Sammanfattning
A microwave-enhanced, palladium-catalyzed protocol for the alpha-arylation of a protected glycine in neat water is described. This reaction proceeds rapidly, under non-inert conditions, to afford a range of phenylglycine derivatives in moderate to good yields. Based on this arylation, a number of aryl L-methionine-SR-sulfoximine (MSO) analogues were prepared and evaluated for their Mycobacterium tuberculosis glutamine synthetase (TB-GS) inhibitory activity.
| Originalspråk | Engelska |
|---|---|
| Sidor (från-till) | 783-789 |
| Antal sidor | 7 |
| Tidskrift | Combinatorial Chemistry and High Throughput Screening |
| Volym | 10 |
| Nummer | 9 |
| DOI | |
| Status | Publicerad - 2007 |
Nyckelord
- arylation
- glutamine synthetase
- microwave
- palladium
- tuberculosis
- water
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