The DOI matches its Crossref record; 83 of the 83 references it cites were found in a registry or an index.
Selective O -acyl ring-opening of β-butyrolactone catalyzed by trifluoromethane sulfonic acid: application to the preparation of well-defined block copolymers
Abstract
HOTf catalyzes ring-opening of β-butyrolactone selectively via O -acyl bond cleavage, enabling efficient copolymerization.
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“One of the reasons of this lack can be explained by the divergent reactivity of monomers according to the catalytic mechanism employed, notably in the case of electrophilic or nucleophilic activations [10, 11].”
From A simple and general approach for the synthesis of biodegradable triblock copolymers by organocatalytic ROP from poly(lactide) macroinitiators (2020) · cites this paper as [11]
Citations
Cites
Controlled Ring-Opening Polymerization of Lactide and Glycolide
Dechy-Cabaret, O., Martin-Vaca, B., & Bourissou, D. (2004) · Chemical Reviews · doi:10.1021/cr040002s · Cited by 2,257
Self-citationOrganocatalytic Ring-Opening Polymerization
Kamber, N. E., Jeong, W., Waymouth, R. M., Pratt, R. C., Lohmeijer, B. G. G., & Hedrick, J. L. (2007) · Chemical Reviews · doi:10.1021/cr068415b · Cited by 1,489
Organocatalysis: Opportunities and Challenges for Polymer Synthesis
Kiesewetter, M. K., Shin, E. J., Hedrick, J. L., & Waymouth, R. M. (2010) · Macromolecules · doi:10.1021/ma9025948 · Cited by 907
Kobayashi, S., Uyama, H., & Kimura, S. (2001) · Chemical Reviews · doi:10.1021/cr990121l · Cited by 883
Thomas, C. M. (2010) · Chem. Soc. Rev. · doi:10.1039/b810065a · Cited by 853
Polymerization of lactide and related cyclic esters by discrete metal complexes
O'Keefe, B. J., Hillmyer, M. A., & Tolman, W. B. (2001) · Journal of the Chemical Society, Dalton Transactions · doi:10.1039/b104197p · Cited by 825
Guanidine and Amidine Organocatalysts for Ring-Opening Polymerization of Cyclic Esters
Lohmeijer, B. G. G., Pratt, R. C., Leibfarth, F., Logan, J. W., Long, D. A., Dove, A. P., Nederberg, F., Choi, J., Wade, C., Waymouth, R. M., et al. (2006) · Macromolecules · doi:10.1021/ma0619381 · Cited by 816
Polymer Synthesis by In Vitro Enzyme Catalysis
Gross, R. A., Kumar, A., & Kalra, B. (2001) · Chemical Reviews · doi:10.1021/cr0002590 · Cited by 695
Organic Catalysis for Ring-Opening Polymerization
Dove, A. P. (2012) · ACS Macro Letters · doi:10.1021/mz3005956 · Cited by 560
Handbook of Ring‐Opening Polymerization
(2009) · doi:10.1002/9783527628407 · Cited by 544
Cited by
Strategies for the synthesis of block copolymers with biodegradable polyester segments
Diaz, C., & Mehrkhodavandi, P. (2021) · Polymer Chemistry · doi:10.1039/d0py01534b · Cited by 74
Wang, X., Liu, J., Xu, S., Xu, J., Pan, X., Liu, J., Cui, S., Li, Z., & Guo, K. (2016) · Polymer Chemistry · doi:10.1039/c6py01107a · Cited by 50
Recent Developments in Lactone Monomers and Polymer Synthesis and Application
Bińczak, J., Dziuba, K., & Chrobok, A. (2021) · Materials · doi:10.3390/ma14112881 · Cited by 43
Toshikj, N., Robin, J.-J., & Blanquer, S. (2020) · European Polymer Journal · doi:10.1016/j.eurpolymj.2020.109599 · Cited by 24
Metadata
- Authors
- Couffin, A., Martín-Vaca, B., Bourissou, D., & Navarro, C.
- Affiliations
- University of Toulouse
- Arkema
- Venue
- Polymer Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2014
- Volume
- 5
- Issue
- 1
- Pages
- 161-168
- ISSN
- 1759-9954
- 1759-9962
- Cited by
- 44
- References
- 83
- Language
- en
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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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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.
