A synthesis of 2- and 4(5)-(2-pyridinyl)imidazoles by palladium-catalysed cross-coupling reactions
โ Scribed by A.S. Bell; D.A. Roberts; K.S. Ruddock
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 198 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Absfrucf N-Substltuted lmldazolylzlnc chlorides were reacted wlth 2bromopyrldlne In the presence of Pd(PPh3)4 and a two-fold excess of ZnCl2 to afford cross-coupled products In 58-93% ylelds. Deprotection provlded convenient routes to 2-or 4(5)-(2-pyrtdlnyl)lmldazoles.
๐ SIMILAR VOLUMES
4-Bromo-and 4-trifluorosulfonyloxypyrrolo[3,4-c]carbazoles were prepared in five steps via a [4+2] cycloaddition and were used as key intermediates in paUadium-catalysed cross coupling reactions allowing the rapid generation of structurally diverse protein kinase C inhibitors.
The synthesis of substituted 5-aryl-2-furfurals from furfurai by three alternative palladium cross coupling strategies are described. The resulting 5-aryl-2-furfurals were converted into their corresponding 5-aryl-2-vinylfurans in good yields by Wittig chemistry.