Reaction of N-(3-oxoalkenyl)chloroacetamides with sodium p-toluenesulfinate – synthesis of 3-tosylpyridin-2(1Н)-ones
Chemistry of Heterocyclic Compounds, ISSN: 1573-8353, Vol: 53, Issue: 12, Page: 1335-1339
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.
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Article Description
[Figure not available: see fulltext.] A series of N-(3-oxoalkenyl)chloroacetamides was prepared by acylation of β-enaminoketones with chloroacetyl chloride. A reaction of these compounds with sodium p-toluenesulfinate in dimethylformamide in the presence of potassium carbonate led to 3-tosylpyridin-2(1H)-ones. The limitations of this reaction were studied.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85040904770&origin=inward; http://dx.doi.org/10.1007/s10593-018-2215-0; http://link.springer.com/10.1007/s10593-018-2215-0; http://link.springer.com/content/pdf/10.1007/s10593-018-2215-0.pdf; http://link.springer.com/article/10.1007/s10593-018-2215-0/fulltext.html; https://dx.doi.org/10.1007/s10593-018-2215-0; https://link.springer.com/article/10.1007/s10593-018-2215-0
Springer Science and Business Media LLC
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