474
M. Akazome and S. Matsumoto
References
1. Akazome, M.: Chiral recognition by inclusion crystals of amino-acid derivatives having trityl
groups, in Tamura R., Miyata M. (eds.) Advances in Organic Crystal Chemistry, pp. 463 −
482, Springer, Japan, (2015)
2. Fogassy, E., Nógrádi, M., Kozma, D., Egri, G., Pálovics, E., Kiss, V.: Optical resolution
methods. Org. Biomol. Chem. 4, 3011–3030 (2006)
3. Siedlecka, R.: Recent developments in optical resolution. Tetrahedron 69, 6331–6363 (2013)
4. Faigel, F., Fogassy, E., Nógrádi, M., Pálovics, E., Schindler, J.: Strategies in optical resolution:
a practical guide. Tetrahedron: Asymmetry 19, 519 − 536 (2008)
5. Toda, F., Bishop, R.: Separations and reactions in organic supramolecular chemistry; perspectives in supramolecular chemistry 8 Wiley, Chichester, (2004)
6. Toda, F. (ed.): Enantiomer separation: Fundamentals and practical methods. Kluwer Academic
Publishers, Dordrecht (2004)
7. Kurilov, D.V., Vinogradov, M.G.: Preparative separation structurally related and racemic
hydroxyl-containing compound through the formation of crystalline molecular complexes.
Russ. Chem. Rev. 77, 621–631 (2008)
8. Toda, F.: comprehensive supramolecular chemistry. in: Lehn J.-M. (ed.) Solid-state supramolecular chemistry: Crystal engineering, pp. 465–516, Pergamon, Oxford, (1996)
9. Batisai, E., Nassimbeni, L.R., Weber, E.: Inclusion compounds of a borneol dumb-bell host
with methylcyclohexanones and 2-butanols: structures and resolutions. CrystEngComm 17,
4205–4209 (2015)
10. Barton, B., Caira, M.R., Hosten, E.C., McCleland, C.W., Weitz, S.: Clathrates of TETROL:
further aspects of the selective inclusion of methylcyclohexanones in their energetically
unfavorable axial methyl conformations. J. Org. Chem. 80, 7184–7192 (2015)
11. Barton, B., Dorfling, S.-L., Hosten, E.C.: Cyclohexanone-driven discriminatory behavior
change of host compound (+)-(2R,3R)-TETROL for isomeric methylcyclohexanone guests.
Cryst. Growth Des. 17, 6725–6732 (2017)
12. Toda, F.: Molecular recognition. Bioorg. Chem. 19, 157–168 (1991)
13. Seebach, D., Beck, A.K., Heckel, A.: TADDOLs, their derivatives, and TADDOL analogues:
versatile chiral auxiliaries. Angew. Chem. Int. Ed. 40, 92–138 (2001)
14. Kaku, H., Ito, M., Horikawa, M., Tsunoda, T.: Deracemization of α-monosubstituted cyclopentanones in the presence of a TADDOL-type host molecule. Tetrahedron 74, 124–129
(2018)
15. Kodama, K., Morita, R., Hirose, T.: Formation of ternary inclusion crystal and enantioseparation
of alkyl aryl sulfoxides by the salt of urea-modified L-phenylalanine and an achiral amine. Cryst.
Growth Des. 16, 5206–5213 (2016)
16. Kodama, K., Kanai, H., Shimomura, Y., Hirose, T.: Enantioseparation of sulfoxides and nitriles
by inclusion crystallization with chiral organic salts based on L-phenylalanine. Eur. J. Org.
Chem. 1726–1729 (2018)
17. Hu, X., Yang, Y., Shi, S., Shan, Z.: Effects of solvent on inclusion complexation of a chiral
dipeptide toward racemic BINOL. Chirality 28, 784–788 (2016)
18. Faigl, F., Fogassy, E., Nógrádi, M., Pálovics, E., Schindler, J.: Separation of non-racemic
mixtures of enantiomers: an essential part of optical resolution. Org. Biomol. Chem. 8, 947–959
(2010)
19. Niess, F., Duplan, V., Sauvage, J.-P.: Molecular muscles: from species in solution to materials
and devices. Chem. Lett. 43, 964–974 (2014)
20. Balzani, V., Credi, A., Raymo, F.M., Stoddart, J.F.: Artificial molecular machines. Angew.
Chem. Int. Ed. 39, 3348–3391 (2000)
21. Kassem, S., van Leeuwen, T., Lubbe, A.S., Wilson, M.R., Feringa, B.L., Leigh, D.A.: Artificial
molecular motors. Chem. Soc. Rev. 46, 2592–2621 (2017)
