Issue 83, 2014

Fluorinative hydrolysis of phosphorothioic acid esters with a binaphthyl group through axis-to-center chirality transfer leading to the formation of P-chiral phosphorothioic monofluoridic acid salts

Abstract

Asymmetric synthesis of P-chiral phosphorothioic monofluoridic acid ammonium salts was achieved via axis-to-center chirality transfer reactions by using phosphorothioic acid O-esters with a binaphthyl group, and the absolute stereochemistry of the salts was determined by X-ray analyses and by comparison of their CD spectra.

Graphical abstract: Fluorinative hydrolysis of phosphorothioic acid esters with a binaphthyl group through axis-to-center chirality transfer leading to the formation of P-chiral phosphorothioic monofluoridic acid salts

Supplementary files

Article information

Article type
Communication
Submitted
07 Jul 2014
Accepted
28 Aug 2014
First published
28 Aug 2014

Chem. Commun., 2014,50, 12473-12475

Author version available

Fluorinative hydrolysis of phosphorothioic acid esters with a binaphthyl group through axis-to-center chirality transfer leading to the formation of P-chiral phosphorothioic monofluoridic acid salts

T. Murai, T. Hayashi, K. Yamada, Y. Maekawa and M. Minoura, Chem. Commun., 2014, 50, 12473 DOI: 10.1039/C4CC05198J

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