1,105
Views
70
CrossRef citations to date
0
Altmetric
Reviews

Recent progress toward organophosphorus compounds based on phosphorus-centered radical difunctionalizations

, &
Pages 589-596 | Received 12 Jan 2017, Accepted 11 Feb 2017, Published online: 25 May 2017
 

GRAPHICAL ABSTRACT

ABSTRACT

Organophosphorus compounds have all along attracted considerable attention as they have broad utilities such as reagents for chemical reactions, ligands for transition metal catalysts, flame retardants, biologically active molecules and building blocks in synthetic chemistry. Compared with metal-catalyzed coupling synthesis, transformations via P-center radicals processes are powerful methods for the synthesis of organophosphorus compounds, as they provide unique routes leading to target molecules in least and concise steps. Generally, homolytic cleavage of P-H bonds serves as a major approach for the generation of P-centered radicals. And the reaction varieties between P-centered radicals and unsaturated compounds including addition reactions, addition/dehydrogenation reactions and difunctionalizations.

This review will focus on the difunctionalization reactions between unsaturated compounds and P-centered radicals origin from P-H compounds published in the period from 2010 to October 2016, by highlighting the reactions' specificity and, where possible, the relevant mechanistic rationale.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.