NMR Identification of Substitutional Isomers in Chelated Polycyclic Aromatic Systems

1963 ◽  
Author(s):  
A. L. Porte ◽  
H. S. Gutowsky
Synthesis ◽  
2006 ◽  
Vol 2006 (14) ◽  
pp. 2313-2318
Author(s):  
María Mirífico ◽  
Esther Svartman ◽  
María Rozas ◽  
Oscar Piro ◽  
Eduardo Castellano

RSC Advances ◽  
2017 ◽  
Vol 7 (82) ◽  
pp. 51858-51863 ◽  
Author(s):  
Ping Huo ◽  
Jingbo Li ◽  
Wanyun Liu ◽  
Guangquan Mei ◽  
Xiaohui He

A nickel catalyst with polycyclic aromatic systems on the backbone exhibits good thermal stability and high activity in norbornene copolymerization.


2020 ◽  
Author(s):  
Alexandra Wahab ◽  
Felix Fleckenstein ◽  
Stefan Feusi ◽  
Renana Poranne

We detail the development of a new Python-based program for automatic generation of NICS-XY-Scans of cata-condensed polycyclic aromatic systems. <div>The program uses an underlying additivity scheme, which enables generation of the Scans using only smaller building blocks within the larger systems, and circumvents the need for quantum mechanical calculations. </div>


2020 ◽  
Author(s):  
Alexandra Wahab ◽  
Felix Fleckenstein ◽  
Stefan Feusi ◽  
Renana Poranne

We detail the development of a new Python-based program for automatic generation of NICS-XY-Scans of cata-condensed polycyclic aromatic systems. <div>The program uses an underlying additivity scheme, which enables generation of the Scans using only smaller building blocks within the larger systems, and circumvents the need for quantum mechanical calculations. </div>


Molecules ◽  
2018 ◽  
Vol 23 (8) ◽  
pp. 2043 ◽  
Author(s):  
Mariusz Kędziorek ◽  
Liliana Dobrzańska

Promising results of an efficient and convenient strategy for the annulation of polycyclic aromatic compounds (PACs), employing orthoquinones as starting material and comprising allylation, pinacol rearrangement, ring-closing metathesis (RCM), and one-pot reduction followed by Wagner-Meerwein rearrangement, are presented. The strategy involves introducing triallylborane prepared in situ in the allylation step. Moreover, a novel expedient method for the preparation of 9,10-diallylphenanthrene was introduced.


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