Palladium-catalyzed synthesis of 1,2-dihydro-4(3H)-carbazolones. Formal total synthesis of murrayaquinone A
Two sequential palladium-catalyzed reactions are the key steps in a novel synthetic route to 1,2-dihydro-4(3H)-carbazolones. The steps are an intermolecular Stille cross-coupling followed by a reductive N-heteroannulation. A formal total synthesis of murrayaquinone A, employing this sequence, is reported.
Scott, Tricia L.,S?derberg, Bj?rn C. G.
p. 6323 - 6332
(2007/10/03)
Novel palladium-catalyzed synthesis of 1,2-dihydro-4(3H)-carbazolones
Two sequential palladium-catalyzed reactions are the key steps in a novel synthetic route to carbazolones, an intermolecular Stille coupling followed by a recently developed palladium-catalyzed reductive N-heteroannulation. A number of functionalized 1,2-dihydro-4(3H)-carbazolones were prepared using this sequence.
Scott, Tricia L.,S?derberg, Bj?rn C.G.
p. 1621 - 1624
(2007/10/03)
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