7682-15-7Relevant articles and documents
Efficient kinetic resolution of amino acids catalyzed by lipase AS 'Amano' via cleavage of an amide bond
Wang, Bo,Liu, Yanfeng,Zhang, Dela,Feng, Yuhong,Li, Jiacheng
, p. 1338 - 1342,5 (2020/09/16)
Herein the efficient kinetic resolution of non-natural alpha-amino acids catalyzed by lipase AS 'Amano' via cleaving the amide bond is reported. The starting materials were the corresponding amino acid amides and the amino acids were generated with ees of up to 99% with E values of >600. These results indicated that the lipase AS 'Amano' could be a powerful amide hydrolase for the kinetic resolution of amino acid starting from the corresponding amino acid amides.
Palladium-catalyzed amidocarbonylation improved by recyclable ionic liquids
Zhu, Bingchun,Jiang, Xuanzhen
, p. 2795 - 2798 (2008/02/11)
Two types of ionic liquids (halide anion ionic liquids and Brensted acidic ionic liquids) were first applied to improve the palladium-catalyzed amidocarbonylation. Both the palladium catalyst and the ionic liquids could be recycled at least five times without significant loss in catalytic activity. Georg Thieme Verlag Stuttgart.
STUDIES ON HYDROCARBOXYLATION OF N-ACETYLIMINES, ENAMINES AND ALLYLAMINES.
Magnus, Philip,Slater, Martin
, p. 2829 - 2832 (2007/10/02)
Treatment of an amide with an aldehyde in the presence of Co2(CO)8/CO/H2 results in N-acyl-α-amino acids. The scope and limitations of this reaction are explored