ChemInform Abstract: Design of Novel Synthetic Peptides Including Cyclic Conformationally and Topographically Constrained Analogues
β Scribed by V. J. HRUBY; G. G. BONNER
- Book ID
- 112021922
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 25 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0931-7597
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Novel Enantioselective Synthesis of trans-Ξ±-(2-Carboxycycloprop-1yl)glycines: Conformationally Constrained L-Glutamate Analogues. -Key step of the described sequence is the oxazaborolidine-catalyzed enantioselective conversion of oxime ethers (V) and (VI) to the corresponding amines. Interestingly,