| Chirality Organization of Aniline Oligomers through Hydrogen Bonds of Amino Acid Moieties. | |
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MedLine Citation:
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PMID: 20958060 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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Aniline oligomers bearing amino acid moieties were designed by the introduction of l/d-Ala-OMe into aniline oligomers to induce chirality organization of the π-conjugated aniline oligomer moieties, wherein the formation of intramolecular hydrogen bonds was demonstrated to play an important role to regulate the aniline oligomer moieties conformationally. |
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Authors:
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Satoshi D Ohmura; Toshiyuki Moriuchi; Toshikazu Hirao |
Publication Detail:
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Type: JOURNAL ARTICLE Date: 2010-10-19 |
Journal Detail:
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Title: The Journal of organic chemistry Volume: - ISSN: 1520-6904 ISO Abbreviation: - Publication Date: 2010 Oct |
Date Detail:
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Created Date: 2010-10-20 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 2985193R Medline TA: J Org Chem Country: - |
Other Details:
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Languages: ENG Pagination: - Citation Subset: - |
Affiliation:
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Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Yamada-oka, Suita, Osaka 565-0871, Japan. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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