A Flexible Route to Indole Scaffolds : Formal Synthesis of (±)-Mersicarpine

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2015
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European Journal of Organic Chemistry ; 2015 (2015), 16. - pp. 3427-3429. - ISSN 1434-193X. - eISSN 0365-5490
Abstract
The formal synthesis of racemic mersicarpine was accomplished in an operationally simple, reliable, and efficient manner in eight isolated steps. The use of a common intermediate increases the degree of synthetic flexibility and allows the construction of two completely different polycyclic alkaloid skeletons.
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540 Chemistry
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Alkaloids, Mersicarpine, Synthesis design, Gassman reaction, Polycycles
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ISO 690PFAFFENBACH, Magnus, Tanja GAICH, 2015. A Flexible Route to Indole Scaffolds : Formal Synthesis of (±)-Mersicarpine. In: European Journal of Organic Chemistry. 2015(16), pp. 3427-3429. ISSN 1434-193X. eISSN 0365-5490. Available under: doi: 10.1002/ejoc.201500309
BibTex
@article{Pfaffenbach2015Flexi-32440,
  year={2015},
  doi={10.1002/ejoc.201500309},
  title={A Flexible Route to Indole Scaffolds : Formal Synthesis of (±)-Mersicarpine},
  number={16},
  volume={2015},
  issn={1434-193X},
  journal={European Journal of Organic Chemistry},
  pages={3427--3429},
  author={Pfaffenbach, Magnus and Gaich, Tanja}
}
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