The racemate-to-homochiral approach to crystal engineering via chiral symmetry breaking

Emergence of a single solid chiral state from a nearly racemic amino acid derivative

Noorduin, W. L., Izumi, T., Millemaggi, A., Leeman, M., Meekes, H., Van Enckevort, W. J. P., Kellogg, R. M., Kaptein, B., Vlieg, E., & Blackmond, D. G. (2008) · Journal of the American Chemical Society · doi:10.1021/ja7106349 · Cited by 459 · see citing works

Amplification of Chirality from Extremely Low to Greater than 99.5 % <i>ee</i> by Asymmetric Autocatalysis

Sato, I., Urabe, H., Ishiguro, S., Shibata, T., & Soai, K. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200390105 · Cited by 232 · see citing works

Spontaneous formation of optically active substances

Havinga, E. (1954) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(54)90300-5 · Cited by 221 · see citing works

A route to enantiopure RNA precursors from nearly racemic starting materials

Hein, J. E., Tse, E., & Blackmond, D. G. (2011) · Nature Chemistry · doi:10.1038/nchem.1108 · Cited by 112 · see citing works

Fast attrition-enhanced deracemization of naproxen by a gradual in situ feed

Noorduin, W. L., Kaptein, B., Meekes, H., van Enckevort, W. J. P., Kellogg, R. M., & Vlieg, E. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200901386 · Cited by 101 · see citing works

Selective chiral symmetry breaking during crystallization: Parity violation or cryptochiral environment in control?

Viedma, C. (2007) · Crystal Growth &amp; Design · doi:10.1021/cg060698d · Cited by 100 · see citing works

Spontaneous Deracemizations

Buhse, T., Cruz, J.-M., Noble-Terán, M. E., Hochberg, D., Ribó, J. M., Crusats, J., & Micheau, J.-C. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00819 · Cited by 189 · see citing works

Possible chemical and physical scenarios towards biological homochirality

Sallembien, Q., Bouteiller, L., Crassous, J., & Raynal, M. (2022) · Chemical Society Reviews · doi:10.1039/d1cs01179k · Cited by 186 · see citing works

Homochiral metal-organic frameworks for enantioseparation.

Liu, J., Mukherjee, S., Wang, F., Fischer, R., & Zhang, J. (2021) · Chemical Society Reviews · doi:10.1039/d0cs01236j · Cited by 63

Supramolecular Interactions Induced Chirality Transmission, Second Harmonic Generation Responses, and Photoluminescent Property of a Pair of Enantiomers from in Situ [2 + 3] Cycloaddition Synthesis

Gao, J.-X., Xiong, J., Xu, Q.-Q., Tan, Y.-H., Liu, Y., Wen, H.-R., & Tang, Y.-Z. (2016) · doi:10.1021/acs.cgd.5b01684 · Cited by 17

Gas-chromatographic separation of enantiomers of 2-chlorobutane and 2-bromobutane on a cyanuric acid-modified Carboblack C adsorbent

Gus'kov, V. Y., Sukhareva, D. A., Arslanova, I. V., & Musabirov, D. (2017) · Journal of Analytical Chemistry · doi:10.1134/s1061934817100069 · Cited by 9 · see citing works

Homochiral zinc benzene-1,3,5-tricarboxylate coordination networks with a chiral nitrogen ligand or template: Spontaneous resolution of a twofold interpenetrated 2D sql (4,4) network and formation of enantiopure 3D sra (SrAl2) networks

Tahli, A., Chamayou, A.-C., Köc, Ü., Brückner, R., Elshaarawy, R. F., Heering, C., & Janiak, C. (2016) · doi:10.1016/j.ica.2016.05.042 · Cited by 9

Non‐stochastic behavior in sodium chlorate crystallization

Cruz, J., Hernández‐Lechuga, K., Domínguez‐Valle, I., Fuentes‐Beltrán, A., Sánchez‐Morales, J. U., Ocampo‐Espindola, J. L., Polanco, C., Micheau, J. C., & Buhse, T. (2019) · Chirality · doi:10.1002/chir.23154 · Cited by 9 · see citing works

Crystal-Packing-Driven Enrichment of Atropoisomers.

Sharafi, M., Campbell, J. P., Rajappan, S., Dudkina, N., Gray, D. L., Woods, T., Li, J.-N., & Schneebeli, S. (2017) · Angewandte Chemie · doi:10.1002/anie.201701876 · Cited by 8

Synthesis, crystal structures, and dye removal properties of a series of discrete and polymeric copper, zinc, cobalt, and cadmium complexes containing bis-pyridyl-bis-amine ligands

Wu, J.-Y., & Chen, C.-W. (2018) · Journal of Solid State Chemistry · doi:10.1016/j.jssc.2018.06.008 · Cited by 7

Synthesis and characterization of multifunctional homochiral 1-D aminoacetic acid potassium metal organic framework

Vadivel, S., Muppidathi, A. L., Jeyaperumal, K. S., & Selvaraj, A. (2018) · Journal of Organometallic Chemistry · doi:10.1016/j.jorganchem.2018.04.032 · Cited by 7

Reversible crystal-to-crystal chiral resolution: making/breaking non-bonding SO interactions.

Mayo, R. A., Sullivan, D. J., Fillion, T., Kycia, S. W., Soldatov, D., & Preuss, K. E. (2017) · Chemical Communications · doi:10.1039/c7cc00907k · Cited by 6 · see citing works

Isomorphism in a Series of Five Homologous Compounds

Andotra, A., Das, S., Killalea, C., Malagreca, F., Zuffa, C., Pandey, P., Khan, S., Liu, J., Fischer, R. C., Dunn, A. S., et al. (2026) · Crystal Growth & Design · doi:10.1021/acs.cgd.6c00230 · Cited by 3 · see citing works

Formation of homochiral 3D frameworks using zinc (II) and rigid achiral ligands

Xu, Z.-X., Shi, M., Li, L.-F., & Gu, J.-N. (2021) · Inorganic Chemistry Communications · doi:10.1016/j.inoche.2021.109167 · Cited by 3

Semi-conductive chiral Co-CPs with helixes based on lactic acid derivatives: Synthesis, structures and photocatalyic properties

Xu, Z.-X., Bai, X., Li, L.-F., & Xu, S. (2020) · doi:10.1016/j.jssc.2020.121524 · Cited by 3

A pair of homochiral porous metal–organic frameworks with a helical metal-carboxylate layer

Xu, Z.-X., Liu, L., & Zhang, J. (2016) · doi:10.1039/c5nj02236c · Cited by 3

Understanding laser desorption with circularly polarized light.

Ristow, F., Scheffel, J., Xu, X., Fehn, N., Oberhofer, K., Riemensberger, J., Mortaheb, F., Kienberger, R., Heiz, U., Kartouzian, A., et al. (2020) · Chirality · doi:10.1002/chir.23279 · Cited by 1 · see citing works

Synthetic Molecular Sequences in Materials Science

Tashiro, K. (2023) · NIMS Monographs · doi:10.1007/978-4-431-56933-6 · Cited by 1

Double Salts and Racemate in Mefloquine–Ibuprofen and Mefloquine–Ketoprofen Systems. A Structural and Thermochemical Analysis

Martins, J. B., Segatto, J. V., Tenorio, J. C., & Carvalho, P. S. (2026) · Chirality · doi:10.1002/chir.70088