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Collect. Czech. Chem. Commun. 1971, 36, 3140-3164
https://doi.org/10.1135/cccc19713140

Stereochemical studies. LXI. The contribution of syn- and anti-elimination to olefin formation in open-chain systems: 5-Decyl and 5-nonyl trimethylammonium bases and tosylates

J. Sicher, J. Závada and M. Pánková

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  • Mohrig Jerry R., Alberg David G., Cartwright Craig H., Pflum Mary Kay H., Aldrich Jeffrey S., Anderson J. Kyle, Anderson Shelby R., Fimmen Ryan L., Snover Amy K.: Stereochemistry of 1,2-elimination reactions at the E2–E1cB interface—tert-butyl 3-tosyloxybutanoate and its thioester. Org. Biomol. Chem. 2008, 6, 1641. <https://doi.org/10.1039/b801592a>
  • SICHER J., ZAVADA J., PANKOVA M.: ChemInform Abstract: STEREOCHEMISCHE UNTERSUCHUNGEN 61. MITT. MECHANISMEN VON ELIMINIERUNGSRK. 20. MITT. ANTEIL DER SYN‐ UND ANTI‐ELIMINIERUNG BEI DER OLEFINBLDG. IN OFFENKETTIGEN SYST., DECYL‐(5)‐TRIMETHYLAMMONIUMBASEN UND ‐TOSYLATE. Chemischer Informationsdienst 1972, 3. <https://doi.org/10.1002/chin.197202105>
  • Svoboda M., Hapala J., Závada J.: The role of base ion-pairing in bimolecular elimination: the effect on the syn-anti dichotomy. Tetrahedron Letters 1972, 13, 265. <https://doi.org/10.1016/S0040-4039(01)84297-0>
  • Závada J., Svoboda M., Pánková M.: The role of base ion-pairing in bimolecular elimination: the effect on the cis- to trans-olefin ratios in the anti- and the syn-pathway. Tetrahedron Letters 1972, 13, 711. <https://doi.org/10.1016/S0040-4039(01)84418-X>
  • Pánková M., Svoboda M., Závada J.: A general occurence of the syn-anti elimination dichotomy under ion-pairing conditions : inessentiality of steric requirements of the leaving group. Tetrahedron Letters 1972, 13, 2465. <https://doi.org/10.1016/S0040-4039(01)84848-6>