Synthesis of per(5-carboxy-5-dehydroxymethyl)-ŕ- and á-cyclodextrins - self-assembly of the per(2,3-di-.I.O./I.-methyl)-protected homologues into highly stable dimers, driven by multiple hydrogen bonds

Name: Synthesis of per(5-carboxy-5-dehydroxymethyl)-ŕ- and á-cyclodextrins - self-assembly of the per(2,3-di-.I.O./I.-methyl)-protected homologues into highly stable dimers, driven by multiple hydrogen bonds
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Kraus, Tomáš; Buděšínský, Miloš; Závada, Jiří

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Synthesis of per(5-carboxy-5-dehydroxymethyl)-ŕ- and á-cyclodextrins - self-assembly of the per(2,3-di-.I.O./I.-methyl)-protected homologues into highly stable dimers, driven by multiple hydrogen bonds

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0193716 - UOCHB-X 20000068 RIV DE eng J - Článek v odborném periodiku
Kraus, Tomáš - Buděšínský, Miloš - Závada, Jiří
Synthesis of per(5-carboxy-5-dehydroxymethyl)-ŕ- and á-cyclodextrins - self-assembly of the per(2,3-di-.I.O./I.-methyl)-protected homologues into highly stable dimers, driven by multiple hydrogen bonds.
European Journal of Organic Chemistry. č. 18 (2000), s. 3133-3137. ISSN 1434-193X. E-ISSN 1099-0690
Grant CEP: GA ČR GA203/00/0138; GA AV ČR KSK2004601
Výzkumný záměr: CEZ:AV0Z4055905
Kód oboru RIV: CC - Organická chemie
Impakt faktor: 2.150, rok: 2000

Synthesis of per(5-carboxy-5-dehydroxymethyl)-ŕ- and á-Cyclodextrins. Self-assembly of the per(2,3-di-O-methyl)-derivatized homologues into highly stable dimers, driven by multiple hydrogen bonds.
Trvalý link: http://hdl.handle.net/11104/0089410

Počet záznamů: 1