Solvent reduced wittig olefination reactions with halo containing conjugated phosphoranes

11Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

The Wittig reaction of carbaldehydes with alkoxycarbonylhalomethylidenetriphenylphosphoranes can be performed with ease in solventless systems. The analogous reaction of carbaldehydes with acylhalomethylidenetriphenylphosphoranes requires a small amount of solvent, such as chloroform, in order for the reaction to proceed. The products of the reaction are versatile precursors for further transformations, such as the Suzuki-Miyaura cross-coupling reaction. © Versita Warsaw and Springer-Verlag Berlin Heidelberg 2006.

Cite

CITATION STYLE

APA

Thiemann, T., Tanaka, Y., Ideta, K., & Mataka, S. (2006). Solvent reduced wittig olefination reactions with halo containing conjugated phosphoranes. Central European Journal of Chemistry, 4(3), 403–427. https://doi.org/10.2478/s11532-006-0024-2

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