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.
SYSNO ASEP 0193716 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Ostatní články Title 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 Author(s) Kraus, Tomáš (UOCHB-X) RID, ORCID
Buděšínský, Miloš (UOCHB-X) RID, ORCID
Závada, Jiří (UOCHB-X)Source Title European Journal of Organic Chemistry - ISSN 1434-193X
č. 18 (2000), s. 3133-3137Number of pages 5 s. Language eng - English Country DE - Germany Subject RIV CC - Organic Chemistry R&D Projects GA203/00/0138 GA ČR - Czech Science Foundation (CSF) KSK2004601 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR) CEZ AV0Z4055905 - UOCHB-X Annotation 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. Workplace Institute of Organic Chemistry and Biochemistry Contact asep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418 Year of Publishing 2001
Number of the records: 1