Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine-Reference-Cited by-同舟云学术

Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine

Published:2016-03 Issue: Volume:183 Page:44-58
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Mikhailovskaya Tatiana F.,Makarov Arkady G.,Selikhova Natalia Yu.,Makarov Alexander Yu.,Pritchina Elena A.,Bagryanskaya Irina Yu.,Vorontsova Elena V.,Ivanov Igor D.,Tikhova Vera D.,Gritsan Nina P.,Slizhov Yuri G.,Zibarev Andrey V.

Funder

Ministry of Education and Science of the Russian Federation

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry

Reference82 articles.

1. Quest for the Rings. In Silico Exploration of Ring Universe To Identify Novel Bioactive Heteroaromatic Scaffolds

2. Benzothiadiazole Derivatives as Fluorescence Imaging Probes: Beyond Classical Scaffolds

3. New fluorinated 1,2-diaminoarenes, quinoxalines, 2,1,3-arenothia(selena)diazoles and related compounds

4. Cu(II)-catalyzed synthesis of quinoxalines from o-phenylenediamines and nitroolefins

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