Development of chiral stabilised azomethine ylids: completing the memory relay
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference10 articles.
1. Development of a chiral stabilised azomethine ylid. A chiral relay system.
2. π-Facial selectivity of the 1,3-dipolar cycloaddition of the parent azomethine ylide to homochiral dipolarophiles
3. Asymmetric synthesis XVII : Facile generation of a chiral azomethine ylide via the CN(R,S) method
4. Metal ion catalysed asymmetric 1,3-dipolar cycloaddition reactions of imines of α-amino esters
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1. α-Quaternary Proline Derivatives by Intramolecular Diastereoselective Arylation of N-Carboxamido Proline Ester Enolates;The Journal of Organic Chemistry;2015-10-16
2. Azomethine Ylides Derived from Alkyl- (3-Oxopiperazin-2-yl)Acetates in 1,3-Dipolar Cycloaddition Reactions with n-Aryl Maleimides;Chemistry of Heterocyclic Compounds;2014-06-14
3. ChemInform Abstract: Development of Chiral Stabilized Azomethine Ylides: Completing the Memory Relay.;ChemInform;2010-08-22
4. Asymmetric 1,3-dipolar cycloadditions of acrylamides;Chem. Soc. Rev.;2010
5. Stereoselective Synthesis of Quaternary Proline Analogues;European Journal of Organic Chemistry;2008-06-23
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