Convenient one pot preparation of acylated phosphinimines and aminophosphonium salts from the versatile triphenylphosphonium and lithium azayldiide Ph3P=N-Li

Article abstract of DOI:10.1080/10426509808545488

Starting from gaseous ammonia, through two multisteps reactions, either acylation or alkylation reactions, we have access to different N-substituted aminophosphonium salts, precursors of amines. Preparation and use of the intermediate, the triphenylphosph

Full text of DOI:10.1080/10426509808545488

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Phosphorus, Sulfur, and
Silicon and the Related
Elements
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Convenient One Pot
Preparation of Acylated
Phosphinimines and
Aminophosphonium
Salts From the Versatile
Triphenylphosphonium
and Lithium Azayldiide
Ph3P=N-Li
Henri-Jean Cristau , Amer Hammami , Eric
Manginot & Eliane Torreilles
a Laboratoire de Chimie Organique E. N. S.
C. M. (ESA 5076 du C.N.R.S.) , 8, Rue de
l'Ecole Normale, 34296 Montpellier, Cedex
5, France
b Laboratoire de Chimie Organique E. N. S.
C. M. (ESA 5076 du C.N.R.S.) , 8, Rue de
l'Ecole Normale, 34296 Montpellier, Cedex
5, France
c Laboratoire de Chimie Organique E. N. S.
C. M. (ESA 5076 du C.N.R.S.) , 8, Rue de
l'Ecole Normale, 34296 Montpellier, Cedex
5, France
d Laboratoire de Chimie Organique E. N. S.
C. M. (ESA 5076 du C.N.R.S.) , 8, Rue de

l'Ecole Normale, 34296 Montpellier, Cedex
5, France
Published online: 17 Mar 2008.
To cite this article: Henri-Jean Cristau , Amer Hammami , Eric Manginot
& Eliane Torreilles (1998) Convenient One Pot Preparation of Acylated
Phosphinimines and Aminophosphonium Salts From the Versatile
Triphenylphosphonium and Lithium Azayldiide Ph3P=N-Li, Phosphorus,
Sulfur, and Silicon and the Related Elements, 134:1, 475-486, DOI:
10.1080/10426509808545488
To link to this article: http://dx.doi.org/10.1080/10426509808545488
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