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Issue 9, 1990
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Synthesis of the indolo[2,3-a]carbazole natural products staurosporinone and arcyriaflavin B

Abstract

Flexible synthetic routes involving double nitrene insertions are described leading to the indolo[2,3-a]carbazole systems present in a growing group of natural products. The methods are exemplified by the total synthesis of two members of this group staurosporinone (9; R = H) and arcyriaflavin B (2).

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Article information


J. Chem. Soc., Perkin Trans. 1, 1990, 2475-2480
Article type
Paper

Synthesis of the indolo[2,3-a]carbazole natural products staurosporinone and arcyriaflavin B

I. Hughes, W. P. Nolan and R. A. Raphael, J. Chem. Soc., Perkin Trans. 1, 1990, 2475
DOI: 10.1039/P19900002475

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