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ChemInform Abstract: Highly Effective and Enantioselective Michael Addition of 4-Hydroxycoumarin to α,β-Unsaturated Ketones Promoted by Simple Chiral Primary Amine Thiourea Bifunctional Catalysts.

✍ Scribed by Ren-Qiang Mei; Xiao-Ying Xu; Yan-Chun Li; Ji-Ya Fu; Qing-Chun Huang; Li-Xin Wang

Publisher: John Wiley and Sons
Year: 2011
Weight: 30 KB
Volume: 42
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201128136

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ChemInform Abstract: Highly Enantioselective Michael Addition of α-Substituted Cyano Ketones to β,γ-Unsaturated α-Keto Esters Using Bifunctional Thiourea-Tertiary Amine Catalysts: An Easy Access to Chiral Dihydropyrans.

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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

Highly Enantioselective Michael Addition

Highly Enantioselective Michael Addition of α-Substituted Cyano Ketones to β,γ-Unsaturated α-Keto Esters using Bifunctional Thiourea-Tertiary Amine Catalysts: An Easy Access to Chiral Dihydropyrans

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