Pauline Adler

20. Catalytic and Sustainable Amide Bond Formation using a DABCO/Dichlorotriazine System
P. Adler,* M. Gras, M. Smietana*
ChemCatChem., 2023, e202300264

19. Cerium(IV)-Mediated Carbon-Carbon Bond Formation for the Synthesis of Spirodienone Lactams.
Adler, P.; Perez, V.; Roupnel, L.; Fadel, A.; Rabasso, N.
Eur. J. Org. Chem. 2022, e202200646. https://doi.org/10.1002/ejoc.202200646.

18. New Biomaterials for Ni Biosorption Turned into Catalysts for Suzuki–Miyaura Cross Coupling of Aryl Iodides in Green Conditions.
Cases, L.; Adler, P.; Pelissier, F.; Diliberto, S.; Boulanger, C.; Grison, C.
RSC Adv. 2021, 11, 28085–28091. https://doi.org/10.1039/D1RA04478H

17. I – Ecologically Responsible and Efficient Recycling of Pd from Aqueous Effluents Using Biosorption on Biomass Feedstock.
Garcia, A.; Deyris, P.-A.; Adler, P.; Pelissier, F.; Dumas, T.; Legrand, Y.-M.; Grison, C.
J. Clean. Prod. 2021, 299, 126895. https://doi.org/10.1016/j.jclepro.2021.126895

16. II- from Ecological Recycling of Pd to Greener Sonogashira Cross-Coupling Reactions.
Adler, P.; Dumas, T.; Deyris, P.-A.; Petit, E.; Diliberto, S.; Boulanger, C.; Grison, C.
J. Clean. Prod. 2021, 293, 126164. https://doi.org/10.1016/j.jclepro.2021.126164

15. A Green Approach for the Reduction of Representative Aryl Functional Groups Using Palladium Ecocatalysts.
Grison, C.; Adler, P.; Deyris, P.-A.; Diliberto, S.; Boulanger, C.
Green Chem. Lett. Rev. 2021, 14, 234–245. https://doi.org/10.1080/17518253.2021.1898682

14. Electrochemical Reduction of α-Amino Allenylphosphonates to α-Amino Allylphosphonates: Electrochemical Reduction of α-Amino Allenylphosphonates to α-Amino Allylphosphonates.
Adler, P.; de Oliveira, P.; Rabasso, N.
Eur. J. Org. Chem. 2020, 3918–3925. https://doi.org/10.1002/ejoc.202000534

13. Unified Approach to the Chemoselective α-Functionalization of Amides with Heteroatom Nucleophiles.
Gonçalves, C. R.; Lemmerer, M.; Teskey, C. J.; Adler, P.; Kaiser, D.; Maryasin, B.; González, L.; Maulide, N.
J. Am. Chem. Soc. 2019, 141, 18437–18443. https://doi.org/10.1021/jacs.9b06956

12. Woody Species: A New Bio-Based Material for Dual Ca/Mg Catalysis with Remarkable Lewis Acidity Properties.
Deyris, P.-A.; Adler, P.; Petit, E.; Legrand, Y.-M.; Grison, C.
Green Chem. 2019, 21, 3133–3142. https://doi.org/10.1039/C9GC00770A

11. α-Fluorination of Carbonyls with Nucleophilic Fluorine.
Adler, P.; Teskey, C. J.; Kaiser, D.; Holy, M.; Sitte, H. H.; Maulide, N.
Nat. Chem. 2019, 11, 329–334. https://doi.org/10.1038/s41557-019-0215-z

10. Bio-Based Catalysts from Biomass Issued after Decontamination of Effluents Rich in Copper—An Innovative Approach towards Greener Copper-Based Catalysis.
Olszewski, T. K.; Adler, P.; Grison, C.
Catalysts 2019, 9, 214. https://doi.org/10.3390/catal9030214

9. Electrophilic Activation of Amides for the Preparation of Polysubstituted Pyrimidines.
Stopka, T.; Adler, P.; Hagn, G.; Zhang, H.; Tona, V.; Maulide, N.
Synthesis 2019, 51, 194–202. https://doi.org/10.1055/s-0037-1610411

8. Chemoselective α,β-Dehydrogenation of Saturated Amides.
Teskey, C. J.; Adler, P.; Gonçalves, C. R.; Maulide, N.
Angew. Chem. Int. Ed. 2019, 58, 447–451. https://doi.org/10.1002/anie.201808794

7. Chemoselective Activation of Diethyl Phosphonates: Modular Synthesis of Biologically Relevant Phosphonylated Scaffolds.
Adler, P.; Pons, A.; Li, J.; Heider, J.; Brutiu, B. R.; Maulide, N.
Angew. Chem. Int. Ed. 2018, 57, 13330–13334. https://doi.org/10.1002/anie.201806343

6. From Acyclic to Cyclic α-Amino Vinylphosphonates by Using Ring-Closing Metathesis.
Adler, P.; Fadel, A.; Prunet, J.; Rabasso, N.
Org. Biomol. Chem. 2017, 15, 387–395. https://doi.org/10.1039/C6OB02548J

5. Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides.
Kaiser, D.; Teskey, C. J.; Adler, P.; Maulide, N.
J. Am. Chem. Soc. 2017, 139, 16040–16043. https://doi.org/10.1021/jacs.7b08813

4. Cerium(IV) Ammonium Nitrate Mediated 5-Endo-Dig Cyclization of α-Amino Allenylphosphonates to Spirodienones.
Adler, P.; Fadel, A.; Rabasso, N.
Chem. Commun. 2015, 51, 3612–3615. https://doi.org/10.1039/C5CC00281H

3. Strategies for the Synthesis of α- and β-Amino Vinylphosphonate.
Adler, P.; Fadel, A.; Rabasso, N.
Tetrahedron 2014, 70, 4437–4456. https://doi.org/10.1016/j.tet.2014.04.086

2. Selective Reduction of Amino Allenephosphonates: Preparation of α-Amino Vinylphosphonates.
Adler, P.; Gomes, F.; Fadel, A.; Rabasso, N.
Eur. J. Org. Chem. 2013, 7546–7555. https://doi.org/10.1002/ejoc.201300904

1. Designing Dye-Nanochannel Antenna Hybrid Materials for Light Harvesting, Transport and Trapping.
Calzaferri, G.; Méallet-Renault, R.; Brühwiler, D.; Pansu, R.; Dolamic, I.; Dienel, T.; Adler, P.; Li, H.; Kunzmann, A.
ChemPhysChem 2011, 12, 580–594. https://doi.org/10.1002/cphc.201000947