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A systematic study of the solid state and solution phase conformational preferences of beta-peptides derived from transpentacin

Abstract:

The solid state and solution phase conformational preferences of a homologous series of β-peptides derived from (S,S)-2- aminocyclopentanecarboxylic acid (transpentacin) have been investigated using a variety of spectroscopic and crystallographic techniques. These studies indicate that the hexamer and pentamer persist as a 12-helix in both the solid state and solution phase. Although the conformational traits of a 12-helix are exhibited by oligomers with as few as three residues in the solid ...

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Publication status:
Published

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Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Role:
Author
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Journal:
TETRAHEDRON-ASYMMETRY
Volume:
21
Issue:
13-14
Pages:
1797-1815
Publication date:
2010-07-14
DOI:
EISSN:
1362-511X
ISSN:
0957-4166
URN:
uuid:5c160e05-18e0-474a-86a2-003b49e2cf10
Source identifiers:
71231
Local pid:
pubs:71231
Language:
English

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