Nickel-Catalyzed Synthesis of Oxazoles via C−S Activation

The synthesis of 2-substituted oxazoles is achieved via nickel-catalyzed cross-coupling reaction of 2-methylthio-oxazole and various organozinc reagents. An extension of this method is demonstrated with a chemoselective, one-pot synthesis of unsymmetrical 2,5-disubstituted oxazoles. This synthesis o...

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Veröffentlicht in:Organic letters 2009-03, Vol.11 (6), p.1457-1459
Hauptverfasser: Lee, Kyoungsoo, Counceller, Carla M, Stambuli, James P
Format: Artikel
Sprache:eng
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Zusammenfassung:The synthesis of 2-substituted oxazoles is achieved via nickel-catalyzed cross-coupling reaction of 2-methylthio-oxazole and various organozinc reagents. An extension of this method is demonstrated with a chemoselective, one-pot synthesis of unsymmetrical 2,5-disubstituted oxazoles. This synthesis of 2- and 2,5-substituted oxazoles using this method provides great advantages over previous methods for these compounds and is highly complementary to current cyclodehydration strategies.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol900260g