Resolution of conglomerates with the assistance of tailor-made impurities. Generality and mechanistic aspects of the "rule of reversal". A new method for assignment of absolute configuration

Processes To Separate Enantiomers

Lorenz, H., & Seidel‐Morgenstern, A. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201302823 · Cited by 526 · see citing works

Molecular Recognition at Crystal Interfaces

Weissbuch, I., Addadi, L., Lahav, M., & Leiserowitz, L. (1991) · Science · doi:10.1126/science.253.5020.637 · Cited by 469 · see citing works

Toward Stereochemical Control, Monitoring, and Understanding of Crystal Nucleation

Weissbuch, I., Lahav, M., & Leiserowitz, L. (2003) · Crystal Growth & Design · doi:10.1021/cg0200560 · Cited by 360 · see citing works

Growth and Dissolution of Organic Crystals with “Tailor‐Made” Inhibitors—Implications in Stereochemistry and Materials Science

Addadi, L., BERKOVITCH‐YELLIN, Z., Weissbuch, I., van Mil, J., Shimon, L. J. W., Lahav, M., & Leiserowitz, L. (1985) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198504661 · Cited by 294 · see citing works

Crystalline Architectures as Templates of Relevance to the Origins of Homochirality

Weissbuch, I., & Lahav, M. (2011) · Chemical Reviews · doi:10.1021/cr1002479 · Cited by 284 · see citing works

A practical guide to pharmaceutical polymorph screening & selection

Lee, E. H. (2014) · Asian Journal of Pharmaceutical Sciences · doi:10.1016/j.ajps.2014.05.002 · Cited by 253 · see citing works

Complete chiral symmetry breaking of an amino acid derivative directed by circularly polarized light

Noorduin, W. L., Bode, A. A. C., van der Meijden, M., Meekes, H., van Etteger, A. F., van Enckevort, W. J. P., Christianen, P. C. M., Kaptein, B., Kellogg, R. M., Rasing, T., et al. (2009) · Nature Chemistry · doi:10.1038/nchem.416 · Cited by 247 · see citing works

Additive controlled crystallization

Song, R., & Cölfen, H. (2011) · CrystEngComm · doi:10.1039/c0ce00419g · Cited by 244 · see citing works

From Ostwald Ripening to Single Chirality

Noorduin, W. L., Vlieg, E., Kellogg, R. M., & Kaptein, B. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200905215 · Cited by 220 · see citing works

Crystallization and Polymorphism of Conformationally Flexible Molecules: Problems, Patterns, and Strategies

Yu, L., Reutzel‐Edens, S. M., & Mitchell, C. A. (2000) · Organic Process Research & Development · doi:10.1021/op000028v · Cited by 194 · 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

Polymer‐Induced Alignment of dl ‐Alanine Nanocrystals to Crystalline Mesostructures

Wohlrab, S., Pinna, N., Antonietti, M., & Cölfen, H. (2005) · Chemistry - A European Journal · doi:10.1002/chem.200400420 · Cited by 164 · see citing works

From parity to chirality: chemical implications revisited

Ávalos, M., Babiano, R., Cintas, P., Jiménez, J. L., & Palacios, J. C. (2000) · Tetrahedron Asymmetry · doi:10.1016/s0957-4166(00)00265-2 · Cited by 161 · see citing works

Stochastic “Mirror Symmetry Breaking” via Self-Assembly, Reactivity and Amplification of Chirality: Relevance to Abiotic Conditions

Weissbuch, I., Leiserowitz, L., & Lahav, M. (2005) · Springer eBooks · doi:10.1007/b137067 · Cited by 155 · see citing works

Bulk Crystals to Surfaces: Combining X-ray Diffraction and Atomic Force Microscopy to Probe the Structure and Formation of Crystal Interfaces

Ward, M. D. (2001) · Chemical Reviews · doi:10.1021/cr000020j · Cited by 150 · see citing works

Calcium sulfate precipitation studies with scale inhibitors for reverse osmosis desalination

Rahman, F. (2013) · Desalination · doi:10.1016/j.desal.2013.03.027 · Cited by 150 · see citing works

Attrition-enhanced deracemization of an amino acid derivative that forms an epitaxial racemic conglomerate

