Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1987, 52, 2961-2970
https://doi.org/10.1135/cccc19872961

A versatile synthesis of oligocrown compounds with hydroxyl groups at the hinge

Martin Bělohradský, Petr Holý, Ivan Stibor and Jiří Závada

Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6

Crossref Cited-by Linking

  • Zarzyka-Niemiec Iwona, Lubczak Jacek: Kinetics and mechanism of addition of parabanic acid (imidazolidine-2,4,5-trione) to oxiranes. Int. J. Chem. Kinet. 2003, 35, 73. <https://doi.org/10.1002/kin.10104>
  • Yu Zaitsev S., Belohradsky M., Zavada J., Möbius D.: Ionic selectivity of the surface-active derivatives of crown ethers in monolayers. This Solid Films 1994, 248, 78. <https://doi.org/10.1016/0040-6090(94)90214-3>
  • Bělohradský Martin, Holý Petr, Koudelka Juraj, Krchňák Viktor, Závada Jiří: Rearrangement of 1,3-bis(azacrown)-2-chloropropanes: the effect of alkali metal ion on neighbouring group participation. J. Chem. Soc., Chem. Commun. 1992, 1745. <https://doi.org/10.1039/C39920001745>
  • BELOHRADSKY M., HOLY P., STIBOR I., ZAVADA J.: ChemInform Abstract: Chemistry of Multidentate Ligands. Part 7. A Versatile Synthesis of Oligocrown Compounds with Hydroxyl Groups at the Hinge. ChemInform 1988, 19. <https://doi.org/10.1002/chin.198813249>