Regioselective synthesis of 2-(1 H -benzimidazol-1-yl)-5-nitro- and 2-(5-nitro-1 H -benzimidazol-1-yl)anilines
Mendeleev Communications, ISSN: 0959-9436, Vol: 33, Issue: 5, Page: 650-652
2023
- 4Citations
- 1Captures
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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
The efficiency of two strategies for the synthesis of N -(2-aminophenyl)-5-nitrobenzimidazole derivatives was studied. The promising route involves the stages of 1-(2,4-dinitro-phenyl)-1 H -benzimidazole monoreduction at 2-positioned nitro group and tandem conversion involving recyclization of the intermediate N -(2-amino-4-nitrophenyl)-5-nitrobenz-imidazole.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0959943623002481; http://dx.doi.org/10.1016/j.mencom.2023.09.020; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85173519444&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S0959943623002481; https://dx.doi.org/10.1016/j.mencom.2023.09.020
OOO Zhurnal "Mendeleevskie Soobshcheniya"
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