One-step biomimetic synthesis of (±)-linderaspirone A and (±)-bi-linderone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. A Pair of Windmill-Shaped Enantiomers from Lindera aggregata with Activity toward Improvement of Insulin Sensitivity
2. Bi-linderone, a Highly Modified Methyl-linderone Dimer from Lindera aggregata with Activity toward Improvement of Insulin Sensitivity in Vitro
3. The [4 + 4] cycloaddition and its strategic application in natural product synthesis
4. Nickel-catalyzed intramolecular [4 + 4]-cycloadditions: a new method for the synthesis of polycycles containing eight-membered rings
5. Nickel-catalyzed intramolecular [4+4] cycloadditions. 4. Enantioselective total synthesis of (+)-asteriscanolide
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1. Investigations on Biomimetic Dimerization in Natural Product Synthesis;Synlett;2023-01-28
2. Linderaspirone A and Bi-linderone;Total Synthesis of Bioactive Natural Products;2019
3. Lindera cyclopentenedione intermediates from the roots of Lindera aggregata;RSC Advances;2018
4. Synthetic Studies toward Bi-linderone Lead To Unexpected 6π-Electrocyclization Reactions: A Facile Construction of Highly Congested Spiro Compounds;Synthesis;2015-08-11
5. Chemical Properties and Biological Activities of Cyclopentenediones: A Review;Mini-Reviews in Medicinal Chemistry;2014-04
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