Phosphinocyclodextrins as confining units for catalytic metal centres. Applications to carbon–carbon bond forming reactions

Matthieu Jouffroy, Rafael Gramage-Doria, David Sémeril, Dominique Armspach, Dominique Matt, Werner Oberhauser and Loïc Toupet
Beilstein J. Org. Chem. 2014, 10, 2388–2405. https://doi.org/10.3762/bjoc.10.249

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Supporting Information File 1: Copies of NMR spectra for compounds 2, 3, 6, 7, 8, 10a and 10b and 11.
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Phosphinocyclodextrins as confining units for catalytic metal centres. Applications to carbon–carbon bond forming reactions
Matthieu Jouffroy, Rafael Gramage-Doria, David Sémeril, Dominique Armspach, Dominique Matt, Werner Oberhauser and Loïc Toupet
Beilstein J. Org. Chem. 2014, 10, 2388–2405. https://doi.org/10.3762/bjoc.10.249

How to Cite

Jouffroy, M.; Gramage-Doria, R.; Sémeril, D.; Armspach, D.; Matt, D.; Oberhauser, W.; Toupet, L. Beilstein J. Org. Chem. 2014, 10, 2388–2405. doi:10.3762/bjoc.10.249

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  • Natarajan, N.; Pierrevelcin, M.-C.; Sémeril, D.; Bauder, C.; Matt, D.; Ramesh, R. Chiral calixarene and resorcinarene derivatives. Conical cavities substituted at their upper rim by two phosphito units and their use as ligands in Rh-catalysed hydroformylation. Catalysis Communications 2019, 118, 70–75. doi:10.1016/j.catcom.2018.09.020
  • Kaya, Z.; Andna, L.; Matt, D.; Bentouhami, E.; Djukic, J.-P.; Armspach, D. Benzimidazolium‐ and Benzimidazolilydene‐Capped Cyclodextrins: New Perspectives in Anion Encapsulation and Gold‐Catalyzed Cycloisomerization of 1,6‐Enynes. Chemistry (Weinheim an der Bergstrasse, Germany) 2018, 24, 17921–17926. doi:10.1002/chem.201804710
  • Yang, J.; Chatelet, B.; Hérault, D.; Dutasta, J.-P.; Martinez, A. Covalent Cages with Inwardly Directed Reactive Centers as Confined Metal and Organocatalysts. European Journal of Organic Chemistry 2018, 2018, 5618–5628. doi:10.1002/ejoc.201800867
  • Harvey, D. Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2013–2014. Mass spectrometry reviews 2018, 37, 353–491. doi:10.1002/mas.21530
  • Sechet, D.; Kaya, Z.; Phan, T. A.; Jouffroy, M.; Bentouhami, E.; Armspach, D.; Matt, D.; Toupet, L. Aza-capped cyclodextrins for intra-cavity metal complexation. Chemical communications (Cambridge, England) 2017, 53, 11717–11720. doi:10.1039/c7cc06434a
  • Wang, B.; Bols, M. Artificial Metallooxidases from Cyclodextrin Diacids. Chemistry (Weinheim an der Bergstrasse, Germany) 2017, 23, 13766–13775. doi:10.1002/chem.201702530
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  • Dindulkar, S. D.; Jeong, D.; Kim, H.; Jung, S. Functionalized β-cyclodextrin as supramolecular ligand and their Pd(OAc)2 complex: highly efficient and reusable catalyst for Mizoroki-Heck cross-coupling reactions in aqueous medium. Carbohydrate research 2016, 430, 85–94. doi:10.1016/j.carres.2016.04.024
  • Macaev, F.; Boldescu, V. Cyclodextrins in Asymmetric and Stereospecific Synthesis. Symmetry 2015, 7, 1699–1720. doi:10.3390/sym7041699
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Patents

  • MATT DOMINIQUE; ARMSPACH DOMINIQUE; JOUFFROY MATTHIEU. AZA-CAPPED CYCLODEXTRINS AND PROCESS OF PREPARING THEM. EP 3281957 A1, Feb 14, 2018.
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