Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1964, 29, 645-651
https://doi.org/10.1135/cccc19640645

Reactivity of 1,1-dialkoxytrimethylamines

Z. Arnold and M. Kornilov

Crossref Cited-by Linking

  • Gloede Jörg, Haase Ludwig, Groβ Hans: Amidacetale, Darstellung und Verwendung. Z. Chem. 2010, 9, 201. <https://doi.org/10.1002/zfch.19690090602>
  • Medvedeva M. I., Tugusheva N. Z., Alekseeva L. M., Evstratova M. I., Kiselev S. S., Chernyshev V. V., Avramenko G. V., Granik V. G.: Substituted 3-and 5-formylpyridin-2-ones in the synthesis of 1-aryl-1, 6-naphthyridinone derivatives. Russ Chem Bull 2009, 58, 2336. <https://doi.org/10.1007/s11172-009-0325-7>
  • Mukhanova T. I., Kukushkin S. Yu., Ivanov P. Yu., Alekseeva L. M., Granik V. G.: A study of the Claisen—Eschenmoser reaction for hydroxymethylbenzofurans and-indoles. Russ Chem Bull 2007, 56, 325. <https://doi.org/10.1007/s11172-007-0053-9>
  • Komarova E. S., Makarov V. A., Alekseeva L. M., Avramenko G. V., Granik V. G.: 4,5-Diamino-1-phenyl-1,7-dihydro-6H-pyrazolo[3,4-b]pyridin-6-one in the synthesis of fused tricyclic systems. Russ Chem Bull 2007, 56, 2337. <https://doi.org/10.1007/s11172-007-0369-5>
  • Ryabova S. Yu., Alekseeva L. M., Lisitsa E. A., Masterova N. S., Kiselev S. S., Evstratova M. I., Granik V. G.: A new approach to the synthesis of pyrrolo[1,2-a]indole derivatives. Russ Chem Bull 2006, 55, 2271. <https://doi.org/10.1007/s11172-006-0582-7>
  • Guthrie J Peter, Gallant Roger T, Jennings Michael C: Preparation and characterization of bicyclic amide acetals and monothioacetals. Can. J. Chem. 2004, 82, 268. <https://doi.org/10.1139/v03-204>
  • Hocková Dana, Buděšínský Miloš, Marek Radek, Marek Jaromír, Holý Antonín: Regioselective Preparation ofN7- andN9-Alkyl Derivatives ofN6-[(Dimethylamino)methylene]adenine Bearing an Active Methylene Group and Their Further Derivatization Leading to α-Branched Acyclic Nucleoside Analogues. Eur. J. Org. Chem. 1999, 1999, 2675. <https://doi.org/10.1002/(SICI)1099-0690(199910)1999:10<2675::AID-EJOC2675>3.0.CO;2-Z>
  • Gusar' N. I., Gul'ko L. I., Gorodetskova N. R., Klebanov B. M.: Synthesis and pharmacological activity of 1-aryl-3-amino-2-pyrazoline derivatives. Pharm Chem J 1994, 28, 255. <https://doi.org/10.1007/BF02219798>
  • Ranganathan Subramania, Kundu Dinabandhu, Mehrotra Sanjiv: The crafting of uracils with enhanced stacking potential. Proc. Indian Acad. Sci. (Chem. Sci.) 1994, 106, 1051. <https://doi.org/10.1007/BF02841916>
  • Mikołajczyk Marian, Graczyk Piotr P., Wiecorek Michał W., Bujacz Grzegorz: A solution and solid state conformation of 2-diphenylphosphinoyl-1,3-dioxanes. The nature of O-C-P anomeric interactions. Tetrahedron 1992, 48, 4209. <https://doi.org/10.1016/S0040-4020(01)92198-2>
  • Castro-Pichel Julia, García-López M. Teresa, De las Heras Federico G., Herranz Rosario: Synthesis of pyrimidine analogues of the nucleoside antibiotic ascamycin. Liebigs Ann. Chem. 1988, 1988, 737. <https://doi.org/10.1002/jlac.198819880805>
  • Castro-Pichel Julia, García-López María Teresa, De las Heras Federico G.: A facile synthesis of ascamycin and related analogues. Tetrahedron 1987, 43, 383. <https://doi.org/10.1016/S0040-4020(01)89967-1>
  • Mohacsi Erno: A New Synthetic Method for the Preparation of N,N-Dimethylformamide DI-Tert-Butyl Acetal. Synthetic Communications 1985, 15, 723. <https://doi.org/10.1080/00397918508063864>
  • Lapuka L. F., Kurbanov D., Pastushenko E. V., Zlot-skii S. S., Rakhmankulov D. L.: Three-dimensional structure of 2-dimethylamino-1,3-dioxacyclanes. Chem Heterocycl Compd 1984, 20, 609. <https://doi.org/10.1007/BF00508665>
