The synthesis of azahelicenes

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F17%3A00491916" target="_blank" >RIV/61388963:_____/17:00491916 - isvavai.cz</a>
Result on the web
<a href="https://www.soc.chim.it/sites/default/files/ths/21/chapter_2.pdf" target="_blank" >https://www.soc.chim.it/sites/default/files/ths/21/chapter_2.pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.17374/targets.2018.21.23" target="_blank" >10.17374/targets.2018.21.23</a>

Result language
angličtina
Original language name
The synthesis of azahelicenes
Original language description
Azahelicenes as heteroanalogues of iconic helically chiral helicenes consist of all-ortho-fused carbocycles (mostly benzene core units) and various nitrogen heterocycles. They have recently attracted increasing attention owing to their remarkable shape and unique chemical and physical properties. The first astonishing applications of azahelicenes to chemistry, physics and biology ranging from enantioselective organocatalysis to circularly polarised light detection have appeared. The present review surveys the recent progress in the synthesis of neutral or cationic azahelicenes and their congeners employing a rich portfolio of synthetic methods. The manifold ways to receive nonracemic azahelicenes are also reviewed.
Czech name
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Czech description
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Project
<a href="/en/project/GA16-08327S" target="_blank" >GA16-08327S: Chiral organic-inorganic hybrid materials and their use in nanoscience</a><br>
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

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