4.4 Article

Direct organocatalytic in situ generation of novel push-pull dienamines: application in tandem Claisen-Schmidt/iso-aromatization reactions

期刊

TETRAHEDRON LETTERS
卷 46, 期 41, 页码 7037-7042

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2005.08.051

关键词

amines; Hagemann's ester; organocatalysis; push-pull dienamine; tandem reactions

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A new, green, regioselective, one-step, tandem reaction of an aldehyde possessing a non-enolizable carbonyl function with a highly substituted cyclohex-2-enone, under amine catalysis afforded highly substituted phenols or 2-arylidenecyclohexanones, respectively. The yields and regioselectivities were good. Evidence for a pathway involving formation of novel push-pull dienamines is presented along with examples demonstrating the amenability of the process to combinatorial chemistry. (c) 2005 Elsevier Ltd. All rights reserved.

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