The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Solid phase peptide synthesis utilizing 9‐fluorenylmethoxycarbonyl amino acids
Abstract
9‐Fluorenylmethoxycarbonyl (Fmoc) amino acids were first used for solid phase peptide synthesis a little more than a decade ago. Since that time, Fmoc solid phase peptide synthesis methodology has been greatly enhanced by the introduction of a variety of solid supports, linkages, and side chain protecting groups, as well as by increased understanding of solvation conditions. These advances have led to many impressive syntheses, such as those of biologically active and isotopically labeled peptides and small proteins. The great variety of conditions under which Fmoc solid phase peptide synthesis may be carried out represents a truly “orthogonal” scheme, and thus offers many unique opportunities for bioorganic chemistry.
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Cites
Tam, J. P. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.15.5409 · Cited by 1,251
Peptide synthesis with carbodiimide
Rebek, J., & Feitler, D. (1975) · International Journal of Peptide and Protein Research · doi:10.1111/j.1399-3011.1975.tb02428.x · Cited by 12
Cited by
N -Methylated Cyclic RGD Peptides as Highly Active and Selective α V β 3 Integrin Antagonists
Dechantsreiter, M. A., Planker, E., Mathä, B., Lohof, E., Hölzemann, G., Jonczyk, A., Goodman, S. L., & Kessler, H. (1999) · Journal of Medicinal Chemistry · doi:10.1021/jm970832g · Cited by 838
Advances in Fmoc solid‐phase peptide synthesis
Behrendt, R., White, P., & Offer, J. (2016) · Journal of Peptide Science · doi:10.1002/psc.2836 · Cited by 760
Combinatorial synthesis — the design of compound libraries and their application to drug discovery
Terrett, N. K., Gardner, M., Gordon, D. W., Kobylecki, R. J., & Steele, J. (1995) · Tetrahedron · doi:10.1016/0040-4020(95)00467-m · Cited by 659
Native Chemical Ligation and Extended Methods: Mechanisms, Catalysis, Scope, and Limitations
Agouridas, V., El Mahdi, O., Diemer, V., Cargoët, M., Monbaliu, J.-C. M., & Melnyk, O. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00712 · Cited by 650
Heilborn, J. D., Nilsson, M. F., Sørensen, O., Ståhle-Bäckdahl, M., Kratz, G., Weber, G., & Borregaard, N. (2003) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2003.12069.x · Cited by 572
Metadata
- Authors
- FIELDS, G. B., & NOBLE, R. L.
- Venue
- International Journal of Peptide and Protein Research
- Publisher
- Wiley
- Published
- 1990-03
- Volume
- 35
- Issue
- 3
- Pages
- 161-214
- ISSN
- 0367-8377 (ISSN-L)
- OpenAlex
- W2037455416
- Cited by
- 2,493
- References
- 2
- FWCI
- 15.40
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Solid phase peptide synthesis utilizing 9‐fluorenylmethoxycarbonyl amino acids. https://app.cochat.ai/papers/10.1111/j.1399-3011.1990.tb00939.x
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- FIELDS, G. B., & NOBLE, R. L. (1990). Solid phase peptide synthesis utilizing 9‐fluorenylmethoxycarbonyl amino acids. International Journal of Peptide and Protein Research. https://doi.org/10.1111/j.1399-3011.1990.tb00939.x
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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