Issue 1, 2018
From the journal:

Natural Product Reports

Natural products and ring-closing metathesis: synthesis of sterically congested olefins

C. Lecourt,a   S. Dhambri, ORCID logo a   L. Allievi,a   Y. Sanogo,a   N. Zeghbib,a   R. Ben Othman,a   M.-I. Lannou, ORCID logo *a   G. Sorin ORCID logo *a  and  J. Ardisson ORCID logo *a  

* Corresponding authors

a Paris Descartes University, Sorbonne Paris Cité, Faculté des Sciences Pharmaceutiques et Biologiques, Unité CNRS UMR 8638 COMÈTE, 4 Avenue de l'observatoire, 75270 Paris Cedex 06, France
E-mail: marie-isabelle.lannou@parisdescartes.fr, geoffroy.sorin@parisdescartes.fr, janick.ardisson@parisdescartes.fr

Abstract

Covering: 2002 to August 2017.

This review highlights recent RCM reactions towards the synthesis of sterically congested natural products. It offers an insight into various synthetic targets and approaches and provides information on the evolution of catalysts as powerful tools enabling the use of increasingly challenging diene precursors.

Graphical abstract: Natural products and ring-closing metathesis: synthesis of sterically congested olefins

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Article information

DOI
https://doi.org/10.1039/C7NP00048K
Article type
Review Article
Submitted
20 Oct 2017
First published
18 Jan 2018

Nat. Prod. Rep., 2018,35, 105-124

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Natural products and ring-closing metathesis: synthesis of sterically congested olefins

C. Lecourt, S. Dhambri, L. Allievi, Y. Sanogo, N. Zeghbib, R. Ben Othman, M.-I. Lannou, G. Sorin and J. Ardisson, Nat. Prod. Rep., 2018, 35, 105 DOI: 10.1039/C7NP00048K

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