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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

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  • Zarzyka‐Niemiec Iwona, Lubczak Jacek: Kinetics and mechanism of addition of parabanic acid (imidazolidine‐2,4,5‐trione) to oxiranes. Int J of Chemical Kinetics 2003, 35, 73. <https://doi.org/10.1002/kin.10104>
  • Katritzky Alan R., Denisko Olga V., Belyakov Sergei A., Schall Otto F., Gokel George W.: Synthesis of New N-Pivot Lariat Crown Ethers Containing a Propylene Linkage in the Side Arm. J. Org. Chem. 1996, 61, 7578. <https://doi.org/10.1021/jo961098w>
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  • 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>