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Quinine-Catalyzed Enantioselective Michael Addition of Diphenyl Phosphite to Nitroolefins: Synthesis of Chiral Precursors of α-Substituted β-Aminophosphonates

✍ Scribed by Jian Wang; Lora D. Heikkinen; Hao Li; Liansuo Zu; Wei Jiang; Hexin Xie; Wei Wang


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
110 KB
Volume
349
Category
Article
ISSN
1615-4150

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✦ Synopsis


Abstract

A quinine‐promoted, enantioselective Michael addition reaction of diphenyl phosphite with nitroalkenes has been developed. This methodology affords a facile access to enantiomerically enriched β‐nitrophosphates, precursors for the preparation of synthetically and biologically useful β‐aminophosphonates.


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