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Smiles rearrangements in Ugi- and Passerini-type couplings: New multicomponent access to O- and N-arylamides

Research output: Contribution to journalArticlepeer-review

Abstract

(Chemical Equation Presented) The use of Smiles rearrangement in Ugi- and Passerini-type couplings with electron-deficient phenols allows very straightforward multicomponent formation of O-aryl- and N-arylamides. Best yields were observed with the highly activated o- and p-nitrophenols, salicylic derivatives giving adducts in lower yields. The scope of these new reactions is further increased by the successful couplings of heterocyclic phenols such as hydroxypyridines and hydroxypyrimidines.

Original languageEnglish
Pages (from-to)4169-4180
Number of pages12
JournalJournal of Organic Chemistry
Volume72
Issue number11
DOIs
Publication statusPublished - 25 May 2007
Externally publishedYes

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