Synthesis of the Bicyclic Moiety of the Miharamycins by Samarium (II) Iodide Induced Ring Closure
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1995-4927.pdf
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Solving the Structural Puzzles of Amipurimycin and Miharamycins Enabled by Stereodivergent Total Synthesis;The Chemical Record;2021-04-09
2. Wittig Reaction: Domino Olefination and Stereoselectivity DFT Study. Synthesis of the Miharamycins’ Bicyclic Sugar Moiety;Organic Letters;2015-11-09
3. ChemInform Abstract: Synthesis of the Bicyclic Moiety of the Miharamycins by Samarium(II) Iodide Induced Ring Closure.;ChemInform;2010-08-17
4. Synthesis of novel purine nucleosides towards a selective inhibition of human butyrylcholinesterase;Bioorganic & Medicinal Chemistry;2009-07
5. Stereochemical Assignment and First Synthesis of the Core of Miharamycin Antibiotics;Chemistry - A European Journal;2008-11-10
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