B. V. Polyakov scite author profile

Synthesis and Reactions of Oximino Derivatives of Acylferrocenes with Electron Donor Substituents in β-Position.-Nitrosation of the acylferrocenes (I) gives the oximes (III) via the corresponding nitroso compounds. The oximes (III) are converted to the derivatives (V), (VII), and (X). Treatment of the diacetylglyoxime (X) with alkali results in cyclization, producing the oxadiazolylferrocene (XI). -(POLYAKOV, B. V.; TVER-DOKHLEBOV, V. P.; TSELINSKII, I. V.; Zh.

show abstract

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.

B. V. Polyakov

ChemInform Abstract: ALKYLATION OF FERROCENE BY HALOMETHYL ETHERS. I. REACTION OF FERROCENE WITH METHYL(CHLOROMETHYL)ETHER

ChemInform Abstract: ALKYLATION OF FERROCENE. I. REACTION OF FERROCENE WITH ETHYLENECHLOROHYDRIN AND DIBROMOETHANE

ChemInform Abstract: NITROSATION OF CARBONYL DERIVATIVES OF FERROCENE

Synthesis of glycidyl ethers on the basis of β-dihydroxy derivatives of ferrocene

ChemInform Abstract: Synthesis and Reactions of Oximino Derivatives of Acylferrocenes with Electron Donor Substituents in β‐Position.

Contact Info

Product

Resources

About