Intramolecular Arylation of 2-Nitrobenzenesulfonamides: A Route to Diverse Nitrogenous Heterocycles

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F17%3A73584708" target="_blank" >RIV/61989592:15110/17:73584708 - isvavai.cz</a>
Alternative codes found
RIV/61989592:15310/17:73584708
Result on the web
<a href="https://link.springer.com/chapter/10.1007%2F7081_2016_5" target="_blank" >https://link.springer.com/chapter/10.1007%2F7081_2016_5</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/7081_2016_5" target="_blank" >10.1007/7081_2016_5</a>

Result language
angličtina
Original language name
Intramolecular Arylation of 2-Nitrobenzenesulfonamides: A Route to Diverse Nitrogenous Heterocycles
Original language description
In addition to being an integral component of numerous drugs, 2- and 4-nitrobenzenesulfonyl (Nos) groups are used as protecting/activating agents for the selective alkylation of primary amines. 2-Nos amides are also useful intermediates for the synthesis of fused nitrogenous heterocycles. This chapter focuses on the use of 2-Nos amides as intramolecular arylation agents and on the application of C- and N-aryl derivatives for the synthesis of diverse heterocycles in the solid phase.
Czech name
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Czech description
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Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Book/collection name
Solid-Phase Synthesis of Nitrogenous Heterocycles. Topics in Heterocyclic Chemistry, vol 52
ISBN
978-3-319-58616-8
Number of pages of the result
28
Pages from-to
139-166
Number of pages of the book
170
Publisher name
Springer, Cham
Place of publication
Switzerland
UT code for WoS chapter
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