Benzhydrylamines via Base-Mediated Intramolecular sp3 C-Arylation of N-Benzyl-2-nitrobenzenesulfonamides-Advanced Intermediates for the Synthesis of Nitrogenous Heterocycles
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F14%3A33151972" target="_blank" >RIV/61989592:15310/14:33151972 - isvavai.cz</a>
Alternative codes found
RIV/61989592:15110/14:33151972
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Benzhydrylamines via Base-Mediated Intramolecular sp3 C-Arylation of N-Benzyl-2-nitrobenzenesulfonamides-Advanced Intermediates for the Synthesis of Nitrogenous Heterocycles
Original language description
N-Benzyl-2-nitrobenzenesulfonamides underwent base-mediated intramolecular arylation at the benzyl sp3 carbon to yield benzhydrylamines. The presence of electron withdrawing groups on the aromatic ring of the benzyl group was required to facilitate the C-arylation. Unsymmetrically substituted benzhydrylamines are advanced intermediates toward nitrogenous heterocycles, as exemplified in the syntheses of indazole oxides and quinazolines.
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
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Continuities
O - Projekt operacniho programu
Others
Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
ACS Combinatorial Science
ISSN
2156-8952
e-ISSN
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Volume of the periodical
16
Issue of the periodical within the volume
10
Country of publishing house
US - UNITED STATES
Number of pages
5
Pages from-to
573-577
UT code for WoS article
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EID of the result in the Scopus database
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