Totalsynthesen des antibakteriellen Naturstoffes Abyssomicin C
- 31 August 2006
- journal article
- highlight
- Published by Wiley in Angewandte Chemie
- Vol. 118 (35) , 5866-5869
- https://doi.org/10.1002/ange.200602409
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- A Diels–Alder Macrocyclization Enables an Efficient Asymmetric Synthesis of the Antibacterial Natural Product Abyssomicin CAngewandte Chemie International Edition in English, 2005
- A Diels–Alder Macrocyclization Enables an Efficient Asymmetric Synthesis of the Antibacterial Natural Product Abyssomicin CAngewandte Chemie, 2005
- Abyssomicin C—A Polycyclic Antibiotic from a Marine Verrucosispora Strain as an Inhibitor of the p‐Aminobenzoic Acid/Tetrahydrofolate Biosynthesis PathwayAngewandte Chemie International Edition in English, 2004
- Abyssomicin C– ein polycyclisches Antibiotikum aus einem marinenVerrucosispora-Stamm als Inhibitor für diep-Aminobenzoesäure/Tetrahydrofolat-BiosyntheseAngewandte Chemie, 2004
- Abyssomicins, Inhibitors of the para-Aminobenzoic Acid Pathway Produced by the Marine Verrucosispora Strain AB-18-032The Journal of Antibiotics, 2004
- Total Synthesis of Pinnatoxin AJournal of the American Chemical Society, 1998
- An intramolecular Diels-Alder approach to the synthesis of chlorothricolide. Synthesis of (.+-.)-24-O-methylchlorothricolideThe Journal of Organic Chemistry, 1990
- Cytochalasan synthesis: total synthesis of cytochalasin GJournal of the Chemical Society, Perkin Transactions 1, 1989
- A simplified total synthesis of cytochalasins via an intramolecular Diels-Alder reactionJournal of the American Chemical Society, 1983
- Formation of macrocyclic structures by use of the diels-alder reactionTetrahedron Letters, 1975