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Enantioselectively catalyzed hydrolysis of p-nitrophenyl esters of N-protected L-amino acids by N-lauroyl L or D-histidine in CTABr micelles.

โœ Scribed by Kimiho Yamada; Hideto Shosenji; Hirotaka Ihara; Yonejiro Otsubo

Book ID
108384838
Publisher
Elsevier Science
Year
1979
Tongue
French
Weight
188 KB
Volume
20
Category
Article
ISSN
0040-4039

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๐Ÿ“œ SIMILAR VOLUMES

Enantioselectively catalyzed oxidation o
Enantioselectively catalyzed oxidation of 3,4-dihydroxy-l-phenylalanine by N-lauroyl L or D-histidine-Cu(II) complex in CTABr micelles.
โœ Kimiho Yamada; Hideto Shosenji; Yonejiro Otsubo; Shuji Ono ๐Ÿ“‚ Article ๐Ÿ“… 1980 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 190 KB

In order to investigate the enzyme model reaction the oxidation of 3,4dihydroxy-L-phenylalanine(L-DOPA) was carried out using optically active catalyst, N-lauroyl L or D-histidine-Cu(I1) complex(L or D-LauHis-Cu(II)), showing appreciable enantioselectivity in the presence of the mixed micelles with

Enantioselectively catalyzed hydrolysis
Enantioselectively catalyzed hydrolysis of p-nitrophenyl esters of N-protected L or D-amino acids by optically active hydroxamic acid and dipeptides
โœ Shuji Ono; Hideto Shosenji; Kimiho Yamada ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 218 KB

Catalyzed hydrolysis of p-nitrophenyl esters of N-protected L or D-phenylalanine by optically active hydroxamic acid or dipeptides in the presence of CTABr micelles showed high enantioselectivity (D/L=5.68 for L-ZLysZ(MHX)), demonstrating control of the direction of the enantioselectivity based on t