Issue 8, 2013

Simple and novel synthesis of 3-(thio)phosphoryl-β-lactams by radical cyclization

Abstract

Radical cyclization of phosphono-acetenamides promoted by manganese(III) acetate leads exclusively to the formation of 3-phosphoryl-β-lactams. The thiophosphoryl analogues were also prepared using this method. In particular, the presented protocol does not require the use of noble metals, while comparable methods do.

Graphical abstract: Simple and novel synthesis of 3-(thio)phosphoryl-β-lactams by radical cyclization

Supplementary files

Article information

Article type
Letter
Submitted
19 Feb 2013
Accepted
14 May 2013
First published
15 May 2013

New J. Chem., 2013,37, 2254-2256

Simple and novel synthesis of 3-(thio)phosphoryl-β-lactams by radical cyclization

P. Punda and S. Makowiec, New J. Chem., 2013, 37, 2254 DOI: 10.1039/C3NJ00192J

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