Synthesis of 1,3,5-Trisubstituted Pyrazole-4-Carboxylates Through 1,3-Dipolar Cycloaddition of Nitrilimines with Allenoates
SSRN Electronic Journal
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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
A strategy for the 1,3-dipolar cycloaddition of nitrilimines to δ-allenoates has been developed to provide various 1,3,5-trisubstituted pyrazole-4-carboxylates and pyrazole-4 -carboxamide derivatives, which have been reported to have excellent anticancer effects. This protocol exhibits characteristics of good yield, mild reaction condition, facile operation process and post-processing steps, as well as moderate tolerance to various functional groups.
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