Abstract
A robust, efficient and scalable method for the synthesis of 12H-indazolo[2,1-a]cinnolin-12-ones was developed. Significantly, a less developed cationic complex [Ru(p-cymene)(MeCN) 3 (SbF 6 ) 2 ] was found to be effective for this transformation. In this reaction, a tandem pathway of C-H ruthenation, Ru(ii)-carbene formation, migratory insertion and condensation was involved. The results of a primary mechanistic study suggested that the C-H activation process might follow an electrophilic-type metalation/deprotonation mechanism.
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CITATION STYLE
Su, L., Yu, Z., Ren, P., Luo, Z., Hou, W., & Xu, H. (2018). Ruthenium(ii)-catalyzed synthesis of indazolone-fused cinnolines via C-H coupling with diazo compounds. Organic and Biomolecular Chemistry, 16(39), 7236–7244. https://doi.org/10.1039/c8ob02071j
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