ArticleThe Journal of organic chemistry2011
Regio- and stereoselective syntheses of the natural product CCR5 antagonist anibamine and its three olefin isomers.
Article in The Journal of organic chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Design and Synthesis of Fluorescence-Labeled TAK779 Analogs as Chemical Probes.Molecules (Basel, Switzerland) · 2025Article
- Anibamine and Its Analogues: Potent Antiplasmodial Agents fromJournal of natural products · 2020Article
- Recent developments in the Suzuki-Miyaura reaction: 2010-2014.Molecules (Basel, Switzerland) · 2015Review
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
The syntheses of the natural product anibamine and its three olefin isomers have been achieved concisely and efficiently via highly regio- and stereoselective reactions. The crucial steps included a regioselective palladium-catalyzed alkynylation by Sonogashira coupling and a stereoselective Suzuki coupling. Further conformation analyses and in vitro calcium mobilization studies were carried out to characterize the compounds' biological properties.
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Registered trials
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