Reintroducing Azidodifluoromethane: Synthesis, Stability and [3+2] Cycloadditions
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F18%3A00495299" target="_blank" >RIV/61388963:_____/18:00495299 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1002/ejoc.201800650" target="_blank" >http://dx.doi.org/10.1002/ejoc.201800650</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/ejoc.201800650" target="_blank" >10.1002/ejoc.201800650</a>
Alternative languages
Result language
angličtina
Original language name
Reintroducing Azidodifluoromethane: Synthesis, Stability and [3+2] Cycloadditions
Original language description
Azidodifluoromethane was prepared in 65% yield from chlorodifluoromethane by a two-step synthesis using tributyl(difluoromethyl)ammonium chloride as an intermediate. The resulting azide was used in Huisgen azide-alkyne reactions and ketone [3+2] cycloadditions to access novel N-difluoromethyl-1,2,3-triazoles.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10401 - Organic chemistry
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
European Journal of Organic Chemistry
ISSN
1434-193X
e-ISSN
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Volume of the periodical
2018
Issue of the periodical within the volume
37
Country of publishing house
DE - GERMANY
Number of pages
4
Pages from-to
5087-5090
UT code for WoS article
000446662900003
EID of the result in the Scopus database
2-s2.0-85054809656