The synthesis of novel aza-1,7-annulated indoles was achieved and these were converted to indolocarbazoles that proved to be potent kinase inhibitors. These compounds were also evaluated in a human colon carcinoma cell line and proved to be good antiproliferative agents.
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| http://dx.doi.org/10.1016/j.bmcl.2004.05.088 | DOI Listing |
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