Recyclization of 5-hydroxy-2-pyrazolines in the reaction with N-nucleophiles

Kuz’menok, N. M.; Koval'chuk, T. A.; Zvonok, A. M.

doi:10.3998/ark.5550190.0009.911

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

Recyclization of 5-hydroxy-2-pyrazolines in the reaction with N-nucleophiles

Abstract: The reactions of 5-hydroxy-1-tosyl-2-pyrazolines with amines or with hydrazine have been investigated. We have shown that these compounds are convenient substrates for the synthesis of 5-aminosubstituted pyrazolines and NH-pyrazoles.

Cited by 2 publications

References 4 publications

Tautomeric origin of dual effects of N1-nicotinoyl-3-(4′-hydroxy-3′-methyl phenyl)-5-[(sub)phenyl]-2-pyrazolines on bacterial and viral strains: POM analyses as new efficient bioinformatics’ platform to predict and optimize bioactivity of drugs

Tautomeric origin of dual effects of N1-nicotinoyl-3-(4′-hydroxy-3′-methyl phenyl)-5-[(sub)phenyl]-2-pyrazolines on bacterial and viral strains: POM analyses as new efficient bioinformatics’ platform to predict and optimize bioactivity of drugs

Pyrazoles

Contact Info

Product

Resources

About