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- W2034374686 abstract "Abstract A highly constrained analogue of l -proline, (1S,2S,4R)-2-phenyl-7-azabicyclo[2.2.1]heptane-1-carboxylic acid, has been incorporated into a model dipeptide. X-Ray diffraction analysis has shown that, in the solid state, this constrained peptide adopts a type I β-turn whereas the analogous dipeptide sequence incorporating l -proline has been shown to accommodate a βII-turn disposition. Attractive interactions involving the middle NH group and either the aromatic rings or the pyramidalised bicycle nitrogen seem to play a role in the stabilisation of the βI-turn conformation observed." @default.
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- W2034374686 date "2003-08-01" @default.
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- W2034374686 title "Stabilisation of the type I β-turn conformation by a bicyclic analogue of proline" @default.
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- W2034374686 doi "https://doi.org/10.1016/s0040-4039(03)01475-8" @default.
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