scholarly journals A covalent organic cage compound acting as a supramolecular shadow mask for the regioselective functionalization of C60

2020 ◽  
Vol 11 (32) ◽  
pp. 8409-8415 ◽  
Author(s):  
Viktoria Leonhardt ◽  
Stefanie Fimmel ◽  
Ana-Maria Krause ◽  
Florian Beuerle

The taming of the Prato reaction: a covalent organic cage compound serves as a supramolecular template for the regioselective functionalization of C60.

2020 ◽  
Author(s):  
Viktoria Leonhardt ◽  
Stefanie Fimmel ◽  
Ana-Maria Krause ◽  
Florian Beuerle

<div><div><div><p>A trigonal-bipyramidal covalent organic cage compound serves as an efficient host to form stable 1:1-complexes with C60 and C70. Fullerene encapsulation has been comprehensively studied by NMR and UV/Vis spectroscopy, mass spectrometry as well as single-crystal X-ray diffraction. Exohedral functionalization of encapsulated C60 via threefold Prato reaction revealed high selectivity for the symmetry-matched all-trans-3 addition pattern.</p></div></div></div>


2020 ◽  
Author(s):  
Viktoria Leonhardt ◽  
Stefanie Fimmel ◽  
Ana-Maria Krause ◽  
Florian Beuerle

<div><div><div><p>A trigonal-bipyramidal covalent organic cage compound serves as an efficient host to form stable 1:1-complexes with C60 and C70. Fullerene encapsulation has been comprehensively studied by NMR and UV/Vis spectroscopy, mass spectrometry as well as single-crystal X-ray diffraction. Exohedral functionalization of encapsulated C60 via threefold Prato reaction revealed high selectivity for the symmetry-matched all-trans-3 addition pattern.</p></div></div></div>


2018 ◽  
Vol 22 (15) ◽  
pp. 1536-1553 ◽  
Author(s):  
Aamer Saeed ◽  
Muhammad Zain-ul-Abideen ◽  
Muhammad N. Mustafa

Synthesis ◽  
2020 ◽  
Author(s):  
Ikyon Kim ◽  
Sung June Kim ◽  
Sunhee Lee

AbstractBroadening of nitrogen-fused heteroaromatic chemical space such as indolizine and pyrrolo[1,2-a]pyrazine was achieved via FeCl­3-catalyzed nucleophilic addition of these N-fused aromatic compounds to a wide range of azolinium systems generated in situ, leading to novel N-fused heteroaromatic scaffolds with dearomatized N-heterocyclic substituents regioselectively. Nucleophilic addition of indolizines and pyrrolo[1,2-a]pyrazines mainly occurred at the C1 position of the isoquinoliniums and at the C4 site of the quinoliniums.


2021 ◽  
Author(s):  
Andreas Hess ◽  
Jan Philip Prohaska ◽  
Sabrina Bettina Doerrich ◽  
Florian Trauner ◽  
Ferdinand Hermann Lutter ◽  
...  

Aryl azoles are ubiquitous as bioactive compounds and their regioselective functionalization is of utmost synthetic importance. Here, we report the development of a toluene-soluble dialkylmagnesium base sBu2Mg. This new reagent...


ChemInform ◽  
2010 ◽  
Vol 26 (9) ◽  
pp. no-no
Author(s):  
A. RICCI ◽  
A. GUERRINI ◽  
G. SECONI ◽  
A. MORDINI ◽  
T. CONSTANTIEUX ◽  
...  

BioResources ◽  
2018 ◽  
Vol 13 (1) ◽  
Author(s):  
Meiyan Lin ◽  
Kunfeng Xia ◽  
Pengbo Lu ◽  
Yanghao Ou ◽  
Lingfeng Su ◽  
...  

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