The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Spontaneous formation of optically active substances
Overview
Integrity signals
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Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Under these circumstances, only monomers with matching chirality to the primary nuclei crystallize leading to SMSB.55,355”
From Possible chemical and physical scenarios towards biological homochirality (2022) · cites this paper as [355]
In the citing paper
“Fourteen supersaturated solutions were gently heated in sealed tubes, then stored at 0 1C to give crystals which were in 12 cases inexplicably more dextrorotatory”
From Possible chemical and physical scenarios towards biological homochirality (2022) · cites this paper as [355]
Citations
Cites
On spontaneous asymmetric synthesis
Frank, F. C. (1953) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(53)90082-1 · Cited by 905
New Procedures for Resolution of Racemic Substances
Powell, H. M. (1952) · Nature · doi:10.1038/170155a0 · Cited by 46
Untersuchung Monomolekularer Filme mit Hilfe von Elektronenstrahlen
Havinga, E., & de Wael, J. (1937) · Recueil des Travaux Chimiques des Pays-Bas · doi:10.1002/recl.19370560410 · Cited by 30
Self-citationTrennung von optischen Antipoden über Komplexverbindungen ohne Zuhilfenahme asymmetrischer Moleküle
SCHLENK, W. J. (1952) · Cellular and Molecular Life Sciences · doi:10.1007/bf02174405 · Cited by 25
Thomas, M. B., & Jones, H. O. (1906) · Journal of the Chemical Society Transactions · doi:10.1039/ct9068900280 · Cited by 12
Research works printed but not linked: 4
- Havinga, 1941, Chem. Weekblad, 38, 642
- Havinga, 1942, C.A., 36, 5790
- Fock, 1902, Z. Krist., 35, 399
- Wedekind, 1903, Ber., 36, 3793
Cited by
Sorted by citations
Items 201–221 of 221
Igarashi, K., & Fujimura, T. (2023) · JOURNAL OF CHEMICAL ENGINEERING OF JAPAN · doi:10.1080/00219592.2023.2197012 · Cited by 1
Yoshida, Y., Mino, T., & Sakamoto, M. (2025) · Springer eBooks · doi:10.1007/978-981-96-5984-5_4 · Cited by 1
N,N′-Dimethyl-N,N′-diphenylethylenediamine
Lennartson, A., Kokoli, T., & Håkansson, M. (2005) · Acta Crystallographica Section E Structure Reports Online · doi:10.1107/s1600536805025298 · Cited by 1
Right-Handed and Left-Handed Molecular Structures
Laforgue, A. (1989) · Topics in molecular organization and engineering · doi:10.1007/978-94-009-1173-4_4 · Cited by 1
Deracemization of sodium chlorate with or without the influence of sodium dithionate
Schindler, M. (2020) · theses.fr (ABES) · doi:10.70675/c335f5c4z01ecz4f47z9627z37dc0e920627 · Cited by 1
Rare, Neglected and Potential Synthetic Methods for the Separation of Enantiomers
Todd, M. H. (2014) · Wiley eBooks · doi:10.1002/9783527650880.ch7
Nonlinear mathematical models for the origin of asymmetry in biological molecules
Hochstim, A. R. (1975) · Journal of Molecular Evolution · doi:10.1007/bf01732294
Miscellaneous Stereo-Differentiating Reaction Systems
Izumi, Y., & Tai, A. (1977) · Elsevier eBooks · doi:10.1016/b978-0-12-377850-5.50009-x
Volkenstein, M. V. (1983) · Elsevier eBooks · doi:10.1016/b978-0-12-723002-3.50008-4
(2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812212-9.16001-4
(2022) · Royal Society of Chemistry eBooks · doi:10.1039/9781839163685-00149
van Leeuwen, P. W. N. M., Freixa, Z., & Cano, I. (2023) · Advances in catalysis · doi:10.1016/bs.acat.2023.10.001
Zhang, X., Luo, S., Chang, X., Zhou, N., Zou, C., & Lu, W. (2025) · Crystal Growth & Design · doi:10.1021/acs.cgd.5c00535
Hosseinalipour, M. S., & Mazzotti, M. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5958958
Discovering Conglomerates for Chiral Resolution by Crystallization
Mbodji, A. (2020) · theses.fr (ABES) · doi:10.70675/f271b8cdz778az4e21zb330z6716467711ab
Solid-state deracemization of a chiral compound: Considerations on scale, solvent and degradation
Hosseinalipour, M. S., Trapp, N., & Mazzotti, M. (2026) · Process Safety and Environmental Protection · doi:10.1016/j.cherd.2026.04.029
Recent advances in synthesis of nitrogen-centered chiral compounds
Wang, Z.-H., Ji, W., & Lin, T. (2026) · RSC Advances · doi:10.1039/d6ra07158a
Metadata
- Authors
- Havinga, E.
- Corresponding author
- Havinga, E.
- Venue
- Biochimica et Biophysica Acta
- Publisher
- Elsevier BV
- Published
- 1954-01
- Volume
- 13
- Issue
- 2
- Pages
- 171-174
- ISSN
- 0006-3002 (ISSN-L)
- OpenAlex
- W1973584973
- Cited by
- 221
- References
- 5
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 4 · 2023: 3 · 2022: 8 · 2021: 10 · 2020: 10 · 2019: 9 · 2018: 3 · 2017: 5 · 2016: 6 · 2015: 10 · 2014: 6 · 2013: 7 · 2012: 3
- FWCI
- 3.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochimica et Biophysica Acta (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Physics and Astronomy › Astronomy and Astrophysics › Origins and Evolution of Life
- Physical Sciences › Chemistry › Organic Chemistry › Chemistry and Stereochemistry Studies
- Physical Sciences › Chemistry › Spectroscopy › Molecular spectroscopy and chirality
- Keywords
- optical activity, chiral molecules, closed systems, origin of life
- MeSH terms
- Chemistry, Organic, Eye, Organic Chemistry Phenomena
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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