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- W2080929467 abstract "Radical cyclizations of di-, tri- and tetrapeptides containing N-2-bromobenzyl,N-methyl-substituted alanine or aspartic acid lead in good yields to α,β-unsaturated γ-lactams. The overall cascade, relying on a hydrogen atom transfer-elimination strategy could serve as a way to incorporate a flat and rigid five-membered ring into the peptide framework." @default.
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- W2080929467 date "2004-12-02" @default.
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- W2080929467 title "Application of the Radical Cascade of Acyclic Peptide-Based Precursors into Analogues of Type I β-Turn" @default.
- W2080929467 doi "https://doi.org/10.1055/s-2004-836054" @default.
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