The preparation of new functionalized [2.2]paracyclophane derivatives with N-containing functional groups

Scholarly Works

• Alshammari, M. B.; Aly, A. A.; Bräse, S.; Nieger, M.; Abd El-Haleem, L. E. Efficient Synthesis of Various Substituted (Thio)Ureas, Semicarbazides, Thiosemicarbazides, Thiazolidones, and Oxadiazole Derived from [2.2]Paracyclophane. ACS omega 2022, 7, 12879–12890. doi:10.1021/acsomega.2c00141
• Hassan, A. A.; Bräse, S.; Aly, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Nieger, M. Stereoselective synthesis of homochiral paracyclophanylindenofuranylimidazo[3.3.3]propellanes. Monatshefte für Chemie - Chemical Monthly 2021, 152, 1571–1579. doi:10.1007/s00706-021-02853-0
• Hassan, A. A.; Bräse, S.; Aly, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Nieger, M. Stereoselective synthesis of homochiral paracyclophanylindenofuranylimidazo[3.3.3]propellanes. Monatshefte Fur Chemie 2021, 152, 1–9.
• Biliz, F.; Cakici, M. Regioselective Synthesis of 4,7,12,15-Tetrasubstituted [2.2]Paracyclophanes: A Modular Route Involving Optical Resolution. European Journal of Organic Chemistry 2021, 2021, 4828–4834. doi:10.1002/ejoc.202100762
• Mungalpara, M. N.; Plieger, P. G.; Rowlands, G. J. The Synthesis of Pyridyl[2.2]paracyclophanes by Palladium‐Catalyzed Cross‐Coupling of Pyridine Sulfinates. Advanced Synthesis & Catalysis 2020, 363, 1069–1080. doi:10.1002/adsc.202001429
• Aly, A. A.; Bräse, S.; Hassan, A. A.; Mohamed, N. K.; El-Haleem, L. E. A.; Nieger, M. Synthesis of New Planar-Chiral Linked [2.2]Paracyclophanes- N-([2.2]-Paracyclophanylcarbamoyl)-4-([2.2]Paracyclophanylcarboxamide, [2.2]Paracyclophanyl-Substituted Triazolthiones and -Substituted Oxadiazoles. Molecules (Basel, Switzerland) 2020, 25, 3315. doi:10.3390/molecules25153315
• Henderson, W. R.; Fagnani, D. E.; Grolms, J.; Abboud, K. A.; Castellano, R. K. Transannular Hydrogen Bonding in Planar-Chiral [2.2]Paracyclophane-Bisamides. Helvetica Chimica Acta 2019, 102. doi:10.1002/hlca.201900047
• Dhami, J. K.; Idzorek, K. M.; Johnson, R. B.; Van Auken, K. S.; Ojala, W. H. Intramolecular geometry and intermolecular interactions of the CNO group of crystalline benzonitrile oxides: a comparison with phenyl cyanates, phenyl isocyanates, and phenyl azides. CrystEngComm 2019, 21, 908–916. doi:10.1039/c8ce02008f
• Loh, Y. K.; Ángeles Fuentes, M.; Vasko, P.; Aldridge, S. Successive Protonation of an N‐Heterocyclic Imine Derived Carbonyl: Superelectrophilic Dication Versus Masked Acylium Ion. Angewandte Chemie 2018, 130, 16797–16801. doi:10.1002/ange.201810709
• Loh, Y. K.; Fuentes, M. Á.; Vasko, P.; Aldridge, S. Successive Protonation of an N-Heterocyclic Imine Derived Carbonyl: Superelectrophilic Dication Versus Masked Acylium Ion. Angewandte Chemie (International ed. in English) 2018, 57, 16559–16563. doi:10.1002/anie.201810709
• Erb, W.; Levanen, G.; Roisnel, T.; Dorcet, V. Application of the Curtius rearrangement to the synthesis of 1′-aminoferrocene-1-carboxylic acid derivatives. New Journal of Chemistry 2018, 42, 3808–3818. doi:10.1039/c7nj05020h
• Braun, C.; Bräse, S.; Schafer, L. L. Planar‐Chiral [2.2]Paracyclophane‐Based Amides as Proligands for Titanium‐ and Zirconium‐Catalyzed Hydroamination. European Journal of Organic Chemistry 2017, 2017, 1760–1764. doi:10.1002/ejoc.201700101
• Jayasundera, K. P.; Kusmus, D. N. M.; Deuilhé, L.; Etheridge, L.; Farrow, Z.; Lun, D. J.; Kaur, G.; Rowlands, G. J. The synthesis of substituted amino[2.2]paracyclophanes. Organic & biomolecular chemistry 2016, 14, 10848–10860. doi:10.1039/c6ob02150f
• Doulcet, J.; Stephenson, G. R. The Use of (−)‐Sparteine/Organolithium Reagents for the Enantioselective Lithiation of 7,8‐Dipropyltetrathia[7]helicene: Single and Double Kinetic Resolution Procedures. Chemistry (Weinheim an der Bergstrasse, Germany) 2015, 21, 18677–18689. doi:10.1002/chem.201502958
• Hopf, H.; Dix, I.; Jones, P. G. Cyclophanes, Part 73: diastereoselective dimerization of an α,β-unsaturated ketone. Structure of all-trans-1,3-dibenzoyl-2,4-di([2.2]paracyclophan-4-yl)cyclobutane. Zeitschrift für Naturforschung B 2015, 70, 573–575. doi:10.1515/znb-2015-0022

Explore citations to this article at