Issue 106, 2014

Suzuki–Miyaura coupling of phosphinoyl-α-allenic alcohols with arylboronic acids catalyzed by a palladium complex “on water”: an efficient method to generate phosphinoyl 1,3-butadienes and derivatives

Abstract

We report here the first palladium-catalyzed Suzuki–Miyaura couplings of phosphinoyl-α-allenic alcohols with arylboronic acids “on water” without phase-transfer catalysts or additives. This new methodology provides a novel approach to generate phosphinoyl 1,3-butadienes and derivatives with medium to excellent yields. A mechanism via initial C(sp3)–OH bond cleavage of the substrate to form π-allyl-palladium intermediates, and transmetallation with arylboronic acid, followed by reductive elimination to afford the product, is proposed.

Graphical abstract: Suzuki–Miyaura coupling of phosphinoyl-α-allenic alcohols with arylboronic acids catalyzed by a palladium complex “on water”: an efficient method to generate phosphinoyl 1,3-butadienes and derivatives

Supplementary files

Article information

Article type
Communication
Submitted
12 Oct 2014
Accepted
27 Oct 2014
First published
29 Oct 2014

RSC Adv., 2014,4, 61722-61726

Author version available

Suzuki–Miyaura coupling of phosphinoyl-α-allenic alcohols with arylboronic acids catalyzed by a palladium complex “on water”: an efficient method to generate phosphinoyl 1,3-butadienes and derivatives

T. Liu, J. Dong, S. Cao, L. Guo and L. Wu, RSC Adv., 2014, 4, 61722 DOI: 10.1039/C4RA12251H

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