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Accueil > Teams > Pharmacognosy - Chemistry of Natural Products > Our books or covers paper > Emergence of diversity and stereochemical outcomes in the biosynthetic pathways of cyclobutane-centered marine alkaloid dimers

Emergence of diversity and stereochemical outcomes in the biosynthetic pathways of cyclobutane-centered marine alkaloid dimers

Mehdi A. Beniddir, Laurent Evanno, Delphine Joseph, Adam Skiredj* and Erwan Poupon*

Dictazoles and sceptrins are singular metabolites of marine origin. The present dichotomic case study provides a comprehensive perspective on these cyclobutane-centered alkaloids and their respective families. Indeed, their upstream and downstream chemistry are both treated herein. Relevant isolation reports and bio-inspired total syntheses are used to decipher the currently admitted biosynthetic hypotheses as well as the emergence of diversity in the two series. This review proposes a transversal vision of the topic, where most aspects of natural product chemistry have a critical importance.

http://pubs.rsc.org/en/content/articlelanding/2016/np/c5np00159e#!divAbstract