The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
The specification of asymmetric configuration in organic chemistry
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Citations
Cites
Determination of the Absolute Configuration of Optically Active Compounds by Means of X-Rays
BIJVOET, J. M., PEERDEMAN, A. F., & van BOMMEL, A. J. (1951) · Nature · doi:10.1038/168271a0 · Cited by 723
Enzymatic Synthesis of the Enantiomorphis of Ethanol-1-d1,2
Loewus, F. A., Westheimer, F. H., & Vennesland, B. (1953) · Journal of the American Chemical Society · doi:10.1021/ja01116a039 · Cited by 134
131. Specification of configuration about quadricovalent asymmetric atoms
Cahn, R. S., & Ingold, C. K. (1951) · Journal of the Chemical Society (Resumed) · doi:10.1039/jr9510000612 · Cited by 131
Self-citation
Research works printed but not linked: 11
- B. Riniker, D. Arigoni, andO. Jeger, Helv. chim. Acta37, 546 (1954). · doi:10.1002/hlca.19540370218
- V. Prelog, M. Wilhelm, andD. Bruce Bright, Helv. chim. Acta37, 221 (1954). · doi:10.1002/hlca.19540370127
- H. Schmid andA. Ebnöther, Helv. chim. Acta34, 1043 (1951).
- M. Przybylska andW. H. Barnes, Acta Cryst.6, 377 (1953). · doi:10.1107/s0365110x53001071
- This is (—)-hydroshikimic acid, whichK. Freudenberg andW. Lwowski cited as an example of a compound which cannot be stereochemically specified on the basis of sub-rule 1 alone [Ann. Chem.594, 76 (1955)]. Actually sub-rules 1 and 2 are required. · doi:10.1002/jlac.19555940109
- C. Martius andG. Schorre, Ann. Chem.570, 140, 143 (1950). · doi:10.1002/jlac.19505700112
- P. E. Wilcox, C. Heidelberger, andV. R. Potter, J. Amer. chem. Soc.72, 5019 (1950). · doi:10.1021/ja01167a054
- A. Streitwieser, J. Amer. chem. Soc.77, 1117 (1955). · doi:10.1021/ja01610a011
- W. Kuhn andR. Rometsch, Helv. chim. Acta27, 1346 (1944). · doi:10.1002/hlca.194402701174
- A. Lüttringhaus andH. Gralheer, Ann. Chem.550, 67 (1941);557, 108, 112 (1947). · doi:10.1002/jlac.19425500105
- D. J. Cram andJ. Abell, J. Amer. chem. Soc.77, 1179 (1955). · doi:10.1021/ja01610a029
Cited by
Specification of Molecular Chirality
Cahn, R. S., Ingold, C., & Prelog, V. (1966) · Angewandte Chemie International Edition in English · doi:10.1002/anie.196603851 · Cited by 1,877
Self-citationLaboratory of Toxicology, F. O. P., Chuong, P.-H., Nguyen, L. A., Department of Pharmacy, L. S. P. C. H., He, H., & Department of Analytical Chemistry, C. P. U. (2006) · International Journal of Biomedical Science · doi:10.59566/ijbs.2006.2085 · Cited by 1,224
Spezifikation der molekularen Chiralität
Cahn, R. S., Ingold, C., & Prelog, V. (1966) · Angewandte Chemie · doi:10.1002/ange.19660780803 · Cited by 719
Self-citationBasic Principles of the CIP‐System and Proposals for a Revision
Prelog, V., & Helmchen, G. (1982) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198205671 · Cited by 592
Self-citationLactate metabolism: historical context, prior misinterpretations, and current understanding
Ferguson, B. S., Rogatzki, M. J., Goodwin, M. L., Kane, D. A., Rightmire, Z., & Gladden, L. B. (2018) · European Journal of Applied Physiology · doi:10.1007/s00421-017-3795-6 · Cited by 441
Metadata
- Authors
- Cahn, R. S., Ingold, C. K., & Prelog, V.
- Venue
- Experientia
- Published
- 1956-03
- Volume
- 12
- Issue
- 3
- Pages
- 81-94
- ISSN
- 1420-682X (ISSN-L)
- 0014-4754
- 1420-9071
- OpenAlex
- W2053032227
- Cited by
- 800
- References
- 3
- FWCI
- 25.67
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
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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.
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- CoChat. (2026). Citation check: The specification of asymmetric configuration in organic chemistry. https://app.cochat.ai/papers/10.1007/bf02157171
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- Cahn, R. S., Ingold, C. K., & Prelog, V. (1956). The specification of asymmetric configuration in organic chemistry. Experientia. https://doi.org/10.1007/bf02157171
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
