CsF-mediated reaction of diazo compounds with 3-nitroindoles: access to cyano- and phosphonylpyrazolo[4,3-b]indoles.

Autor: Kumar, Sandeep, Gupta, Ashis Kumar, Vaishanv, Narendra Kumar, Kant, Ruchir, Mohanan, Kishor
Předmět:
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