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Preparation of Chiral Amino Esters by Asymmetric Phase-Transfer Catalyzed Alkylations of Schiff Bases in a Ball Mill

Chemistry : a European journal, 2012-03, Vol.18 (12), p.3773-3779

2012

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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

Accounts of chemical research, 2021-02, Vol.54 (3), p.685-696

2021

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N-Pyrrolidine-based α/β-peptides incorporating ABOC, a constrained bicyclic β-amino acid, for asymmetric aldol reaction catalysis

Tetrahedron, 2016-03, Vol.72 (13), p.1706-1715

2016

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Turning Peptide Sequences into Ribbon Foldamers by a Straightforward Multicyclization Reaction

Angewandte Chemie (International ed.), 2015-11, Vol.54 (47), p.13966-13970

International ed. in English, 2015

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12/14/14-Helix Formation in 2:1 α/β-Hybrid Peptides Containing Bicyclo[2.2.2]octane Ring Constraints

Chemistry : a European journal, 2016-08, Vol.22 (34), p.11986-11990

2016

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Robust Helix Formation in a New Family of Oligoureas Based on a Constrained Bicyclic Building Block

Angewandte Chemie (International ed.), 2012-11, Vol.51 (45), p.11267-11270

International ed. in English, 2012

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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

Tetrahedron letters, 2021-01, Vol.63, p.152706, Article 152706

2021

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Synthesis and changes in affinity for NOP and opioid receptors of novel hexapeptides containing β(2)-tryptophan analogues

Bioorganic & medicinal chemistry letters, 2013-07, Vol.23 (14), p.4052-4055

2013

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A bicyclic unit reversal to stabilize the 12/14-helix in mixed homochiral oligoureas

Chemical communications (Cambridge, England), 2020-07, Vol.56 (57), p.7921-7924

2020

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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

Journal of organic chemistry, 2017-03, Vol.82 (6), p.3144-3151

2017

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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, 2018-01, Vol.2018 (2), p.178-187

2018

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Straightforward Approach for Cellular‐Uptake Quantification

Angewandte Chemie (International ed.), 2010-10, Vol.49 (44), p.8240-8243

2010

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Synthesis of Enantiopure 1,2-Diaminobicyclo[2.2.2]octane Derivatives, C1-Symmetric Chiral 1,2-Diamines with a Rigid Bicyclic Backbone

Journal of organic chemistry, 2017-03, Vol.82 (6), p.3144-3151

2017

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Crystal structure of Boc-( S )-ABOC-( S )-Ala-( S )-ABOC-( S )-Phe-OBn chloroform monosolvate

Acta crystallographica. Section E, Crystallographic communications, 2015-10, Vol.71 (10), p.1193-1195

2015

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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

European journal of organic chemistry, 2018-01, Vol.2018 (2), p.178-187

2018

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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

Chemistry : a European journal, 2018-12, Vol.24 (70), p.18795-18800

2018

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A Straightforward Approach for Cellular‐Uptake Quantification

Angewandte Chemie, 2010-10, Vol.122 (44), p.8416-8419

2010

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Turning Peptide Sequences into Ribbon Foldamers by a Straightforward Multicyclization Reaction

Angewandte Chemie, 2015-11, Vol.127 (47), p.14172-14176

2015

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Asymmetric Synthesis of β2-Tryptophan Analogues via Friedel–Crafts Alkylation of Indoles with a Chiral Nitroacrylate

Journal of organic chemistry, 2011-08, Vol.76 (15), p.6116-6124

2011

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The iodolactone approach to enantiopure oxiranes of constrained chiral cyclic β-amino acids

Tetrahedron: asymmetry, 2008-09, Vol.19 (18), p.2135-2139

2008

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Unprecedented Chain-Length-Dependent Conformational Conversion Between 11/9 and 18/16 Helix in α/β-Hybrid Peptides

Angewandte Chemie (International ed.), 2014-11, Vol.53 (48), p.13131-13135

2014

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Asymmetric Diels-Alder Cycloaddition of 1-Aminocyclohexadiene to Chiral Acrylate: Synthesis of Enantiopure Bridgehead-Aminobicyclo[2.2.2]octane-2-carboxylic Acid Derivatives

