Issue 63, 2016

A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds

Abstract

A synthetic approach to diverse scaffolds was developed that was inspired by diterpene biosynthesis. Initial scaffolds, generated using Diels–Alder reactions of furyl-functionalised amines, were transformed into alternative scaffolds using cleavage, ring expansion, annulation and rearrangement reactions. In total, 25 diverse scaffolds were prepared that were shown to have high natural product-likeness.

Graphical abstract: A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds

Supplementary files

Article information

Article type
Communication
Submitted
03 Jun 2016
Accepted
13 Jul 2016
First published
18 Jul 2016
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2016,52, 9837-9840

Author version available

A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds

J. D. Firth, P. G. E. Craven, M. Lilburn, A. Pahl, S. P. Marsden and A. Nelson, Chem. Commun., 2016, 52, 9837 DOI: 10.1039/C6CC04662B

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