The article highlighted on the cover of Issue 7 is a communication from Hans-Joachim Knölker and co-workers describing the syntheses of O-methylmurrayamine A and 7-methoxymurrayacine and first asymmetric synthesis of (−)-trans-dihydroxygirinimbine.
Pyrano[3,2-a]carbazole alkaloids are an interesting class of molecule with pharmacological potential, which has lead to an effort to develop efficient synthetic routes towards them. Here the authors report an iron-mediated route to the pyrano[3,2-a]carbazole skeleton with high efficiencies.
The article comes highly recommended by our referees, so why not download the article today – it’s free to access for 6 weeks!
Efficient iron-mediated approach to pyrano[3,2-a]carbazole alkaloids—first total syntheses of O-methylmurrayamine A and 7-methoxymurrayacine, first asymmetric synthesis and assignment of the absolute configuration of (−)-trans-dihydroxygirinimbine
Konstanze K. Gruner, Thomas Hopfmann, Kazuhiro Matsumoto, Anne Jäger, Tsutomu Katsuki and Hans-Joachim Knölker
Org. Biomol. Chem., 2011, 9, 2057-2061
DOI: 10.1039/C0OB01088J