Anionic ring expansion reactions of oxabicyclo[4.2.1]heptenones. An efficient entry into the carbon framework of oxygenated cembranoids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Aromatization of 2,2,5-trialkyl-substituted 2,5-dihydrofurans and factors affecting their stabilization;Chemistry of Heterocyclic Compounds;2018-04
2. Tandem Metathesis Reactions of Oxabicyclo[2.2.1]heptenes: Studies on the Spirocyclic Core of Cyclopamine;Organic Letters;2011-04-01
3. ChemInform Abstract: Anionic Ring Expansion Reactions of Oxabicyclo[4.2.1]heptenones. An Efficient Entry into the Carbon Framework of Oxygenated Cembranoids.;ChemInform;2010-05-23
4. Asymmetric Synthesis of a Hydroxylated Nine-membered Lactone from Tartaric Acid using the Claisen Rearrangement;Australian Journal of Chemistry;2010
5. Synthesis of a 10-membered ring with eleutheside functionality by Nozaki–Hiyama–Kishi coupling;Tetrahedron;2007-11
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