1,3-Dipolar cycloaddition of vinyloxy quinolines with α-alkoxy carbonyl aldonitrones or cyclic surrogates: A comparative study for an asymmetric access to trans 4-quinolinoxy oxaprolines-Reference-Cited by-同舟云学术

1,3-Dipolar cycloaddition of vinyloxy quinolines with α-alkoxy carbonyl aldonitrones or cyclic surrogates: A comparative study for an asymmetric access to trans 4-quinolinoxy oxaprolines

Published:2019-01 Issue:3 Volume:75 Page:429-440
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Hamdi Abdelrahman,Laurent Mathieu Y.,Hémon-Ribaud Annie,Mostafa Amany S.,Massoud Mohammed A.M.,Selim Khalid B.,Dujardin Gilles

Funder

Egypt-France Scientific and Technological Cooperation Program

Academy of Scientific Research and Technology

French Embassy in Egypt

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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3. The discovery and characterization of a novel scaffold as a potent hepatitis C virus inhibitor

4. Evaluating the Role of Macrocycles in the Susceptibility of Hepatitis C Virus NS3/4A Protease Inhibitors to Drug Resistance

5. The Discovery of Asunaprevir (BMS-650032), An Orally Efficacious NS3 Protease Inhibitor for the Treatment of Hepatitis C Virus Infection

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