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ChemInform Abstract: Enantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to α,β-Unsaturated Aldehydes by Redox Oxidation.

✍ Scribed by Zi-Qiang Rong; Min-Qiang Jia; Shu-Li You

Publisher: John Wiley and Sons
Year: 2011
Weight: 36 KB
Volume: 42
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201150117

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## Abstract Enals react with various 1,3‐dicarbonyl compounds as redox‐activated Michael acceptors in the presence of TAZ as NHC precursor and a bisphenol derived quinone TBQ as the organic oxidant to produce dihydropyranones.

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

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