22. Mislow, K.: Stereochemical consequences of correlated rotation in molecular propellers. Acc.
Chem. Res. 9, 26–33 (1976)
M. Akazome and S. Matsumoto
References
1. Akazome, M.: Chiral recognition by inclusion crystals of amino-acid derivatives having trityl
groups, in Tamura R., Miyata M. (eds.) Advances in Organic Crystal Chemistry, pp. 463 −
482, Springer, Japan, (2015)
2. Fogassy, E., Nógrádi, M., Kozma, D., Egri, G., Pálovics, E., Kiss, V.: Optical resolution
methods. Org. Biomol. Chem. 4, 3011–3030 (2006)
3. Siedlecka, R.: Recent developments in optical resolution. Tetrahedron 69, 6331–6363 (2013)
4. Faigel, F., Fogassy, E., Nógrádi, M., Pálovics, E., Schindler, J.: Strategies in optical resolution:
a practical guide. Tetrahedron: Asymmetry 19, 519 − 536 (2008)
5. Toda, F., Bishop, R.: Separations and reactions in organic supramolecular chemistry; perspectives in supramolecular chemistry 8 Wiley, Chichester, (2004)
6. Toda, F. (ed.): Enantiomer separation: Fundamentals and practical methods. Kluwer Academic
Publishers, Dordrecht (2004)
7. Kurilov, D.V., Vinogradov, M.G.: Preparative separation structurally related and racemic
hydroxyl-containing compound through the formation of crystalline molecular complexes.
Russ. Chem. Rev. 77, 621–631 (2008)
8. Toda, F.: comprehensive supramolecular chemistry. in: Lehn J.-M. (ed.) Solid-state supramolecular chemistry: Crystal engineering, pp. 465–516, Pergamon, Oxford, (1996)
9. Batisai, E., Nassimbeni, L.R., Weber, E.: Inclusion compounds of a borneol dumb-bell host
with methylcyclohexanones and 2-butanols: structures and resolutions. CrystEngComm 17,
4205–4209 (2015)
10. Barton, B., Caira, M.R., Hosten, E.C., McCleland, C.W., Weitz, S.: Clathrates of TETROL:
further aspects of the selective inclusion of methylcyclohexanones in their energetically
unfavorable axial methyl conformations. J. Org. Chem. 80, 7184–7192 (2015)
11. Barton, B., Dorfling, S.-L., Hosten, E.C.: Cyclohexanone-driven discriminatory behavior
change of host compound (+)-(2R,3R)-TETROL for isomeric methylcyclohexanone guests.
Cryst. Growth Des. 17, 6725–6732 (2017)
12. Toda, F.: Molecular recognition. Bioorg. Chem. 19, 157–168 (1991)
13. Seebach, D., Beck, A.K., Heckel, A.: TADDOLs, their derivatives, and TADDOL analogues:
versatile chiral auxiliaries. Angew. Chem. Int. Ed. 40, 92–138 (2001)
14. Kaku, H., Ito, M., Horikawa, M., Tsunoda, T.: Deracemization of α-monosubstituted cyclopentanones in the presence of a TADDOL-type host molecule. Tetrahedron 74, 124–129
(2018)
15. Kodama, K., Morita, R., Hirose, T.: Formation of ternary inclusion crystal and enantioseparation
of alkyl aryl sulfoxides by the salt of urea-modified L-phenylalanine and an achiral amine. Cryst.
Growth Des. 16, 5206–5213 (2016)
16. Kodama, K., Kanai, H., Shimomura, Y., Hirose, T.: Enantioseparation of sulfoxides and nitriles
by inclusion crystallization with chiral organic salts based on L-phenylalanine. Eur. J. Org.
Chem. 1726–1729 (2018)
17. Hu, X., Yang, Y., Shi, S., Shan, Z.: Effects of solvent on inclusion complexation of a chiral
dipeptide toward racemic BINOL. Chirality 28, 784–788 (2016)
18. Faigl, F., Fogassy, E., Nógrádi, M., Pálovics, E., Schindler, J.: Separation of non-racemic
mixtures of enantiomers: an essential part of optical resolution. Org. Biomol. Chem. 8, 947–959
(2010)
19. Niess, F., Duplan, V., Sauvage, J.-P.: Molecular muscles: from species in solution to materials
and devices. Chem. Lett. 43, 964–974 (2014)
20. Balzani, V., Credi, A., Raymo, F.M., Stoddart, J.F.: Artificial molecular machines. Angew.
Chem. Int. Ed. 39, 3348–3391 (2000)
21. Kassem, S., van Leeuwen, T., Lubbe, A.S., Wilson, M.R., Feringa, B.L., Leigh, D.A.: Artificial
molecular motors. Chem. Soc. Rev. 46, 2592–2621 (2017)
22. Mislow, K.: Stereochemical consequences of correlated rotation in molecular propellers. Acc.
Chem. Res. 9, 26–33 (1976)