Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear PdI Catalysis

56Citations
Citations of this article
36Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

S-aryl phosphorothioates are privileged motifs in pharmaceuticals, agrochemicals, and catalysts; yet, the challenge of devising a straightforward synthetic route to enantioenriched S-aryl phosphorothioates has remained unsolved to date. We demonstrate herein the first direct C−SP(=O)(OR′)(OR′′) coupling of diverse and chiral phosphorothioate salts with aryl iodides, enabled by an air- and moisture-stable PdI dimer. Our mechanistic and computational data suggest distinct dinuclear PdI catalysis to be operative, which allows for operationally simple couplings with broad scope and full retention of stereochemistry.

Cite

CITATION STYLE

APA

Chen, X. Y., Pu, M., Cheng, H. G., Sperger, T., & Schoenebeck, F. (2019). Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear PdI Catalysis. Angewandte Chemie - International Edition, 58(33), 11395–11399. https://doi.org/10.1002/anie.201906063

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