GUANOSINE. Nucleosides, Nucleotides and Nucleic Acids 2001, 20, 1761. <https://doi.org/10.1081/NCN-100107188>
  • Takagi Kaname, Hubert-Habart Michel: Ring transformation of 5-acylpyrimidines and 5-acyluracils into pyrazoles with hydrazines in acidic medium. Journal of Heterocyclic Chemistry 1996, 33, 1003. <https://doi.org/10.1002/jhet.5570330401>
  • Reichardt Christian, Budnik Ulrich, Harms Klaus, Schäfer Gerhard, Stein Jörg: Chiral polymethine dyes, V. syntheses, absolute configuration, spectroscopic, and chiroptical properties of chiral dinuclear tri- and pentamethinium as well as trinuclear [2.2.2]heptamethinediium cyanine dyes with 3-sec-butyl-1,3-dimethylindolyl end groups. Liebigs Ann. 1995, 1995, 329. <https://doi.org/10.1002/jlac.199519950241>
  • Takagi Kaname, Bajnati Abdelilah, Hubert-Habart Michel: Formation of pyrimidine-5-carboxaldehydes, 1-aminoethylene-2,2-dicarboxaldehyde and 2-amino-4-anilino-1,3,5-triazine from triformylmethane and amidines. Journal of Heterocyclic Chemistry 1994, 31, 973. <https://doi.org/10.1002/jhet.5570310446>
  • Marson Charles M.: Reactions of carbonyl compounds with (monohalo) methyleniminium salts (vilsmeier reagents). Tetrahedron 1992, 48, 3659. <https://doi.org/10.1016/S0040-4020(01)92263-X>
  • Adams Florian, Gompper Rudolf: Di(4-pyridinio)-, Di(2-benzothiazolio)-, Di(2-[1,3-dithiolylio])- and Diformyltetraaza[14]annulenes and Tetraaza[14]annulenylene-Homologous Tetrathiafulvalenes. Angew. Chem. Int. Ed. Engl. 1989, 28, 1063. <https://doi.org/10.1002/anie.198910631>
  • Arnold Z., Kryshtal G.V., Král V., Dvorˇák D., Yanovskaya L.A.: The first general synthetic approach to aikylidenemalonaldehydes. Tetrahedron Letters 1988, 29, 2861. <https://doi.org/10.1016/0040-4039(88)85231-6>
  • Taylor Edward C., Yoon Cheol-Min: A Convenant Synthesis of 6-Formyl-5-Deazapterin. Synthetic Communications 1988, 18, 1187. <https://doi.org/10.1080/00397918808060909>
  • Reichardt Christian, Knecht Josef, Morsek Walter, Plaas Dietrich, Allmann Rudolf, Kucharczyk Damian: Synthesen mit aliphatischen Dialdehyden, XXXVII. Darstellung, Struktur und Eigenschaften eines [3.3.3]Decamethinium‐Cyaninfarbstoffes mit Indolin‐Endgruppen. Chem. Ber. 1983, 116, 1982. <https://doi.org/10.1002/cber.19831160525>
  • Knorr Rudolf, Weiß Alfons: Synthesen und Eigenschaften hochsubstituierter Vinamidine. Chem. Ber. 1982, 115, 139. <https://doi.org/10.1002/cber.19821150115>
  • Lloyd Douglas, McNab Hamish: Vinamidine und Vinamidiniumsalze — Beispiele stabilisierter Push-Pull-Alkene. Angew. Chem. 1976, 88, 496. <https://doi.org/10.1002/ange.19760881503>
  • Lloyd Douglas, McNab Hamish: Vinamidines and Vinamidinium Salts?Examples of Stabilized Push-Pull Alkenes. Angew. Chem. Int. Ed. Engl. 1976, 15, 459. <https://doi.org/10.1002/anie.197604591>
  • Pulst Manfred, Weißenfels Manfred: Die Chemie der β‐Chlorvinylaldehyde. Zeitschrift für Chemie 1976, 16, 337. <https://doi.org/10.1002/j.0044-2402.1976.tb00209.x>
  • Reichardt Christian, Mormann Werner: Synthesen mit substituierten Malondialdehyden, XI. γ‐Formyl‐tetramethinmerocyanin‐, γ‐Formyl‐pentamethincyanin‐ und [2.2.2]Heptamethincyanin‐Farbstoffe. Chem. Ber. 1972, 105, 1815. <https://doi.org/10.1002/cber.19721050606>
  • Reichardt Christian, Halbritter Klaus: Synthesen mit substituierten Malondialdehyden, X. γ‐Fluor‐pentamethincyanin‐Farbstoffe. Chem. Ber. 1971, 104, 822. <https://doi.org/10.1002/cber.19711040319>
  • Nikolajewski Hans Edmund, Dähne Siegfried, Hirsch Bodo: Neue Polymethinsynthesen, II. Vilsmeier‐Formylierung von Polyenaldehyden. Chem. Ber. 1967, 100, 2616. <https://doi.org/10.1002/cber.19671000822>
  • Reichardt Chr.: Synthesen mit substituierten malondialdehyden III trinucleare pentamethincyanin-farbstoffe. Tetrahedron Letters 1967, 8, 4327. <https://doi.org/10.1016/S0040-4039(01)89684-2>
  • Knunyants I. L., Cheburkov Yu. A., Bargamova M. D.: Action of triethylamine on 3,3,3-trifluoro-2-(trifluoromethyl)propionyl fluoride. Russ Chem Bull 1966, 15, 1000. <https://doi.org/10.1007/BF00846055>
  • Bredereck H., Effenberger F., Gleiter R., Hirsch K. A.: Synthese und Reaktionen von 1,3-Bisdimethylamino-3-methoxypropen und 1,3,3-Trisdimethylaminopropen. Angew. Chem. 1965, 77, 1010. <https://doi.org/10.1002/ange.19650772206>
  • Jutz C., Amschler H.: Tris-dibenzofulvenyl-methyl-Anion, ein extrem stabiles, farbiges Carbanion [3]. Angew. Chem. 1964, 76, 302. <https://doi.org/10.1002/ange.19640760707>