A solid-state trimerisation of a diene diacid affords a bicyclobutyl: Reactant structure from X-ray powder data and product separation and structure determination via co-crystallisation
Chemical Communications, ISSN: 1364-548X, Vol: 47, Issue: 1, Page: 236-238
2011
- 21Citations
- 14Captures
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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
- Citations21
- Citation Indexes21
- 21
- CrossRef20
- Captures14
- Readers14
- 14
Article Description
A bicyclobutyl that bears six carboxylic acid groups results from a trimerisation of a diene diacid in the solid state. Powder X-ray diffraction and a co-crystallisation are used to solve the structure of the diene and elucidate the stereochemistry of the bicyclobutyl, respectively. © 2010 The Royal Society of Chemistry.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=78649840961&origin=inward; http://dx.doi.org/10.1039/c0cc02204g; http://www.ncbi.nlm.nih.gov/pubmed/20820530; https://xlink.rsc.org/?DOI=C0CC02204G; http://xlink.rsc.org/?DOI=C0CC02204G; http://pubs.rsc.org/en/content/articlepdf/2011/CC/C0CC02204G; https://dx.doi.org/10.1039/c0cc02204g; https://pubs.rsc.org/en/content/articlelanding/2011/cc/c0cc02204g
Royal Society of Chemistry (RSC)
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