Synthesis of novel conformationally locked carbocyclic nucleosides derived from 5,5- and 6,6-bis(hydroxymethyl)bicyclo[2.2.1]heptan-2-ol

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F05%3A00021591" target="_blank" >RIV/61388963:_____/05:00021591 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Synthesis of novel conformationally locked carbocyclic nucleosides derived from 5,5- and 6,6-bis(hydroxymethyl)bicyclo[2.2.1]heptan-2-ol

Original language description

Novel racemic nucleoside analogues derived from 5,5- and 6,6-bis(hydroxymethyl)bicyclo[2.2.1]heptan-2-ol were synthesized. The target compounds were tested for cytotoxic activity.

Czech name

Syntéza nových konformačně uzamčených karbocyklických nukleosidů odvozených od 5,5- a 6,6-bis(hydroxymethyl)bicyklo[2.2.1]heptan-2-olu

Czech description

Byla syntetizována nová racemická analoga nukleosidů odvozená od 5,5- and 6,6-bis(hydroxymethyl)bicyklo[2.2.1]heptan-2-olu. Cílové látky byly testovány na cytotoxickou aktivitu.

Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

<a href="/en/project/GA203%2F05%2F0132" target="_blank" >GA203/05/0132: Carbocyclic nucleoside analogues containing substituted norbornanes: compounds with potential biological effects</a><br>

Continuities

Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2005

Confidentiality

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

Name of the periodical

Collection of Czechoslovak Chemical Communications

ISSN

0010-0765

e-ISSN

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Volume of the periodical

70

Issue of the periodical within the volume

4

Country of publishing house

CZ - CZECH REPUBLIC

Number of pages

20

Pages from-to

519-538

UT code for WoS article

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EID of the result in the Scopus database

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