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Asymmetric α-Fluoroalkyl-α-Amino Acids: Recent Advances in Their Synthesis and Applications
Nathan Picois
,
Yazid Boutahri
,
Pierre Milbeo
,
Chiara Zanato
,
Nathalie Lensen
,
et al.
Article dans une revue
hal-04516441v1
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N-Pyrrolidine-based alpha/beta-peptides incorporating ABOC, a constrained bicyclic beta-amino acid, for asymmetric aldol reaction catalysis
Pierre Milbeo
,
Kelly Maurent
,
Laure Moulat
,
Aurelien Lebrun
,
Claude Didierjean
,
et al.
Article dans une revue
hal-01532027v1
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C 1 -Symmetric 1,2-Diaminobicyclo[2.2.2]octane Ligands in Copper-Catalyzed Asymmetric Henry Reaction: Catalyst Development and DFT Studies
Pierre Milbeo
,
Laure Moulat
,
Claude Didierjean
,
Emmanuel Aubert
,
Jean Martinez
,
et al.
Article dans une revue
hal-02419329v1
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Synthesis of Enantiopure 1,2-Diaminobicyclo[2.2.2]octane Derivatives, C 1 -Symmetric Chiral 1,2-Diamines with a Rigid Bicyclic Backbone
Pierre Milbeo
,
Laure Moulat
,
Claude Didierjean
,
Emmanuel Aubert
,
Jean Martinez
,
et al.
Article dans une revue
hal-01552321v1
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A bicyclic unit reversal to stabilize the 12/14-helix in mixed homochiral oligoureas
Pierre Milbeo
,
Matthieu Simon
,
Claude Didierjean
,
Emmanuel Wenger
,
Emmanuel Aubert
,
et al.
Article dans une revue
hal-03080580v1
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1-Aminobicyclo[2.2.2]octane-2-carboxylic acid and derivatives as chiral constrained bridged scaffolds for foldamers and chiral catalysts
Pierre Milbeo
,
Jean Martinez
,
Muriel Amblard
,
Monique Calmès
,
Baptiste Legrand
Article dans une revue
hal-03371473v1
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12/10‐Helix in Mixed β‐Peptides Alternating Bicyclic and Acyclic β‐Amino Acids: Probing the Relationship between Bicyclic Side Chain and Helix Stability
Matthieu Simon
,
Pierre Milbeo
,
Hongtao Liu
,
Christophe Andre
,
Emmanuel Wenger
,
et al.
Article dans une revue
hal-02403147v1
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Synthesis, characterisation and cytotoxic activity evaluation of new metal-salen complexes based on the 1,2-bicyclo[2.2.2]octane bridge
Pierre Milbeo
,
François Quintin
,
Laure Moulat
,
Claude Didierjean
,
Jean Martinez
,
et al.
Article dans une revue
hal-03103305v1
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