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Mehdi A. Beniddir

Researcher at Université Paris-Saclay

Publications -  94
Citations -  1338

Mehdi A. Beniddir is an academic researcher from Université Paris-Saclay. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 17, co-authored 71 publications receiving 859 citations. Previous affiliations of Mehdi A. Beniddir include University of Paris-Sud & Institut de Chimie des Substances Naturelles.

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Natural products targeting strategies involving molecular networking: different manners, one goal

TL;DR: This review illustrates through selected cornerstone studies the new thinking in natural product isolation by drawing a parallel between the different underlying philosophies behind the use of molecular networking in targeting natural products.
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The Value of Universally Available Raw NMR Data for Transparency, Reproducibility, and Integrity in Natural Product Research

James B. McAlpine, +74 more
TL;DR: In this article, the authors present a comprehensive review of the scientific value of disseminating raw nuclear magnetic resonance (NMR) data, independently of, and in parallel with, classical publishing outlets.
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Unified biomimetic assembly of voacalgine A and bipleiophylline via divergent oxidative couplings

TL;DR: A unified oxidative coupling protocol between indole derivatives and 2,3-dihydroxybenzoic acid, mediated by silver oxide, has been developed to produce the core of bipleiophylline and of its biosynthetic precursor, voacalgine A.
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Emergence of diversity and stereochemical outcomes in the biosynthetic pathways of cyclobutane-centered marine alkaloid dimers.

TL;DR: The present dichotomic case study provides a comprehensive perspective on these cyclobutane-centered alkaloids and their respective families and proposes a transversal vision of the topic.
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Acridone alkaloids from Glycosmis chlorosperma as DYRK1A inhibitors.

TL;DR: Two new acridone alkaloids were isolated from the stem bark of Glycosmis chlorosperma, together with the known atalaphyllidine and acrifoline, and molecular docking calculations provided structural details for the interaction between these compounds and DYRK1A.