Pierre Milbeo
Affiliations: | Trinity College, Dublin, Dublin, County Dublin, Ireland |
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Parents
Sign in to add mentorMonique Calmès | grad student | University of Montpellier, France | |
Eoin M. Scanlan | post-doc | 2018-2020 | Trinity College Dublin (University of Dublin) (Ireland) |
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Publications
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Picois N, Boutahri Y, Milbeo P, et al. (2024) Asymmetric α-Fluoroalkyl-α-Amino Acids: Recent Advances in Their Synthesis and Applications. Molecules (Basel, Switzerland). 29 |
Picois N, Bodero L, Milbeo P, et al. (2024) Bimodal use of chiral α-Trifluoromethylalanine in Aib Foldamers: study of the position impact towards the helical screw-sense preference. Chemistry (Weinheim An Der Bergstrasse, Germany). e202400540 |
Milbeo P, Lebrêne A, Savchuk M, et al. (2023) An Organocatalytic and Stereoselective Vinylogous Domino Process Towards Thiochromans. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301311 |
Milbeo P, Martinez J, Amblard M, et al. (2021) 1-Aminobicyclo[2.2.2]octane-2-carboxylic Acid and Derivatives As Chiral Constrained Bridged Scaffolds for Foldamers and Chiral Catalysts. Accounts of Chemical Research |
Milbeo P, Simon M, Didierjean C, et al. (2020) A bicyclic unit reversal to stabilize the 12/14-helix in mixed homochiral oligoureas. Chemical Communications (Cambridge, England) |
Calmes M, Legrand B, Simon M, et al. (2018) 12/10-helix in mixed b-peptides alternating bicyclic and acyclic b-amino acids: probing the relationship between bicyclic side chain and helix stability. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Milbeo P, Moulat L, Didierjean C, et al. (2018) C1‐Symmetric 1,2‐Diaminobicyclo[2.2.2]octane Ligands in Copper‐Catalyzed Asymmetric Henry Reaction: Catalyst Development and DFT Studies European Journal of Organic Chemistry. 2018: 178-187 |
Milbeo P, Moulat L, Didierjean C, et al. (2017) Synthesis of enantiopure DABO derivatives, C1-symmetric chiral 1,2-diamines with a rigid bicyclic backbone. The Journal of Organic Chemistry |
Milbeo P, Maurent K, Moulat L, et al. (2016) N-Pyrrolidine-based α/β-peptides incorporating ABOC, a constrained bicyclic β-amino acid, for asymmetric aldol reaction catalysis Tetrahedron. 72: 1706-1715 |