Chiral Bambusurils for Enantioselective Recognition of Carboxylate Anion Guests

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F18%3A00101604" target="_blank" >RIV/00216224:14310/18:00101604 - isvavai.cz</a>

Result on the web

<a href="https://onlinelibrary.wiley.com/doi/full/10.1002/chem.201802748" target="_blank" >https://onlinelibrary.wiley.com/doi/full/10.1002/chem.201802748</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1002/chem.201802748" target="_blank" >10.1002/chem.201802748</a>

Result language

angličtina

Original language name

Chiral Bambusurils for Enantioselective Recognition of Carboxylate Anion Guests

Original language description

Synthesis of the first enantiomerically pure chiral bambusurils is reported. The bambusurils were prepared on the gram scale without using any chromatography techniques. The bambusurils formed supramolecular complexes with all tested chiral carboxylates including amino acids and drug molecules with the enantioselectivity ranging from 1.1 to 3.2.

Czech name

—

Czech description

—

Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

—

OECD FORD branch

10400 - Chemical sciences

Project

Result was created during the realization of more than one project. More information in the Projects tab.

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2018

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Chemistry - A European Journal

ISSN

0947-6539

e-ISSN

—

Volume of the periodical

24

Issue of the periodical within the volume

58

Country of publishing house

DE - GERMANY

Number of pages

4

Pages from-to

15482-15485

UT code for WoS article

000447636000006

EID of the result in the Scopus database

—