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ChemInform Abstract: Asymmetric Synthesis of Fluorinated Flavanone Derivatives by an Organocatalytic Tandem Intramolecular Oxa-Michael Addition/Electrophilic Fluorination Reaction by Using Bifunctional Cinchona Alkaloids.

✍ Scribed by Hai-Feng Wang; Hai-Feng Cui; Zhuo Chai; Peng Li; Chang-Wu Zheng; Ying-Quan Yang; Gang Zhao

Publisher: John Wiley and Sons
Year: 2010
Weight: 76 KB
Volume: 41
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201019125

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Asymmetric Synthesis of Fluorinated Flav

Asymmetric Synthesis of Fluorinated Flavanone Derivatives by an Organocatalytic Tandem Intramolecular Oxa-Michael Addition/Electrophilic Fluorination Reaction by Using Bifunctional Cinchona Alkaloids

✍ Hai-Feng Wang; Hai-Feng Cui; Zhuo Chai; Peng Li; Chang-Wu Zheng; Ying-Quan Yang; 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 290 KB

Supporting information for this article is available on the WWW under http://dx.doi.org/10.1002/chem.200902303. Scheme 1. Organocatalyzed tandem intramolecular oxa-Michael addition/ electrophilic fluorination reaction to access chiral fluorinated flavanones.

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