Facile total synthesis of (±)-α-herbertenol, (±)-α-cuparenone and (±)-HM-1 methyl ether involving alkylation of hindered esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. Structures of ent-herbertane sesquiterpenoids displaying antifungal properties from the liverwort Herberta adunca
2. Novel Phenolics from Phytopathogenic FungusHelicobasidium mompa
3. A short and efficient total synthesis of (±) α-cuparenone
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1. The Krapcho Dealkoxycarbonylation Reaction of Esters with α-Electron-Withdrawing Substituents;Organic Reactions;2013-05-30
2. Formal Synthesis of Racemic Herbertene, α-Herbertenol, β-Herbertenol and Herbertenone via Gold(I)-Catalyzed Cyclization of 5-Phenyl-5-siloxy-3-en-1-ynes;Bulletin of the Korean Chemical Society;2013-01-20
3. A chiral pool based approach to antipodes of α-cuparenone;Tetrahedron: Asymmetry;2012-11
4. A highly diastereoselective total synthesis of (±)-heritonin and (±)-heritol;Tetrahedron;2012-10
5. ChemInform Abstract: Facile Total Synthesis of (.+-.)-α-Herbertenol, (.+-.)-α-Cuparenone and (.+-.)-HM-1 Methyl Ether Involving Alkylation of Hindered Esters.;ChemInform;2010-06-14
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