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Regioselective Halogenations and Subsequent Suzuki-Miyaura Coupling onto Bicyclic 2-Pyridones

Bengtsson, Christoffer (author)
Umeå universitet,Kemiska institutionen
Almqvist, Fredrik (author)
Umeå universitet,Kemiska institutionen
 (creator_code:org_t)
2009-12-21
2010
English.
In: The Journal of organic chemistry. - : American Chemical Society. - 1520-6904 .- 0022-3263. ; 75:3, s. 972-5
  • Journal article (peer-reviewed)
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  • A selective synthesis of 6-bromo-8-iodo dihydro thiazolo ring-fused 2-pyridones is described. These halogenated 2-pyridones are selectively arylated by sequential Suzuki-Miyaura couplings. This approach can advantageously be used to synthesize focused libraries of substituted ring-fused 2-pyridones, a class of compounds with novel antibacterial properties.

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