Enamine-Mediated Azide-Ketone [3+2] Cycloaddition of Azidoperfluoroalkanes

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F18%3A00491878" target="_blank" >RIV/61388963:_____/18:00491878 - isvavai.cz</a>

Alternative codes found

RIV/00216208:11310/18:10378077

Result on the web

<a href="http://dx.doi.org/10.1002/slct.201801344" target="_blank" >http://dx.doi.org/10.1002/slct.201801344</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1002/slct.201801344" target="_blank" >10.1002/slct.201801344</a>

Result language

angličtina

Original language name

Enamine-Mediated Azide-Ketone [3+2] Cycloaddition of Azidoperfluoroalkanes

Original language description

An effective synthesis of highly functionalized N-perfluoroalkyl-1,2,3-triazoles from azidoperfluoroalkanes has been achieved. In situ generated enamines readily participate in the azide-carbonyl [3 + 2] cycloaddition, providing a facile way to fully substituted triazole frameworks in good to excellent yields. The synthetic value of these triazoles was shown in the synthesis of perfluorinated 1,5-disubstituted triazoles by hydrolysis and decarboxylation.

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

10401 - Organic chemistry

Project

—

Continuities

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2018

Confidentiality

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

Name of the periodical

ChemistrySelect

ISSN

2365-6549

e-ISSN

—

Volume of the periodical

3

Issue of the periodical within the volume

25

Country of publishing house

DE - GERMANY

Number of pages

4

Pages from-to

7045-7048

UT code for WoS article

000437504200002

EID of the result in the Scopus database

2-s2.0-85049599318