Leading the way: The novel thiostrepton analogue 1 and its 5S, 6S diastereomer were synthesized through macrolactamization reactions. Forays towards the total synthesis of the natural product itself should follow a similar strategy.
Synthetic studies on thiostrepton: Construction of thiostrepton analogues with the thiazoline-containing macrocycle / K. C., Nicolaou; Marta, Nevalainen; Mark, Zak; Stephan, Bulat; Bella, Marco; Brian S., Safina. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION. - ISSN 1433-7851. - 42:29(2003), pp. 3418-3424. [10.1002/anie.200351745]
Synthetic studies on thiostrepton: Construction of thiostrepton analogues with the thiazoline-containing macrocycle
BELLA, Marco;
2003
Abstract
Leading the way: The novel thiostrepton analogue 1 and its 5S, 6S diastereomer were synthesized through macrolactamization reactions. Forays towards the total synthesis of the natural product itself should follow a similar strategy.File allegati a questo prodotto
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