Pauline Adler
25. Towards Improved Peptidic α-Ketoamide Inhibitors of the Plasmodial Subtilisin-Like SUB1: Exploration of N-Terminal Extensions and Cyclic Constraints.
A. K. Puszko, F. A. Batista, A. Ejjoummany, A. Bouillon, M. Maurel, P. Adler, A. Legru, M. Martinez, L. Ortega Varga, M. Hadjadj, P. M. Alzari, A. Blondel, A. Haouz, J.-C. Barale, J.-F. Hernandez
ChemMedChem. 2025, e202400924
24. Reduction of C=X to CH2
P. Adler
Reference Module in Chemistry, Molecular Sciences and Chemical Engineering 2024
23. Peptide–Oligonucleotide Conjugates: Catalytic Preparation in Aqueous Solution or On-Column
M. Gras, M. Smietana, P. Adler
Current Protocols, 2025, 5, e70154
22. Insights from structure-activity relationships and the binding mode of peptidic α-ketoamide inhibitors of the malaria drug target subtilisin-like SUB1. A. Legru, F. A. Batista, A. K. Puszko, A. Bouillon, M. Maurel, M. Martinez, A. Ejjoummany, L. Ortega Varga, P. Adler, A. Méchaly, M. Hadjadj, P. Sosnowski, G. Hopfgartner, P. M. Alzari, A. Blondel, A. Haouz, J.-C. Barale, J.-F. Hernandez
Eur. J. Med. Chem.2024, 269, 116308.
21. A Catalytic Approach for the Synthesis of Peptide–Oligonucleotides Conjugates in Aqueous Solution or On-Column
M. Gras, P. Adler, M. Smietana
Chem. Eur. J., 2024, e202401069
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
