An attractive intermediate in the total synthesis of eleutherobin has been synthesised. The key step of this synthesis is an intramolecular Diels-Alder reaction, which leads to intermediate possessing rings A and C of the eleutherobin skeleton.
Intramolecular Diels-Alder strategy in a synthetic approach to the eleutherobin core
SAMARITANI, SIMONA;
2005-01-01
Abstract
An attractive intermediate in the total synthesis of eleutherobin has been synthesised. The key step of this synthesis is an intramolecular Diels-Alder reaction, which leads to intermediate possessing rings A and C of the eleutherobin skeleton.File in questo prodotto:
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