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Novel conformationally-constrained beta-peptides characterized by 1H NMR chemical shifts.

Authors
Type
Published Article
Journal
Chemical communications (Cambridge, England)
Publication Date
Issue
20
Pages
2534–2535
Identifiers
PMID: 14594267
Source
Medline
License
Unknown

Abstract

For a novel family of oxanorbornene beta-peptides, density functional theory computations of the three-dimensional structure and 1H NMR chemical shifts predict that the dimer and trimer form consecutive 8-membered hydrogen-bonded ring helices, which is supported by excellent agreement with experimental solution NMR data.

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