Regioselective 1,4-conjugate aza-Michael addition of dienones with benzotriazole
Heterocyclic Communications, ISSN: 0793-0283, Vol: 23, Issue: 4, Page: 287-291
2017
- 12Citations
- 12Captures
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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
The regioselective 1,4-conjugate aza-Michael addition of dienones with benzotriazole catalyzed by potassium acetate is described. A series of 3-(benzotriazol-1-yl)-1,5-diarylpent-4-en-1-ones were efficiently synthesized under mild conditions. This protocol has advantages of transition-metal free catalyst, high yield and high regioselectivity.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85027157642&origin=inward; http://dx.doi.org/10.1515/hc-2016-0182; https://www.degruyter.com/document/doi/10.1515/hc-2016-0182/html; http://www.degruyter.com/view/j/hc.2017.23.issue-4/hc-2016-0182/hc-2016-0182.xml; https://www.degruyter.com/view/j/hc.2017.23.issue-4/hc-2016-0182/hc-2016-0182.xml
Walter de Gruyter GmbH
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