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dc.contributor.authorLI, Xuesong
dc.contributor.authorQI, Ting
dc.contributor.authorSRINIVAS, Kolupula
dc.contributor.authorMASSIP, Stephane
dc.contributor.authorMAURIZOT, Victor
dc.contributor.authorHUC, Ivan
dc.date.accessioned2020-09-03T07:56:12Z
dc.date.available2020-09-03T07:56:12Z
dc.date.issued2016
dc.identifier.issn1523-7060
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/10846
dc.description.abstractEnThe synthesis of very long helical aromatic amide foldamers was thought to be limited by steric hindrance associated with stable folded conformations. This difficulty may be overcome by using pure reagents, relatively high concentrations, and long reaction times. Bromine substituents and careful identification and elimination of anhydride byproducts both greatly improve chromatographic purification, giving access to pure products amenable to a segment-doubling synthesis of sequences composed of up to 96 monomers. An efficient one-pot multibromination of helical oligomers is also reported.
dc.language.isoen
dc.title.enSynthesis and Multibromination of Nanosized Helical Aromatic Amide Foldamers via Segment-Doubling Condensation
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.orglett.6b00165
dc.subject.halChimie/Matériaux
bordeaux.journalOrganic Letters
bordeaux.page1044-1047
bordeaux.volume18
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248*
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN, UMR 5248)
bordeaux.issue5
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionBordeaux INP
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Organic%20Letters&rft.date=2016&rft.volume=18&rft.issue=5&rft.spage=1044-1047&rft.epage=1044-1047&rft.eissn=1523-7060&rft.issn=1523-7060&rft.au=LI,%20Xuesong&QI,%20Ting&SRINIVAS,%20Kolupula&MASSIP,%20Stephane&MAURIZOT,%20Victor&rft.genre=article


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