The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
Peptide coupling of unprotected amino acids through in situ p-nitrophenyl ester formation
Overview
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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
“Unfortunately, such ideal strategies have been limited to the synthesis of dipeptides because N → C peptide elongation involves the iterative repetition of activation and aminolysis of peptidyl acids, the racemization/epimerization tendency of which is usually 35–110 times higher than that of the corresponding N-carbamate-protected amino acids.20”
From Ynamide Coupling Reagents: Origin and Advances (2024) · cites this paper as [20]
In the citing paper
“Unfortunately, such ideal strategies have been limited to the synthesis of dipeptides because N → C peptide elongation involves the iterative repetition of activation and aminolysis of peptidyl acids, the racemization/epimerization tendency of which is usually 35–110 times higher than that of the corresponding N-carbamate-protected amino acids.20”
From Ynamide Coupling Reagents: Origin and Advances (2024) · cites this paper as [20]
Citations
Cites
Synthesis of Peptides by Aminolysis of Nitrophenyl Esters
BODÁNSZKY, M. (1955) · Nature · doi:10.1038/175685a0 · Cited by 270
Kim, S., Lee, J. I., & Kim, Y. C. (1985) · The Journal of Organic Chemistry · doi:10.1021/jo00205a004 · Cited by 130
The chemical synthesis of peptides
(1992) · Choice Reviews Online · doi:10.5860/choice.29-5704 · Cited by 103
Solid-Phase Peptide Synthesis in the Reverse (N → C) Direction
Thieriet, N., Guibé, F., & Alberício, F. (2000) · Organic Letters · doi:10.1021/ol0058341 · Cited by 63
Bodanszky, M., Deshmane, S. S., & Martínez, J. (1979) · The Journal of Organic Chemistry · doi:10.1021/jo01324a008 · Cited by 50
Bodanszky, M., Sheehan, J. T., Ondetti, M. A., & Lande, S. (1963) · Journal of the American Chemical Society · doi:10.1021/ja00890a036 · Cited by 45
BODANSZKY, A. A., Bodanszky, M., Chandramouli, N., Kwei, J. Z., Martínez, J., & Tolle, J. C. (1980) · The Journal of Organic Chemistry · doi:10.1021/jo01289a016 · Cited by 43
Peptide synthesis with benzisoxazolium salts—III
Kemp, D. S., Wrobel, S., Wang, S.-W., BERNSTEIN, Z., & REBEK, J. J. (1974) · Tetrahedron · doi:10.1016/s0040-4020(01)97372-7 · Cited by 29
Wharton, C. W. (1974) · Biochemical Journal · doi:10.1042/bj1430575 · Cited by 29
Klieger, E., & Gibian, H. (1961) · Justus Liebig s Annalen der Chemie · doi:10.1002/jlac.19616490121 · Cited by 25
Research works printed but not linked: 1
- Clayton, 1957, Peptides, 1399
Cited by
Ynamide Coupling Reagents: Origin and Advances
Hu, L., & Zhao, J. (2024) · Accounts of Chemical Research · doi:10.1021/acs.accounts.3c00743 · Cited by 89
Inverse Peptide Synthesis Using Transient Protected Amino Acids
Liu, T., Peng, Z., Lai, M., Hu, L., & Zhao, J. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.4c00314 · Cited by 58
Metadata
- Authors
- Gagnon, P., Huang, X., Therrien, E., & Keillor, J. W.
- Affiliations
- Université de Montréal (CA)
- Corresponding author
- Keillor, Jeffrey W.
- ORCID
- Keillor, Jeffrey W.
- Venue
- Tetrahedron Letters
- Publisher
- Elsevier BV
- Published
- 2002-10
- Volume
- 43
- Issue
- 43
- Pages
- 7717-7719
- ISSN
- 0040-4039 (ISSN-L)
- OpenAlex
- W2119945849
- Cited by
- 40
- References
- 11
- Citations by year
- 2025: 1 · 2024: 6 · 2023: 1 · 2022: 3 · 2021: 1 · 2020: 2 · 2019: 1 · 2017: 2 · 2016: 1 · 2015: 3 · 2014: 3 · 2013: 1 · 2012: 1
- FWCI
- 0.46
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- Locations
- Tetrahedron Letters (publishedVersion)
- Funders
- Université de Montréal
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Analysis
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Reactions
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Synthetic Organic Chemistry
- Keywords
- peptide coupling, unprotected amino acids, p-nitrophenyl esters, in situ activation, dipeptides, tripeptides, N-protected amino acids, racemization, peptide synthesis
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Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Peptide coupling of unprotected amino acids through in situ p-nitrophenyl ester formation. https://app.cochat.ai/papers/10.1016/s0040-4039(02)01840-3
- The paper
- Gagnon, P., Huang, X., Therrien, E., & Keillor, J. W. (2002). Peptide coupling of unprotected amino acids through in situ p-nitrophenyl ester formation. Tetrahedron Letters. https://doi.org/10.1016/s0040-4039(02)01840-3
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.
