Extremely Facile Formation of the Pavine Alkaloid Skeleton by the Photoreaction between Isoquinoline and Benzyltrifluoroborate
Author:
Affiliation:
1. Department of Chemistry, Graduate School of Natural Science, Shimane University, 1060 Nishikawatsu-cho, Matsue, Shimane 690-8504, Japan
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/cl.190809
Reference22 articles.
1. Benzylisoquinoline Alkaloid Metabolism: A Century of Discovery and a Brave New World
2. Antiviral potential of Bulgarian medicinal plants
3. Synthesis of new TNF-α Inhibitors and their biological properties
4. (−)-Neocaryachine, an Antiproliferative Pavine Alkaloid from Cryptocarya laevigata, Induces DNA Double-Strand Breaks
5. Cardiac electrophysiologic and antiarrhythmic actions of a pavine alkaloid derivative,O-methyl-neocaryachine, in rat heart
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1. Diastereoselective dearomative bifunctionalization of isoquinolinium salts to access bridged tetrahydroisoquinolines;New Journal of Chemistry;2024
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3. Photo-induced Benzylation of Quinolines with Tetra-coordinate Benzylboron Reagents;Chemistry Letters;2023-03-05
4. Photochemical Synthesis of Benzylisoquinoline Alkaloids Using Tetra-coordinate Benzylboron Reagents: Application to Berberine Type Alkaloids;Chemistry Letters;2022-02-05
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