Fsp-rich and diverse fragments inspired by natural products as a collection to enhance fragment-based drug discovery
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 ea...
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2020-02, Vol.56 (15), p.228-2283 |
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| container_end_page | 2283 |
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| container_issue | 15 |
| container_start_page | 228 |
| container_title | Chemical communications (Cambridge, England) |
| container_volume | 56 |
| creator | Hanby, Abigail R Troelsen, Nikolaj S Osberger, Thomas J Kidd, Sarah L Mortensen, Kim T Spring, David R |
| description | 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.
Herein, we describe the natural product inspired synthesis of 38 complex small molecules based upon 20 unique frameworks suitable for fragment-based screening. |
| doi_str_mv | 10.1039/c9cc09796a |
| format | Article |
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| ispartof | Chemical communications (Cambridge, England), 2020-02, Vol.56 (15), p.228-2283 |
| issn | 1359-7345 1364-548X |
| language | eng |
| recordid | cdi_rsc_primary_c9cc09796a |
| source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| title | Fsp-rich and diverse fragments inspired by natural products as a collection to enhance fragment-based drug discovery |
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