An efficient method for the synthesis of 6-vinylindazolo[3,2-a]isoquinolines via rhodium(III)-catalysed C-H bond activation/subsequent [4+2] cyclization starting from easily available 3-aryl-1-H-indazoles and propargyl alcohols has been developed. A series of vinyl-annulated...
An efficient approach for the synthesis of Nsubstituted indenoisoquinolinones via rhodium(III)-catalyzed C− H bond activation/subsequent [4 + 2] cyclization starting from easily available 2-phenyloxazolines and 2-diazo-1,3-indandiones has been developed. A series of indeno[1,2-c]isoquinolinones were obtained in up to 93% yield through C−H functionalization, followed by intramolecular annulation, elimination, and ringopening in a "one pot manner" under mild reaction conditions. This protocol features excellent atom-and step-economy and provides a novel strategy for the synthesis of N-substituted indenoisoquinolinones and a chance to study their biological activities.
A mild and efficient tool to construct structurally diverse N/O spiroheterocyclics via Rh(III)-catalyzed [3 + 3] cascade spiroannulation of benzoxazines with 1-diazonaphthalen-2(1H)-ones has been developed. The desired spirooxazine-pyrans could be...
A convenient method for the alkylation of 3-arylbenzo[d]isoxazoles with maleimides under the redox neutral conditions has been developed, giving a series of substituted succinimides in up to 99% yield. This...
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