Facile and convenient syntheses of 6,11-dihydro-5H-indeno[1,2-c] isoquinolin-5-ones and 6,11-dihydro-5H-indolo[3,2-c]isoquinolin-5-one

Prakash G. Jagtap, Erkan Baloglu, Garry Southan, William Williams, Aloka Roy, Alexander Nivorozhkin, Nelson Landrau, Kevin Desisto, Andrew L. Salzman, Csaba Szabó

    Research output: Contribution to journalArticle

    38 Scopus citations

    Abstract

    (Chemical Equation Presented) The synthesis of 6,11-dihydro-5H-indeno[1,2- c]isoquinolin-5-ones from the base-promoted condensation reaction of homophthalic anhydride and 2-(bromomethyl)-benzonitrile and a convenient method for the synthesis of indolo[3,2-c]isoquinolinones are described.

    Original languageEnglish (US)
    Pages (from-to)1753-1756
    Number of pages4
    JournalOrganic Letters
    Volume7
    Issue number9
    DOIs
    StatePublished - Apr 28 2005

    ASJC Scopus subject areas

    • Biochemistry
    • Physical and Theoretical Chemistry
    • Organic Chemistry

    Fingerprint Dive into the research topics of 'Facile and convenient syntheses of 6,11-dihydro-5H-indeno[1,2-c] isoquinolin-5-ones and 6,11-dihydro-5H-indolo[3,2-c]isoquinolin-5-one'. Together they form a unique fingerprint.

  • Cite this

    Jagtap, P. G., Baloglu, E., Southan, G., Williams, W., Roy, A., Nivorozhkin, A., Landrau, N., Desisto, K., Salzman, A. L., & Szabó, C. (2005). Facile and convenient syntheses of 6,11-dihydro-5H-indeno[1,2-c] isoquinolin-5-ones and 6,11-dihydro-5H-indolo[3,2-c]isoquinolin-5-one. Organic Letters, 7(9), 1753-1756. https://doi.org/10.1021/ol050331m