Abstract
The expedient synthesis of compounds enriched in sp3 character is key goal in modern drug discovery. Herein, we report how a single pot Suzuki-Miyaura-hydrogenation can be used to furnish lead and fragment-like products in good to excellent yields. The approach has been successfully applied in formats amenable to parallel synthesis, in an asymmetric sense, and in the preparation of molecules with annotated biological activity.
Original language | English |
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Number of pages | 4 |
Journal | Chemical Communications (London) |
Early online date | 27 Nov 2017 |
DOIs | |
Publication status | E-pub ahead of print - 27 Nov 2017 |
Keywords
- synthesis
- sp3
- drug discovery