Strychnine as Target, Samarium Diiodide as Tool: A Personal Story
Author:
Affiliation:
1. Leibniz Institute for Natural Product Research and Infection Biology e.V.; Hans-Knöll-Institute (HKI); Beutenbergstrasse 11a 07745 Jena Germany
2. Institut für Chemie und Biochemie; Freie Universität Berlin; Takustrasse 3 14195 Berlin Germany
Publisher
Wiley
Subject
Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry
Reference127 articles.
1. Die Strychnos-Alkaloide Ein Überblick über ein halbes Jahrhundert Alkaloidforschung
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2. “For Its Size, the Most Complex Natural Product Known.” Who Deserves Credit for Determining the Structure of Strychnine?;ACS Central Science;2022-06-08
3. Samarium(II)‐Promoted Cyclizations of Nonactivated Indolyl Sulfinyl Imines to Polycyclic Tertiary Carbinamines;European Journal of Organic Chemistry;2022-04-06
4. Synthesis and Evaluation of Enantiopure HMPA Analogs in Samarium‐Diiodide‐Promoted Dearomatizations of N‐Acylated Indole Derivatives;European Journal of Organic Chemistry;2021-10-20
5. Mechanistic Vistas of Trivalent Nitrogen Compound Reduction by Samarium Diiodide;European Journal of Organic Chemistry;2020-12-29
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