Synthesis of the AB ring system of clifednamide utilizing Claisen rearrangement and Diels-Alder reaction as key steps
| Autor: | Aman Bhasin, Andreas Köhn, Aruna Raja, Inga Loke, Rainer Schobert, Julia Holz, Guillaume Bentzinger, Sabine Laschat, Florenz Sasse |
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| Přispěvatelé: | Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7, 38124 Braunschweig, Germany. |
| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
Stereochemistry
Sigmatropic reaction 010402 general chemistry Ring (chemistry) 01 natural sciences Biochemistry Heterocyclic Compounds 4 or More Rings Silyl ether chemistry.chemical_compound Mannitol Physical and Theoretical Chemistry Diels–Alder reaction Cycloaddition Reaction Molecular Structure 010405 organic chemistry Chemistry Organic Chemistry fungi Stereoisomerism Carroll rearrangement Pyrrolidinones 0104 chemical sciences Claisen rearrangement Intramolecular force Quantum Theory Enone |
| Popis: | In order to construct the functionalized AB ring system of clifednamide, member of the class of macrocyclic tetramic acid lactams, a synthesis was developed which utilized an Ireland-Claisen rearrangement and an intramolecular Diels-Alder reaction. Starting from di-O-isopropylidene-d-mannitol the allyl carboxylate precursor for the sigmatropic rearrangement was prepared. This rearrangement proceeded diastereoselectively only in the presence of an allyl silyl ether instead of the parent enone in the side chain, as suggested by deuteration experiments. A subsequent Diels-Alder reaction yielded the target ethyl hexahydro-1H-indene-carboxylate with high diastereoselectivity. Quantum-chemical investigations of this intramolecular Diels-Alder reaction support the proposed configuration of the final product. |
| Databáze: | OpenAIRE |
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