The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Апрель 13, 2025
Pyrazolo[1,2-a]indazoles and pyrazolo[1,2-a]cinnolines can be constructed selectively via catalytic system-controlled C(sp2)-H activation/[4 + 1] cyclization 2] reaction, utilizing pyrazolidinones diazo indandiones. Employing two different Rh(III) catalysts, we successfully synthesized distinct types of nitrogen-containing heterocyclic compounds, pyrazolo[1,2-a]indazoles pyrazolo[1,2-a]cinnolines, respectively. Moreover, an inexpensive Ru(II) catalyst could also effectively generate with moderate to good yields. Overall, these methodologies offer advantages such as regioselectivity, broad substrate scope, operational simplicity, product availability.
Язык: Английский