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
Synthesis of Two Optically Active N-Acetyl Dipeptides by the p-Nitrophenyl Ester Method
✍ Scribed by Cash, William D.
- Book ID
- 126931714
- Publisher
- American Chemical Society
- Year
- 1962
- Tongue
- English
- Weight
- 429 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0022-3263
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