The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
Synthetic foldamers
Abstract
Foldamers are artificial folded molecular architectures inspired by the structures and functions of biopolymers. This highlight focuses on important developments concerning foldamers produced by chemical synthesis and on the perspectives that these new self-organized molecular scaffolds offer. Progress in the field has led to synthetic objects that resemble small proteins in terms of size and complexity yet that may not contain any α-amino acids. Foldamers have introduced new tools and concepts to develop biologically active substances, synthetic receptors and novel materials.
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Cites
Sequence-Selective Recognition of DNA by Strand Displacement with a Thymine-Substituted Polyamide
Nielsen, P. E., Egholm, M., Berg, R. H., & Buchardt, O. (1991) · Science · doi:10.1126/science.1962210 · Cited by 3,332
Gellman, S. H. (1998) · Accounts of Chemical Research · doi:10.1021/ar960298r · Cited by 2,506
Hill, D. J., Mio, M. J., Prince, R. B., Hughes, T. S., & Moore, J. S. (2001) · Chemical Reviews · doi:10.1021/cr990120t · Cited by 2,239
Helicates as Versatile Supramolecular Complexes
Piguet, C., Bernardinelli, G., & Hopfgartner, G. (1997) · Chemical Reviews · doi:10.1021/cr960053s · Cited by 1,711
Helical Polymers: Synthesis, Structures, and Functions
Yashima, E., Maeda, K., Iida, H., Furusho, Y., & Nagai, K. (2009) · Chemical Reviews · doi:10.1021/cr900162q · Cited by 1,666
Peptoids: a modular approach to drug discovery.
Simon, R. J., Kania, R. S., Zuckermann, R. N., Huebner, V. D., Jewell, D. A., Banville, S., Ng, S., Wang, L., Rosenberg, S., & Marlowe, C. K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.20.9367 · Cited by 953
Solvophobically Driven Folding of Nonbiological Oligomers
Nelson, J. C., Saven, J. G., Moore, J. S., & Wolynes, P. G. (1997) · Science · doi:10.1126/science.277.5333.1793 · Cited by 825
Seebach, D., Overhand, M., Kühnle, F. N. M., Martinoni, B., Oberer, L., Hommel, U., & Widmer, H. (1996) · Helvetica Chimica Acta · doi:10.1002/hlca.19960790402 · Cited by 734
Interconversion of single and double helices formed from synthetic molecular strands
Berl, V., Huc, I., Khoury, R. G., Krische, M. J., & Lehn, J.-M. (2000) · Nature · doi:10.1038/35037545 · Cited by 723
Self-citationβ-Peptide Foldamers: Robust Helix Formation in a New Family of β-Amino Acid Oligomers
Appella, D. H., Christianson, L. A., Karle, I. L., Powell, D. R., & Gellman, S. H. (1996) · Journal of the American Chemical Society · doi:10.1021/ja963290l · Cited by 705
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Single-chain technology using discrete synthetic macromolecules
Ouchi, M., Badi, N., Lutz, J.-F., & Sawamoto, M. (2011) · Nature Chemistry · doi:10.1038/nchem.1175 · Cited by 386
New Modalities for Challenging Targets in Drug Discovery
Valeur, E., Guéret, S. M., Adihou, H., Gopalakrishnan, R., Lemurell, M., Waldmann, H., Grossmann, T. N., & Plowright, A. T. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201611914 · Cited by 382
Macrocycles as Ion Pair Receptors
He, Q., Vargas-Zúñiga, G. I., Kim, S. H., Kim, S. K., & Sessler, J. L. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00734 · Cited by 319
Cametti, M., & Rissanen, K. (2013) · Chem. Soc. Rev. · doi:10.1039/c2cs35439j · Cited by 281
Targeting protein–protein interactions, a wide open field for drug design
Bakail, M., & Ochsenbein, F. (2016) · Comptes Rendus. Chimie · doi:10.1016/j.crci.2015.12.004 · Cited by 117
Metadata
- Authors
- Guichard, G., & Huc, I.
- Venue
- Chemical Communications
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2011
- Volume
- 47
- Issue
- 21
- Pages
- 5933
- ISSN
- 1359-7345 (ISSN-L)
- 1364-548X
- OpenAlex
- W4234803768
- Cited by
- 769
- References
- 70
- FWCI
- 23.75
- Type
- journal article
- Language
- en
- Open access
- closed
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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.