Asymmetric total synthesis of (+)-carneic acid A and structure revision of its natural form
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Carneic Acids A and B, Chemotaxonomically Significant Antimicrobial Agents from the Xylariaceous Ascomycete Hypoxylon carneum
2. First Total Synthesis of Antimitotic Compound, (+)-Phomopsidin
3. Alternative synthetic approach for (+)-phomopsidin via the highly stereoselective TADA reaction
4. Asymmetric total synthesis of MK8383: the iron-mediated coupling reaction is the only effective method for the construction of the (Z)-trisubstituted side-chain alkene
5. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions
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3. Research on Liebeskind-Srogl coupling/intramolecular Diels-Alder reaction cascade;Tetrahedron Letters;2018-03
4. A highly stereoselective intramolecular Diels–Alder reaction for construction of the AB ring moiety of bruceantin;Tetrahedron Letters;2015-03
5. Lenormandins A—G, new azaphilones from Hypoxylon lenormandii and Hypoxylon jaklitschii sp. nov., recognised by chemotaxonomic data;Fungal Diversity;2015-01-20
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