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

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

Chemical communications (Cambridge, England) (2006-09-14)
Wen-Xiong Zhang, Masayoshi Nishiura, Zhaomin Hou
RÉSUMÉ

Organo alkali metal compounds such as (n)BuLi 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.

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Sigma-Aldrich
Lithium bis(trimethylsilyl)amide, 97%