Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes

Carmine Gaeta, Carmen Talotta and Placido Neri
Beilstein J. Org. Chem. 2018, 14, 2112–2124. https://doi.org/10.3762/bjoc.14.186

Supporting Information

Supporting Information File 1: VT NMR studies of hexyloxycalix[6]arene 1, 2D COSY and HSQC spectra of atropoisomeric pseudorotaxanes, details of DFT calculations and atomic coordinates.
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Calix[6]arene-based atropoisomeric pseudo[2]rotaxanes
Carmine Gaeta, Carmen Talotta and Placido Neri
Beilstein J. Org. Chem. 2018, 14, 2112–2124. https://doi.org/10.3762/bjoc.14.186

How to Cite

Gaeta, C.; Talotta, C.; Neri, P. Beilstein J. Org. Chem. 2018, 14, 2112–2124. doi:10.3762/bjoc.14.186

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Scholarly Works

  • Iuliano, V.; Talotta, C.; Della Sala, P.; De Rosa, M.; Soriente, A.; Neri, P.; Gaeta, C. Hexahexyloxycalix[6]arene, a Conformationally Adaptive Host for the Complexation of Linear and Branched Alkylammonium Guests. Molecules (Basel, Switzerland) 2023, 28, 4749. doi:10.3390/molecules28124749
  • Mockler, N. M.; Ramberg, K. O.; Guagnini, F.; Raston, C. L.; Crowley, P. B. Noncovalent Protein-Pseudorotaxane Assembly Incorporating an Extended Arm Calix[8]arene with α-Helical Recognition Properties. Crystal growth & design 2021, 21, 1424–1427. doi:10.1021/acs.cgd.0c01717
  • Iuliano, V.; Talotta, C.; Gaeta, C.; Hickey, N.; Geremia, S.; Vatsouro, I.; Kovalev, V.; Neri, P. Influence of exo-Adamantyl Groups and endo-OH Functions on the Threading of Calix[6]arene Macrocycle. The Journal of organic chemistry 2020, 85, 12585–12593. doi:10.1021/acs.joc.0c01769
  • Bakić, M. T.; Iuliano, V.; Talotta, C.; Geremia, S.; Hickey, N.; Spinella, A.; De Rosa, M.; Soriente, A.; Gaeta, C.; Neri, P. Threading of Conformationally Stable Calix[6]arene Wheels Substituted at the Methylene Bridges. The Journal of organic chemistry 2019, 84, 11922–11927. doi:10.1021/acs.joc.9b01779
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