Abstract
The reductive amination of several carbonyl compounds (Leuckart reaction) has been performed using Nmethylformamide
and microwave technology. Under these conditions, a new mechanism is proposed via
the initial formation of an imine, followed by reduction to the amine by ‘in situ’ generated formic acid,
and further formylation of the amine. Using this methodology, the formyl derivatives of several secondary
amines were obtained in good to excellent yields.
Journal Title
Journal ISSN
Volume Title
Publisher
ELSERVIER
Date
Description
Citation
Tetrahedron Letters 54 (2013) 1835–1838



