Nickel-catalyzed highly regioselective hydrocyanation of alkenes with Zn(CN)2

24Citations
Citations of this article
12Readers
Mendeley users who have this article in their library.

Abstract

The first general and regioselective nickel-catalyzed hydrocyanation of terminal alkenes with Zn(CN)2 using an air-stable and inexpensive nickel(ii) salt as the precatalyst has been established. The strategy avoids the use of the volatile and hazardous reagent HCN. Aryl/heteroaryl alkenes are effectively converted to branched nitrile derivatives, while aliphatic alkenes or active alkenes are transformed to linear nitriles with good to excellent regioselectivity.

Cite

CITATION STYLE

APA

Wang, G., Xie, X., Xu, W., & Liu, Y. (2019). Nickel-catalyzed highly regioselective hydrocyanation of alkenes with Zn(CN)2. Organic Chemistry Frontiers, 6(12), 2037–2042. https://doi.org/10.1039/c9qo00396g

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free