886853-77-6Relevant articles and documents
Rapid, robust, clean, catalyst-free synthesis of 2-halo-3-carboxyindoles
Kunzer, Aaron R.,Wendt, Michael D.
supporting information; experimental part, p. 1815 - 1818 (2011/05/05)
A novel synthesis of 2-halo-3-carboxyindoles from 2-(2,2-dihalovinyl) anilines was discovered. Reaction conditions and substrate applicability were studied. Optimally, the reaction takes only minutes when these substrates are heated in DMSO at 120 °C in t
SUBSTITUTED INDOLO-PYRIDINONE COMPOUNDS
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Page/Page column 54-55, (2010/10/19)
The present invention relates to substituted indolo-pyridinone compounds and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing substituted indolo-pyridinone compounds and methods of treat
Efficient syntheses of KDR kinase inhibitors using a Pd-catalyzed tandem C-N/suzuki coupling as the key step
Fang, Yuan-Qing,Karisch, Robert,Lautens, Mark
, p. 1341 - 1346 (2007/10/03)
(Chemical Equation Presented) A family of four potent KDR kinase inhibitors containing an indol-2-yl quinolin-2-one structure was utilizing a Pd-catalyzed tandem C-N and C-C coupling sequence.