Assignment of absolute configuration of the α,β-unsaturated γ-methyl-γ-lactone of the annonaceous acetogenins by a simple enzymatic method
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Progress in the Chemistry of Organic Natural Products: Acetogenins from Annonaceae;Cavé,1996
2. Annonaceous Acetogenins: A Review
3. Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives
4. Studies in Natural Products;Ramirez,1995
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1. ChemInform Abstract: Acetogenins from Annonaceae. Part 53. Assignment of Absolute Configuration of the α,β-Unsaturated γ-Methyl-γ- Lactone of the Annonaceous Acetogenins by a Simple Enzymatic Method.;ChemInform;2010-08-04
2. Semisynthesis and Screening of a Small Library of Pro-Apoptotic Squamocin Analogues: Selection and Study of a Benzoquinone Hybrid with an Improved Biological Profile.;ChemMedChem;2006-01-16
3. Semisynthesis of heterocyclic analogues of squamocin, a cytotoxic annonaceous acetogenin, by an unusual oxidative decarboxylation reaction;Bioorganic & Medicinal Chemistry;2003-08-05
4. NMR Determination of Absolute Configuration of Butenolides of Annonaceous Type;Chemistry - A European Journal;2002-12-16
5. Cohibins C and D, Two Important Metabolites in the Biogenesis of Acetogenins from Annona muricata and Annona nutans;Journal of Natural Products;2000-07-26
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