Issue 5, 2016

Synthesis of the first metal-free phosphanylphosphonate and its use in the “phospha–Wittig–Horner” reaction

Abstract

The synthesis of the first phophanylphosphonate, Mes*PH–PO(OEt)2 (2-H), in which the P(III) centre is not coordinated by a M(CO)5 (M = W, Mo, Cr) fragment is reported. The title compound reacts with LDA under the formation of 2-Li which is best described as the enolate form with a high double bond character between the two phosphorus centres. 2-Li is shown to engage in the phospha–Wittig–Horner reaction and converts aldehydes into phosphaalkenes that are metal-free and thus available for future manipulations at the phophorus lone pair. Using a selection of aldehydes with aliphatic, aromatic or vinylic substituents as substrates, phosphaalkene formation proceeds in high yields and high E-selectivity. The selectivity is however compromised during purification on standard silica which was found to promote E/Z isomerization.

Graphical abstract: Synthesis of the first metal-free phosphanylphosphonate and its use in the “phospha–Wittig–Horner” reaction

Supplementary files

Article information

Article type
Paper
Submitted
21 септ. 2015
Accepted
26 окт. 2015
First published
09 ноем. 2015

Dalton Trans., 2016,45, 2201-2207

Author version available

Synthesis of the first metal-free phosphanylphosphonate and its use in the “phospha–Wittig–Horner” reaction

K. Esfandiarfard, A. I. Arkhypchuk, A. Orthaber and S. Ott, Dalton Trans., 2016, 45, 2201 DOI: 10.1039/C5DT03686K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements