Issue 4, 2004

Microwave-assisted synthesis of allylic amines: considerable rate acceleration in the hydrozirconation–transmetalation–aldimine addition sequence

Abstract

The hydrozirconation of alkynes with zirconocene hydrochloride and the dimethylzinc-mediated addition of alkenylzirconocenes to diphenylphosphinoyl imines can be greatly accelerated with microwave irradiation, resulting in a convenient and rapid one-pot process for the preparation of synthetically useful allylic amines.

Graphical abstract: Microwave-assisted synthesis of allylic amines: considerable rate acceleration in the hydrozirconation–transmetalation–aldimine addition sequence

Supplementary files

Article information

Article type
Communication
Submitted
23 Dec 2003
Accepted
19 Jan 2004
First published
28 Jan 2004

Org. Biomol. Chem., 2004,2, 443-445

Microwave-assisted synthesis of allylic amines: considerable rate acceleration in the hydrozirconation–transmetalation–aldimine addition sequence

P. Wipf, J. Janjic and C. R. J. Stephenson, Org. Biomol. Chem., 2004, 2, 443 DOI: 10.1039/B316741K

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