Synthesis of 2 H -3,1-pyrazolo[3,4- e ]oxazines via a new conversion of Friedländer reaction
Chinese Chemical Letters, ISSN: 1001-8417, Vol: 18, Issue: 6, Page: 636-638
2007
- 16Citations
- 6Captures
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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.
Article Description
2H -3,1-Pyrazolo[3,4- e ]oxazines ( 5a – c ) and tacrine analogies ( 6a – c ) were designed and prepared using 5-amino-4-cyanopyrazole ( 7 ) and cycloketones ( 2a – c ) as reactants. The study demonstrated that the new conversion existed in the Friedländer reaction of o -aminocyanopyrazole with cycloketones.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1001841707001519; http://dx.doi.org/10.1016/j.cclet.2007.04.015; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=34249806695&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S1001841707001519; https://api.elsevier.com/content/article/PII:S1001841707001519?httpAccept=text/xml; https://api.elsevier.com/content/article/PII:S1001841707001519?httpAccept=text/plain; https://dx.doi.org/10.1016/j.cclet.2007.04.015
Elsevier BV
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