Kaptein, B., Noorduin, W. L., Meekes, H., van Enckevort, W. J. P., Kellogg, R. M., & Vlieg, E. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200802468 · Cited by 134 · see citing works

Strategies for chiral separation: from racemate to enantiomer

Sui, J., Wang, N., Wang, J., Huang, X., Wang, T., Zhou, L., & Hao, H. (2023) · Chemical Science · doi:10.1039/d3sc01630g · Cited by 133 · see citing works

Complete Deracemization by Attrition‐Enhanced Ostwald Ripening Elucidated

Noorduin, W. L., Meekes, H., van Enckevort, W. J. P., Millemaggi, A., Leeman, M., Kaptein, B., Kellogg, R. M., & Vlieg, E. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200801846 · Cited by 126 · see citing works

A Link Between Macroscopic Phenomena and Molecular Chirality: Crystals as Probes for the Direct Assignment of Absolute Configuration of Chiral Molecules

Addadi, L., BERKOVITCH‐YELLIN, Z., Weissbuch, I., Lahav, M., & Leiserowitz, L. (1986) · Topics in stereochemistry · doi:10.1002/9780470147252.ch1 · Cited by 107 · see citing works

The influence of impurities and solvents on crystallization

Meenan, P. A., Anderson, S. R., & Klug, D. L. (2002) · Elsevier eBooks · doi:10.1016/b978-075067012-8/50005-7 · Cited by 104 · see citing works

Enantioseparation by crystallization using magnetic substrates

Tassinari, F., Steidel, J., Paltiel, S., Fontanesi, C., Lahav, M., Paltiel, Y., & Naaman, R. (2019) · Chemical Science · doi:10.1039/c9sc00663j · Cited by 101 · see citing works

Resolution of Seven‐Coordinate Complexes

Lennartson, A., Vestergren, M., & Håkansson, M. (2005) · Chemistry - A European Journal · doi:10.1002/chem.200401019 · Cited by 101 · see citing works

Racemic leucine separation by hollow‐fiber extraction

Ding, H. B., Carr, P. W., & Cussler, E. L. (1992) · AIChE Journal · doi:10.1002/aic.690381002 · Cited by 99 · see citing works

The kinetics of crystal growth in the presence of tailor-made additives

Black, S. N., Davey, R. J., & Halcrow, M. A. (1986) · Journal of Crystal Growth · doi:10.1016/0022-0248(86)90552-x · Cited by 96 · see citing works

Enantioselective Crystallization on Chiral Polymeric Microspheres

Medina, D. D., Goldshtein, J., Margel, S., & Mastai, Y. (2007) · Advanced Functional Materials · doi:10.1002/adfm.200600408 · Cited by 93 · see citing works

Catalytic Deracemization Reactions

Huang, M., Pan, T., Jiang, X., & Luo, S. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c02622 · Cited by 90 · see citing works

Enantioselective crystallization on nanochiral surfaces

Mastai, Y. (2009) · Chemical Society Reviews · doi:10.1039/b812587m · Cited by 89 · see citing works

Impurity incorporation in solution crystallization: diagnosis, prevention, and control

Capellades, G., Bonsu, J. O., & Myerson, A. S. (2022) · CrystEngComm · doi:10.1039/d1ce01721g · Cited by 87 · see citing works

Opportunities in asymmetric synthesis: An industrial prospect

Kotha, S. (1994) · Tetrahedron · doi:10.1016/s0040-4020(01)90388-6 · Cited by 87 · see citing works

Complete Deracemization by Attrition‐Enhanced Ostwald Ripening Elucidated

Noorduin, W. L., Meekes, H., van Enckevort, W. J. P., Millemaggi, A., Leeman, M., Kaptein, B., Kellogg, R. M., & Vlieg, E. (2008) · Angewandte Chemie · doi:10.1002/ange.200801846 · Cited by 87 · see citing works

Recent developments in optical resolution

Siedlecka, R. (2013) · Tetrahedron · doi:10.1016/j.tet.2013.05.035 · Cited by 83 · see citing works

Viedma Ripening of Conglomerate Crystals of Achiral Molecules Monitored Using Solid-State Circular Dichroism

