Regioselective multi-component synthesis of 1H-pyrazolo[3,4-d]pyrimidine- 6(7H)-thiones
Molecular Diversity, ISSN: 1381-1991, Vol: 16, Issue: 3, Page: 591-600
2012
- 8Citations
- 13Captures
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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.
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Metrics Details
- Citations8
- Citation Indexes8
- CrossRef6
- Captures13
- Readers13
- 13
Article Description
A variety of pyrazolo[3,4-d]pyrimidine-6(7H)-thione derivatives were easily synthesized with a novel, simple, efficient, and regioselective method via three-component condensation reaction of 5-methyl-1H-pyrazol-3-amine, arylisothiocyanates, and aldehydes in the presence of catalytic amount of p-toluenesulfonic acid (p-TSA) in 1-butyl-3-methylimidazolium bromide ionic liquidwith excellent yields and short reaction times. © Springer Science+Business Media B.V. 2012.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84869498890&origin=inward; http://dx.doi.org/10.1007/s11030-012-9391-0; http://www.ncbi.nlm.nih.gov/pubmed/22926535; http://link.springer.com/10.1007/s11030-012-9391-0; https://dx.doi.org/10.1007/s11030-012-9391-0; https://link.springer.com/article/10.1007/s11030-012-9391-0; http://www.springerlink.com/index/10.1007/s11030-012-9391-0; http://www.springerlink.com/index/pdf/10.1007/s11030-012-9391-0
Springer Science and Business Media LLC
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