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Diels–Alder “click” reactions: recent applications in polymer and material science
Abstract
The “click” chemistry concept is based on utilizing rapid reactions which are efficient, versatile, and selective. Indeed, Diels–Alder (DA) reactions fulfill most of the requirements for the “click” chemistry concept. In this review, we discuss the recent reports concerned with the use of DA “click” reactions in the synthesis of various macromolecular architectures, bioconjugates and hybrid materials.
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Tornøe, C. W., Christensen, C., & Meldal, M. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo011148j · Cited by 8,696
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Self-Healing Injectable Hydrogels for Tissue Regeneration
Bertsch, P., Diba, M., Mooney, D. J., & Leeuwenburgh, S. C. G. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00179 · Cited by 892
Click Chemistry in Materials Science
Xi, W., Scott, T. F., Kloxin, C. J., & Bowman, C. N. (2014) · Advanced Functional Materials · doi:10.1002/adfm.201302847 · Cited by 677
Design Challenges in Polymeric Scaffolds for Tissue Engineering
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Yu, F., Cao, X., Du, J., Wang, G., & Chen, X. (2015) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5b06896 · Cited by 359
Metadata
- Authors
- Tasdelen, M. A.
- Venue
- Polymer Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2011
- Volume
- 2
- Issue
- 10
- Pages
- 2133
- ISSN
- 1759-9954 (ISSN-L)
- 1759-9962
- OpenAlex
- W2037776133
- Cited by
- 582
- References
- 1
- FWCI
- 14.96
- 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.
