New synthetic routes to optically active α-quaternary α-aryl amino acid derivatives via the diastereoselective Stevens and Sommelet–Hauser rearrangements
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2008/OB/B811162F
Reference18 articles.
1. Recent Developments in the Catalytic Asymmetric Cyanation of Ketimines
2. Asymmetric Activation oftropos 2,2′-Biphenol with Cinchonine Generates an Effective Catalyst for the Asymmetric Strecker Reaction ofN-Tosyl-Protected Aldimines and Ketoimines
3. Enantioselective Strecker Reaction of Phosphinoyl Ketoimines Catalyzed by in Situ Prepared Chiral N,N‘-Dioxides
4. Assembly State of Catalytic Modules as Chiral Switches in Asymmetric Strecker Amino Acid Synthesis
5. Asymmetric Strecker Reaction of Ketoimines Catalyzed by a Novel Chiral BifunctionalN,N′-Dioxide
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