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- W2329385087 endingPage "3753" @default.
- W2329385087 startingPage "3740" @default.
- W2329385087 abstract "Lewis acid catalyzed quaternary ammonium salt mediated highly regioselective ring-opening of chiral activated aziridines and azetidines with alcohols to nonracemic β- and γ-amino ethers has been developed. The reaction mainly proceeds via an SN2 pathway, and the partial racemization of the starting substrate was effectively controlled by using quaternary ammonium salts. β- and γ-amino ethers are obtained with high enantio- and diastereospecificity (ee up to >99%, de up to 99%). The methodology was further extended to synthesize morpholines and their homologues with high enantiospecificity (ee up to 90%) when halo alcohols were employed as the nucleophiles." @default.
- W2329385087 created "2016-06-24" @default.
- W2329385087 creator A5006491428 @default.
- W2329385087 creator A5035436985 @default.
- W2329385087 creator A5085283251 @default.
- W2329385087 date "2012-04-05" @default.
- W2329385087 modified "2023-09-25" @default.
- W2329385087 title "Syntheses of Chiral β- and γ-Amino Ethers, Morpholines, and Their Homologues via Nucleophilic Ring-Opening of Chiral Activated Aziridines and Azetidines" @default.
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