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Dearomatising rearrangements of lithiated thiophenecarboxamides
Authors:Clayden Jonathan  Turnbull Rachel  Helliwell Madeleine  Pinto Ivan
Institution:Department of Chemistry, University of Manchester, Oxford Road, Manchester, UK M13 9PL. j.p.clayden@man.ac.uk
Abstract:Thiophene-3-carboxamides bearing allyl or benzyl substituents at nitrogen undergo dearomatising cyclisation on treatment with LDA. Rearrangements transform the dearomatised products into pyrrolinones, azepinones or partially saturated azepinothiophenes.
Keywords:
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