Issue 22, 2002
From the journal:

Chemical Communications

Dialkyl aluminium amides: new reagents for the conversion of C[double bond, length as m-dash]O into C[double bond, length as m-dash]NR functionalities†

John C. Gordon,*a   Piyush Shukla,b   Alan H. Cowley,b   Jamie N. Jones,b   D. Webster Keoghc  and  Brian L. Scotta  

* Corresponding authors

a Los Alamos National Laboratory, Chemistry Division, MS J514, Los Alamos, New Mexico, USA
E-mail: jgordon@lanl.gov

b Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, Texas, USA

c Los Alamos National Laboratory, Chemistry Division, MS G739, Los Alamos, New Mexico, USA
E-mail: jgordon@lanl.gov

Abstract

A new methodology for the preparation of α-diimines and β-aminoenones has been devised and represents an alternative route to these and related nitrogenous ligands bearing highly electronegative substituents.

Graphical abstract: Dialkyl aluminium amides: new reagents for the conversion of C [[double bond, length as m-dash]] O into C [[double bond, length as m-dash]] NR functionalities

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Article information

DOI
https://doi.org/10.1039/B203693B
Article type
Communication
Submitted
16 Apr 2002
Accepted
01 Oct 2002
First published
18 Oct 2002

Chem. Commun., 2002, 2710-2711

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Dialkyl aluminium amides: new reagents for the conversion of C[double bond, length as m-dash]O into C[double bond, length as m-dash]NR functionalities

J. C. Gordon, P. Shukla, A. H. Cowley, J. N. Jones, D. W. Keogh and B. L. Scott, Chem. Commun., 2002, 2710 DOI: 10.1039/B203693B

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