Number of the records: 1
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
- 1.0193716 - UOCHB-X 20000068 RIV DE eng J - Journal Article
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
R&D Projects: GA ČR GA203/00/0138; GA AV ČR KSK2004601
Institutional research plan: CEZ:AV0Z4055905
Subject RIV: CC - Organic Chemistry
Impact factor: 2.150, year: 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.
Permanent Link: http://hdl.handle.net/11104/0089410
Number of the records: 1