Issue 7, 2016

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

Abstract

Covering: up to 2016

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.

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

Article information

Article type
Review Article
Submitted
21 Dec 2015
First published
25 May 2016

Nat. Prod. Rep., 2016,33, 820-842

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

M. A. Beniddir, L. Evanno, D. Joseph, A. Skiredj and E. Poupon, Nat. Prod. Rep., 2016, 33, 820 DOI: 10.1039/C5NP00159E

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