Stereochemical revision of communiols D and H through synthesis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Communiols A–D: new mono- and bis-tetrahydrofuran derivatives from the coprophilous fungus Podospora communis
2. Communiols E−H: New Polyketide Metabolites from the Coprophilous Fungus Podospora communis
3. Acetogenins from Annonaceae: recent progress in isolation, synthesis and mechanisms of action
4. New Trimethylenemethane Dianion Synthons: Application to the Preparation of Substituted Perhydrofuro[2,3-b]furans
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1. Stereospecific [3+2] cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4: an efficient synthesis of multi-substituted perhydrofuro[2,3-b]furans and perhydrofuro[2,3-b]pyrans;Chem. Commun.;2014
2. A new approach to the synthesis of ethyl (4E)-alkenoates;Russian Journal of General Chemistry;2013-11
3. InCl3 Catalyzed Highly Diastereoselective [3 + 2] Cycloaddition of 1,2-Cyclopropanated Sugars with Aldehydes: A Straightforward Synthesis of Persubstituted Bis-Tetrahydrofurans and Perhydrofuro[2,3-b]pyrans;Organic Letters;2013-10-04
4. Straightforward and highly diastereoselective synthesis of 2,2-di-substituted perhydrofuro[2,3-b]pyran (and furan) derivatives promoted by BiCl3;Chemical Communications;2013
5. Stereoselective Synthesis of the C1–C16 Fragment of Goniodomin A;Bulletin of the Chemical Society of Japan;2012-09-15
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