Peptides: The Wave of the Future 2001
DOI: 10.1007/978-94-010-0464-0_9
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Two Novel and Efficient Approaches to Synthesis of Enantiopure Dipeptide β-Turn Mimetics: Indolizidinone Amino Acids

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“…with novel α, β, and γ substituents. In a similar manner, we are seeking also to develop mimics for the key secondary structures of peptides and proteins, i.e., α-helix, β-sheet, β-turn, and extended structures. Our most recent efforts are directed toward bicyclic heterocyclic systems that constrain putative β-turns both in φ−ψ space and in χ space. The challenge of exploring all the available topographical space with 16, 32, or even more isomers is substantial, but certainly can be aided by combinatorial chemistry such as the one-bead, one-compound method …”
Section: Future Perspectivesmentioning
confidence: 99%
“…with novel α, β, and γ substituents. In a similar manner, we are seeking also to develop mimics for the key secondary structures of peptides and proteins, i.e., α-helix, β-sheet, β-turn, and extended structures. Our most recent efforts are directed toward bicyclic heterocyclic systems that constrain putative β-turns both in φ−ψ space and in χ space. The challenge of exploring all the available topographical space with 16, 32, or even more isomers is substantial, but certainly can be aided by combinatorial chemistry such as the one-bead, one-compound method …”
Section: Future Perspectivesmentioning
confidence: 99%