The first 2,3-heterodifunctionalized β-cyclodextrin derivatives as artificial enzymes
Chemical Communications, ISSN: 1364-548X, Vol: 51, Issue: 13, Page: 2601-2604
2015
- 23Citations
- 25Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations23
- Citation Indexes23
- CrossRef23
- 23
- Captures25
- Readers25
- 25
Article Description
Novel 2,3-heterodisubstituted β-cyclodextrin derivatives were designed as artificial enzymes to degrade chemical warfare agents. One of them reduced the acetylcholinesterase inhibitory potential by soman faster than its monosubstituted analog. This journal is
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84922647475&origin=inward; http://dx.doi.org/10.1039/c4cc09189b; http://www.ncbi.nlm.nih.gov/pubmed/25572650; http://xlink.rsc.org/?DOI=C4CC09189B; http://pubs.rsc.org/en/content/articlepdf/2015/CC/C4CC09189B; https://xlink.rsc.org/?DOI=C4CC09189B; https://dx.doi.org/10.1039/c4cc09189b; https://pubs.rsc.org/en/content/articlelanding/2015/cc/c4cc09189b
Royal Society of Chemistry (RSC)
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