Towards the stereoselective synthesis of inherently chiral pseudorotaxanes

Pierre Mobian, Natalie Banerji, Gérald Bernardinelli and Jérôme Lacour

Org. Biomol. Chem., 2006, 4, 224
DOI: 10.1039/B513562A

C-hexaphenyl-substituted trianglamine as a chiral solvating agent for carboxylic acids

Andrea Gualandi, Stefano Grilli, Diego Savoia, Marcin Kwit and Jacek Gawroński

Org. Biomol. Chem., 2011, 9, 4234
DOI: 10.1039/c0ob01192d

Chiral anion-mediated asymmetric ion pairing chemistry

Jérôme Lacour and Delphine Moraleda

Chem. Commun., 2009, 7073
DOI: 10.1039/b912530b

Structural analyses of isolated cyclic tetrapeptides with varying amino acid residues

A. Stamm, D. Maué, A. Schaly, S. Schlicher, J. Bartl, S. Kubik and M. Gerhards

Phys. Chem. Chem. Phys., 2017, 19, 10718
DOI: 10.1039/C6CP08696A

A widely applicable concept for predictable induction of preferred configuration in C3-symmetric systems

Gebhard Haberhauer, Thomas Oeser and Frank Rominger

Chem. Commun., 2005, 2799
DOI: 10.1039/b502158h

Synthesis of triazole cages containing C3-symmetric α-cyclic tripeptide scaffold

Subrata Chakraborty and Dar-Fu Tai

Tetrahedron Letters, 2014, 55, 2274
DOI: 10.1016/j.tetlet.2014.02.089

Synthesis of Rigid Receptors Based on Triphenylene Ketals

Matthias C. Schopohl, Andreas Faust, Daniela Mirk, Roland Fröhlich, Olga Kataeva and Siegfried R. Waldvogel

Eur J Org Chem, 2005, 2005, 2987
DOI: 10.1002/ejoc.200500108

Sugar derived hexacoordinated phosphates: Chiral anionic auxiliaries with general asymmetric efficiency

Céline Pérollier, Gérald Bernardinelli and Jérôme Lacour

Chirality, 2008, 20, 313
DOI: 10.1002/chir.20441

Supramolecular Control for the Modular Synthesis of Pseudopeptidic Macrocycles through an Anion-Templated Reaction

Ignacio Alfonso, Michael Bolte, Miriam Bru, M. Isabel Burguete, Santiago V. Luis and Jenifer Rubio

J. Am. Chem. Soc., 2008, 130, 6137
DOI: 10.1021/ja710132c

Synthesis of chiral threefold and sixfold functionalized macrocyclic imidazole peptides

Áron Pintér and Gebhard Haberhauer

Tetrahedron, 2009, 65, 2217
DOI: 10.1016/j.tet.2009.01.047

Triptycene‐Based Chiral Macrocyclic Hosts for Highly Enantioselective Recognition of Chiral Guests Containing a Trimethylamino Group

Geng‐Wu Zhang, Peng‐Fei Li, Zheng Meng, Han‐Xiao Wang, Ying Han and Chuan‐Feng Chen

Angew Chem Int Ed, 2016, 55, 5304
DOI: 10.1002/anie.201600911

Synthesis and conformational aspects of 20- and 40-membered macrocyclic mono and dinuclear uranyl complexes incorporating salen and (R)-BINOL units

Maria E. Amato, Francesco P. Ballistreri, Andrea Pappalardo, Domenico Sciotto, Gaetano A. Tomaselli and Rosa Maria Toscano

Tetrahedron, 2007, 63, 9751
DOI: 10.1016/j.tet.2007.07.014

Rapid Access to Chiral and Tripodal Cavitands from β‐Pinene

Xiuze Wang, Radoslav Z. Pavlović, Tyler J. Finnegan, Pratik Karmakar, Curtis E. Moore and Jovica D. Badjić

Chemistry A European J, 2022, 28
DOI: 10.1002/chem.202202416

Chiral hexacoordinated phosphates: From pioneering studies to modern uses in stereochemistry

