A Two-Step Approach to a Hexacyclic Lamellarin Core via 1,3-Dipolar Cycloaddition of Isoquinolinium Ylides to Nitrostilbenes
Author:
Affiliation:
1. N. D. Zelinsky Institute of Organic Chemistry RAS, 47 Leninsky Prospect, 119991 Moscow, Russian Federation
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c00312
Reference93 articles.
1. Lamellarin alkaloids: Isolation, synthesis, and biological activity
2. An Overview of the Multifaceted Lessons Learned from Marine-Derived Bioactive Lamellarin Natural Products
3. Anticancer Properties of Lamellarins
4. Assessing the drug-likeness of lamellarins, a marine-derived natural product class with diverse oncological activities
5. Recent Advances in Lamellarin Alkaloids: Isolation, Synthesis and Activity
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2. Cascade Synthesis of Pyrrolo[1,2-a]quinolines and Pyrrolo[2,1-a]isoquinolines via Formal [3 + 2]-Cycloaddition of Push–Pull Nitro Heterocycles with Carbonyl-Stabilized Quinolinium/Isoquinolinium Ylides;The Journal of Organic Chemistry;2024-06-25
3. Base-Mediated Cascade Lactonization/1,3-Dipolar Cycloaddition Pathway for the One-Pot Assembly of Coumarin-Functionalized Pyrrolo[2,1-a]isoquinolines;The Journal of Organic Chemistry;2024-06-05
4. Progress on synthesis and structure-activity relationships of lamellarins over the past decade;European Journal of Medicinal Chemistry;2024-04
5. Visible‐Light‐Catalyzed Formal [3+2] Annulation‐Aromatization of Amidines with Isoquinolinium N‐Ylides: Access to Imidazo[2,1‐a]isoquinolines;Advanced Synthesis & Catalysis;2023-09-29
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