Raman and IR spectral studies ofD-phenylglycinium perchlorate
Author:
Publisher
Wiley
Subject
Spectroscopy,General Materials Science
Reference33 articles.
1. Substrate specificity of immobilized penicillin-G acylase towards penicillin and cephalosporin derivatives was studied. The phenylacetyl moiety can be altered at the α-position with several small substituents. Depending on polarity and size of the substituent, enzyme activity decreases or increases. Insertion or deletion of atoms between the aromatic nucleus of the phenylacetyl group and the center of hydrolysis leads to substrates that are no longer recognized by the enzyme.
2. Structure-Activity Studies of Antitumor Taxanes: Synthesis of Novel C-13 Side Chain Homologated Taxol and Taxotere Analogs
3. Design, Synthesis, and Evaluation of Latent Alkylating Agents Activated by Glutathione S-Transferase
4. Crystalline Complexes Involving Amino Acids. II. (R)-(−)-1-Phenylglycinium Hydrogen Squarate Monohydrate
5. D-Phenylglycine Hydrochloride
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