McLaughlin, D. T., Nguyen, T. P. T., Mengnjo, L., Bian, C., Leung, Y. H., Goodfellow, E., Ramrup, P., Woo, S., & Cuccia, L. A. (2014) · Crystal Growth & Design · doi:10.1021/cg401577m · Cited by 82 · see citing works

Complete chiral resolution using additive-induced crystal size bifurcation during grinding

Noorduin, W. L., van der Asdonk, P., Meekes, H., van Enckevort, W. J. P., Kaptein, B., Leeman, M., Kellogg, R. M., & Vlieg, E. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200806214 · Cited by 79 · see citing works

Interfacial Effect of Molecules on Nucleation Kinetics

Liu, X. (2001) · The Journal of Physical Chemistry B · doi:10.1021/jp010671z · Cited by 77 · see citing works

Crystallization of Amino Acids on Self-Assembled Monolayers of Rigid Thiols on Gold

Lee, A. Y., Ulman, A., & Myerson, A. S. (2002) · Langmuir · doi:10.1021/la025704w · Cited by 71 · see citing works

Interactions Between Acidic Macromolecules and Structured Crystal Surfaces. Stereochemistry and Biomineralization

Addadi, L., & Weiner, S. (1986) · Molecular crystals and liquid crystals · doi:10.1080/00268948608079592 · Cited by 69 · see citing works

Parity Violating Energetic Difference and Enantiomorphous Crystalsp-Caveats; Reinvestigation of Tyrosine Crystallization

Lahav, M., Weissbuch, I., Shavit, E., Reiner, C., NICHOLSON, G. J., & Schurig, V. (2006) · Origins of Life and Evolution of Biospheres · doi:10.1007/s11084-005-9000-7 · Cited by 67 · see citing works

Total Spontaneous Resolution by Deracemization of Isoindolinones

Yagishita, F., Ishikawa, H., Onuki, T., Hachiya, S., Mino, T., & Sakamoto, M. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201205097 · Cited by 65 · see citing works

State of the Art in Crystallization‐Induced Diastereomer Transformations

Kolarovič, A., & Jakubec, P. (2021) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.202100473 · Cited by 60 · see citing works

A Cyclic Continuous Process for Converting Conglomerates into Optically Pure Enantiomers by Crystallization and Dissolution with the Assistance of ‘Tailor-made’ Polymers

Zbaida, D., Lahav, M., Drauz, K., Knaup, G. L., & Kottenhahn, M. (2000) · Tetrahedron · doi:10.1016/s0040-4020(00)00465-8 · Cited by 59 · see citing works

Molecular recognition at the interface between crystals and biology: generation, manifestation and detection of chirality at crystal surfacesThis article is based (partly) on a presentation which will be made at the European Research Conference (EURESCO) on "Molecular Crystal Engineering - EuroConference on Design and Preparation of Molecular Materials" (Acquafredda di Maratea, Italy, 31 May - 5 June 2003) organised by the European Science Foundation and supported by the European Commission, Research DG, Human Potential Programme, High-Level Scientific Conferences, Contract HPCF-CT-2002-00270. This information is the sole responsibility of the author(s) and does not reflect the ESF or Community's opinion. The ESF and the Community are not responsible for any use that might be made of data appearing in this publication.

Addadi, L., & Geva, M. (2003) · CrystEngComm · doi:10.1039/b304061e · Cited by 58 · see citing works

Enantioenrichment by Iterative Retro‐Aldol/Aldol Reaction Catalyzed by an Achiral or Racemic Base

Flock, A. M., Reucher, C. M. M., & Bolm, C. (2010) · Chemistry - A European Journal · doi:10.1002/chem.200903497 · Cited by 57 · see citing works

Tailor-made auxiliaries for the control of nucleation, growth and dissolution of two- and three-dimensional crystals

Lahav, M., & Leiserowitz, L. (1993) · Journal of Physics D Applied Physics · doi:10.1088/0022-3727/26/8b/003 · Cited by 55 · see citing works

Crystal doping aided by rapid expansion of supercritical solutions

Vemavarapu, C., Mollan, M. J., & Needham, T. E. (2002) · AAPS PharmSciTech · doi:10.1208/pt030429 · Cited by 54 · see citing works

Recent advances in the field of chiral crystallization

Putman, J. I., & Armstrong, D. W. (2022) · Chirality · doi:10.1002/chir.23492 · Cited by 53 · see citing works

