Reductive acid-catalyzed rearrangement of 3-(2-nitrobenzyl)quinoxalin-2(1Н)-ones in the presence of NaSO – effective method for the synthesis of 2-(indol-2-yl)benzimidazoles
Chemistry of Heterocyclic Compounds, ISSN: 1573-8353, Vol: 53, Issue: 9, Page: 1033-1044
2017
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Article Description
[Figure not available: see fulltext.] An effective one-step method is proposed for the synthesis of 2-(indol-2-yl)benzimidazoles from 3-(2-nitrobenzyl)quinoxalin-2(1Н)-ones without using metal catalysts and reagents. This method is based on the Mamedov rearrangement of 3-(2-aminobenzyl)quinoxalin-2(1Н)-ones, formed in situ by the action of NaSO, giving 2-(indol-2-yl)benzimidazoles as the products.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85033434831&origin=inward; http://dx.doi.org/10.1007/s10593-017-2166-x; http://link.springer.com/10.1007/s10593-017-2166-x; http://link.springer.com/content/pdf/10.1007/s10593-017-2166-x.pdf; http://link.springer.com/article/10.1007/s10593-017-2166-x/fulltext.html; https://dx.doi.org/10.1007/s10593-017-2166-x; https://link.springer.com/article/10.1007/s10593-017-2166-x
Springer Science and Business Media LLC
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