Dynamic kinetic resolution of racemic N-phthalyl amino acids using (S)-α-methylpantolactone as the chiral auxiliary

Tetrahedron Asymmetry

Volumn 11, Issue 3, 2000, Pages 737-741

  Calmes, Monique ^a   Glot, Christéle ^a   Michel, Thibaut ^a   Rolland, Marc ^a   Martinez, Jean ^a  

^a UNIVERSITÉ DE MONTPELLIER   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE;

ARTICLE; CHEMICAL REACTION KINETICS; CHIRALITY; ESTERIFICATION; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 0034712183     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(00)00017-3     Document Type: Article

References (32)

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27. All new described products were isolated by chromatography on silica gel, or by recrystallization, and satisfactory analytical data have been obtained.
28. 6′), 166.2 (CO), 173.0 (CO), 178.3 (CO).
29. -3, T=298 K, final R=0.032, final Rw=0.045. Details of the crystal structure determination have been deposited at the Cambridge Crystallographic Data Centre (deposition number CCDC137179).
30. 5), 180.6 (CO).
31. 3) by integration of the α-methyl signal of the pantolactonyl moiety of the pair of diastereoisomers and/or by HPLC (Chiraspher column (Merck)).
32. Marfey, P. Carlsberg Res. Commun. 1984, 49, 591.