Benzyl-4,5-dihydroisoxazoles from benzylcyclo-propanes: regioselective insertion of an n=o fragment into the three-membered carbocycle of benzylcyclopropanes by the action of nitrous acid

Gazzaeva, R. A.; Трофимова, Е. В.; Каджаева, А. З.; Федотов, А. Н.; Mochalov, S. S.

doi:10.1007/s10593-012-1125-9

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.

Benzyl-4,5-dihydroisoxazoles from benzylcyclo-propanes: regioselective insertion of an n=o fragment into the three-membered carbocycle of benzylcyclopropanes by the action of nitrous acid

Cited by 2 publications

References 7 publications

ChemInform Abstract: Benzyl‐4,5‐dihydroisoxazoles from Benzylcyclopropanes: Regioselective Insertion of an N=O Fragment into the Three‐Membered Carbocycle of Benzylcyclopropanes by the Action of Nitrous Acid.

ChemInform Abstract: Benzyl‐4,5‐dihydroisoxazoles from Benzylcyclopropanes: Regioselective Insertion of an N=O Fragment into the Three‐Membered Carbocycle of Benzylcyclopropanes by the Action of Nitrous Acid.

Isoxazoles

Contact Info

Product

Resources

About