Hanby, AR, Troelsen, NS, Osberger, TJ et al. (3 more authors) (2020) Fsp3-rich and diverse fragments inspired by natural products as a collection to enhance fragment-based drug discovery. Chemical Communications, 56 (15). pp. 2280-2283. ISSN 1359-7345
Abstract
Herein, we describe the natural product inspired synthesis of 38 complex small molecules based upon 20 unique frameworks suitable for fragment-based screening. Utilising an efficient strategy, two key building block diastereomers were harnessed to generate novel, three-dimensional fragments which each possess numerous synthetically accessible fragment growth positions.
Metadata
| Item Type: | Article | 
|---|---|
| Authors/Creators: | 
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| Copyright, Publisher and Additional Information: | © The Royal Society of Chemistry 2020. This is an author produced version of an article published in Chemical Communications. Uploaded in accordance with the publisher's self-archiving policy. | 
| Dates: | 
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| Institution: | The University of Leeds | 
| Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) > Organic Chemistry (Leeds) | 
| Depositing User: | Symplectic Publications | 
| Date Deposited: | 20 Apr 2020 11:13 | 
| Last Modified: | 20 Jan 2021 01:39 | 
| Status: | Published | 
| Publisher: | Royal Society of Chemistry (RSC) | 
| Identification Number: | 10.1039/c9cc09796a | 
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:159627 | 
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