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Collect. Czech. Chem. Commun. 1970, 35, 2810-2830
https://doi.org/10.1135/cccc19702810

Ganglionic blocking agents. XV. Synthesis and activity of some tertiary hexylamines

Z. J. Vejdělek, V. Trčka, M. Vaněček, B. Kakáč and J. Holubek

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  • Beaudegnies Renaud, Lamberth Clemens: A general synthesis of novel acyclic chiral α-tertiary amines. Tetrahedron Letters 2020, 61, 152463. <https://doi.org/10.1016/j.tetlet.2020.152463>
  • Svoboda Jan, Pelcová Monika, Nevěčná Taťjana, Pytela Oldřich: Kinetics and Mechanism of Acetoxymercuration and Acid-Catalysed Hydration of α-Alkylstyrenes. IJMS 2005, 6, 30. <https://doi.org/10.3390/i6010030>
  • Schwesinger Reinhard, Willaredt Jürgen, Schlemper Helmut, Keller Manfred, Schmitt Dieter, Fritz Hans: Novel, Very Strong, Uncharged Auxiliary Bases; Design and Synthesis of Monomeric and Polymer‐Bound Triaminoiminophosphorane Bases of Broadly Varied Steric Demand. Chem. Ber. 1994, 127, 2435. <https://doi.org/10.1002/cber.19941271215>
  • Schwesinger Reinhard, Hasenfratz Christian, Schlemper Helmut, Walz Leonhard, Peters Eva‐Maria, Peters Karl, Von Schnering Hans Georg: Wie stark und wie gehindert können ungeladene Phosphazenbasen sein?. Angewandte Chemie 1993, 105, 1420. <https://doi.org/10.1002/ange.19931050940>
  • Schwesinger Reinhard, Hasenfratz Christian, Schlemper Helmut, Walz Leonhard, Peters Eva‐Maria, Peters Karl, von Schnering Hans Georg: How Strong and How Hindered Can Uncharged Phosphazene Bases Be?. Angew. Chem. Int. Ed. Engl. 1993, 32, 1361. <https://doi.org/10.1002/anie.199313611>
  • Elliott Michael, Farnham Andrew W., Janes Norman F., Johnson Diana M., Pulman David A.: Synthesis and insecticidal activity of lipophilic amides. Part 5: Influence on activity of varying the substituent on nitrogen. Pestic. Sci. 1987, 18, 229. <https://doi.org/10.1002/ps.2780180403>
  • VEJDELEK Z. J., TRCKA V., VANECEK M., KAKAC B., HOLUBEK J.: ChemInform Abstract: GANGLIENBLOCKIERENDE AGENZIEN 15. MITT. SYNTHESE UND AKTIVITAET EINIGER TERTIAERER HEXYLAMINE. Chemischer Informationsdienst. Organische Chemie 1971, 2. <https://doi.org/10.1002/chin.197101244>