Concise Access to a Model of the Marine Alkaloid Halicyclamine A through Macrocycle-Forming Addition of a 5-Aminopenta-2,4-dienal onto a 2,3-Dihydropyridinium Salt
Author:
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201000142/fullpdf
Reference34 articles.
1. Manzamine A, a novel antitumor alkaloid from a sponge
2. Polycyclic Amine Alkaloids (3-Alkylpiperidine Alkaloids) – Novel Marine Bioactive Compounds: Structure, Synthesis and Biochemical Aspects
3. THE MANZAMINE ALKALOIDS
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1. Synthesis of a Halicyclamine-Type Macrocyclic Scaffold via Biomimetic Transannular Cyclization;Organic Letters;2023-04-12
2. Total Synthesis of the Tetracyclic Pyridinium Alkaloid epi ‐Tetradehydrohalicyclamine B;Angewandte Chemie International Edition;2022-09-02
3. Total Synthesis of the Tetracyclic Pyridinium Alkaloid epi ‐Tetradehydrohalicyclamine B;Angewandte Chemie;2022-09-02
4. Regiocontrolled Dimerization of Densely Functionalized 1,6-Dihydropyridines for the Biomimetic Synthesis of a Halicyclamine-type Scaffold by Preventing Disproportionation;The Journal of Organic Chemistry;2022-04-14
5. Theoretical insights into the static chemical reactivity and NLO properties of some conjugated carbonyl compounds: case of 5-aminopenta-2,4-dienal derivatives;Monatshefte für Chemie - Chemical Monthly;2020-07
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