Highly distorted Cone calix[4]arenes through intramolecular mc murry coupling reaction
Tetrahedron, ISSN: 0040-4020, Vol: 51, Issue: 29, Page: 7951-7958
1995
- 29Citations
- 10Captures
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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
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.
Article Description
Highly distorted and rigid cone conformers of calix[4]arene have been synthesized by low-valent titanium promoted intra -molecular coupling of aldehydes 1 a-d. The reaction outcome strongly depends on the substituents present at the upper rim and reaction time. In all cases examined infra-molecular coupled compounds, having a bridge only two atoms long, were obtained in about 30% yield.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/004040209500411Z; http://dx.doi.org/10.1016/0040-4020(95)00411-z; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0029004184&origin=inward; http://linkinghub.elsevier.com/retrieve/pii/004040209500411Z; http://api.elsevier.com/content/article/PII:004040209500411Z?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:004040209500411Z?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/004040209500411Z; https://api.elsevier.com/content/article/PII:004040209500411Z?httpAccept=text/xml; https://api.elsevier.com/content/article/PII:004040209500411Z?httpAccept=text/plain; http://dx.doi.org/10.1016/0040-4020%2895%2900411-z; https://dx.doi.org/10.1016/0040-4020%2895%2900411-z
Elsevier BV
Provide Feedback
Have ideas for a new metric? Would you like to see something else here?Let us know