  • Schenone Pietro, Mosti Luisa, Menozzi Giulia: Reaction of 2-dimethylaminomethylene-1,3-diones with dinucleophiles. I. Synthesis of 1,5-disubstituted 4-acylpyrazoles. Journal of Heterocyclic Chemistry 1982, 19, 1355. <https://doi.org/10.1002/jhet.5570190620>
  • Kantlehner Willi, Kienitz Lutz, Jaus Horst, Bredereck Hellmut: Orthoamide, XXX. Darstellung von Orthoamidderivaten der Kohlensäure. Liebigs Ann. Chem. 1979, 1979, 2089. <https://doi.org/10.1002/jlac.197919791219>
  • Corley L.S., Vogl O.: Haloaldehyde polymers: 16. Stabilization of anionically-prepared polychloral by end-capping with decomposable cations and other additives. Polymer 1979, 20, 1535. <https://doi.org/10.1016/0032-3861(79)90022-3>
  • Abdulla R.F., Brinkmeyer R.S.: The chemistry of formamide acetals. Tetrahedron 1979, 35, 1675. <https://doi.org/10.1016/0040-4020(79)88001-1>
  • Costisella B., Gross H.: ?-Substituierte Phosphonate. XXII. Synthese und NMR-Spektren offenkettiger und cyclischer Acetale von Formyl-phosphons�ureestern und Formyl-diphenylphosphinoxid. J. Prakt. Chem. 1977, 319, 8. <https://doi.org/10.1002/prac.19773190103>
  • Anteunis Marc, Gelan J., Van Cauwenberghe R.: NMR experiments on acetals. 300 MHz spectrum and conformational aspects of the 1-aza-4,6-dioxabicyclo[3.3.0]octane system. Org. Magn. Reson. 1974, 6, 362. <https://doi.org/10.1002/mrc.1270060614>
  • Kantlehner Willi, Speh Peter: Orthoamide, XXI. Reaktionen von Dialkylamino‐methoxy‐acetonitrilen und Bis‐dimethylamino‐acetonitril mit Alkalialkoholaten. Eine neue Synthese von Säureamidacetalen und Aminalestern. Chem. Ber. 1972, 105, 1340. <https://doi.org/10.1002/cber.19721050424>
  • Gualtieri F., Johnson H., Maibach H., Skidmore D., Skinner W.: Topical Mosquito Repellents IV: Alicyclic, Bicyclic, and Unsaturated Acetals, Aminoacetals, and Carboxamide Acetals. Journal of Pharmaceutical Sciences 1972, 61, 577. <https://doi.org/10.1002/jps.2600610417>
  • Holý A.: Transformation of nucleosides into their 5′-deoxy derivatives. Tetrahedron Letters 1972, 13, 585. <https://doi.org/10.1016/S0040-4039(01)84384-7>
  • Martini Thomas: Die umsetzung von fluorolefinen mit diäthanolamin. Tetrahedron Letters 1972, 13, 3957. <https://doi.org/10.1016/S0040-4039(01)94207-8>
  • Bredereck Hellmut, Simchen Gerhard, Kantlehner Willi: Orthoamide, XVII. Reaktionen von Dimethylamino‐alkoxy‐acetonitrilen. Chem. Ber. 1971, 104, 932. <https://doi.org/10.1002/cber.19711040332>
  • Kantlehner Willi, Speh Peter: Säureamid‐Reaktionen, LI. Notiz zur Darstellung von N . N . N ′. N ′‐Tetramethylformamidiniumchlorid. Chem. Ber. 1971, 104, 3714. <https://doi.org/10.1002/cber.19711041136>
  • Bredereck Hellmut, Simchen Gerhard, Rebsdat Siegfried, Kantlehner Willi, Horn Peter, Wahl Rudolf, Hoffmann Horst, Grieshaber Peter: Säureamid‐Reaktionen, L; Orthoamide, I Darstellung und Eigenschaften der Amidacetale und Aminalester. Chem. Ber. 1968, 101, 41. <https://doi.org/10.1002/cber.19681010108>
  • Seeliger W., Aufderhaar E., Diepers W., Feinauer R., Nehring R., Thier W., Hellmann H.: Neuere Synthesen und Reaktionen cyclischer Imidsäureester. Angew. Chem. 1966, 78, 913. <https://doi.org/10.1002/ange.19660782002>
  • Feinauer Roland, Seeliger Wolfgang: Über die Anlagerung von Epoxiden an cyclische Iminoester. Justus Liebigs Ann. Chem. 1966, 698, 174. <https://doi.org/10.1002/jlac.19666980120>
  • Lustig Ernest., Moniz William B.: Nuclear Magnetic Resonance Spectrometry. Anal. Chem. 1966, 38, 331. <https://doi.org/10.1021/ac60237a023>
  • Brechbühler H., Büchi H., Hatz E., Schreiber J., Eschenmoser A.: Die Reaktion von Carbonsäuren mit Acetalen des N, N-Dimethylformamids: eine Veresterungsmethode. HCA 1965, 48, 1746. <https://doi.org/10.1002/hlca.19650480734>