96861-91-5Relevant articles and documents
Palladium-Catalyzed Synthesis of Pyrayaquinones, Murrayaquinones, and Murrayafoline-B
Kutz, Sebastian K.,Schmidt, Arndt W.,Kn?lker, Hans-Joachim
, p. 275 - 292 (2016/12/24)
We describe the total synthesis of murrayafoline-B and seven carbazole-1,4-quinone alkaloids. A palladium(II)-catalyzed oxidative cyclization is used to construct the carbazole skeleton. Pyran annulation and oxidation provide pyrayaquinone-A, -B, and -C. DIBAL-H-promoted reductive ring opening of pyrano[3,2-a]carbazole precursors leads to the prenylated and geranylated carbazole-1,4-quinone alkaloids murrayaquinone-B, -C, -D, and -E and to murrayafoline-B.
Synthesis of some carbazolequinone alkaloids and their analogues. Facile palladium-assisted intramolecular ring closure of arylamino-1,4-benzoquinones to carbazole-1,4-quinones
Yogo,Ito,Furukawa
, p. 328 - 334 (2007/10/02)
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