185684-93-9Relevant academic research and scientific papers
Transition Metal Complexes in Organic Synthesis, Part 71:1 First Total Synthesis of Furoclausine-A
Kn?lker, Hans-Joachim,Krahl, Micha P.
, p. 528 - 530 (2004)
The first total synthesis of the furo[3,2-a]carbazole alkaloid furoclausine-A is described using an iron-mediated construction of the carbazole framework and an acid-catalyzed annulation of the furan ring as key steps.
Transition metals in organic synthesis, part 104. Iron-mediated total synthesis of furoclausine-A
Krahl, Micha P.,Schmidt, Arndt W.,Knoelker, Hans-Joachim
, p. 357 - 370 (2013/08/23)
Using iron-mediated coupling reactions a convergent seven-step synthesis of the furo[3,2-a]carbazole alkaloid furoclausine-A is achieved.
Transition metal complexes in organic synthesis, part 63;1 convergent iron-mediated syntheses of the furo[3,2-a]carbazole alkaloid furostifoline
Knolker,Frohner
, p. 2131 - 2136 (2007/10/03)
Two highly efficient routes to the furo[3,2-a]carbazole alkaloid furostifoline are described. Both syntheses use the iron-mediated arylamine cyclization as the key-step and lead to the natural product in seven and five steps, respectively.
Transition metal complexes in organic synthesis, Part 35. First total synthesis of furostifoline
Knoelker, Hans-Joachim,Froehner, Wolfgang
, p. 9183 - 9186 (2007/10/03)
The first total synthesis of the furo[3,2-a]carbazole alkaloid furostifoline was achieved using a convergent iron-mediated construction of the carbazole nucleus.
