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A proline-based macrocyclic amide with S-4 symmetry

Authors
Ahn, Hee ChoonYun, Sun-miChoi, Kihang
Issue Date
5-1월-2008
Publisher
CHEMICAL SOC JAPAN
Citation
CHEMISTRY LETTERS, v.37, no.1, pp.10 - 11
Indexed
SCIE
SCOPUS
Journal Title
CHEMISTRY LETTERS
Volume
37
Number
1
Start Page
10
End Page
11
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/124446
DOI
10.1246/cl.2008.10
ISSN
0366-7022
Abstract
A new square-shaped macrocyclic amide was prepared from N-(4-amino-2-nitrophenyl)proline (ANPP). The two enantiomers of ANPP were connected in an alternating sequence and then cyclized to the corresponding macrocyclic tetramer with S-4 symmetry. In this design, there is a central cavity approximately 7 angstrom in diameter and rigid aromatic rings and intramolecular hydrogen bonding help to reduce the conformational flexibility of the molecule.
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