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
Metal ion and micellar triggering of enantioselectivity in the hydrolysis of N-protected amino acid esters
โ Scribed by John G.J. Weijnen; Arie Koudijs; Johan F.J. Engbersen
- Publisher
- Elsevier Science
- Year
- 1992
- Weight
- 324 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0304-5102
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