In recent years, tailor-made c-constrained amino acids have emerged as critically important key structural units in the de novo design of peptide-based drugs with enhanced receptor selectivity and stability to metabolic degradation. [1, Incorporation of these amino acids in strategic positions of a
β¦ LIBER β¦
A Practical Asymmetric Synthesis of Enantiomerically Pure 3-Substituted Pyroglutamic Acids and Related Compounds
β Scribed by Vadim A. Soloshonok; Chaozhong Cai; Victor J. Hruby
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 106 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0044-8249
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