The DOI matches its Crossref record; 72 of the 72 references it cites were found in a registry or an index.
Traceless switch organocatalysis enables multiblock ring-opening copolymerizations of lactones, carbonates, and lactides: by a one plus one approach in one pot
Abstract
A switch of organocatalysis from cationic to base/conjugate-acid bifunctional mechanisms made ring-opening copolymerizations of lactones/carbonates to lactides success.
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In the citing paper
“To overcome this orthogonal activation, Wang et al. have recently developed the 'traceless switching organocatalysis' [10], which was the first efficient approach to generate biodegradable multiblock copolymers with organocatalysis.”
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 [10]
In the citing paper
“As we mentioned in the introduction, block copolymerization by sequential polymerization using organocatalysis is not frequent in the literature especially due to the divergent reactivity between the monomers/catalysts couples [10].”
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 [10]
In the citing paper
“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 [10]
Citations
Cites
Small-Molecule H-Bond Donors in Asymmetric Catalysis
Doyle, A. G., & Jacobsen, E. N. (2007) · Chemical Reviews · doi:10.1021/cr068373r · Cited by 2,634
Organocatalytic 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
Lewis Base Catalysis in Organic Synthesis
Denmark, S. E., & Beutner, G. L. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200604943 · Cited by 1,281
Seayad, J., & List, B. (2005) · Organic & Biomolecular Chemistry · doi:10.1039/b415217b · Cited by 1,134
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
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
Hong, M., & Chen, E. Y.-X. (2016) · Nature Chemistry · doi:10.1038/nchem.2391 · Cited by 677
Ring-opening copolymerization (ROCOP): synthesis and properties of polyesters and polycarbonates
Paul, S., Zhu, Y., Romain, C., Brooks, R., Saini, P. K., & Williams, C. K. (2015) · Chemical Communications · doi:10.1039/c4cc10113h · Cited by 593
Recent advances in the synthesis of aliphatic polyesters by ring-opening polymerization☆
JEROME, C., & LECOMTE, P. (2008) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2008.02.008 · Cited by 590
Organic Catalysis for Ring-Opening Polymerization
Dove, A. P. (2012) · ACS Macro Letters · doi:10.1021/mz3005956 · Cited by 560
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
Toshikj, N., Robin, J.-J., & Blanquer, S. (2020) · European Polymer Journal · doi:10.1016/j.eurpolymj.2020.109599 · Cited by 24
Metadata
- Authors
- Wang, X., Liu, J., Xu, S., Xu, J., Pan, X., Liu, J., Cui, S., Li, Z., & Guo, K.
- Affiliations
- State Key Laboratory of Materials-Oriented Chemical Engineering
- Venue
- Polymer Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2016
- Volume
- 7
- Issue
- 41
- Pages
- 6297-6308
- ISSN
- 1759-9954
- 1759-9962
- Cited by
- 50
- References
- 72
- Language
- en
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- This page
- CoChat. (2026). Citation check: Traceless switch organocatalysis enables multiblock ring-opening copolymerizations of lactones, carbonates, and lactides: by a one plus one approach in one pot. https://app.cochat.ai/papers/10.1039/c6py01107a
- The paper
- Wang, X., Liu, J., Xu, S., Xu, J., Pan, X., Liu, J., Cui, S., Li, Z., & Guo, K. (2016). Traceless switch organocatalysis enables multiblock ring-opening copolymerizations of lactones, carbonates, and lactides: by a one plus one approach in one pot. Polymer Chemistry. https://doi.org/10.1039/c6py01107a
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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.