European Journal of Organic Chemistry, 2007-07, Vol.2007 (19), p.3166-3172

2007

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12/14/14-Helix Formation in 2:1 [alpha]/[beta]-Hybrid Peptides Containing Bicyclo[2.2.2]octane Ring Constraints

Chemistry : a European journal, 2016-08, Vol.22 (34), p.11986

2016

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(S)-ABOC: A Rigid Bicyclic β-Amino Acid as Turn Inducer

Organic letters, 2012-02, Vol.14 (4), p.960-963

2012

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New 1,3-amino alcohols derived from enantiopure bridgehead β-aminobicyclo[2.2.2]oct-5-ene-2-carboxylic acids

Amino acids, 2012-07, Vol.43 (1), p.415-421

2012

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Preparation of Chiral Amino Esters by Asymmetric Phase-Transfer Catalyzed Alkylations of Schiff Bases in a Ball Mill

1‑Aminobicyclo[2.2.2]octane-2-carboxylic Acid and Derivatives As Chiral Constrained Bridged Scaffolds for Foldamers and Chiral Catalysts

N-Pyrrolidine-based α/β-peptides incorporating ABOC, a constrained bicyclic β-amino acid, for asymmetric aldol reaction catalysis

Turning Peptide Sequences into Ribbon Foldamers by a Straightforward Multicyclization Reaction

12/14/14-Helix Formation in 2:1 α/β-Hybrid Peptides Containing Bicyclo[2.2.2]octane Ring Constraints

Robust Helix Formation in a New Family of Oligoureas Based on a Constrained Bicyclic Building Block

Synthesis, characterisation and cytotoxic activity evaluation of new metal-salen complexes based on the 1,2-bicyclo[2.2.2]octane bridge

Synthesis and changes in affinity for NOP and opioid receptors of novel hexapeptides containing β(2)-tryptophan analogues

A bicyclic unit reversal to stabilize the 12/14-helix in mixed homochiral oligoureas

Synthesis of Enantiopure 1,2-Diaminobicyclo[2.2.2]octane Derivatives, C 1‑Symmetric Chiral 1,2-Diamines with a Rigid Bicyclic Backbone

C1‐Symmetric 1,2‐Diaminobicyclo[2.2.2]octane Ligands in Copper‐Catalyzed Asymmetric Henry Reaction: Catalyst Development and DFT Studies

Straightforward Approach for Cellular‐Uptake Quantification

Synthesis of Enantiopure 1,2-Diaminobicyclo[2.2.2]octane Derivatives, C1-Symmetric Chiral 1,2-Diamines with a Rigid Bicyclic Backbone

Crystal structure of Boc-( S )-ABOC-( S )-Ala-( S )-ABOC-( S )-Phe-OBn chloroform monosolvate

C 1 ‐Symmetric 1,2‐Diaminobicyclo[2.2.2]octane Ligands in Copper‐Catalyzed Asymmetric Henry Reaction: Catalyst Development and DFT Studies

12/10‐Helix in Mixed β‐Peptides Alternating Bicyclic and Acyclic β‐Amino Acids: Probing the Relationship between Bicyclic Side Chain and Helix Stability

A Straightforward Approach for Cellular‐Uptake Quantification

Turning Peptide Sequences into Ribbon Foldamers by a Straightforward Multicyclization Reaction

Asymmetric Synthesis of β2-Tryptophan Analogues via Friedel–Crafts Alkylation of Indoles with a Chiral Nitroacrylate

The iodolactone approach to enantiopure oxiranes of constrained chiral cyclic β-amino acids

Unprecedented Chain-Length-Dependent Conformational Conversion Between 11/9 and 18/16 Helix in α/β-Hybrid Peptides

Asymmetric Diels-Alder Cycloaddition of 1-Aminocyclohexadiene to Chiral Acrylate: Synthesis of Enantiopure Bridgehead-Aminobicyclo[2.2.2]octane-2-carboxylic Acid Derivatives

12/14/14-Helix Formation in 2:1 [alpha]/[beta]-Hybrid Peptides Containing Bicyclo[2.2.2]octane Ring Constraints

(S)-ABOC: A Rigid Bicyclic β-Amino Acid as Turn Inducer

New 1,3-amino alcohols derived from enantiopure bridgehead β-aminobicyclo[2.2.2]oct-5-ene-2-carboxylic acids

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