Chirality: An inescapable concept for the pharmaceutical, bio‐pharmaceutical, food, and cosmetic industries

Kandula, J. S., Rayala, V. V. S. P. K., & Radhakrishnanand, P. (2023) · Separation Science Plus · doi:10.1002/sscp.202200131 · Cited by 52 · see citing works

Secondary nucleation that leads to chiral symmetry breaking in stirred crystallization

Kondepudi, D. K., & Sabanayagam, C. R. (1994) · Chemical Physics Letters · doi:10.1016/0009-2614(93)e1392-t · Cited by 52 · see citing works

Chiral soluble polymers and microspheres for enantioselective crystallization

Menahem, T., & Mastai, Y. (2006) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.21376 · Cited by 51 · see citing works

Dutch Resolution of Racemates and the Roles of Solid Solution Formation and Nucleation Inhibition

Kellogg, R. M., Kaptein, B., & Vries, T. R. (2007) · Topics in current chemistry · doi:10.1007/128_2006_095 · Cited by 50 · see citing works

Helical Chirality of Supramolecular Columns and Spheres Self‐Organizes Complex Liquid Crystals, Crystals, and Quasicrystals

Percec, V., & Xiao, Q. (2021) · Israel Journal of Chemistry · doi:10.1002/ijch.202100057 · Cited by 48 · see citing works

Enantioselective Symmetry Breaking Directed by the Order of Process Steps

Noorduin, W. L., Meekes, H., van Enckevort, W. J. P., Kaptein, B., Kellogg, R. M., & Vlieg, E. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200907231 · Cited by 48 · see citing works

Attrition‐Enhanced Deracemization of an Amino Acid Derivative That Forms an Epitaxial Racemic Conglomerate

Kaptein, B., Noorduin, W. L., Meekes, H., van Enckevort, W. J. P., Kellogg, R. M., & Vlieg, E. (2008) · Angewandte Chemie · doi:10.1002/ange.200802468 · Cited by 48 · see citing works

Von der Ostwald‐Reifung zur Homochiralität

Noorduin, W. L., Vlieg, E., Kellogg, R. M., & Kaptein, B. (2009) · Angewandte Chemie · doi:10.1002/ange.200905215 · Cited by 47 · see citing works

Autocatalytic Enantiomerisation at the Crystal Surface in Deracemisation of Scalemic Conglomerates

Wei, S., Mauksch, M., & Tsogoeva, S. B. (2009) · Chemistry - A European Journal · doi:10.1002/chem.200900979 · Cited by 45 · see citing works

Wachstum und Auflösung Organischer Kristalle in Gegenwart von Additiven ‐ ein Beitrag zu Stereochemie und Materialwissenschaften

Addadi, L., BERKOVITCH‐YELLIN, Z., Weissbuch, I., van Mil, J., Shimon, L. J. W., Lahav, M., & Leiserowitz, L. (1985) · Angewandte Chemie · doi:10.1002/ange.19850970607 · Cited by 45 · see citing works

Complete Chiral Resolution Using Additive‐Induced Crystal Size Bifurcation During Grinding

Noorduin, W. L., van der Asdonk, P., Meekes, H., van Enckevort, W. J. P., Kaptein, B., Leeman, M., Kellogg, R. M., & Vlieg, E. (2009) · Angewandte Chemie · doi:10.1002/ange.200806214 · Cited by 43 · see citing works

Lamellar Racemic Twinning as an Obstacle for the Resolution of Enantiomers by Crystallization: The Case of Me(All)N + (CH 2 Ph)Ph X - (X = Br, I) Salts

Torbeev, V. Y., Lyssenko, K. A., Kharybin, O. N., Antipin, M. Y., & Kostyanovsky, R. G. (2003) · The Journal of Physical Chemistry B · doi:10.1021/jp035588l · Cited by 43 · see citing works

Directional Crystal Jumping Controlled by Chirality

Chen, Y., Zhang, J., Zhang, J., & Wan, X. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.3c13416 · Cited by 42 · see citing works

Enabling Enantiopurity: Combining Racemization and Dual-Drug Co-crystal Resolution

