Journal
TETRAHEDRON
Volume 68, Issue 11, Pages 2496-2508Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2012.01.060
Keywords
Diazodicarbonyls; beta-Enaminoamides; Wolff rearrangement; Uracil
Categories
Funding
- Ministry of Knowledge Economy (MKE) [RTI04-01-04]
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This paper describes simple and efficient approaches for the preparation of beta-enaminoamides through thermal Wolff rearrangement of cyclic diazodicarbonyls followed by trapping with various amines. The synthesized beta-enaminoamides were readily converted into uracil derivatives. (C) 2012 Elsevier Ltd. All rights reserved.
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