Organic Chemistry Portal

Abstracts

Search:

A Mild and Efficient Route to 2-Azetidinones Using the Cyanuric Chloride-DMF Complex

Maaroof Zarei, Aliasghar Jarrahpour*

*Department of Chemistry, College of Sciences, Shiraz University, Shiraz 71454, Iran, Email: jarrahsusc.ac.ir

M. Zarei, A. Jarrahpour, Synlett, 2011, 2572-2576.

DOI: 10.1055/s-0030-1289517


Abstract

Efficient conversion of Schiff bases and carboxylic acids to β-lactams can be carried out at room temperature in CH2Cl2, using a cyanuric chloride-N,N-dimethyl formamide complex. The complex is easily prepared by reaction of cyanuric chloride and DMF at room temperature.

see article for more examples


While ads financed 62% of the published abstracts in 2024, donations allowed us to publish additional 12%. 26% of the abstracts have been published voluntarly. If you kindly donate, we can publish more freely accessible information and help the chemical community even more:

If you don't like pawalls or a flood of more and more advertising, then you can send a clear signal here!


Key Words

2-azetidinones, β-lactams, Staudinger synthesis, cyanuric chloride, Schiff base


ID: J60-Y2011-3150