A short, enantiospecific synthesis of a protected seco acid precursor to (R,R)-(−)-pyrenophorin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
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2. Synthesis of (±)-pyrenophorin utilizing 1,3-dipolar cycloaddition of silyl nitronate for the construction of 16-membered ring
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4. An optically active allene macrodiolide: A versatile key intermediate leading to (−)-pyrenophorin and (+)-dibenzomacrodiolides
5. A Short Asymmetric Synthesis of (R,R)-(-)-Pyrenophorin
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2. Regioselective Addition of 1,3-Dicarbonyl Dianions to Carbonyl Compounds: One Pot Lactonization and Ketalization of δ-Hydroxy-β-keto Esters to Protected Pyrone Derivatives;Australian Journal of Chemistry;2012
3. Macrocyclisation of Macrodiolide with Dimethylaluminium Methaneselenolate;European Journal of Organic Chemistry;2010-11-12
4. ChemInform Abstract: A Short, Enantiospecific Synthesis of a Protected Seco Acid Precursor to (R,R)-(-) Pyrenophorin.;ChemInform;2010-08-05
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