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

Pfaffenbach, Magnus; Gaich, Tanja

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

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Date

2015

Publication type

Journal article

Publication status

Published

Published in

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.

Subject (DDC)

540 Chemistry

Keywords

Alkaloids, Mersicarpine, Synthesis design, Gassman reaction, Polycycles

Cite This

ISO 690

PFAFFENBACH, 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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Bibliography of Konstanz

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