Harmsen, B., & Leyssens, T. (2018) · Crystal Growth & Design · doi:10.1021/acs.cgd.8b00438 · Cited by 42 · see citing works

Chiral crystallization of glutamic acid on self assembled films of cysteine

Dressler, D. H., & Mastai, Y. (2007) · Chirality · doi:10.1002/chir.20389 · Cited by 39 · see citing works

Self‐Reporting Inhibitors: A Single Crystallization Process To Obtain Two Optically Pure Enantiomers

Ye, X., Cui, J., Li, B., Li, N., Zhang, J., & Wan, X. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201803480 · Cited by 38 · see citing works

Crystals and Crystal Growth

Lee, A. Y., Erdemir, D., & Myerson, A. S. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139026949.002 · Cited by 38 · see citing works

The Origin of Life and the Crystallization of Aspartic Acid in Water

Lee, T., & Lin, Y. K. (2010) · Crystal Growth & Design · doi:10.1021/cg901219f · Cited by 37 · see citing works

Solvent dependent assembly and disassembly of a hydrogen bonded helical structure in a Co–Mo bimetallic complex

Khatua, S., Harada, T., Kuroda, R., & Bhattacharjee, M. (2007) · Chemical Communications · doi:10.1039/b705891h · Cited by 37 · see citing works

Structural Aspects of Nucleation Inhibitors for Diastereomeric Resolutions and the Relationship to Dutch Resolution

Leeman, M., Brasile, G., Gelens, E., Vries, T. R., Kaptein, B., & Kellogg, R. M. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200704021 · Cited by 36 · see citing works

Tuning crystallization and stability of the metastable polymorph of dl -methionine by a structurally similar additive

Li, Z., Shi, P., Yang, Y., Sun, P., Wang, Y., Xu, S., & Gong, J. (2019) · CrystEngComm · doi:10.1039/c9ce00009g · Cited by 36 · see citing works

Stereochemical studies on chiral systems in two dimensions

Weissbuch, I., Kuzmenko, I., Berfeld, M., Leiserowitz, L., & Lahav, M. (2000) · Journal of Physical Organic Chemistry · doi:10.1002/1099-1395(200007)13:7 · Cited by 36 · see citing works

Noncovalently Functionalized Commodity Polymers as Tailor‐Made Additives for Stereoselective Crystallization

Ye, X., Wang, Z., Zhang, J., & Wan, X. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202106603 · Cited by 35 · see citing works

Direct assignment of the absolute configuration of molecules from crystal morphology

Weissbuch, I., Leiserowitz, L., & Lahav, M. (2008) · Chirality · doi:10.1002/chir.20498 · Cited by 34 · see citing works

Verfahren zur Enantiomerentrennung

Lorenz, H., & Seidel‐Morgenstern, A. (2014) · Angewandte Chemie · doi:10.1002/ange.201302823 · Cited by 34 · see citing works

Impurity Occurrence and Removal in Crystalline Products from Process Reactions

Moynihan, H. A., & Horgan, D. E. (2017) · Organic Process Research & Development · doi:10.1021/acs.oprd.6b00403 · Cited by 33 · see citing works

Temperature cycle induced deracemization

Intaraboonrod, K., Lerdwiriyanupap, T., Hoquante, M., Coquerel, G., & Flood, A. E. (2020) · Mendeleev Communications · doi:10.1016/j.mencom.2020.07.002 · Cited by 32 · see citing works

Selective Crystallization of d -Mannitol Polymorphs Using Surfactant Self-Assembly

Penha, F. M., Gopalan, A. V., Meijlink, J. C., İbiş, F., & Eral, H. B. (2021) · Crystal Growth & Design · doi:10.1021/acs.cgd.1c00243 · Cited by 32 · see citing works

Controlled ice nucleation in microsized water droplet

Du, N., & Liu, X. (2002) · Applied Physics Letters · doi:10.1063/1.1492849 · Cited by 32 · see citing works

Role of Additives during Deracemization Using Temperature Cycling

Belletti, G., Meekes, H., Rutjes, F. P. J. T., & Vlieg, E. (2018) · Crystal Growth & Design · doi:10.1021/acs.cgd.8b00856 · Cited by 31 · see citing works

