Matches in SemOpenAlex for { <https://semopenalex.org/work/W2023166213> ?p ?o ?g. }
- W2023166213 endingPage "6047" @default.
- W2023166213 startingPage "6038" @default.
- W2023166213 abstract "A practically simple three-component Strecker reaction for the asymmetric synthesis of enantiopure α-arylglycines has been developed. Addition of a range of aryl-aldehydes to a solution of sodium cyanide and (S)-1-(4-methoxyphenyl)ethylamine affords highly crystalline (S,S)-α-aminonitriles that are easily obtained in diastereomerically pure form. Heating the resultant (S,S)-α-aminonitriles in 6 M aqueous HCl at reflux resulted in cleavage of their chiral auxiliary fragments and concomitant hydrolysis of their nitrile groups to afford enantiopure (S)-α-arylglycines. The enantiopurities of these (S)-α-arylglycines were determined via derivatization of their corresponding methyl esters with 2-formylphenylboronic acid and (S)-BINOL, followed by (1)H NMR spectroscopic analysis of the resultant mixtures of diastereomeric iminoboronate esters." @default.
- W2023166213 created "2016-06-24" @default.
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- W2023166213 creator A5025662974 @default.
- W2023166213 creator A5059671002 @default.
- W2023166213 creator A5084137468 @default.
- W2023166213 date "2011-06-27" @default.
- W2023166213 modified "2023-10-17" @default.
- W2023166213 title "Asymmetric Strecker Synthesis of α-Arylglycines" @default.
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