Published July 23, 2019
| Version v1
Journal article
Synthesis, Structure, and Cytotoxicity of Urukthapelstatin A Polyazole Cyclopeptide Analogs
- Others:
- Institut für Organische Chemie und Makromolekulare Chemie ; Friedrich-Schiller-Universität = Friedrich Schiller University Jena [Jena, Germany]
- Institut de Chimie de Nice (ICN) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)
Description
Analogs of the natural product urukthapelstatin A that belongs to the rare family of polyazole cyclopeptides were synthesized and their cytotoxic activities were determined to gather data toward structure-activity relationships. Crucial steps within the convergent syntheses were a macrothiolacton-ization and a subsequent aza-Wittig reaction to install the het-erocyclic backbone. The synthesis design was proven to be generally suitable for the formation of these azole containing cyclo
Abstract
International audience
Additional details
- URL
- https://hal.archives-ouvertes.fr/hal-02414497
- URN
- urn:oai:HAL:hal-02414497v1
- Origin repository
- UNICA