Mild and efficient trimethylsilylcyanation of ketones catalysed by PNP chloride

35Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Mild & green: The commercially and readily available PNPCl behaves as a very effective catalyst for the synthesis of various trimethylsilyl cyanohydrins from a wide range of aliphatic, cyclic, α,β-unsaturated and aromatic ketones. The method proceeds at room temperature in solvent-free conditions, in the presence of very small amounts of catalyst (see scheme). Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Cite

CITATION STYLE

APA

Lacour, M. A., Rahier, N. J., & Taillefer, M. (2011). Mild and efficient trimethylsilylcyanation of ketones catalysed by PNP chloride. Chemistry - A European Journal, 17(44), 12276–12279. https://doi.org/10.1002/chem.201101195

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