C−H Activation Enables a Concise Total Synthesis of Quinine and Analogues with Enhanced Antimalarial Activity

We report a novel approach to the classical natural product quinine that is based on two stereoselective key steps, namely a C−H activation and an aldol reaction, to unite the two heterocyclic moieties of the target molecule. This straightforward and flexible strategy enables a concise synthesis of...

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Detalles Bibliográficos
Autores principales: O' Donovan, Daniel H., Aillard, Paul, Berger, Martin, de la Torre, Aurélien, Petkova, Desislava, Knittl‐Frank, Christian, Geerdink, Danny, Kaiser, Marcel, Maulide, Nuno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146912/
https://www.ncbi.nlm.nih.gov/pubmed/29761878
http://dx.doi.org/10.1002/anie.201804551

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146912/
https://www.ncbi.nlm.nih.gov/pubmed/29761878
http://dx.doi.org/10.1002/anie.201804551

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