Cycloaddition Reactions of Deoxyribosylpropynoates

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F14%3A10277930" target="_blank" >RIV/00216208:11310/14:10277930 - isvavai.cz</a>

Alternative codes found

RIV/61388963:_____/14:00428607

Result on the web

<a href="http://dx.doi.org/10.1080/00397911.2013.848896" target="_blank" >http://dx.doi.org/10.1080/00397911.2013.848896</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1080/00397911.2013.848896" target="_blank" >10.1080/00397911.2013.848896</a>

Result language

angličtina

Original language name

Cycloaddition Reactions of Deoxyribosylpropynoates

Original language description

Pure anomers of either alpha or beta 3-(2-deoxyribofuranosyl)propynoates reacted with the tetramethylcyclobutadiene-aluminum trichloride complex to yield the corresponding diastereoisomeric Dewar benzenes. Thermal- or ultraviolet light-initiated rearrangement gave rise to highly substituted C-aryldeoxyribosides as single anomers. The same compounds as well as other substituted deoxyribosides were obtained also by transition metal-mediated cycloaddition reactions.

Czech name

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Czech description

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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

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Continuities

Z - Vyzkumny zamer (s odkazem do CEZ)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2014

Confidentiality

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

Name of the periodical

Synthetic Communications

ISSN

0039-7911

e-ISSN

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Volume of the periodical

44

Issue of the periodical within the volume

9

Country of publishing house

US - UNITED STATES

Number of pages

8

Pages from-to

1232-1239

UT code for WoS article

000334071900005

EID of the result in the Scopus database

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