Particle Engineering: Fundamentals of Particle Formation and Crystal Growth

Lee, A. Y., & Myerson, A. S. (2006) · MRS Bulletin · doi:10.1557/mrs2006.207 · Cited by 31 · see citing works

Studies in chiral symmetry breaking crystallization I: The effects of stirring and evaporation rates

Kondepudi, D. K., Digits, J. A., & Bullock, K. L. (1995) · Chirality · doi:10.1002/chir.530070203 · Cited by 31 · see citing works

Disorder and twinning in molecular crystals: impurity‐induced effects in adipic acid

Seton, L., Davey, R. J., Lieberman, H. F., & Pritchard, R. G. (2000) · Journal of Pharmaceutical Sciences · doi:10.1002/(sici)1520-6017(200003)89:3 · Cited by 29 · see citing works

Replication of α-amino acids via Strecker synthesis with amplification and multiplication of chiral intermediate aminonitriles

Aiba, S., Takamatsu, N., Sasai, T., Tokunaga, Y., & Kawasaki, T. (2016) · Chemical Communications · doi:10.1039/c6cc05544c · Cited by 29 · see citing works

Amino acid directed mirror symmetry breaking and chiral amplification of ethylenediammonium sulfate crystals

Cheung, P. S. M., & Cuccia, L. A. (2009) · Chemical Communications · doi:10.1039/b823029c · Cited by 27 · see citing works

Chiral Polymers and Polymeric Particles for Enantioselective Crystallization

Medina, D. D., & Mastai, Y. (2018) · Israel Journal of Chemistry · doi:10.1002/ijch.201800174 · Cited by 27 · see citing works

Kinetics of chiral resolution in stirred crystallization of D/L-glutamic acid

Buhse, T., Kondepudi, D. K., & Hoskins, B. J. (1999) · Chirality · doi:10.1002/(sici)1520-636x(1999)11:4 · Cited by 27 · see citing works

Aspects of additives in precipitation processes: Performance of polycarboxylates in gypsum growth prevention

van der Leeden, M. C., & van Rosmalen, G. M. (1987) · Desalination · doi:10.1016/0011-9164(87)90204-9 · Cited by 25 · see citing works

Solid‐Phase Conversion of Four Stereoisomers into a Single Enantiomer

Engwerda, A. H. J., Mertens, J. C. J., Tinnemans, P., Meekes, H., Rutjes, F. P. J. T., & Vlieg, E. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201808913 · Cited by 24 · see citing works

Potential of Chiral Solvents for Enantioselective Crystallization. 2. Evaluation of Kinetic Effects

Tulashie, S. K., Lorenz, H., & Seidel‐Morgenstern, A. (2009) · Crystal Growth & Design · doi:10.1021/cg801286s · Cited by 24 · see citing works

Tuning organic crystal chirality by the molar masses of tailored polymeric additives

Ye, X., Li, B., Wang, Z., Li, J., Zhang, J., & Wan, X. (2021) · Nature Communications · doi:10.1038/s41467-021-27236-1 · Cited by 23 · see citing works

Effects of Homochiral Molecules of (S)-(+)-Ibuprofen and (S)-(−)-Sodium Ibuprofen Dihydrate on the Crystallization Kinetics of Racemic (R,S)-(±)-Sodium Ibuprofen Dihydrate

Lee, T., Chen, Y. H., & Wang, Y. W. (2007) · Crystal Growth & Design · doi:10.1021/cg070045c · Cited by 23 · see citing works

Directing the Viedma ripening of ethylenediammonium sulfate using “Tailor-made” chiral additives

Nguyễn, T. P. T., Cheung, P. S. M., Werber, L., Gagnon, J., Sivakumar, R., Lennox, C. B., Sossin, A., Mastai, Y., & Cuccia, L. A. (2016) · Chemical Communications · doi:10.1039/c6cc06534a · Cited by 22 · see citing works

High‐performance nano‐splitters containing aggregation‐induced emission luminogens for stereoselective crystallization obtained via polymerization‐induced self‐assembly

Li, B., Li, N., Wang, Z., Ye, X., Zhang, J., & Wan, X. (2021) · Aggregate · doi:10.1002/agt2.129 · Cited by 22 · see citing works

Scale Formation and Control in Thermal Desalination Systems

Rahman, F., & Amjad, Z. (2010) · CRC Press eBooks · doi:10.1201/9781420071450-c14 · Cited by 22 · see citing works

