D-hexopyranosides; nitrogen-containing functionalities; glucosamine; aminoglycoside antibiotics; neuraminidase inhibitors; aziridine ring-opening; Michael addition; activated hydroxyl group

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F24%3A73626670" target="_blank" >RIV/61989592:15310/24:73626670 - isvavai.cz</a>

Výsledek na webu

<a href="https://www.mdpi.com/1420-3049/29/15/3465" target="_blank" >https://www.mdpi.com/1420-3049/29/15/3465</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.3390/molecules29153465" target="_blank" >10.3390/molecules29153465</a>

Jazyk výsledku

angličtina

Název v původním jazyce

D-hexopyranosides; nitrogen-containing functionalities; glucosamine; aminoglycoside antibiotics; neuraminidase inhibitors; aziridine ring-opening; Michael addition; activated hydroxyl group

Popis výsledku v původním jazyce

Various substituted D-hexopypyranosides units with nitrogen-containing functionalities are present in many important natural compounds and pharmaceutical substances. Since their complex structural diversity contributes to a broad spectrum of biological functions and activities, these derivatives are frequently studied. This review covers syntheses of D-hexopyranosides with vicinal nitrogen-containing functionalities since the 1960s, when the first articles emerged. The syntheses are arranged according to the positions of substitutions, to form a relative configuration of vicinal functionalities, and synthetic methodologies.

Název v anglickém jazyce

D-hexopyranosides; nitrogen-containing functionalities; glucosamine; aminoglycoside antibiotics; neuraminidase inhibitors; aziridine ring-opening; Michael addition; activated hydroxyl group

Popis výsledku anglicky

Various substituted D-hexopypyranosides units with nitrogen-containing functionalities are present in many important natural compounds and pharmaceutical substances. Since their complex structural diversity contributes to a broad spectrum of biological functions and activities, these derivatives are frequently studied. This review covers syntheses of D-hexopyranosides with vicinal nitrogen-containing functionalities since the 1960s, when the first articles emerged. The syntheses are arranged according to the positions of substitutions, to form a relative configuration of vicinal functionalities, and synthetic methodologies.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10401 - Organic chemistry

Projekt

—

Návaznosti

S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2024

Kód důvěrnosti údajů

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

Název periodika

MOLECULES

ISSN

1420-3049

e-ISSN

—

Svazek periodika

29

Číslo periodika v rámci svazku

15

Stát vydavatele periodika

CH - Švýcarská konfederace

Počet stran výsledku

28

Strana od-do

"3465-1"-"3465-28"

Kód UT WoS článku

001286944100001

EID výsledku v databázi Scopus

2-s2.0-85200720363