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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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Cite the Following Article
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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Scholarly Works
- Tilloy, S.; Monflier, E. doi:10.1002/9783527832033.ch34
- Kaya, Z.; Bentouhami, E.; Pelzer, K.; Armspach, D. Cavity-shaped ligands for asymmetric metal catalysis. Coordination Chemistry Reviews 2021, 445, 214066. doi:10.1016/j.ccr.2021.214066
- Tazawa, T.; Phanopoulos, A.; Nozaki, K. doi:10.1002/0471264180.or107.01
- Chakrabortty, S.; Almasalma, A. A.; de Vries, J. G. Recent developments in asymmetric hydroformylation. Catalysis Science & Technology 2021, 11, 5388–5411. doi:10.1039/d1cy00737h
- Molnár, Á. Synthetic Application of Cyclodextrins in Combination with Metal Ions, Complexes, and Metal Particles. ChemCatChem 2020, 13, 1424–1474. doi:10.1002/cctc.202001610
- Matt, D.; Harrowfield, J. Phosphines and other P(III)-derivatives with Cavity-shaped Subunits: Valuable Ligands for Supramolecular Metal Catalysis, Metal Confinement and Subtle Steric Control. ChemCatChem 2020, 13, 153–168. doi:10.1002/cctc.202001242
- Bauder, C.; Sémeril, D. Styrene hydroformylation with cavity‐shaped ligands. European Journal of Inorganic Chemistry 2019, 2019, 4951–4965. doi:10.1002/ejic.201900974
- 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
- Natarajan, N.; Brenner, E.; Sémeril, D.; Matt, D.; Harrowfield, J. The Use of Resorcinarene Cavitands in Metal‐Based Catalysis. European Journal of Organic Chemistry 2017, 2017, 6100–6113. doi:10.1002/ejoc.201700725
- Fankhauser, D.; Easton, C. J. Chirality in Supramolecular Assemblies; Wiley, 2016; pp 307–342. doi:10.1002/9781118867334.ch11
- Jouffroy, M.; Armspach, D.; Matt, D.; Osakada, K.; Takeuchi, D. Synthesis of Optically Active Polystyrene Catalyzed by Monophosphine Pd Complexes. Angewandte Chemie 2016, 128, 8507–8510. doi:10.1002/ange.201603191
- Jouffroy, M.; Armspach, D.; Matt, D.; Osakada, K.; Takeuchi, D. Synthesis of Optically Active Polystyrene Catalyzed by Monophosphine Pd Complexes. Angewandte Chemie (International ed. in English) 2016, 55, 8367–8370. doi:10.1002/anie.201603191
- 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
- Jouffroy, M.; Armspach, D.; Matt, D. Cyclodextrin and phosphorus(III): a versatile combination for coordination chemistry and catalysis. Dalton transactions (Cambridge, England : 2003) 2015, 44, 12942–12969. doi:10.1039/c5dt00667h
Patents
- MATT DOMINIQUE; ARMSPACH DOMINIQUE; JOUFFROY MATTHIEU. AZA-CAPPED CYCLODEXTRINS AND PROCESS OF PREPARING THEM. EP 3281957 A1, Feb 14, 2018.