Synthesis of SF5-containing benzisoxazoles, quinolines, and quinazolines by the Davis reaction of nitro-(pentafluorosulfanyl)benzenes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F13%3A00391782" target="_blank" >RIV/61388963:_____/13:00391782 - isvavai.cz</a>
Result on the web
<a href="https://www.beilstein-journals.org/bjoc/single/articleFullText.htm?vt=f&publicId=1860-5397-9-43&tpn=1&bpn=singleVolume&vn=9" target="_blank" >https://www.beilstein-journals.org/bjoc/single/articleFullText.htm?vt=f&publicId=1860-5397-9-43&tpn=1&bpn=singleVolume&vn=9</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3762/bjoc.9.43" target="_blank" >10.3762/bjoc.9.43</a>
Alternative languages
Result language
angličtina
Original language name
Synthesis of SF5-containing benzisoxazoles, quinolines, and quinazolines by the Davis reaction of nitro-(pentafluorosulfanyl)benzenes
Original language description
Meta- or para-nitro-(pentafluorosulfonyl)benzenes underwent the Davis reaction with arylacetonitriles to provide the SF5-containing benzisoxazoles. Good yields were obtained with arylacetonitriles containing the electron-neutral or electron-donor group,while those with the electron-acceptor group were found to be unreactive. Reductions of the benzisoxazoles gave ortho-aminobenzophenones in high yields. Their synthetic utility was demonstrated by condensation reactions with carbonyl compounds or aminesto provide SF5-containing quinolines and quinazolines, respectively.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GAP207%2F12%2F0072" target="_blank" >GAP207/12/0072: Development of new methodologies towards (pentafluorosulfanyl)benzenes.</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Beilstein Journal of Organic Chemistry
ISSN
1860-5397
e-ISSN
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Volume of the periodical
9
Issue of the periodical within the volume
Feb 21
Country of publishing house
DE - GERMANY
Number of pages
6
Pages from-to
411-416
UT code for WoS article
000315411800001
EID of the result in the Scopus database
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