Fine Tuning Reactivity: Synthesis and Isolation of 1,2,3,12b-Tetrahydroimidazo[1,2-f]phenanthridines
Author:
Affiliation:
1. WestCHEM, Department of Chemistry, University of Glasgow, Glasgow G12 8QQ, United Kingdom
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo901622e
Reference41 articles.
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3. Total Synthesis of Amaryllidaceae Pyrrolophenanthridinium Alkaloids via the Ziegler−Ullmann Reaction: Tortuosine, Criasbetaine, and Ungeremine
4. Antileukemic activity of ungeremine and related compounds. Preparation of analogs of ungeremine by a practical photochemical reaction
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1. Stereoselective Synthesis of Hexahydroimidazo[1,2-a]quinolines via SN2-Type Ring-Opening Hydroarylation–Hydroamination Cascade Cyclization of Activated Aziridines with N-Propargylanilines;Organic Letters;2020-09-28
2. Phenanthridine derivatives as promising new anticancer agents: synthesis, biological evaluation and binding studies;Future Medicinal Chemistry;2020-04
3. One-pot synthesis of 2,3-diphenyl-6,7-dihydroimidazo[1,2-f]phenanthridin-8(5H)-ones catalyzed by CuI/l-proline;Monatshefte für Chemie - Chemical Monthly;2018-01-19
4. Synthesis of Electron‐Deficient Tetrahydro‐ and Dihydroimidazo[1,2‐ f ]phenanthridines by Microwave‐Mediated IMDAF Reactions;European Journal of Organic Chemistry;2017-04-20
5. Come-back of phenanthridine and phenanthridinium derivatives in the 21st century;Beilstein Journal of Organic Chemistry;2014-12-10
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