Issue 20, 2022

Reactivities of allenic and olefinic Michael acceptors towards phosphines

Abstract

The kinetics of the reactions of tributylphosphine with allenic and olefinic Michael acceptors in dichloromethane at 20 °C was followed by photometric and NMR spectroscopic methods. Combination with DFT-calculated methyl anion affinities revealed the relevance of retroaddition barriers in phosphine-catalysed reactions when mixtures of allenic and olefinic substrates are used.

Graphical abstract: Reactivities of allenic and olefinic Michael acceptors towards phosphines

Supplementary files

Article information

Article type
Communication
Submitted
02 Dec 2021
Accepted
21 Jan 2022
First published
21 Feb 2022
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2022,58, 3358-3361

Reactivities of allenic and olefinic Michael acceptors towards phosphines

F. An, H. Jangra, Y. Wei, M. Shi, H. Zipse and A. R. Ofial, Chem. Commun., 2022, 58, 3358 DOI: 10.1039/D1CC06786A

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