ReviewChemistry (Weinheim an der Bergstrasse, Germany)2015
Recent Advances on the Total Syntheses of Communesin Alkaloids and Perophoramidine.
Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
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Who cites it
18 citing papers in PubMed.
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- Application of Hosomi-Sakurai allylation reaction in total synthesis of biologically active natural products.Frontiers in chemistry · 2025Review
- A biofertilizing fungal endophyte of cranberry plants suppresses the plant pathogenFrontiers in microbiology · 2024Article
- Finding activity through rigidity: syntheses of natural products containing tricyclic bridgehead carbon centers.Natural product reports · 2023Review
- Natural product anticipation through synthesis.Nature reviews. Chemistry · 2022Article
- Synthesis of tetracyclic spiroindolines by an interrupted Bischler-Napieralski reaction: total synthesis of akuammicine.Organic & biomolecular chemistry · 2021Article
- Taming Radical Pairs in the Crystalline Solid State: Discovery and Total Synthesis of Psychotriadine.Journal of the American Chemical Society · 2021Article
- Discovery and Total Synthesis of a Bis(cyclotryptamine) Alkaloid Bearing the Elusive Piperidinoindoline Scaffold.Journal of the American Chemical Society · 2020Article
- Enzyme-Catalyzed Azepinoindole Formation in Clavine Alkaloid Biosynthesis.Organic letters · 2020Article
- Total Synthesis and Anti-Cancer Activity of All Known Communesin Alkaloids and Related Derivatives.Journal of the American Chemical Society · 2019Article
- Synthesis of the ABCDG ring skeleton of communesin F based on carboborylation of 1,3-diene and Bi(OTf)The Journal of antibiotics · 2019Article
- 1-Alkyl-3-alkylindolin-2-imine hydrochlorides as useful building blocks in the copper-catalyzed synthesis of polycyclic indoline scaffolds.RSC advances · 2019Article
- Synthesis of 3,3'-Disubstituted Indolenines Utilizing the Lewis Acid Catalyzed Alkylation of 2,3-Disubstituted Indoles with Trichloroacetimidates.Synlett : accounts and rapid communications in synthetic organic chemistry · 2017Article
- Expedient Synthesis of Indolo[2,3-ACS omega · 2017Article
- Pardon the Interruption: A Modification of Fischer's Venerable Reaction for the Synthesis of Heterocycles and Natural Products.Synlett : accounts and rapid communications in synthetic organic chemistry · 2017Article
- Convergent and Biomimetic Enantioselective Total Synthesis of (-)-Communesin F.Journal of the American Chemical Society · 2016Article
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2 authors.
Funding
Abstract
The communesin alkaloids are a diverse family of Penicillium-derived alkaloids. Their caged-polycyclic structure and intriguing biological profiles have made these natural products attractive targets for total synthesis. Similarly, the ascidian-derived alkaloid, perophoramidine, is structurally related to the communesins and has also become a popular target for total synthesis. This review serves to summarize the many elegant approaches that have been developed to access the communesin alkaloids and perophoramidine. Likewise, strategies to access the communesin ring system are reviewed.
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