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Cover Feature: Base-Mediated Generation of Ketenimines from Ynamides: Direct Access to Azetidinimines by an Imino-Staudinger Synthesis (Chem. Eur. J. 53/2017).

Authors :
Romero, Eugénie
Minard, Corinne
Benchekroun, Mohamed
Ventre, Sandrine
Retailleau, Pascal
Dodd, Robert H.
Cariou, Kevin
Source :
Chemistry - A European Journal. 9/21/2017, Vol. 23 Issue 53, p12956-12956. 1p.
Publication Year :
2017

Abstract

Ynamides were used as precursors for the in situ generation of highly reactive ketenimines which were trapped with imines in a [2+2] cycloaddition under microwave irradiation. Twenty novel azetidinimines have been prepared in this straightforward and operationally simple manner. Furthermore, the products arising from this imino‐Staudinger synthesis were functionalized using a wide range of protocols that leave the four‐membered amidine ring intact. (Illustration by E. Menneteau, CNRS‐PRC 2017). More information can be found in the Communication by R. H. Dodd, K. Cariou et al. on page 12991. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09476539
Volume :
23
Issue :
53
Database :
Academic Search Index
Journal :
Chemistry - A European Journal
Publication Type :
Academic Journal
Accession number :
125257379
Full Text :
https://doi.org/10.1002/chem.201703248