Document Detail

Chirality Organization of Aniline Oligomers through Hydrogen Bonds of Amino Acid Moieties.
MedLine Citation:
PMID:  20958060     Owner:  NLM     Status:  In-Data-Review    
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.
Satoshi D Ohmura; Toshiyuki Moriuchi; Toshikazu Hirao
Publication Detail:
Type:  Journal Article     Date:  2010-10-19
Journal Detail:
Title:  The Journal of organic chemistry     Volume:  75     ISSN:  1520-6904     ISO Abbreviation:  J. Org. Chem.     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2014-02-04     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  2985193R     Medline TA:  J Org Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  7909-12     Citation Subset:  IM    
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