MORPHOLOGY ENGINEERING OF ORGANIC CRYSTALS WITH THE ASSISTANCE OF “TAILOR-MADE” GROWTH INHIBITORS

Addadi, L., BERKOVITCH‐YELLIN, Z., Weissbuch, I., Lahav, M., & Leiserowitz, L. (1983) · Molecular crystals and liquid crystals · doi:10.1080/00268948308074685 · Cited by 22 · see citing works

Designing single chirality via crystallization method: spontaneous chiral symmetry breaking and deracemization

Zhang, B., Sun, X., & Du, P. (2023) · Materials Today Chemistry · doi:10.1016/j.mtchem.2023.101636 · Cited by 21 · see citing works

Enantioselective crystallization of histidine on chiral self-assembled films of cysteine

Dressler, D. H., & Mastai, Y. (2007) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2007.02.028 · Cited by 21 · see citing works

Stereochemical Discrimination at Organic Crystal Surfaces 1: The Systems Serine/Threonine and Serine/Allothreonine

Weissbuch, I., Shimon, L. J. W., Addadi, L., BERKOVITCH‐YELLIN, Z., Weinstein, S., Lahav, M., & Leiserowitz, L. (1985) · Israel Journal of Chemistry · doi:10.1002/ijch.198500057 · Cited by 21 · see citing works

Effect of additives on the preferential crystallization of L-asparagine monohydrate

Kongsamai, P., Maneedaeng, A., Flood, C., ter Horst, J. H., & Flood, A. E. (2017) · The European Physical Journal Special Topics · doi:10.1140/epjst/e2016-60257-3 · Cited by 20 · see citing works

Efficient Havinga–Kondepudi resolution of conglomerate amino acid derivatives by slow cooling and abrasive grinding

Leeman, M., Noorduin, W. L., Millemaggi, A., Vlieg, E., Meekes, H., van Enckevort, W. J. P., Kaptein, B., & Kellogg, R. M. (2010) · CrystEngComm · doi:10.1039/c0ce00140f · Cited by 20 · see citing works

The Nanoscale Aspects of Chirality in Crystal Growth: Structure and Heterogeneous Equilibria

Coquerel, G., & Amabilino, D. B. (2009) · Wiley eBooks · doi:10.1002/9783527625345.ch10 · Cited by 19 · see citing works

Total Spontaneous Resolution by Deracemization of Isoindolinones

Yagishita, F., Ishikawa, H., Onuki, T., Hachiya, S., Mino, T., & Sakamoto, M. (2012) · Angewandte Chemie · doi:10.1002/ange.201205097 · Cited by 18 · see citing works

ChemInform Abstract: RESOLUTION OF CONGLOMERATES WITH THE ASSISTANCE OF TAILOR‐MADE IMPURITIES. GENERALITY AND MECHANISTIC ASPECTS OF THE “RULE OF REVERSAL”. A NEW METHOD FOR ASSIGNMENT OF ABSOLUTE CONFIGURATION

Addadi, L., Weinstein, S., Gati, E., Weissbuch, I., & Lahav, M. (1982) · ChemInform · doi:10.1002/chin.198247076

Useful impurities for optical resolutions. 3. An improved Pasteur-type resolution of conglomerates and a new empirical method for assignment of absolute configuration

Addadi, L., Gati, E., & Lahav, M. (1981) · Journal of the American Chemical Society · doi:10.1021/ja00395a060 · Cited by 32 · see citing works

Pruning the conformational dependence in the determination of the absolute configuration and the proposal of an algorithm to assign the absolute configuration

Bultinck, P., & Kuppens, T. (2003) · Ghent University Academic Bibliography (Ghent University)

Erroneous conclusion based on a misinterpretation of the International Union of Pure and Applied Chemistry (IUPAC) rules for designating absolute configurations

Legg, J. I. (1971) · Inorganic Chemistry · doi:10.1021/ic50104a072 · Cited by 3 · see citing works

Thematic issue on determination of absolute configuration

Allenmark, S. G., Gawronski, J. K., & Berova, N. D. (2007) · Chirality · doi:10.1002/chir.20523 · Cited by 3 · see citing works