Rearrangements of 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans reactions of paulownin and wodeshiol with triethylsilane and BF3-etherate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference3 articles.
1. A general synthesis of 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans applicable to unsymmetrically substituted compounds
2. Pelter A.; Ward, R. S.; Venkateswarlu, R.; Kamakshi, C. unpublished results.
3. Acid catalysed rearrangements of arboreol: A biomimetic synthesis of gmelanone
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1. Novel lignan-based compounds via click chemistry: paulownin isolation, structural modifications and cytotoxic activity evaluations;Natural Product Research;2020-03-16
2. Stereospecific synthesis of endo-endo-3,7-dioxabicyclo[3.3.0]octane lignans using 1,6-bis(dipropylboryl)-2,4-hexadiene;Russian Chemical Bulletin;2011-11
3. ChemInform Abstract: Rearrangements of 2,6-Diaryl-3,7-dioxabicyclo(3.3.0)octane Lignans. Reactions of Paulownin (I) and Wodeshiol (III) with Triethylsilane and BF3-Etherate.;ChemInform;2010-08-21
4. Ionic and Organometallic-Catalyzed Organosilane Reductions;Organic Reactions;2008-08-11
5. Boron Trifluoride Etherate;Encyclopedia of Reagents for Organic Synthesis;2007-03-15
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