Jérôme Lacour

Comptes Rendus. Chimie, 2010, 13, 985
DOI: 10.1016/j.crci.2010.02.009

Chiral nitrogen-containing calix[4]crown—an excellent receptor for chiral recognition of mandelic acid

Xian-Xian Liu and Yan-Song Zheng

Tetrahedron Letters, 2006, 47, 6357
DOI: 10.1016/j.tetlet.2006.07.002

Ring-expanded chiral rhombamine macrocycles for efficient NMR enantiodiscrimination of carboxylic acid derivatives

Koichi Tanaka, Tomoharu Iwashita, Chihiro Sasaki and Hiroki Takahashi

Tetrahedron: Asymmetry, 2014, 25, 602
DOI: 10.1016/j.tetasy.2014.03.009

Vibrational and electronic circular dichroism of Δ-TRISPHAT [tris(tetrachlorobenzenediolato)phosphate(V)] anion

Delphine Bas, Thomas Bürgi, Jerôme Lacour, Jerôme Vachon and Jacques Weber

Chirality, 2005, 17, S143
DOI: 10.1002/chir.20131

Molecular recognition of organic ammonium ions in solution using synthetic receptors

Andreas Späth and Burkhard König

Beilstein J. Org. Chem., 2010, 6
DOI: 10.3762/bjoc.6.32

Synthetic Receptors Based on Abiotic Cyclo(pseudo)peptides

Stefan Kubik

Molecules, 2022, 27, 2821
DOI: 10.3390/molecules27092821

Diastereomeric discrimination by achiral substances: the effect of diverse ions in the stability of amphi-ionophore cystine-based cyclopeptide stereoisomers

Samaneh Ahmadi, Hossein A. Dabbagh, Saeid Ebrahimi and Hossein Farrokhpour

Molecular Physics, 2019, 117, 557
DOI: 10.1080/00268976.2018.1527408

Ion‐Pairing Effects in the Self‐Assembly of a Fluorescent Pseudorotaxane

Miguel Clemente‐León, Chiara Pasquini, Virginie Hebbe‐Viton, Jerome Lacour, Antonella Dalla Cort and Alberto Credi

Eur J Org Chem, 2006, 2006, 105
DOI: 10.1002/ejoc.200500479

Highly Selective Recognition of α‐Chiral Primary Organoammonium Ions by C3‐Symmetric Peptide Receptors

Markus Schnopp and Gebhard Haberhauer

Eur J Org Chem, 2009, 2009, 4458
DOI: 10.1002/ejoc.200900510

Tuning Chloride Binding, Encapsulation, and Transport by Peripheral Substitution of Pseudopeptidic Tripodal Small Cages

Inés Martí, Jenifer Rubio, Michael Bolte, M. Isabel Burguete, Cristian Vicent, Roberto Quesada, Ignacio Alfonso and Santiago V. Luis

Chemistry A European J, 2012, 18, 16728
DOI: 10.1002/chem.201202182

Triptycene‐Based Chiral Macrocyclic Hosts for Highly Enantioselective Recognition of Chiral Guests Containing a Trimethylamino Group

Geng‐Wu Zhang, Peng‐Fei Li, Zheng Meng, Han‐Xiao Wang, Ying Han and Chuan‐Feng Chen

Angewandte Chemie, 2016, 128, 5390
DOI: 10.1002/ange.201600911

Kinetic Control in the Chiral Recognition of Three‐Bladed Propellers

Clément Bonnot, Emmanuel Aubert, Natalie Banerji, Jérôme Lacour, Enrique Espinosa and Jean‐Claude Chambron

Chemistry A European J, 2010, 16, 5706
DOI: 10.1002/chem.200903058

Backbone-modified Cyclic Peptides: New Scaffolds for Supramolecular Chemistry

Katrina A. Jolliffe

Supramolecular Chemistry, 2005, 17, 81
DOI: 10.1080/10610270412331328970

Exceptional Chiral Recognition of Racemic Carboxylic Acids by Calix[4]arenes Bearing Optically Pure α,β-Amino Alcohol Groups

Yan-Song Zheng and Chun Zhang

Org. Lett., 2004, 6, 1189
DOI: 10.1021/ol036122o