, Supramolecular Chemistry

T. Brotin and J. Dutasta, Chem. Rev, pp.88-130, 2009.

P. Satha, G. T. Illa, S. Hazra, C. S. Purohit-;-a, S. H. Joseph et al., Encapsulation of neutral species, Angew. Chem. Int. Ed, vol.2, pp.2866-2868, 2013.

C. Li, C. Huang, S. Lai, . A. Chiu-;-m, J. Little et al., Angew. Chem. Int. Ed, vol.14, pp.4511-4513, 2011.

T. Bouchet, D. Brotin, T. Cavagnat, . Buffeteau, . Chem et al., Supramolecular Chemistry, vol.16, pp.870-890, 2010.

K. E. Chaffee, H. A. Fogarty, T. Brotin, B. M. Goodson, J. Dutasta et al., J. Phys. Chem. A, vol.113, pp.13675-13684, 2009.

K. Bartik, M. Luhmer, J. Dutasta, A. Collet, J. Reisse et al., Chem. Soc, vol.128, 2006.

L. Garel, L. , J. Dutasta, and A. Collet, Angew. Chem. Int. Ed. Engl, vol.120, pp.1169-1171, 1993.

F. Bregier, O. Hudecek, F. Chaux, and M. J. , Encapsulation of charged species, see for instance: a)

J. C. Penouilh, P. Chambron, E. Lhotak, E. Aubert, and . Espinosa, Eur. J. Org. chem, pp.3795-3811, 2017.

T. Brotin, S. Goncalves, P. Berthault, D. Cavagnat, and T. Buffeteau, J. Phys. Chem. B, p.117, 2013.

). T. Brotin, R. Montserret, A. Bouchet, D. Cavagnat, M. Linares et al., Supramolacular chemistry, vol.77, pp.11652-11653, 1198.

G. Milanole, B. Gao, A. Paoletti, G. Pieters, C. Dugave et al., Bioorg. Med.chem, vol.25, pp.5542-5548, 2015.

N. Rousseau-;-d)-n.-tassali, C. Kotera, E. Boutin, and Y. Léonce, Chem. Commun, vol.51, pp.11482-11484, 2015.

B. Boulard, E. Rousseau, F. Dubost, T. Taran, J. Brotin et al., Anal. Chem, vol.86, pp.1783-1788, 2014.

;. T. Francis, K. K. Stevens, R. M. Palaniappan, M. B. Ramirez, D. E. Francis et al., Angew. Chem. Int. Ed, vol.52, pp.1245-1252, 2013.

Y. Seward, N. S. Bai, I. J. Khan, . K. Dmochowski-;-g, and Y. Seward, Chem. Sci, vol.2, pp.1103-1110, 2011.

N. S. Bai, I. J. Khan, ;. Dmochowski, T. Hilty, and D. Lowery, Chem. Sci, vol.2, pp.1103-1110, 2011.

A. Wemmer and . Pines, Angew. Chem. Int. Ed, vol.45, pp.446-449, 2006.

J. Canceill, A. Collet, G. Gotarelli, and P. Palmieri, J. Am. Chem. Soc, vol.109, pp.6454-6464, 1987.

T. Brotin, R. Barbe, M. Darzac, and J. Dutasta, Chem. Eur. J, vol.9, pp.5784-5792, 2003.

P. Soulard, P. Asselin, A. Cuisset, J. R. Moreno, T. R. Huet et al.,

X. Freedman, L. A. Cao, and . Nafie, J. Crassous, PhysChemChemPhys, vol.8, pp.79-92, 2006.

A. Lacombe and . Collet, J. Am. Chem. Soc, vol.107, pp.6993-6996, 1985.

A. Bouchet, T. Brotin, M. Linares, H. Ågren, D. Cavagnat et al., J. Org. Chem, vol.76, pp.4178-4181, 2011.

, (-) of methyloxirane refers to the specific optical rotation (SOR) of the neat compound. For this compound, it has been shown that the sign of the SOR values is solvent dependent. See for instance, Bull. Chem. Soc. Jpn, vol.43, pp.3920-3921, 1970.

A. Bouchet, T. Brotin, M. Linares, H. Ågren, D. Cavagnat et al., J. Org. Chem, vol.76, pp.1372-1383, 2011.

M. Darzac, T. Brotin, D. Bouchu, and J. Dutasta, Chem. Commun, pp.48-49, 2002.

T. Brotin, D. Cavagnat, P. Berthault, R. Montserret, and T. Buffeteau, J. Phys. Chem. B, vol.116, p.10905, 2012.

Y. H. Zhao, M. H. Abraham, and A. M. Zissimos, J. Org. Chem, vol.68, pp.7368-7373, 2003.

M. A. Robbins, P. N. Devine, and T. Oh, Org. Synth, vol.76, pp.101-109, 1999.

N. Daugey, N. De-rycke, T. Brotin, and T. Buffeteau, Chirality, 2018.