Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5276309 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
β-Enamino ketones were successfully synthesized by reaction of endo glycals with primary or secondary amines in the presence of hypervalent iodine reagent in one pot. After the oxidation and protonation taking place on hypervalent iodine agent in acidic condition, endo glucals were effectively converted into the uncyclic β-alkoxyvinyl ketones. Further substitution of β-alkoxyvinyl ketones with primary or secondary amines provided the corresponding β-enamino ketone derivatives in 57-67% yields.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zi-Ping Lin, Hsu-Hsuan Wu, Masayuki Kimura, Kimiyoshi Kaneko, Hiroyuki Takayama, Fung Fuh Wong, Jin Bin Wu, Hui-Chang Lin,