نتایج جستجو برای: n substituted pyrroles

تعداد نتایج: 1008175  

2015
Mohamed Yacine Ameur Messaoud Ghenia Bentabed-Ababsa Madani Hedidi Aïcha Derdour Floris Chevallier Yury S Halauko Oleg A Ivashkevich Vadim E Matulis Laurent Picot Valérie Thiéry Thierry Roisnel Vincent Dorcet Florence Mongin

The synthesis of N-arylated pyrroles and indoles is documented, as well as their functionalization by deprotonative metallation using the base in situ prepared from LiTMP and ZnCl2·TMEDA (1/3 equiv). With N-phenylpyrrole and -indole, the reactions were carried out in hexane containing TMEDA which regioselectively afforded the 2-iodo derivatives after subsequent iodolysis. With pyrroles and indo...

Journal: :Chemical communications 2016
Pradeep Sadhu Tharmalingam Punniyamurthy

A copper(II)-mediated regioselective N-arylation of azoles has been developed using 8-aminoquinoline amide as a directing group. This reaction shows a broad substrate scope with different azoles such as pyrroles, indoles, pyrazoles and carbazole with good yields.

Journal: :The Journal of organic chemistry 2015
Taejoo Jeong Sangil Han Neeraj Kumar Mishra Satyasheel Sharma Seok-Yong Lee Joa Sub Oh Jong Hwan Kwak Young Hoon Jung In Su Kim

The rhodium(III)-catalyzed direct amidation of indoles and pyrroles with aryl and alkyl isocyanates is described. These transformations provide a facile and efficient construction of C2-amidated N-heterocyclic scaffolds.

2001
Jonathan L. Sessler Rebecca S. Zimmerman Christophe Bucher Vladimír Král Bruno Andrioletti

Calixphyrins are a class of hybrid molecules that lie at the structural crossroads between porphyrins and calixpyrroles. Porphyrins, long known for their versatile metal cation coordination chemistry, are macrocycles that contain only sp2-hybridized bridging meso carbon atoms within their framework. Calix[n]pyrroles, on the other hand, are porphyrin analogs that contain pyrroles bridged exclusi...

Journal: :European Journal of Organic Chemistry 2021

Calix[4]pyrroles can be obtained from the efficient preprogrammed condensation between acetone and pyrrole. This reaction forms attractive macrocycle resembling in its constitution, but not oxidation state, to porphyrin structure, prominently present vital “pigments of life”. Calix[2]pyrrolidine[2]pyrrole calix[4]pyrrolidine, partially totally reduced version macrocycle, became accessible throu...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Pablo Ballester Guzmán Gil-Ramírez

Calix[4]pyrroles having extended aromatic cavities have been functionalized with 4 ureas in the para position of their meso phenyl substituents. This elaboration of the upper rim was completed in 2 synthetic steps starting from the alpha,alpha,alpha,alpha-tetranitro isomer of the calix[4]pyrrole obtained in the acid catalyzed condensation of p-nitrophenyl methyl ketone and pyrrole. In dichlorom...

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