Abstract
The chemical space explored in drug discovery programs is restricted by a narrow reaction toolkit and the frequent failure of even these reactions with polar and functionalized substrates. Recently, high-throughput reaction optimization has been integrated into discovery workflows, thereby increasing the value of specific reaction classes in the toolkit. It is likely that high-throughput experimentation will enable expansion of the synthetic chemistry that is widely exploited in discovery, thereby increasing innovation in medicinal chemistry.
| Original language | English |
|---|---|
| Pages (from-to) | 3591–3593 |
| Number of pages | 3 |
| Journal | Journal of Medicinal Chemistry |
| Volume | 60 |
| Issue number | 9 |
| Early online date | 24 Mar 2017 |
| DOIs |
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| Publication status | Published - 11 May 2017 |
Funding
We thank EPSRC (Grant EP/N025652/1) for funding.
Keywords
- drug discovery
- substitution reactions
- solvents
- optimization
- medicinal chemistry
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