Efficient Microwave Access to Polysubstituted Amidines from Imidoylbenzotriazoles
Alan R. Katritzky,* Chunming Cai and Sandeep K. Singh
*Center for Heterocyclic Compounds, Department of Chemistry, University of
Florida, Gainesville, Florida 32611-7200, Email: katritzky
chem.ufl.edu
A. R. Katritzky, C. Cai, S. K. Singh, J. Org. Chem., 2006, 71, 3375-3380.
DOI: 10.1021/jo052443x
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Abstract
Microwave reactions of primary and secondary amines with imidoylbenzotriazoles gave various polysubstituted amidines in good yields. Convenient preparations of a variety of amides and imidoylbenzotriazoles have also been developed using microwave irradiation under mild conditions and short reaction times.
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A. R. Katritzky, H.-Y. He, K. Suzuki, J. Org. Chem., 2000, 65, 8210-8213.
Efficient Conversion of Carboxylic Acids into N-Acylbenzotriazoles
A. R. Katritzky, N. Kirichenko, B. V. Rogovoy, Synthesis, 2003, 2777-2780.
Key Words
Amides, Amidines, Microwave Synthesis
ID: J42-Y2006-1080
