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2-Aryltetrahydropyridines formed by anionic cyclization or ring-closing metathesis were converted to their N′-aryl urea derivatives. Depending on the position of the unsaturation within the tetrahydropyridine ring, metalation by deprotonative lithiation or carbolithiation led to migration of the N′-aryl substituent to the 2- or 6-position via intramolecular nucleophilic attack of a benzylic organolithium on the aryl ring. The products are a range of 2,2-, 2,2,3-, and 2,6-polysubstituted piperidine derivatives. Related chemistry was observed in pyrroline homologues.
|Number of pages||4|
|Early online date||18 Feb 2015|
|Publication status||Published - 6 Mar 2015|
FingerprintDive into the research topics of '2,2- and 2,6-diarylpiperidines by aryl migration within lithiated urea derivatives of tetrahydropyridines'. Together they form a unique fingerprint.
- 1 Finished
alpha-Arylation and alpha-Vinylation of Enolates: New Reactivity from the Urea Linkage.
1/07/15 → 31/05/18