Issue 36, 2006

Alkali-metal-catalyzed addition of primary and secondary phosphines to carbodiimides. A general and efficient route to substituted phosphaguanidines

Abstract

Organo alkali metal compounds such as nBuLi and (Me3Si)2NK act as excellent catalyst precursors for the addition of phosphine P–H bonds to carbodiimides, offering a general and atom-economical route to substituted phosphaguanidines, with excellent tolerability to aromatic C–Br and C–Cl bonds.

Graphical abstract: Alkali-metal-catalyzed addition of primary and secondary phosphines to carbodiimides. A general and efficient route to substituted phosphaguanidines

Supplementary files

Article information

Article type
Communication
Submitted
29 Jun 2006
Accepted
18 Jul 2006
First published
02 Aug 2006

Chem. Commun., 2006, 3812-3814

Alkali-metal-catalyzed addition of primary and secondary phosphines to carbodiimides. A general and efficient route to substituted phosphaguanidines

W. Zhang, M. Nishiura and Z. Hou, Chem. Commun., 2006, 3812 DOI: 10.1039/B609198A

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