Autor: |
Kumar, Sandeep, Gupta, Ashis Kumar, Vaishanv, Narendra Kumar, Kant, Ruchir, Mohanan, Kishor |
Předmět: |
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Zdroj: |
New Journal of Chemistry; 10/28/2024, Vol. 48 Issue 40, p17670-17675, 6p |
Abstrakt: |
A CsF-promoted synthesis of cyanopyrazolo[4,3-b]indoles via a [3+2] cycloaddition reaction of diazoacetonitrile with N-substituted 3-nitroindoles and subsequent elimination of the nitro group has been devised. This protocol delivers diverse cyano-containing pyrazole-fused indoles in good to excellent yields under mild conditions. Besides diazoacetonitrile, the Seyferth–Gilbert reagent (SGR) readily participated in this reaction to provide facile access to phosphonylated pyrazolo[4,3-b]indoles. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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